{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T22:07:40Z","timestamp":1791151660939,"version":"4.1.0"},"reference-count":338,"publisher":"Frontiers Media SA","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Front. Genet."],"DOI":"10.3389\/fgene.2015.00003","type":"journal-article","created":{"date-parts":[[2015,2,3]],"date-time":"2015-02-03T16:02:35Z","timestamp":1422979355000},"source":"Crossref","is-referenced-by-count":127,"title":["Disorders of phospholipid metabolism: an emerging class of mitochondrial disease due to defects in nuclear genes"],"prefix":"10.3389","volume":"6","author":[{"given":"Ya-Wen","family":"Lu","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Steven M.","family":"Claypool","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1965","published-online":{"date-parts":[[2015,2,3]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","first-page":"86","DOI":"10.1016\/j.mito.2008.12.001","article-title":"Distinct effects of tafazzin deletion in differentiated and undifferentiated mitochondria.","volume":"9","author":"Acehan","year":"2009","journal-title":"Mitochondrion"},{"key":"B2","doi-asserted-by":"publisher","first-page":"2184","DOI":"10.1016\/j.bpj.2011.03.031","article-title":"Cardiolipin affects the supramolecular organization of ATP synthase in mitochondria.","volume":"100","author":"Acehan","year":"2011a","journal-title":"Biophys. J."},{"key":"B3","doi-asserted-by":"publisher","first-page":"899","DOI":"10.1074\/jbc.M110.171439","article-title":"Cardiac and skeletal muscle defects in a mouse model of human Barth syndrome.","volume":"286","author":"Acehan","year":"2011b","journal-title":"J. Biol. Chem."},{"key":"B4","doi-asserted-by":"publisher","first-page":"40","DOI":"10.1038\/labinvest.3700480","article-title":"Comparison of lymphoblast mitochondria from normal subjects and patients with Barth syndrome using electron microscopic tomography.","volume":"87","author":"Acehan","year":"2007","journal-title":"Lab. Invest."},{"key":"B5","doi-asserted-by":"publisher","first-page":"529","DOI":"10.1016\/j.molcel.2008.10.021","article-title":"Respiratory active mitochondrial supercomplexes.","volume":"32","author":"Acin-Perez","year":"2008","journal-title":"Mol. Cell"},{"key":"B6","doi-asserted-by":"publisher","first-page":"290","DOI":"10.1097\/MOL.0b013e328354fcf4","article-title":"Lysophospholipid acyltransferases: 1-acylglycerol-3-phosphate O-acyltransferases. From discovery to disease.","volume":"23","author":"Agarwal","year":"2012","journal-title":"Curr. Opin. Lipidol."},{"key":"B7","doi-asserted-by":"publisher","first-page":"4096","DOI":"10.1074\/jbc.273.7.4096","article-title":"Characterization of a human lysophosphatidic acid acyltransferase that is encoded by a gene located in the class III region of the human major histocompatibility complex.","volume":"273","author":"Aguado","year":"1998","journal-title":"J. Biol. Chem."},{"key":"B8","doi-asserted-by":"publisher","first-page":"960","DOI":"10.1002\/humu.22071","article-title":"Identification of a truncation mutation of acylglycerol kinase (AGK) gene in a novel autosomal recessive cataract locus.","volume":"33","author":"Aldahmesh","year":"2012","journal-title":"Hum. Mutat."},{"key":"B9","doi-asserted-by":"publisher","first-page":"4652","DOI":"10.1038\/emboj.2011.324","article-title":"Arrangement of electron transport chain components in bovine mitochondrial supercomplex I1III2IV1.","volume":"30","author":"Althoff","year":"2011","journal-title":"EMBO J."},{"key":"B10","doi-asserted-by":"publisher","first-page":"457","DOI":"10.1038\/290457a0","article-title":"Sequence and organization of the human mitochondrial genome.","volume":"290","author":"Anderson","year":"1981","journal-title":"Nature"},{"key":"B11","doi-asserted-by":"crossref","first-page":"18797","DOI":"10.1016\/S0021-9258(17)30583-5","article-title":"Mitochondrial contact sites. Lipid composition and dynamics.","volume":"265","author":"Ardail","year":"1990","journal-title":"J. Biol. Chem."},{"key":"B12","doi-asserted-by":"publisher","first-page":"11497","DOI":"10.1074\/jbc.M113.531921","article-title":"Phosphatidic acid (PA)-preferring phospholipase A1 regulates mitochondrial dynamics.","volume":"289","author":"Baba","year":"2014","journal-title":"J. Biol. Chem."},{"key":"B13","doi-asserted-by":"publisher","first-page":"151","DOI":"10.1007\/s11010-013-1563-4","article-title":"A lysophospholipid acyltransferase antagonist, CI-976, creates novel membrane tubules marked by intracellular phospholipase A1 KIAA0725p.","volume":"376","author":"Baba","year":"2013","journal-title":"Mol. Cell. Biochem."},{"key":"B14","doi-asserted-by":"publisher","first-page":"25","DOI":"10.1016\/j.chemphyslip.2013.10.008","article-title":"The topology and regulation of cardiolipin biosynthesis and remodeling in yeast.","volume":"179","author":"Baile","year":"2014a","journal-title":"Chem. Phys. Lipids"},{"key":"B15","doi-asserted-by":"publisher","first-page":"1768","DOI":"10.1074\/jbc.M113.525733","article-title":"Unremodeled and remodeled cardiolipin are functionally indistinguishable in yeast.","volume":"289","author":"Baile","year":"2014b","journal-title":"J. Biol. Chem."},{"key":"B16","doi-asserted-by":"publisher","first-page":"2008","DOI":"10.1091\/mbc.E13-03-0121","article-title":"Deacylation on the matrix side of the mitochondrial inner membrane regulates cardiolipin remodeling.","volume":"24","author":"Baile","year":"2013","journal-title":"Mol. Biol. Cell"},{"key":"B17","doi-asserted-by":"publisher","first-page":"2113","DOI":"10.1093\/hmg\/ddq088","article-title":"OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation.","volume":"19","author":"Ban","year":"2010","journal-title":"Hum. Mol. Genet."},{"key":"B18","doi-asserted-by":"publisher","first-page":"327","DOI":"10.1016\/0022-510X(83)90209-5","article-title":"An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes.","volume":"62","author":"Barth","year":"1983","journal-title":"J. Neurol. Sci."},{"key":"B19","doi-asserted-by":"publisher","first-page":"349","DOI":"10.1002\/ajmg.a.20660","article-title":"X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update.","author":"Barth","year":"2004","journal-title":"Am. J. Med. Genet. A"},{"key":"B20","doi-asserted-by":"publisher","first-page":"157","DOI":"10.1007\/BF01799418","article-title":"X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts.","volume":"19","author":"Barth","year":"1996","journal-title":"J. Inherit. Metab. Dis."},{"key":"B21","doi-asserted-by":"publisher","first-page":"801","DOI":"10.1083\/jcb.200407123","article-title":"A novel acylglycerol kinase that produces lysophosphatidic acid modulates cross talk with EGFR in prostate cancer cells.","volume":"169","author":"Bektas","year":"2005","journal-title":"J. Cell Biol."},{"key":"B22","doi-asserted-by":"publisher","first-page":"11572","DOI":"10.1074\/jbc.M805511200","article-title":"Identification of a cardiolipin-specific phospholipase encoded by the gene CLD1 (YGR110W) in yeast.","volume":"284","author":"Beranek","year":"2009","journal-title":"J. Biol. Chem."},{"key":"B23","doi-asserted-by":"publisher","first-page":"3821","DOI":"10.1021\/bi00336a001","article-title":"ADP\/ATP carrier protein from beef heart mitochondria has high amounts of tightly bound cardiolipin, as revealed by 31P nuclear magnetic resonance.","volume":"24","author":"Beyer","year":"1985","journal-title":"Biochemistry"},{"key":"B24","doi-asserted-by":"publisher","first-page":"385","DOI":"10.1038\/ng0496-385","article-title":"A novel X-linked gene, G4.5. is responsible for Barth syndrome.","volume":"12","author":"Bione","year":"1996","journal-title":"Nat. Genet."},{"key":"B25","doi-asserted-by":"publisher","first-page":"335","DOI":"10.1038\/labinvest.3780427","article-title":"Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle.","volume":"82","author":"Bissler","year":"2002","journal-title":"Lab. Invest."},{"key":"B26","doi-asserted-by":"publisher","first-page":"2205","DOI":"10.1093\/emboj\/16.9.2205","article-title":"Multiple interactions of components mediating preprotein translocation across the inner mitochondrial membrane.","volume":"16","author":"Bomer","year":"1997","journal-title":"EMBO J."},{"key":"B27","doi-asserted-by":"publisher","first-page":"567","DOI":"10.1002\/ana.20416","article-title":"Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).","volume":"57","author":"Bouslam","year":"2005","journal-title":"Ann. Neurol."},{"key":"B28","doi-asserted-by":"publisher","first-page":"5202","DOI":"10.1091\/mbc.E05-03-0256","article-title":"Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: implications for Barth syndrome.","volume":"16","author":"Brandner","year":"2005","journal-title":"Mol. Biol. Cell"},{"issue":"e102738","key":"B29","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0102738","article-title":"Specific interaction with cardiolipin triggers functional activation of Dynamin-Related Protein 1.","volume":"9","author":"Bustillo-Zabalbeitia","year":"2014","journal-title":"PLoS ONE"},{"issue":"118ra110","key":"B30","doi-asserted-by":"publisher","DOI":"10.1126\/scitranslmed.3003310","article-title":"Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.","volume":"4","author":"Calvo","year":"2012","journal-title":"Sci. Transl. Med."},{"key":"B31","doi-asserted-by":"publisher","first-page":"25","DOI":"10.1146\/annurev-genom-082509-141720","article-title":"The mitochondrial proteome and human disease.","volume":"11","author":"Calvo","year":"2010","journal-title":"Annu. Rev. Genomics Hum. Genet."},{"key":"B32","doi-asserted-by":"publisher","first-page":"31727","DOI":"10.1074\/jbc.M402930200","article-title":"A novel cardiolipin-remodeling pathway revealed by a gene encoding an endoplasmic reticulum-associated acyl-CoA:lysocardiolipin acyltransferase (ALCAT1) in mouse.","volume":"279","author":"Cao","year":"2004","journal-title":"J. Biol. Chem."},{"key":"B33","doi-asserted-by":"publisher","first-page":"E647","DOI":"10.1152\/ajpendo.90761.2008","article-title":"ALCAT1 is a polyglycerophospholipid acyltransferase potently regulated by adenine nucleotide and thyroid status.","volume":"296","author":"Cao","year":"2009","journal-title":"Am. J. Physiol. Endocrinol. Metab."},{"key":"B34","doi-asserted-by":"publisher","first-page":"443","DOI":"10.1016\/0006-291X(92)90501-B","article-title":"Human liver long-chain 3-hydroxyacyl-coenzyme A dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondria.","volume":"183","author":"Carpenter","year":"1992","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"B35","doi-asserted-by":"publisher","first-page":"628","DOI":"10.1016\/j.cell.2009.08.005","article-title":"Importing mitochondrial proteins: machineries and mechanisms.","volume":"138","author":"Chacinska","year":"2009","journal-title":"Cell"},{"key":"B36","doi-asserted-by":"publisher","first-page":"817","DOI":"10.1016\/j.cell.2005.01.011","article-title":"Mitochondrial presequence translocase: switching between TOM tethering and motor recruitment involves Tim21 and Tim17.","volume":"120","author":"Chacinska","year":"2005","journal-title":"Cell"},{"key":"B37","doi-asserted-by":"publisher","first-page":"9829","DOI":"10.1074\/jbc.273.16.9829","article-title":"The PEL1 gene (renamed PGS1) encodes the phosphatidylglycero-phosphate synthase of Saccharomyces cerevisiae.","volume":"273","author":"Chang","year":"1998a","journal-title":"J. Biol. Chem."},{"key":"B38","doi-asserted-by":"publisher","first-page":"14933","DOI":"10.1074\/jbc.273.24.14933","article-title":"Isolation and characterization of the gene (CLS1) encoding cardiolipin synthase in Saccharomyces cerevisiae.","volume":"273","author":"Chang","year":"1998b","journal-title":"J. Biol. Chem."},{"key":"B39","doi-asserted-by":"publisher","first-page":"169","DOI":"10.1042\/BJ20060303","article-title":"Identification and functional characterization of hCLS1, a human cardiolipin synthase localized in mitochondria.","volume":"398","author":"Chen","year":"2006","journal-title":"Biochem. J."},{"key":"B40","doi-asserted-by":"publisher","first-page":"R169","DOI":"10.1093\/hmg\/ddp326","article-title":"Mitochondrial dynamics \u00e2\u20ac\u201c fusion, fission, movement, and mitophagy \u00e2\u20ac\u201c in neurodegenerative diseases.","volume":"18","author":"Chen","year":"2009","journal-title":"Hum. Mol. Genet."},{"key":"B41","doi-asserted-by":"publisher","first-page":"10048","DOI":"10.1074\/jbc.M708151200","article-title":"AGPAT6 is a novel microsomal glycerol-3-phosphate acyltransferase.","volume":"283","author":"Chen","year":"2008","journal-title":"J. Biol. Chem."},{"key":"B42","doi-asserted-by":"publisher","first-page":"123","DOI":"10.1016\/0014-5793(83)80429-3","article-title":"The mitochondrial phosphate carrier reconstituted in liposomes is inhibited by doxorubicin.","volume":"159","author":"Cheneval","year":"1983","journal-title":"FEBS Lett."},{"key":"B43","doi-asserted-by":"crossref","first-page":"13003","DOI":"10.1016\/S0021-9258(17)38828-2","article-title":"Adriamycin as a probe for the transversal distribution of cardiolipin in the inner mitochondrial membrane.","volume":"260","author":"Cheneval","year":"1985","journal-title":"J. Biol. Chem."},{"key":"B44","doi-asserted-by":"publisher","first-page":"5869","DOI":"10.1021\/bi7023282","article-title":"Shotgun lipidomics reveals the temporally dependent, highly diversified cardiolipin profile in the mammalian brain: temporally coordinated postnatal diversification of cardiolipin molecular species with neuronal remodeling.","volume":"47","author":"Cheng","year":"2008","journal-title":"Biochemistry"},{"key":"B45","doi-asserted-by":"publisher","first-page":"C33","DOI":"10.1152\/ajpcell.00243.2006","article-title":"Role of cardiolipin alterations in mitochondrial dysfunction and disease.","volume":"292","author":"Chicco","year":"2007","journal-title":"Am. J. Physiol. Cell Physiol."},{"key":"B46","doi-asserted-by":"publisher","first-page":"1255","DOI":"10.1038\/ncb1487","article-title":"A common lipid links Mfn-mediated mitochondrial fusion and SNARE-regulated exocytosis.","volume":"8","author":"Choi","year":"2006","journal-title":"Nat. Cell Biol."},{"key":"B47","doi-asserted-by":"publisher","first-page":"3845","DOI":"10.1128\/MCB.05393-11","article-title":"Stomatin-like protein 2 binds cardiolipin and regulates mitochondrial biogenesis and function.","volume":"31","author":"Christie","year":"2011","journal-title":"Mol. Cell. Biol."},{"key":"B48","doi-asserted-by":"publisher","first-page":"1197","DOI":"10.1038\/ncb2837","article-title":"Cardiolipin externalization to the outer mitochondrial membrane acts as an elimination signal for mitophagy in neuronal cells.","volume":"15","author":"Chu","year":"2013","journal-title":"Nat. Cell Biol."},{"key":"B49","doi-asserted-by":"publisher","first-page":"373","DOI":"10.1007\/s00415-013-7206-6","article-title":"Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis.","volume":"261","author":"Citterio","year":"2014","journal-title":"J. Neurol."},{"key":"B50","doi-asserted-by":"publisher","first-page":"2059","DOI":"10.1016\/j.bbamem.2009.04.020","article-title":"Cardiolipin, a critical determinant of mitochondrial carrier protein assembly and function.","volume":"1788","author":"Claypool","year":"2009","journal-title":"Biochim. Biophys. Acta"},{"key":"B51","doi-asserted-by":"publisher","first-page":"32","DOI":"10.1016\/j.tibs.2011.09.003","article-title":"The complexity of cardiolipin in health and disease.","volume":"37","author":"Claypool","year":"2012","journal-title":"Trends Biochem. Sci."},{"key":"B52","doi-asserted-by":"publisher","first-page":"379","DOI":"10.1083\/jcb.200605043","article-title":"Mitochondrial mislocalization and altered assembly of a cluster of Barth syndrome mutant tafazzins.","volume":"174","author":"Claypool","year":"2006","journal-title":"J. Cell Biol."},{"key":"B53","doi-asserted-by":"publisher","first-page":"937","DOI":"10.1083\/jcb.200801152","article-title":"Cardiolipin defines the interactome of the major ADP\/ATP carrier protein of the mitochondrial inner membrane.","volume":"182","author":"Claypool","year":"2008","journal-title":"J. Cell Biol."},{"key":"B54","doi-asserted-by":"publisher","first-page":"447","DOI":"10.1083\/jcb.201008177","article-title":"Barth syndrome mutations that cause tafazzin complex lability.","volume":"192","author":"Claypool","year":"2011","journal-title":"J. Cell Biol."},{"key":"B55","doi-asserted-by":"publisher","first-page":"462","DOI":"10.1016\/0005-2736(71)90123-4","article-title":"Enzymic characterization and lipid composition of rat liver subcellular membranes.","volume":"249","author":"Colbeau","year":"1971","journal-title":"Biochim. Biophys. Acta"},{"key":"B56","doi-asserted-by":"publisher","first-page":"815","DOI":"10.1126\/science.1225625","article-title":"Intramitochondrial transport of phosphatidic acid in yeast by a lipid transfer protein.","volume":"338","author":"Connerth","year":"2012","journal-title":"Science"},{"key":"B57","doi-asserted-by":"publisher","first-page":"1779","DOI":"10.1016\/j.febslet.2009.12.049.","article-title":"Transbilayer (flip-flop) lipid motion and lipid scrambling in membranes.","volume":"584","author":"Contreras","year":"2010","journal-title":"FEBS Lett."},{"key":"B58","doi-asserted-by":"publisher","first-page":"115","DOI":"10.1016\/j.ymgme.2012.01.015","article-title":"Barth syndrome in a female patient.","volume":"106","author":"Cosson","year":"2012","journal-title":"Mol. Genet. Metab."},{"key":"B59","doi-asserted-by":"publisher","first-page":"915","DOI":"10.1083\/jcb.200604016","article-title":"Structural and functional features and significance of the physical linkage between ER and mitochondria.","volume":"174","author":"Csordas","year":"2006","journal-title":"J. Cell Biol."},{"key":"B60","doi-asserted-by":"publisher","first-page":"121","DOI":"10.1016\/j.molcel.2010.06.029","article-title":"Imaging interorganelle contacts and local calcium dynamics at the ER-mitochondrial interface.","volume":"39","author":"Csordas","year":"2010","journal-title":"Mol. Cell"},{"key":"B61","doi-asserted-by":"publisher","first-page":"393","DOI":"10.1016\/j.cub.2014.01.007","article-title":"Mitochondria and melanosomes establish physical contacts modulated by Mfn2 and involved in organelle biogenesis.","volume":"24","author":"Daniele","year":"2014","journal-title":"Curr. Biol."},{"issue":"118","key":"B62","doi-asserted-by":"publisher","DOI":"10.1186\/1471-2350-14-118","article-title":"Targeted exome sequencing for mitochondrial disorders reveals high genetic heterogeneity.","volume":"14","author":"DaRe","year":"2013","journal-title":"BMC Med. Genet."},{"key":"B63","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1016\/0304-4157(85)90002-4","article-title":"Lipids of mitochondria.","volume":"822","author":"Daum","year":"1985","journal-title":"Biochim. Biophys. Acta"},{"key":"B64","doi-asserted-by":"publisher","first-page":"103","DOI":"10.1016\/S0163-7827(97)00006-4","article-title":"Import of lipids into mitochondria.","volume":"36","author":"Daum","year":"1997","journal-title":"Prog. Lipid Res."},{"key":"B65","doi-asserted-by":"publisher","first-page":"385","DOI":"10.1136\/jmg.2005.036657","article-title":"Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition.","volume":"43","author":"Davey","year":"2006","journal-title":"J. Med. Genet."},{"key":"B66","doi-asserted-by":"publisher","first-page":"605","DOI":"10.1038\/nature07534","article-title":"Mitofusin 2 tethers endoplasmic reticulum to mitochondria.","volume":"456","author":"de Brito","year":"2008","journal-title":"Nature"},{"key":"B67","doi-asserted-by":"publisher","first-page":"108","DOI":"10.1016\/S0005-2736(96)00240-4","article-title":"Phospholipid composition of highly purified mitochondrial outer membranes of rat liver and Neurospora crassa. Is cardiolipin present in the mitochondrial outer membrane?","volume":"1325","author":"de Kroon","year":"1997","journal-title":"Biochim. Biophys. Acta"},{"key":"B68","doi-asserted-by":"publisher","first-page":"222","DOI":"10.1080\/07853890510007368","article-title":"Mitochondrial DNA and disease.","volume":"37","author":"Dimauro","year":"2005","journal-title":"Ann. Med."},{"issue":"7132","key":"B69","doi-asserted-by":"publisher","DOI":"10.1038\/srep07132","article-title":"Late-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation.","volume":"4","author":"Doi","year":"2014","journal-title":"Sci. Rep."},{"key":"B70","doi-asserted-by":"publisher","first-page":"424","DOI":"10.1091\/mbc.E07-08-0748","article-title":"Interaction of the J-protein heterodimer Pam18\/Pam16 of the mitochondrial import motor with the translocon of the inner membrane.","volume":"19","author":"D\u00e2\u20ac\u2122Silva","year":"2008","journal-title":"Mol. Biol. Cell"},{"key":"B71","doi-asserted-by":"publisher","first-page":"12419","DOI":"10.1073\/pnas.0505969102","article-title":"Role of Pam16\u00e2\u20ac\u2122s degenerate J domain in protein import across the mitochondrial inner membrane.","volume":"102","author":"D\u00e2\u20ac\u2122Silva","year":"2005","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B72","doi-asserted-by":"publisher","first-page":"806","DOI":"10.1016\/j.scr.2013.05.005","article-title":"Cardiolipin deficiency affects respiratory chain function and organization in an induced pluripotent stem cell model of Barth syndrome.","volume":"11","author":"Dudek","year":"2013","journal-title":"Stem Cell Res."},{"key":"B73","doi-asserted-by":"publisher","DOI":"10.1177\/0883073814541474","article-title":"MEGDEL syndrome in a child from palestine: report of a novel mutation in SERAC1 gene.","author":"Dweikat","year":"2014","journal-title":"J. Child Neurol."},{"key":"B74","doi-asserted-by":"crossref","first-page":"19434","DOI":"10.1016\/S0021-9258(17)45391-9","article-title":"Tightly associated cardiolipin in the bovine heart mitochondrial ATP synthase as analyzed by 31P nuclear magnetic resonance spectroscopy.","volume":"265","author":"Eble","year":"1990","journal-title":"J. Biol. Chem."},{"key":"B75","doi-asserted-by":"crossref","first-page":"3423","DOI":"10.1016\/S0021-9258(19)42589-1","article-title":"The reacylation of deacylated derivatives of diphosphatidylglycerol by microsomes and mitochondria from rat liver.","volume":"249","author":"Eichberg","year":"1974","journal-title":"J. Biol. Chem."},{"key":"B76","doi-asserted-by":"publisher","first-page":"95","DOI":"10.1016\/j.devcel.2014.06.007","article-title":"A dynamic interface between vacuoles and mitochondria in yeast.","volume":"30","author":"Elbaz-Alon","year":"2014","journal-title":"Dev. Cell"},{"key":"B77","doi-asserted-by":"publisher","first-page":"718","DOI":"10.1016\/j.bbrc.2013.12.043","article-title":"A novel lysophosphatidic acid acyltransferase enzyme (LPAAT4) with a possible role for incorporating docosahexaenoic acid into brain glycerophospholipids.","volume":"443","author":"Eto","year":"2014","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"B78","doi-asserted-by":"publisher","first-page":"307","DOI":"10.1007\/s00401-013-1115-8","article-title":"Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.","volume":"126","author":"Fink","year":"2013","journal-title":"Acta Neuropathol."},{"key":"B79","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1016\/j.jns.2012.03.025","article-title":"Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance.","volume":"318","author":"Finsterer","year":"2012","journal-title":"J. Neurol. Sci."},{"key":"B80","doi-asserted-by":"publisher","first-page":"8608","DOI":"10.1021\/bi100742w","article-title":"Structural and functional characterization of the recombinant human mitochondrial trifunctional protein.","volume":"49","author":"Fould","year":"2010","journal-title":"Biochemistry"},{"key":"B81","author":"Foundation","year":"2014","journal-title":"The United Mitochondrial Disease Foundation."},{"key":"B82","doi-asserted-by":"publisher","first-page":"226","DOI":"10.1038\/nsmb735","article-title":"Pam16 has an essential role in the mitochondrial protein import motor.","volume":"11","author":"Frazier","year":"2004","journal-title":"Nat. Struct. Mol. Biol."},{"key":"B83","doi-asserted-by":"publisher","first-page":"214","DOI":"10.1016\/0005-2736(94)00287-Y","article-title":"Characterization of a microsomal subfraction associated with mitochondria of the yeast, Saccharomyces cerevisiae. Involvement in synthesis and import of phospholipids into mitochondria.","volume":"1234","author":"Gaigg","year":"1995","journal-title":"Biochim. Biophys. Acta"},{"key":"B84","doi-asserted-by":"publisher","first-page":"1594","DOI":"10.1007\/s11064-010-0337-6","article-title":"Biological function of the cellular lipid BMP-BMP as a key activator for cholesterol sorting and membrane digestion.","volume":"36","author":"Gallala","year":"2011","journal-title":"Neurochem. Res."},{"key":"B85","doi-asserted-by":"crossref","first-page":"627","DOI":"10.1042\/bj3240627","article-title":"Asymmetrical distribution of cardiolipin in yeast inner mitochondrial membrane triggered by carbon catabolite repression.","volume":"324(Pt 2)","author":"Gallet","year":"1997","journal-title":"Biochem. J."},{"key":"B86","doi-asserted-by":"publisher","first-page":"61","DOI":"10.1016\/S0005-2736(99)00022-X","article-title":"Transbilayer movement and distribution of spin-labelled phospholipids in the inner mitochondrial membrane.","volume":"1418","author":"Gallet","year":"1999","journal-title":"Biochim. Biophys. Acta"},{"key":"B87","doi-asserted-by":"publisher","first-page":"2133","DOI":"10.1016\/j.cub.2009.10.074","article-title":"Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome.","volume":"19","author":"Gebert","year":"2009","journal-title":"Curr. Biol."},{"key":"B88","doi-asserted-by":"publisher","first-page":"507","DOI":"10.1016\/S0092-8674(02)01073-5","article-title":"The mitochondrial presequence translocase: an essential role of Tim50 in directing preproteins to the import channel.","volume":"111","author":"Geissler","year":"2002","journal-title":"Cell"},{"key":"B89","doi-asserted-by":"publisher","first-page":"331","DOI":"10.1038\/35042526","article-title":"Functional genomic analysis of cell division in C. elegans using RNAi of genes on chromosome III.","volume":"408","author":"Gonczy","year":"2000","journal-title":"Nature"},{"key":"B90","doi-asserted-by":"publisher","first-page":"1214","DOI":"10.1038\/ejhg.2013.29","article-title":"Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54).","volume":"21","author":"Gonzalez","year":"2013","journal-title":"Eur. J. Hum. Genet."},{"key":"B91","doi-asserted-by":"publisher","first-page":"1194","DOI":"10.1016\/j.bbadis.2013.03.005","article-title":"Barth syndrome: cellular compensation of mitochondrial dysfunction and apoptosis inhibition due to changes in cardiolipin remodeling linked to tafazzin (TAZ) gene mutation.","volume":"1832","author":"Gonzalvez","year":"2013","journal-title":"Biochim. Biophys. Acta"},{"key":"B92","doi-asserted-by":"publisher","first-page":"614","DOI":"10.1038\/sj.cdd.4401571","article-title":"tBid interaction with cardiolipin primarily orchestrates mitochondrial dysfunctions and subsequently activates Bax and Bak.","volume":"12","author":"Gonzalvez","year":"2005","journal-title":"Cell Death Differ."},{"key":"B93","doi-asserted-by":"publisher","first-page":"681","DOI":"10.1083\/jcb.200803129","article-title":"Cardiolipin provides an essential activating platform for caspase-8 on mitochondria.","volume":"183","author":"Gonzalvez","year":"2008","journal-title":"J. Cell Biol."},{"key":"B94","doi-asserted-by":"publisher","first-page":"626","DOI":"10.1126\/science.1099320","article-title":"The pathophysiology of mitochondrial cell death.","volume":"305","author":"Green","year":"2004","journal-title":"Science"},{"key":"B95","doi-asserted-by":"publisher","first-page":"3665","DOI":"10.1073\/pnas.82.11.3665","article-title":"Intrinsic curvature hypothesis for biomembrane lipid composition: a role for nonbilayer lipids.","volume":"82","author":"Gruner","year":"1985","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B96","doi-asserted-by":"publisher","first-page":"149","DOI":"10.1046\/j.1365-2958.2003.03802.x","article-title":"Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndrome.","volume":"51","author":"Gu","year":"2004","journal-title":"Mol. Microbiol."},{"key":"B97","doi-asserted-by":"publisher","first-page":"1587","DOI":"10.1126\/science.1140494","article-title":"A slicer-mediated mechanism for repeat-associated siRNA 5\u00e2\u20ac\u2122 end formation in","volume":"315","author":"Gunawardane","year":"2007","journal-title":"Drosophila. Science"},{"issue":"119","key":"B98","doi-asserted-by":"publisher","DOI":"10.1186\/s13023-014-0119-3","article-title":"Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients.","volume":"9","author":"Haghighi","year":"2014","journal-title":"Orphanet J. Rare Dis."},{"key":"B99","doi-asserted-by":"publisher","first-page":"35","DOI":"10.1016\/S0014-5793(02)03292-1","article-title":"Cardiolipin: a proton trap for oxidative phosphorylation.","volume":"528","author":"Haines","year":"2002","journal-title":"FEBS Lett."},{"key":"B100","doi-asserted-by":"publisher","first-page":"170","DOI":"10.1111\/j.1749-6632.1982.tb21415.x","article-title":"Glycerolipid biosynthesis in peroxisomes via the acyl dihydroxyacetone phosphate pathway.","volume":"386","author":"Hajra","year":"1982","journal-title":"Ann. N. Y. Acad. Sci."},{"key":"B101","doi-asserted-by":"publisher","first-page":"864","DOI":"10.1194\/jlr.D500044-JLR200","article-title":"Shotgun lipidomics of cardiolipin molecular species in lipid extracts of biological samples.","volume":"47","author":"Han","year":"2006","journal-title":"J. Lipid Res."},{"key":"B102","doi-asserted-by":"publisher","first-page":"305","DOI":"10.1016\/0003-9861(81)90153-3","article-title":"Asymmetrical orientation of phospholipids and their interactions with marker enzymes in pig heart mitochondrial inner membrane.","volume":"208","author":"Harb","year":"1981","journal-title":"Arch. Biochem. Biophys."},{"key":"B103","doi-asserted-by":"publisher","first-page":"4356","DOI":"10.1038\/emboj.2011.379","article-title":"The mitochondrial contact site complex, a determinant of mitochondrial architecture.","volume":"30","author":"Harner","year":"2011","journal-title":"EMBO J."},{"key":"B104","doi-asserted-by":"publisher","first-page":"2302","DOI":"10.1128\/MCB.00189-13","article-title":"MCJ\/DnaJC15, an endogenous mitochondrial repressor of the respiratory chain that controls metabolic alterations.","volume":"33","author":"Hatle","year":"2013","journal-title":"Mol. Cell. Biol."},{"key":"B105","doi-asserted-by":"publisher","first-page":"H210","DOI":"10.1152\/ajpheart.00098.2010","article-title":"Tafazzin knockdown causes hypertrophy of neonatal ventricular myocytes.","volume":"299","author":"He","year":"2010","journal-title":"Am. J. Physiol. Heart Circ. Physiol."},{"issue":"654198","key":"B106","doi-asserted-by":"publisher","DOI":"10.1155\/2014\/654198","article-title":"Mitochondria-targeted antioxidant prevents cardiac dysfunction induced by tafazzin gene knockdown in cardiac myocytes.","volume":"2014","author":"He","year":"2014","journal-title":"Oxid. Med. Cell. Longev."},{"key":"B107","doi-asserted-by":"publisher","first-page":"901","DOI":"10.1530\/REP-08-0494","article-title":"Small RNA molecules in the regulation of spermatogenesis.","volume":"137","author":"He","year":"2009","journal-title":"Reproduction"},{"key":"B108","doi-asserted-by":"publisher","first-page":"9574","DOI":"10.1073\/pnas.91.20.9574","article-title":"Identification of a phosphatidic acid-preferring phospholipase A1 from bovine brain and testis.","volume":"91","author":"Higgs","year":"1994","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B109","doi-asserted-by":"publisher","first-page":"5468","DOI":"10.1074\/jbc.273.10.5468","article-title":"Cloning of a phosphatidic acid-preferring phospholipase A1 from bovine testis.","volume":"273","author":"Higgs","year":"1998","journal-title":"J. Biol. Chem."},{"key":"B110","doi-asserted-by":"publisher","first-page":"210","DOI":"10.1136\/jmg.24.4.210","article-title":"Endocardial fibroelastosis: possible X linked inheritance.","volume":"24","author":"Hodgson","year":"1987","journal-title":"J. Med. Genet."},{"key":"B111","doi-asserted-by":"publisher","first-page":"717","DOI":"10.1038\/331717a0","article-title":"Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.","volume":"331","author":"Holt","year":"1988","journal-title":"Nature"},{"key":"B112","doi-asserted-by":"publisher","first-page":"86","DOI":"10.1016\/j.devcel.2014.06.006","article-title":"Cellular metabolism regulates contact sites between vacuoles and mitochondria.","volume":"30","author":"Honscher","year":"2014","journal-title":"Dev. Cell"},{"key":"B113","doi-asserted-by":"publisher","first-page":"4181","DOI":"10.1021\/bi00436a009","article-title":"Phospholipid asymmetry in large unilamellar vesicles induced by transmembrane pH gradients.","volume":"28","author":"Hope","year":"1989","journal-title":"Biochemistry"},{"key":"B114","doi-asserted-by":"publisher","first-page":"323","DOI":"10.1083\/jcb.201107053","article-title":"A mitochondrial-focused genetic interaction map reveals a scaffold-like complex required for inner membrane organization in mitochondria.","volume":"195","author":"Hoppins","year":"2011","journal-title":"J. Cell Biol."},{"key":"B115","doi-asserted-by":"publisher","first-page":"590","DOI":"10.1016\/j.plipres.2013.07.002","article-title":"Lipids of mitochondria.","volume":"52","author":"Horvath","year":"2013","journal-title":"Prog. Lipid Res."},{"key":"B116","doi-asserted-by":"publisher","first-page":"382","DOI":"10.1016\/0005-2760(75)90106-X","article-title":"Further studies on the formation of cardiolipin and phosphatidylglycerol in rat liver mitochondria. Effect of divalent cations and the fatty acid composition of CDP-diglyceride.","volume":"380","author":"Hostetler","year":"1975","journal-title":"Biochim. Biophys. Acta"},{"key":"B117","doi-asserted-by":"publisher","first-page":"3059","DOI":"10.1016\/j.febslet.2006.04.054","article-title":"Identification and characterization of human cardiolipin synthase.","volume":"580","author":"Houtkooper","year":"2006","journal-title":"FEBS Lett."},{"key":"B118","doi-asserted-by":"publisher","first-page":"230","DOI":"10.1016\/j.ab.2009.01.032","article-title":"Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography-mass spectrometry as a diagnostic test for Barth syndrome.","volume":"387","author":"Houtkooper","year":"2009a","journal-title":"Anal. Biochem."},{"key":"B119","doi-asserted-by":"publisher","first-page":"2003","DOI":"10.1016\/j.bbamem.2009.07.009","article-title":"The enigmatic role of tafazzin in cardiolipin metabolism.","volume":"1788","author":"Houtkooper","year":"2009b","journal-title":"Biochim. Biophys. Acta"},{"key":"B120","doi-asserted-by":"publisher","first-page":"2493","DOI":"10.1007\/s00018-008-8030-5","article-title":"Cardiolipin, the heart of mitochondrial metabolism.","volume":"65","author":"Houtkooper","year":"2008","journal-title":"Cell. Mol. Life Sci."},{"key":"B121","doi-asserted-by":"publisher","first-page":"217","DOI":"10.1016\/0005-2736(90)90036-N","article-title":"Improved methods to isolate and subfractionate rat liver mitochondria. Lipid composition of the inner and outer membrane.","volume":"1021","author":"Hovius","year":"1990","journal-title":"Biochim. Biophys. Acta"},{"key":"B122","doi-asserted-by":"publisher","first-page":"71","DOI":"10.1016\/0014-5793(93)80922-H","article-title":"Phospholipid asymmetry of the outer membrane of rat liver mitochondria. Evidence for the presence of cardiolipin on the outside of the outer membrane.","volume":"330","author":"Hovius","year":"1993","journal-title":"FEBS Lett."},{"issue":"e59267","key":"B123","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0059267","article-title":"Assessing phospholipase A2 activity toward cardiolipin by mass spectrometry.","volume":"8","author":"Hsu","year":"2013","journal-title":"PLoS ONE"},{"key":"B124","doi-asserted-by":"publisher","first-page":"376","DOI":"10.1016\/j.devcel.2011.01.004","article-title":"piRNA-associated germline nuage formation and spermatogenesis require MitoPLD profusogenic mitochondrial-surface lipid signaling.","volume":"20","author":"Huang","year":"2011","journal-title":"Dev. Cell"},{"key":"B125","doi-asserted-by":"publisher","first-page":"1997","DOI":"10.1194\/jlr.M700154-JLR200","article-title":"De novo biosynthesis of the late endosome lipid, bis(monoacylglycero)phosphate.","volume":"48","author":"Hullin-Matsuda","year":"2007","journal-title":"J. Lipid Res."},{"key":"B126","doi-asserted-by":"publisher","first-page":"313","DOI":"10.1016\/j.plefa.2009.09.006","article-title":"Bis(monoacylglycero)phosphate, a peculiar phospholipid to control the fate of cholesterol: implications in pathology.","volume":"81","author":"Hullin-Matsuda","year":"2009","journal-title":"Prostaglandins Leukot. Essent. Fatty Acids"},{"key":"B127","doi-asserted-by":"publisher","first-page":"332","DOI":"10.1016\/j.molcel.2014.06.003","article-title":"Proteomic mapping of the human mitochondrial intermembrane space in live cells via ratiometric APEX tagging.","volume":"55","author":"Hung","year":"2014","journal-title":"Mol. Cell"},{"key":"B128","doi-asserted-by":"publisher","first-page":"1256","DOI":"10.1161\/01.CIR.103.9.1256","article-title":"Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome.","volume":"103","author":"Ichida","year":"2001","journal-title":"Circulation"},{"key":"B129","doi-asserted-by":"publisher","first-page":"347","DOI":"10.1016\/0005-2760(94)90064-7","article-title":"Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein.","volume":"1215","author":"IJlst","year":"1994","journal-title":"Biochim. Biophys. Acta"},{"key":"B130","doi-asserted-by":"publisher","first-page":"14924","DOI":"10.1073\/pnas.1413706111","article-title":"The hereditary spastic paraplegia-related enzyme DDHD2 is a principal brain triglyceride lipase.","volume":"111","author":"Inloes","year":"2014","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B131","doi-asserted-by":"publisher","first-page":"312","DOI":"10.1016\/j.tig.2005.04.003","article-title":"Nuclear genes and mitochondrial translation: a new class of genetic disease.","volume":"21","author":"Jacobs","year":"2005","journal-title":"Trends Genet."},{"issue":"e55250","key":"B132","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0055250","article-title":"Caspase-8 binding to cardiolipin in giant unilamellar vesicles provides a functional docking platform for bid.","volume":"8","author":"Jalmar","year":"2013","journal-title":"PLoS ONE"},{"issue":"e103","key":"B133","doi-asserted-by":"publisher","DOI":"10.1038\/cddis.2010.81","article-title":"Giant unilamellar vesicles (GUVs) as a new tool for analysis of caspase-8\/Bid-FL complex binding to cardiolipin and its functional activity.","volume":"1","author":"Jalmar","year":"2010","journal-title":"Cell Death Dis."},{"key":"B134","doi-asserted-by":"publisher","first-page":"22387","DOI":"10.1074\/jbc.M909868199","article-title":"Absence of cardiolipin in the crd1 null mutant results in decreased mitochondrial membrane potential and reduced mitochondrial function.","volume":"275","author":"Jiang","year":"2000","journal-title":"J. Biol. Chem."},{"key":"B135","doi-asserted-by":"publisher","first-page":"1543","DOI":"10.1091\/mbc.E04-08-0697","article-title":"The mitochondrial inner membrane protein mitofilin controls cristae morphology.","volume":"16","author":"John","year":"2005","journal-title":"Mol. Biol. Cell"},{"key":"B136","doi-asserted-by":"publisher","first-page":"C689","DOI":"10.1152\/ajpcell.00108.2006","article-title":"Tissue heterogeneity of the mammalian mitochondrial proteome.","volume":"292","author":"Johnson","year":"2007","journal-title":"Am. J. Physiol. Cell Physiol."},{"key":"B137","doi-asserted-by":"publisher","first-page":"1053","DOI":"10.1086\/301604","article-title":"Mutation characterization and genotype-phenotype correlation in Barth syndrome.","volume":"61","author":"Johnston","year":"1997","journal-title":"Am. J. Hum. Genet."},{"key":"B138","doi-asserted-by":"publisher","first-page":"95","DOI":"10.1002\/ana.10214","article-title":"Adenine nucleotide translocator 1 deficiency associated with Sengers syndrome.","volume":"52","author":"Jordens","year":"2002","journal-title":"Ann. Neurol."},{"key":"B139","doi-asserted-by":"publisher","first-page":"212","DOI":"10.1016\/j.bbamcr.2008.07.024","article-title":"Cellular functions of cardiolipin in yeast.","volume":"1793","author":"Joshi","year":"2009","journal-title":"Biochim. Biophys. Acta"},{"key":"B140","doi-asserted-by":"publisher","first-page":"1392","DOI":"10.1016\/S0301-472X(01)00749-4","article-title":"Identification and characterization of Magmas, a novel mitochondria-associated protein involved in granulocyte-macrophage colony-stimulating factor signal transduction.","volume":"29","author":"Jubinsky","year":"2001","journal-title":"Exp. Hematol."},{"key":"B141","doi-asserted-by":"publisher","first-page":"585","DOI":"10.1177\/002215540305100504","article-title":"Developmental expression of Magmas in murine tissues and its co-expression with the GM-CSF receptor.","volume":"51","author":"Jubinsky","year":"2003","journal-title":"J. Histochem. Cytochem."},{"key":"B142","doi-asserted-by":"publisher","first-page":"223","DOI":"10.1038\/nchembio727","article-title":"Cytochrome c acts as a cardiolipin oxygenase required for release of proapoptotic factors.","volume":"1","author":"Kagan","year":"2005","journal-title":"Nat. Chem. Biol."},{"key":"B143","first-page":"56","article-title":"Increased reactive oxygen species (ROS) production and low catalase level in fibroblasts of a girl with MEGDEL association (Leigh syndrome, deafness, 3-methylglutaconic aciduria).","volume":"49","author":"Karkucinska-Wieckowska","year":"2011","journal-title":"Folia Neuropathol."},{"key":"B144","doi-asserted-by":"publisher","first-page":"738","DOI":"10.1016\/S0022-3476(05)80289-6","article-title":"X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria.","volume":"119","author":"Kelley","year":"1991","journal-title":"J. Pediatr."},{"key":"B145","doi-asserted-by":"publisher","first-page":"201","DOI":"10.1161\/01.RES.0000233378.95325.ce","article-title":"A zebrafish model of human Barth syndrome reveals the essential role of tafazzin in cardiac development and function.","volume":"99","author":"Khuchua","year":"2006","journal-title":"Circ. Res."},{"key":"B146","doi-asserted-by":"publisher","first-page":"1312","DOI":"10.1194\/jlr.M034728","article-title":"Dysfunctional cardiac mitochondrial bioenergetic, lipidomic, and signaling in a murine model of Barth syndrome.","volume":"54","author":"Kiebish","year":"2013","journal-title":"J. Lipid Res."},{"key":"B147","doi-asserted-by":"publisher","first-page":"113","DOI":"10.1038\/10084","article-title":"Late endosomal membranes rich in lysobisphosphatidic acid regulate cholesterol transport.","volume":"1","author":"Kobayashi","year":"1999","journal-title":"Nat. Cell Biol."},{"key":"B148","doi-asserted-by":"publisher","first-page":"193","DOI":"10.1038\/32440","article-title":"A lipid associated with the antiphospholipid syndrome regulates endosome structure and function.","volume":"392","author":"Kobayashi","year":"1998","journal-title":"Nature"},{"key":"B149","doi-asserted-by":"publisher","first-page":"2673","DOI":"10.1021\/bi036200f","article-title":"Transbilayer movement of phospholipids in biogenic membranes.","volume":"43","author":"Kol","year":"2004","journal-title":"Biochemistry"},{"key":"B150","doi-asserted-by":"publisher","first-page":"10500","DOI":"10.1021\/bi010627+","article-title":"Membrane-spanning peptides induce phospholipid flop: a model for phospholipid translocation across the inner membrane of","volume":"40","author":"Kol","year":"2001","journal-title":"E. coli. Biochemistry"},{"key":"B151","doi-asserted-by":"publisher","first-page":"221","DOI":"10.1080\/10409230701380452","article-title":"Protein degradation within mitochondria: versatile activities of AAA proteases and other peptidases.","volume":"42","author":"Koppen","year":"2007","journal-title":"Crit. Rev. Biochem. Mol. Biol."},{"key":"B152","doi-asserted-by":"publisher","first-page":"477","DOI":"10.1126\/science.1175088","article-title":"An ER-mitochondria tethering complex revealed by a synthetic biology screen.","volume":"325","author":"Kornmann","year":"2009","journal-title":"Science"},{"key":"B153","doi-asserted-by":"publisher","first-page":"14151","DOI":"10.1073\/pnas.1111314108","article-title":"The conserved GTPase Gem1 regulates endoplasmic reticulum-mitochondria connections.","volume":"108","author":"Kornmann","year":"2011","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B154","doi-asserted-by":"publisher","first-page":"234","DOI":"10.1038\/nsmb734","article-title":"The J domain-related cochaperone Tim16 is a constituent of the mitochondrial TIM23 preprotein translocase.","volume":"11","author":"Kozany","year":"2004","journal-title":"Nat. Struct. Mol. Biol."},{"key":"B155","doi-asserted-by":"crossref","first-page":"5308","DOI":"10.1016\/S0021-9258(18)50596-2","article-title":"Asymmetric distribution of phospholipids in the inner membrane of beef heart mitochondria.","volume":"254","author":"Krebs","year":"1979","journal-title":"J. Biol. Chem."},{"key":"B156","doi-asserted-by":"crossref","first-page":"1277","DOI":"10.1096\/fasebj.9.13.7557017","article-title":"The biochemistry of programmed cell death.","volume":"9","author":"Kroemer","year":"1995","journal-title":"FASEB J."},{"key":"B157","doi-asserted-by":"crossref","first-page":"901","DOI":"10.1128\/jb.165.3.901-910.1986","article-title":"Subcellular and submitochondrial localization of phospholipid-synthesizing enzymes in Saccharomyces cerevisiae.","volume":"165","author":"Kuchler","year":"1986","journal-title":"J. Bacteriol."},{"key":"B158","doi-asserted-by":"publisher","first-page":"1213","DOI":"10.1083\/jcb.200806048","article-title":"The translocator maintenance protein Tam41 is required for mitochondrial cardiolipin biosynthesis.","volume":"183","author":"Kutik","year":"2008","journal-title":"J. Cell Biol."},{"key":"B159","doi-asserted-by":"publisher","first-page":"331","DOI":"10.1016\/S0092-8674(02)01036-X","article-title":"Bid, Bax, and lipids cooperate to form supramolecular openings in the outer mitochondrial membrane.","volume":"111","author":"Kuwana","year":"2002","journal-title":"Cell"},{"issue":"e1001969","key":"B160","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pbio.1001969","article-title":"A conserved endoplasmic reticulum membrane protein complex (EMC) facilitates phospholipid transfer from the ER to mitochondria.","volume":"12","author":"Lahiri","year":"2014","journal-title":"PLoS Biol."},{"key":"B161","doi-asserted-by":"publisher","first-page":"482","DOI":"10.1055\/s-2008-1050858","article-title":"[Infantile cataract, hypertrophic cardiomyopathy and lactic acidosis following minor muscular exertion \u00e2\u20ac\u201c a little known metabolic disease]","volume":"189","author":"Lalive D\u00e2\u20ac\u2122Epinay","year":"1986","journal-title":"Klin. Monbl. Augenheilkd."},{"key":"B162","doi-asserted-by":"publisher","first-page":"1567","DOI":"10.1126\/science.1230381","article-title":"Supercomplex assembly determines electron flux in the mitochondrial electron transport chain.","volume":"340","author":"Lapuente-Brun","year":"2013","journal-title":"Science"},{"key":"B163","doi-asserted-by":"publisher","first-page":"976","DOI":"10.1021\/bi00895a023","article-title":"On the structure of cardiolipin.","volume":"3","author":"Lecocq","year":"1964","journal-title":"Biochemistry"},{"key":"B164","doi-asserted-by":"publisher","first-page":"13488","DOI":"10.1074\/jbc.M314032200","article-title":"Identification of a new glycerol-3-phosphate acyltransferase isoenzyme, mtGPAT2, in mitochondria.","volume":"279","author":"Lewin","year":"2004","journal-title":"J. Biol. Chem."},{"key":"B165","doi-asserted-by":"publisher","first-page":"2069","DOI":"10.1016\/j.bbamem.2009.03.014","article-title":"The physicochemical properties of cardiolipin bilayers and cardiolipin-containing lipid membranes.","volume":"1788","author":"Lewis","year":"2009","journal-title":"Biochim. Biophys. Acta"},{"key":"B166","doi-asserted-by":"publisher","first-page":"6975","DOI":"10.1073\/pnas.1120043109","article-title":"Lysocardiolipin acyltransferase 1 (ALCAT1) controls mitochondrial DNA fidelity and biogenesis through modulation of MFN2 expression.","volume":"109","author":"Li","year":"2012","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B167","doi-asserted-by":"publisher","first-page":"154","DOI":"10.1016\/j.cmet.2010.07.003","article-title":"Cardiolipin remodeling by ALCAT1 links oxidative stress and mitochondrial dysfunction to obesity.","volume":"12","author":"Li","year":"2010","journal-title":"Cell Metab."},{"key":"B168","doi-asserted-by":"crossref","first-page":"13998","DOI":"10.1016\/S0021-9258(18)71632-3","article-title":"A human muscle adenine nucleotide translocator gene has four exons, is located on chromosome 4, and is differentially expressed.","volume":"264","author":"Li","year":"1989","journal-title":"J. Biol. Chem."},{"key":"B169","doi-asserted-by":"publisher","first-page":"1789","DOI":"10.1007\/s00415-014-7418-4","article-title":"Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations.","volume":"261","author":"Liguori","year":"2014","journal-title":"J. Neurol."},{"key":"B170","doi-asserted-by":"publisher","first-page":"1491","DOI":"10.1016\/j.bbamcr.2012.05.009","article-title":"The role of mitochondria in cellular iron-sulfur protein biogenesis and iron metabolism.","volume":"1823","author":"Lill","year":"2012","journal-title":"Biochim. Biophys. Acta"},{"key":"B171","first-page":"1153","article-title":"Phospholipid scramblase 3 is the mitochondrial target of protein kinase C delta-induced apoptosis.","volume":"63","author":"Liu","year":"2003a","journal-title":"Cancer Res."},{"key":"B172","first-page":"892","article-title":"Phospholipid scramblase 3 controls mitochondrial structure, function, and apoptotic response.","volume":"1","author":"Liu","year":"2003b","journal-title":"Mol. Cancer Res."},{"key":"B173","doi-asserted-by":"publisher","first-page":"4493","DOI":"10.1128\/MCB.01092-12","article-title":"Ablation of ALCAT1 mitigates hypertrophic cardiomyopathy through effects on oxidative stress and mitophagy.","volume":"32","author":"Liu","year":"2012","journal-title":"Mol. Cell. Biol."},{"key":"B174","doi-asserted-by":"publisher","first-page":"469","DOI":"10.1042\/BJ20041348","article-title":"Cloning and characterization of murine 1-acyl-sn-glycerol 3-phosphate acyltransferases and their regulation by PPARalpha in murine heart.","volume":"385","author":"Lu","year":"2005","journal-title":"Biochem. J."},{"key":"B175","doi-asserted-by":"publisher","first-page":"1140","DOI":"10.1194\/jlr.C600004-JLR200","article-title":"Cloning and characterization of a cDNA encoding human cardiolipin synthase (hCLS1).","volume":"47","author":"Lu","year":"2006","journal-title":"J. Lipid Res."},{"key":"B176","doi-asserted-by":"publisher","first-page":"929","DOI":"10.1038\/cdd.2008.9","article-title":"Contributions to Bax insertion and oligomerization of lipids of the mitochondrial outer membrane.","volume":"15","author":"Lucken-Ardjomande","year":"2008","journal-title":"Cell Death Differ."},{"key":"B177","doi-asserted-by":"publisher","first-page":"1776","DOI":"10.1172\/JCI104637","article-title":"A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study.","volume":"41","author":"Luft","year":"1962","journal-title":"J. Clin. Invest."},{"key":"B178","doi-asserted-by":"publisher","first-page":"75","DOI":"10.1007\/8904_2014_322","article-title":"The expanding MEGDEL phenotype: optic nerve atrophy, microcephaly, and myoclonic epilepsy in a child with SERAC1 mutations.","volume":"16","author":"Lumish","year":"2014","journal-title":"JIMD Rep."},{"key":"B179","doi-asserted-by":"publisher","first-page":"e25","DOI":"10.1111\/ene.12305","article-title":"Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum.","volume":"21","author":"Magariello","year":"2014","journal-title":"Eur. J. Neurol."},{"key":"B180","doi-asserted-by":"publisher","first-page":"2337","DOI":"10.1073\/pnas.0811224106","article-title":"Role of calcium-independent phospholipase A2 in the pathogenesis of Barth syndrome.","volume":"106","author":"Malhotra","year":"2009a","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B181","doi-asserted-by":"publisher","first-page":"314","DOI":"10.1016\/j.bbalip.2009.01.004","article-title":"Formation of molecular species of mitochondrial cardiolipin. 1. A novel transacylation mechanism to shuttle fatty acids between sn-1 and sn-2 positions of multiple phospholipid species.","volume":"1791","author":"Malhotra","year":"2009b","journal-title":"Biochim. Biophys. Acta"},{"key":"B182","doi-asserted-by":"publisher","first-page":"9937","DOI":"10.1074\/jbc.275.14.9937","article-title":"The genomic organization, complete mRNA sequence, cloning, and expression of a novel human intracellular membrane-associated calcium-independent phospholipase A(2).","volume":"275","author":"Mancuso","year":"2000","journal-title":"J. Biol. Chem."},{"key":"B183","doi-asserted-by":"publisher","first-page":"34611","DOI":"10.1074\/jbc.M707795200","article-title":"Genetic ablation of calcium-independent phospholipase A2gamma leads to alterations in mitochondrial lipid metabolism and function resulting in a deficient mitochondrial bioenergetic phenotype.","volume":"282","author":"Mancuso","year":"2007","journal-title":"J. Biol. Chem."},{"key":"B184","doi-asserted-by":"publisher","first-page":"2399","DOI":"10.1172\/JCI107052","article-title":"Lipids of alveolar macrophages, polymorphonuclear leukocytes, and their phagocytic vesicles.","volume":"51","author":"Mason","year":"1972","journal-title":"J. Clin. Invest."},{"key":"B185","doi-asserted-by":"publisher","first-page":"322","DOI":"10.1016\/j.bbrc.2013.02.099","article-title":"Tespa1 is a novel component of mitochondria-associated endoplasmic reticulum membranes and affects mitochondrial calcium flux.","volume":"433","author":"Matsuzaki","year":"2013","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"B186","doi-asserted-by":"publisher","first-page":"670","DOI":"10.1007\/s00018-004-4464-6","article-title":"Hsp70 chaperones: cellular functions and molecular mechanism.","volume":"62","author":"Mayer","year":"2005","journal-title":"Cell. Mol. Life Sci."},{"key":"B187","doi-asserted-by":"publisher","first-page":"314","DOI":"10.1016\/j.ajhg.2011.12.005","article-title":"Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome.","volume":"90","author":"Mayr","year":"2012","journal-title":"Am. J. Hum. Genet."},{"key":"B188","doi-asserted-by":"publisher","first-page":"462","DOI":"10.1016\/j.jmb.2006.06.057","article-title":"Mitochondrial respiratory chain supercomplexes are destabilized in Barth syndrome patients.","volume":"361","author":"McKenzie","year":"2006","journal-title":"J. Mol. Biol."},{"issue":"e1004311","key":"B189","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pgen.1004311","article-title":"The impairment of MAGMAS function in human is responsible for a severe skeletal dysplasia.","volume":"10","author":"Mehawej","year":"2014","journal-title":"PLoS Genet."},{"key":"B190","doi-asserted-by":"publisher","first-page":"476","DOI":"10.1101\/gad.460708","article-title":"Prohibitins control cell proliferation and apoptosis by regulating OPA1-dependent cristae morphogenesis in mitochondria.","volume":"22","author":"Merkwirth","year":"2008","journal-title":"Genes Dev."},{"key":"B191","doi-asserted-by":"publisher","first-page":"1165","DOI":"10.1016\/j.cell.2008.12.005","article-title":"Mitofusin 2 builds a bridge between ER and mitochondria.","volume":"135","author":"Merkwirth","year":"2008","journal-title":"Cell"},{"key":"B192","doi-asserted-by":"publisher","first-page":"14264","DOI":"10.1074\/jbc.275.19.14264","article-title":"The human nm23-H4 gene product is a mitochondrial nucleoside diphosphate kinase.","volume":"275","author":"Milon","year":"2000","journal-title":"J. Biol. Chem."},{"key":"B193","doi-asserted-by":"publisher","first-page":"222","DOI":"10.1034\/j.1600-0854.2003.00072.x","article-title":"Recycling compartments and the internal vesicles of multivesicular bodies harbor most of the cholesterol found in the endocytic pathway.","volume":"4","author":"Mobius","year":"2003","journal-title":"Traffic"},{"key":"B194","doi-asserted-by":"publisher","first-page":"4945","DOI":"10.1093\/emboj\/cdg485","article-title":"Tim14, a novel key component of the import motor of the TIM23 protein translocase of mitochondria.","volume":"22","author":"Mokranjac","year":"2003","journal-title":"EMBO J."},{"key":"B195","doi-asserted-by":"publisher","first-page":"31608","DOI":"10.1074\/jbc.M502397200","article-title":"The import motor of the yeast mitochondrial TIM23 preprotein translocase contains two different J proteins, Tim14 and Mdj2.","volume":"280","author":"Mokranjac","year":"2005","journal-title":"J. Biol. Chem."},{"key":"B196","doi-asserted-by":"publisher","first-page":"889","DOI":"10.1016\/j.cell.2010.08.017","article-title":"Membrane remodeling induced by the dynamin-related protein Drp1 stimulates Bax oligomerization.","volume":"142","author":"Montessuit","year":"2010","journal-title":"Cell"},{"key":"B197","doi-asserted-by":"publisher","first-page":"629","DOI":"10.1016\/S0092-8674(03)00926-7","article-title":"Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria.","volume":"115","author":"Mootha","year":"2003","journal-title":"Cell"},{"key":"B198","doi-asserted-by":"publisher","first-page":"467","DOI":"10.1007\/s00431-004-1465-2","article-title":"Congenital hypertrophic cardiomyopathy, cataract, mitochondrial myopathy and defective oxidative phosphorylation in two siblings with Sengers-like syndrome.","volume":"163","author":"Morava","year":"2004","journal-title":"Eur. J. Pediatr."},{"key":"B199","doi-asserted-by":"publisher","first-page":"26620","DOI":"10.1074\/jbc.M109.038869","article-title":"Intracellular phospholipase A1gamma (iPLA1gamma) is a novel factor involved in coat protein complex I- and Rab6-independent retrograde transport between the endoplasmic reticulum and the Golgi complex.","volume":"284","author":"Morikawa","year":"2009","journal-title":"J. Biol. Chem."},{"key":"B200","doi-asserted-by":"publisher","first-page":"6874","DOI":"10.1074\/jbc.M107935200","article-title":"Mitochondrial protein import: molecular basis of the ATP-dependent interaction of MtHsp70 with Tim44.","volume":"277","author":"Moro","year":"2002","journal-title":"J. Biol. Chem."},{"key":"B201","doi-asserted-by":"publisher","first-page":"3667","DOI":"10.1093\/emboj\/18.13.3667","article-title":"The TIM17.23 preprotein translocase of mitochondria: composition and function in protein transport into the matrix.","volume":"18","author":"Moro","year":"1999","journal-title":"EMBO J."},{"key":"B202","doi-asserted-by":"publisher","first-page":"748","DOI":"10.1002\/jcp.22177","article-title":"Caenorhabditis elegans mitofilin homologs control the morphology of mitochondrial cristae and influence reproduction and physiology.","volume":"224","author":"Mun","year":"2010","journal-title":"J. Cell. Physiol."},{"key":"B203","doi-asserted-by":"publisher","first-page":"823","DOI":"10.1194\/jlr.M700592-JLR200","article-title":"Identification of a novel sn-glycerol-3-phosphate acyltransferase isoform, GPAT4, as the enzyme deficient in Agpat6\u00e2\u20ac\u201c\/\u00e2\u20ac\u201c mice.","volume":"49","author":"Nagle","year":"2008","journal-title":"J. Lipid Res."},{"key":"B204","doi-asserted-by":"publisher","first-page":"11329","DOI":"10.1074\/jbc.M111092200","article-title":"A novel phospholipase A1 with sequence homology to a mammalian Sec23p-interacting protein, p125.","volume":"277","author":"Nakajima","year":"2002","journal-title":"J. Biol. Chem."},{"key":"B205","doi-asserted-by":"publisher","first-page":"351","DOI":"10.1016\/j.mito.2004.07.002","article-title":"Developing a systematic approach to the diagnosis and classification of mitochondrial disease.","volume":"4","author":"Naviaux","year":"2004","journal-title":"Mitochondrion"},{"key":"B206","doi-asserted-by":"publisher","first-page":"880","DOI":"10.1111\/j.1600-0854.2012.01352.x","article-title":"Gem1 and ERMES do not directly affect phosphatidylserine transport from ER to mitochondria or mitochondrial inheritance.","volume":"13","author":"Nguyen","year":"2012","journal-title":"Traffic"},{"key":"B207","doi-asserted-by":"publisher","first-page":"229","DOI":"10.1016\/0005-2728(90)90255-3","article-title":"The role of contact sites between inner and outer mitochondrial membrane in energy transfer.","volume":"1018","author":"Nicolay","year":"1990","journal-title":"Biochim. Biophys. Acta"},{"key":"B208","doi-asserted-by":"publisher","first-page":"98","DOI":"10.1379\/1466-1268(2000)0050098:MHDHCO2.0.CO;2","article-title":"Mammalian HSP40\/DNAJ homologs: cloning of novel cDNAs and a proposal for their classification and nomenclature.","volume":"5","author":"Ohtsuka","year":"2000","journal-title":"Cell Stress Chaperones"},{"key":"B209","doi-asserted-by":"publisher","first-page":"432","DOI":"10.1038\/pr.2012.92","article-title":"New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies.","volume":"72","author":"Ojala","year":"2012","journal-title":"Pediatr. Res."},{"key":"B210","doi-asserted-by":"publisher","first-page":"1457","DOI":"10.1086\/302095","article-title":"X chromosome inactivation in carriers of Barth syndrome.","volume":"63","author":"Orstavik","year":"1998","journal-title":"Am. J. Hum. Genet."},{"key":"B211","doi-asserted-by":"publisher","first-page":"583","DOI":"10.1083\/jcb.200810189","article-title":"The genetic interactome of prohibitins: coordinated control of cardiolipin and phosphatidylethanolamine by conserved regulators in mitochondria.","volume":"184","author":"Osman","year":"2009a","journal-title":"J. Cell Biol."},{"key":"B212","doi-asserted-by":"publisher","first-page":"3823","DOI":"10.1242\/jcs.037655","article-title":"Prohibitins and the functional compartmentalization of mitochondrial membranes.","volume":"122","author":"Osman","year":"2009b","journal-title":"J. Cell Sci."},{"key":"B213","doi-asserted-by":"publisher","first-page":"1976","DOI":"10.1038\/emboj.2010.98","article-title":"A mitochondrial phosphatase required for cardiolipin biosynthesis: the PGP phosphatase Gep4.","volume":"29","author":"Osman","year":"2010","journal-title":"EMBO J."},{"key":"B214","doi-asserted-by":"publisher","first-page":"7","DOI":"10.1083\/jcb.201006159","article-title":"Making heads or tails of phospholipids in mitochondria.","volume":"192","author":"Osman","year":"2011","journal-title":"J. Cell Biol."},{"key":"B215","doi-asserted-by":"publisher","first-page":"112","DOI":"10.1016\/j.cell.2008.06.016","article-title":"A mitochondrial protein compendium elucidates complex I disease biology.","volume":"134","author":"Pagliarini","year":"2008","journal-title":"Cell"},{"key":"B216","doi-asserted-by":"publisher","first-page":"851","DOI":"10.1016\/j.devcel.2007.03.022","article-title":"Zucchini and squash encode two putative nucleases required for rasiRNA production in the Drosophila germline.","volume":"12","author":"Pane","year":"2007","journal-title":"Dev. Cell"},{"key":"B217","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1016\/S0021-9258(18)72683-5","article-title":"Isolation and purification of a serologically active phospholipid from beef heart.","volume":"143","author":"Pangborn","year":"1942","journal-title":"J. Biol. Chem."},{"key":"B218","doi-asserted-by":"publisher","first-page":"643","DOI":"10.1016\/j.ceca.2009.03.012","article-title":"Role of cardiolipin peroxidation and Ca2+ in mitochondrial dysfunction and disease.","volume":"45","author":"Paradies","year":"2009","journal-title":"Cell Calcium"},{"key":"B219","doi-asserted-by":"publisher","first-page":"1335","DOI":"10.2174\/156802608786141124","article-title":"Protein synthesis and assembly in mitochondrial disorders.","volume":"8","author":"Perez-Martinez","year":"2008","journal-title":"Curr. Top. Med. Chem."},{"key":"B220","doi-asserted-by":"publisher","first-page":"1083","DOI":"10.1083\/jcb.201401006","article-title":"Uniform nomenclature for the mitochondrial contact site and cristae organizing system.","volume":"204","author":"Pfanner","year":"2014","journal-title":"J. Cell Biol."},{"key":"B221","doi-asserted-by":"publisher","first-page":"52873","DOI":"10.1074\/jbc.M308366200","article-title":"Cardiolipin stabilizes respiratory chain supercomplexes.","volume":"278","author":"Pfeiffer","year":"2003","journal-title":"J. Biol. Chem."},{"issue":"e000455","key":"B222","doi-asserted-by":"publisher","DOI":"10.1161\/JAHA.111.000455","article-title":"Tafazzin knockdown in mice leads to a developmental cardiomyopathy with early diastolic dysfunction preceding myocardial noncompaction.","volume":"1","author":"Phoon","year":"2012","journal-title":"J. Am. Heart Assoc."},{"key":"B223","doi-asserted-by":"publisher","first-page":"513","DOI":"10.1203\/00006450-199603000-00021","article-title":"Familial cardiomyopathy with cataracts and lactic acidosis: a defect in complex I (NADH-dehydrogenase) of the mitochondria respiratory chain.","volume":"39","author":"Pitkanen","year":"1996","journal-title":"Pediatr. Res."},{"key":"B224","doi-asserted-by":"crossref","first-page":"4596","DOI":"10.1016\/S0021-9258(17)33243-X","article-title":"Studies on the subcellular localization and properties of bis(monoacylglyceryl)phosphate biosynthesis in rat liver.","volume":"251","author":"Poorthuis","year":"1976","journal-title":"J. Biol. Chem."},{"key":"B225","doi-asserted-by":"publisher","first-page":"287","DOI":"10.1016\/j.cmet.2013.07.008","article-title":"TRIAP1\/PRELI complexes prevent apoptosis by mediating intramitochondrial transport of phosphatidic acid.","volume":"18","author":"Potting","year":"2013","journal-title":"Cell Metab."},{"key":"B226","doi-asserted-by":"publisher","first-page":"2888","DOI":"10.1038\/emboj.2010.169","article-title":"Regulation of mitochondrial phospholipids by Ups1\/PRELI-like proteins depends on proteolysis and Mdm35.","volume":"29","author":"Potting","year":"2010","journal-title":"EMBO J."},{"issue":"74","key":"B227","doi-asserted-by":"publisher","DOI":"10.3389\/fphys.2013.00074","article-title":"Diminished exercise capacity and mitochondrial bc1 complex deficiency in Tafazzin-knockdown mice.","volume":"4","author":"Powers","year":"2013","journal-title":"Front. Physiol."},{"key":"B228","doi-asserted-by":"publisher","first-page":"451","DOI":"10.1194\/jlr.M007575","article-title":"Enzymatic activities of the human AGPAT isoform 3 and isoform 5: localization of AGPAT5 to mitochondria.","volume":"52","author":"Prasad","year":"2011","journal-title":"J. Lipid Res."},{"key":"B229","doi-asserted-by":"publisher","first-page":"S109","DOI":"10.1194\/jlr.R800052-JLR200","article-title":"Lipin proteins and metabolic homeostasis.","author":"Reue","year":"2009","journal-title":"J. Lipid Res."},{"key":"B230","doi-asserted-by":"publisher","first-page":"1328","DOI":"10.1126\/science.1230593","article-title":"Proteomic mapping of mitochondria in living cells via spatially restricted enzymatic tagging.","volume":"339","author":"Rhee","year":"2013","journal-title":"Science"},{"key":"B231","doi-asserted-by":"publisher","first-page":"158","DOI":"10.1016\/j.cmet.2014.04.016","article-title":"DNAJC19, a mitochondrial cochaperone associated with cardiomyopathy, forms a complex with prohibitins to regulate cardiolipin remodeling.","volume":"20","author":"Richter-Dennerlein","year":"2014","journal-title":"Cell Metab."},{"key":"B232","doi-asserted-by":"publisher","first-page":"428","DOI":"10.1016\/j.ymgme.2012.09.013","article-title":"Intrafamilial variability for novel TAZ gene mutation: Barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle.","volume":"107","author":"Ronvelia","year":"2012","journal-title":"Mol. Genet. Metab."},{"key":"B233","doi-asserted-by":"publisher","first-page":"79","DOI":"10.1002\/ar.1091900108","article-title":"Ultrastructural characterization of nuage in spermatocytes of the rat testis.","volume":"190","author":"Russell","year":"1978","journal-title":"Anat. Rec."},{"key":"B234","doi-asserted-by":"publisher","first-page":"2204","DOI":"10.1002\/ajmg.a.36059","article-title":"Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations in SERAC1.","volume":"161","author":"Sarig","year":"2013","journal-title":"Am. J. Med. Genet. A"},{"key":"B235","doi-asserted-by":"publisher","first-page":"4389","DOI":"10.1016\/j.febslet.2010.09.047","article-title":"Golgi-localized KIAA0725p regulates membrane trafficking from the Golgi apparatus to the plasma membrane in mammalian cells.","volume":"584","author":"Sato","year":"2010","journal-title":"FEBS Lett."},{"key":"B236","doi-asserted-by":"publisher","first-page":"35","DOI":"10.1002\/ana.21217","article-title":"Prevalence of mitochondrial DNA disease in adults.","volume":"63","author":"Schaefer","year":"2008","journal-title":"Ann. Neurol."},{"key":"B237","doi-asserted-by":"publisher","first-page":"1777","DOI":"10.1093\/emboj\/19.8.1777","article-title":"Supercomplexes in the respiratory chains of yeast and mammalian mitochondria.","volume":"19","author":"Schagger","year":"2000","journal-title":"EMBO J."},{"key":"B238","doi-asserted-by":"publisher","first-page":"862","DOI":"10.1038\/nchembio.1064","article-title":"The physical state of lipid substrates provides transacylation specificity for tafazzin.","volume":"8","author":"Schlame","year":"2012a","journal-title":"Nat. Chem. Biol."},{"key":"B239","doi-asserted-by":"publisher","first-page":"512","DOI":"10.1016\/j.chemphyslip.2012.03.001","article-title":"Comparison of cardiolipins from Drosophila strains with mutations in putative remodeling enzymes.","volume":"165","author":"Schlame","year":"2012b","journal-title":"Chem. Phys. Lipids"},{"key":"B240","doi-asserted-by":"publisher","first-page":"727","DOI":"10.1111\/j.1432-1033.1993.tb17711.x","article-title":"Mitochondrial cardiolipin in diverse eukaryotes. Comparison of biosynthetic reactions and molecular acyl species.","volume":"212","author":"Schlame","year":"1993","journal-title":"Eur. J. Biochem."},{"key":"B241","doi-asserted-by":"crossref","first-page":"74","DOI":"10.1016\/S0021-9258(18)54116-8","article-title":"Cardiolipin is synthesized on the matrix side of the inner membrane in rat liver mitochondria.","volume":"268","author":"Schlame","year":"1993","journal-title":"J. Biol. Chem."},{"key":"B242","doi-asserted-by":"publisher","first-page":"1994","DOI":"10.1016\/j.jacc.2003.06.015","article-title":"Phospholipid abnormalities in children with Barth syndrome.","volume":"42","author":"Schlame","year":"2003","journal-title":"J. Am. Coll. Cardiol."},{"key":"B243","doi-asserted-by":"publisher","first-page":"290","DOI":"10.1016\/0003-2697(91)90332-N","article-title":"Analysis of cardiolipin molecular species by high-performance liquid chromatography of its derivative 1,3-bisphosphatidyl-2-benzoyl-sn-glycerol dimethyl ester.","volume":"195","author":"Schlame","year":"1991","journal-title":"Anal. Biochem."},{"key":"B244","doi-asserted-by":"publisher","first-page":"38","DOI":"10.1016\/j.chemphyslip.2005.08.002","article-title":"Molecular symmetry in mitochondrial cardiolipins.","volume":"138","author":"Schlame","year":"2005","journal-title":"Chem. Phys. Lipids"},{"key":"B245","doi-asserted-by":"publisher","first-page":"257","DOI":"10.1016\/S0163-7827(00)00005-9","article-title":"The biosynthesis and functional role of cardiolipin.","volume":"39","author":"Schlame","year":"2000","journal-title":"Prog. Lipid Res."},{"key":"B246","doi-asserted-by":"crossref","first-page":"589","DOI":"10.1042\/bj2720589","article-title":"Lysocardiolipin formation and reacylation in isolated rat liver mitochondria.","volume":"272","author":"Schlame","year":"1990","journal-title":"Biochem. J."},{"key":"B247","doi-asserted-by":"publisher","first-page":"111","DOI":"10.1074\/jbc.M112.408633","article-title":"Dual function of mitochondrial Nm23-H4 protein in phosphotransfer and intermembrane lipid transfer: a cardiolipin-dependent switch.","volume":"288","author":"Schlattner","year":"2013","journal-title":"J. Biol. Chem."},{"key":"B248","doi-asserted-by":"publisher","first-page":"32","DOI":"10.1016\/j.chemphyslip.2013.12.008","article-title":"Mitochondrial cardiolipin\/phospholipid trafficking: the role of membrane contact site complexes and lipid transfer proteins.","volume":"179","author":"Schlattner","year":"2014","journal-title":"Chem. Phys. Lipids"},{"key":"B249","doi-asserted-by":"publisher","first-page":"661","DOI":"10.1016\/j.bbrc.2010.05.149","article-title":"Membrane topology of human AGPAT3 (LPAAT3).","volume":"397","author":"Schmidt","year":"2010","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"B250","doi-asserted-by":"publisher","first-page":"768","DOI":"10.1038\/371768a0","article-title":"Mitochondrial Hsp70\/MIM44 complex facilitates protein import.","volume":"371","author":"Schneider","year":"1994","journal-title":"Nature"},{"key":"B251","doi-asserted-by":"publisher","first-page":"1348","DOI":"10.1093\/hmg\/dds541","article-title":"Methylation-controlled J-protein MCJ acts in the import of proteins into human mitochondria.","volume":"22","author":"Schusdziarra","year":"2013","journal-title":"Hum. Mol. Genet."},{"key":"B252","doi-asserted-by":"publisher","first-page":"1073","DOI":"10.1016\/j.ajhg.2012.10.017","article-title":"Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia.","volume":"91","author":"Schuurs-Hoeijmakers","year":"2012","journal-title":"Am. J. Hum. Genet."},{"key":"B253","doi-asserted-by":"publisher","first-page":"1588","DOI":"10.1016\/j.bbabio.2012.04.015","article-title":"The stability and activity of respiratory Complex II is cardiolipin-dependent.","volume":"1817","author":"Schwall","year":"2012","journal-title":"Biochim. Biophys. Acta"},{"key":"B254","doi-asserted-by":"publisher","first-page":"873","DOI":"10.1016\/S0022-3476(75)80217-4","article-title":"Congenital cataract and mitochondrial myopathy of skeletal and heart muscle associated with lactic acidosis after exercise.","volume":"86","author":"Sengers","year":"1975","journal-title":"J. Pediatr."},{"key":"B255","doi-asserted-by":"publisher","first-page":"789","DOI":"10.1074\/jbc.271.2.789","article-title":"The CDS1 gene encoding CDP-diacylglycerol synthase in Saccharomyces cerevisiae is essential for cell growth.","volume":"271","author":"Shen","year":"1996","journal-title":"J. Biol. Chem."},{"key":"B256","doi-asserted-by":"publisher","first-page":"1713","DOI":"10.1038\/sj.emboj.7601618","article-title":"Structures and physiological roles of 13 integral lipids of bovine heart cytochrome c oxidase.","volume":"26","author":"Shinzawa-Itoh","year":"2007","journal-title":"EMBO J."},{"key":"B257","doi-asserted-by":"crossref","first-page":"10047","DOI":"10.1016\/S0021-9258(18)99184-2","article-title":"Mitochondrial membrane contact sites of yeast. Characterization of lipid components and possible involvement in intramitochondrial translocation of phospholipids.","volume":"266","author":"Simbeni","year":"1991","journal-title":"J. Biol. Chem."},{"key":"B258","doi-asserted-by":"publisher","first-page":"607","DOI":"10.1007\/BF02531048","article-title":"Species variations in phospholipid class distribution of organs. II. Heart and skeletal muscle.","volume":"4","author":"Simon","year":"1969","journal-title":"Lipids"},{"key":"B259","doi-asserted-by":"publisher","first-page":"841","DOI":"10.1073\/pnas.92.3.841","article-title":"The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy.","volume":"92","author":"Sims","year":"1995","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B260","doi-asserted-by":"publisher","first-page":"1248","DOI":"10.1093\/hmg\/ddq002","article-title":"Role of magmas in protein transport and human mitochondria biogenesis.","volume":"19","author":"Sinha","year":"2010","journal-title":"Hum. Mol. Genet."},{"key":"B261","doi-asserted-by":"publisher","first-page":"1757","DOI":"10.1128\/MCB.01527-13","article-title":"Unraveling the intricate organization of mammalian mitochondrial presequence translocases: existence of multiple translocases for maintenance of mitochondrial function.","volume":"34","author":"Sinha","year":"2014","journal-title":"Mol. Cell. Biol."},{"key":"B262","doi-asserted-by":"publisher","first-page":"40","DOI":"10.1016\/j.ymgme.2012.11.282","article-title":"Mitochondrial citrate synthase crystals: novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations.","volume":"108","author":"Siriwardena","year":"2013","journal-title":"Mol. Genet. Metab."},{"key":"B263","doi-asserted-by":"publisher","first-page":"656","DOI":"10.1007\/BF00441527","article-title":"Fatal neonatal cardiomyopathy associated with cataract and mitochondrial myopathy.","volume":"148","author":"Smeitink","year":"1989","journal-title":"Eur. J. Pediatr."},{"key":"B264","doi-asserted-by":"publisher","first-page":"865","DOI":"10.1089\/hum.2010.199","article-title":"Characterization of a transgenic short hairpin RNA-induced murine model of Tafazzin deficiency.","volume":"22","author":"Soustek","year":"2011","journal-title":"Hum. Gene Ther."},{"key":"B265","doi-asserted-by":"publisher","first-page":"290","DOI":"10.1097\/FJC.0b013e31819b5461","article-title":"Cardiolipin remodeling in the heart.","volume":"53","author":"Sparagna","year":"2009","journal-title":"J. Cardiovasc. Pharmacol."},{"key":"B266","doi-asserted-by":"publisher","first-page":"215","DOI":"10.1017\/S1047951107000042","article-title":"Cardiac features of a novel autosomal recessive dilated cardiomyopathic syndrome due to defective importation of mitochondrial protein.","volume":"17","author":"Sparkes","year":"2007","journal-title":"Cardiol. Young"},{"key":"B267","doi-asserted-by":"publisher","first-page":"227","DOI":"10.1016\/0005-2736(88)90397-5","article-title":"Lipid topology and physical properties of the outer mitochondrial membrane of the yeast, Saccharomyces cerevisiae.","volume":"946","author":"Sperka-Gottlieb","year":"1988","journal-title":"Biochim. Biophys. Acta"},{"key":"B268","doi-asserted-by":"publisher","first-page":"1719","DOI":"10.1126\/science.1220270","article-title":"Leucine-tRNA initiates at CUG start codons for protein synthesis and presentation by MHC class I.","volume":"336","author":"Starck","year":"2012","journal-title":"Science"},{"key":"B269","doi-asserted-by":"publisher","first-page":"2623","DOI":"10.1194\/jlr.M036285","article-title":"Dietary macronutrients modulate the fatty acyl composition of rat liver mitochondrial cardiolipins.","volume":"54","author":"Stavrovskaya","year":"2013","journal-title":"J. Lipid Res."},{"key":"B270","doi-asserted-by":"publisher","first-page":"970","DOI":"10.1002\/pd.2599","article-title":"Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth.","volume":"30","author":"Steward","year":"2010","journal-title":"Prenat. Diagn."},{"key":"B271","doi-asserted-by":"publisher","first-page":"1154","DOI":"10.1038\/emboj.2008.35","article-title":"Dimer ribbons of ATP synthase shape the inner mitochondrial membrane.","volume":"27","author":"Strauss","year":"2008","journal-title":"EMBO J."},{"key":"B272","doi-asserted-by":"publisher","first-page":"709","DOI":"10.1016\/j.cmet.2013.03.018","article-title":"Tam41 is a CDP-diacylglycerol synthase required for cardiolipin biosynthesis in mitochondria.","volume":"17","author":"Tamura","year":"2013","journal-title":"Cell Metab."},{"key":"B273","doi-asserted-by":"publisher","first-page":"631","DOI":"10.1083\/jcb.200603087","article-title":"Identification of Tam41 maintaining integrity of the TIM23 protein translocator complex in mitochondria.","volume":"174","author":"Tamura","year":"2006","journal-title":"J. Cell Biol."},{"key":"B274","doi-asserted-by":"publisher","first-page":"2875","DOI":"10.1038\/emboj.2010.149","article-title":"Mdm35p imports Ups proteins into the mitochondrial intermembrane space by functional complex formation.","volume":"29","author":"Tamura","year":"2010","journal-title":"EMBO J."},{"key":"B275","doi-asserted-by":"publisher","first-page":"15205","DOI":"10.1074\/jbc.M111.338665","article-title":"Role for two conserved intermembrane space proteins, Ups1p and Ups2p, [corrected] in intra-mitochondrial phospholipid trafficking.","volume":"287","author":"Tamura","year":"2012","journal-title":"J. Biol. Chem."},{"key":"B276","doi-asserted-by":"publisher","first-page":"248","DOI":"10.1091\/mbc.E04-09-0807","article-title":"Formation of membrane-bound ring complexes by prohibitins in mitochondria.","volume":"16","author":"Tatsuta","year":"2005","journal-title":"Mol. Biol. Cell"},{"key":"B277","doi-asserted-by":"publisher","first-page":"281","DOI":"10.1038\/nbt793","article-title":"Characterization of the human heart mitochondrial proteome.","volume":"21","author":"Taylor","year":"2003","journal-title":"Nat. Biotechnol."},{"key":"B278","doi-asserted-by":"publisher","first-page":"12716","DOI":"10.1074\/jbc.M210329200","article-title":"Purification and characterization of monolysocardiolipin acyltransferase from pig liver mitochondria.","volume":"278","author":"Taylor","year":"2003","journal-title":"J. Biol. Chem."},{"key":"B279","doi-asserted-by":"publisher","first-page":"30360","DOI":"10.1074\/jbc.M109.048322","article-title":"Identification of the human mitochondrial linoleoyl-coenzyme A monolysocardiolipin acyltransferase (MLCL AT-1).","volume":"284","author":"Taylor","year":"2009","journal-title":"J. Biol. Chem."},{"issue":"e48628","key":"B280","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0048628","article-title":"Human trifunctional protein alpha links cardiolipin remodeling to beta-oxidation.","volume":"7","author":"Taylor","year":"2012","journal-title":"PLoS ONE"},{"key":"B281","doi-asserted-by":"publisher","first-page":"1051","DOI":"10.1016\/j.ajhg.2012.11.001","article-title":"Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.","volume":"91","author":"Tesson","year":"2012","journal-title":"Am. J. Hum. Genet."},{"key":"B282","doi-asserted-by":"publisher","first-page":"26198","DOI":"10.1074\/jbc.M803132200","article-title":"The nucleoside diphosphate kinase D (NM23-H4) binds the inner mitochondrial membrane with high affinity to cardiolipin and couples nucleotide transfer with respiration.","volume":"283","author":"Tokarska-Schlattner","year":"2008","journal-title":"J. Biol. Chem."},{"key":"B283","doi-asserted-by":"publisher","first-page":"11447","DOI":"10.1074\/jbc.274.17.11447","article-title":"Mammalian diacylglycerol kinases, a family of lipid kinases with signaling functions.","volume":"274","author":"Topham","year":"1999","journal-title":"J. Biol. Chem."},{"key":"B284","doi-asserted-by":"publisher","first-page":"73","DOI":"10.1016\/j.ymgme.2013.04.021","article-title":"Exome sequencing identifies a new mutation in SERAC1 in a patient with 3-methylglutaconic aciduria.","volume":"110","author":"Tort","year":"2013","journal-title":"Mol. Genet. Metab."},{"key":"B285","doi-asserted-by":"publisher","first-page":"707","DOI":"10.1083\/jcb.200308004","article-title":"A J-protein is an essential subunit of the presequence translocase-associated protein import motor of mitochondria.","volume":"163","author":"Truscott","year":"2003","journal-title":"J. Cell Biol."},{"key":"B286","doi-asserted-by":"publisher","first-page":"433","DOI":"10.1038\/sj.emboj.7601963","article-title":"Fission and selective fusion govern mitochondrial segregation and elimination by autophagy.","volume":"27","author":"Twig","year":"2008","journal-title":"EMBO J."},{"key":"B287","doi-asserted-by":"crossref","first-page":"1034","DOI":"10.1016\/S0021-9258(18)48391-3","article-title":"Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. II. Purification and properties of enoyl-coenzyme A (CoA) hydratase\/3-hydroxyacyl-CoA dehydrogenase\/3-ketoacyl-CoA thiolase trifunctional protein.","volume":"267","author":"Uchida","year":"1992","journal-title":"J. Biol. Chem."},{"key":"B288","doi-asserted-by":"publisher","first-page":"85","DOI":"10.1007\/978-90-481-2813-6_7","article-title":"Mitochondrial disorders due to nuclear OXPHOS gene defects.","volume":"652","author":"Ugalde","year":"2009","journal-title":"Adv. Exp. Med. Biol."},{"key":"B289","first-page":"979","article-title":"Molecular characterization of mitochondrial trifunctional protein deficiency: formation of the enzyme complex is important for stabilization of both alpha- and beta-subunits.","volume":"58","author":"Ushikubo","year":"1996","journal-title":"Am. J. Hum. Genet."},{"key":"B290","doi-asserted-by":"publisher","first-page":"1182","DOI":"10.1194\/jlr.M500056-JLR200","article-title":"Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosis.","volume":"46","author":"Valianpour","year":"2005","journal-title":"J. Lipid Res."},{"key":"B291","doi-asserted-by":"publisher","first-page":"729","DOI":"10.1067\/mpd.2002.129174","article-title":"Cardiolipin deficiency in X-linked cardioskeletal myopathy and neutropenia (Barth syndrome, MIM 302060): a study in cultured skin fibroblasts.","volume":"141","author":"Valianpour","year":"2002","journal-title":"J. Pediatr."},{"key":"B292","doi-asserted-by":"publisher","first-page":"103","DOI":"10.1042\/BJ20060373","article-title":"Phospholipid scramblase-3 regulates cardiolipin de novo biosynthesis and its resynthesis in growing HeLa cells.","volume":"401","author":"Van","year":"2007","journal-title":"Biochem. J."},{"key":"B293","doi-asserted-by":"crossref","first-page":"7248","DOI":"10.1016\/S0021-9258(19)39106-9","article-title":"Phospholipid synthesis in a membrane fraction associated with mitochondria.","volume":"265","author":"Vance","year":"1990","journal-title":"J. Biol. Chem."},{"key":"B294","doi-asserted-by":"publisher","first-page":"185","DOI":"10.1016\/j.tcb.2012.01.004","article-title":"Role of MINOS in mitochondrial membrane architecture and biogenesis.","volume":"22","author":"van der Laan","year":"2012","journal-title":"Trends Cell Biol."},{"key":"B295","doi-asserted-by":"publisher","first-page":"1152","DOI":"10.1038\/ncb1635","article-title":"Motor-free mitochondrial presequence translocase drives membrane integration of preproteins.","volume":"9","author":"van der Laan","year":"2007","journal-title":"Nat. Cell Biol."},{"key":"B296","doi-asserted-by":"publisher","first-page":"255","DOI":"10.1007\/BF01956157","article-title":"A retrospective study of patients with the hereditary syndrome of congenital cataract, mitochondrial myopathy of heart and skeletal muscle and lactic acidosis.","volume":"152","author":"van Ekeren","year":"1993","journal-title":"Eur. J. Pediatr."},{"key":"B297","doi-asserted-by":"publisher","first-page":"2346","DOI":"10.1194\/jlr.D600024-JLR200","article-title":"Monolysocardiolipin in cultured fibroblasts is a sensitive and specific marker for Barth syndrome.","volume":"47","author":"van Werkhoven","year":"2006","journal-title":"J. Lipid Res."},{"key":"B298","doi-asserted-by":"publisher","first-page":"267","DOI":"10.1016\/S1074-7613(00)80609-3","article-title":"Targeted disruption of the mouse Caspase 8 gene ablates cell death induction by the TNF receptors, Fas\/Apo1, and DR3 and is lethal prenatally.","volume":"9","author":"Varfolomeev","year":"1998","journal-title":"Immunity"},{"key":"B299","doi-asserted-by":"publisher","first-page":"43089","DOI":"10.1074\/jbc.M305956200","article-title":"Only one splice variant of the human TAZ gene encodes a functional protein with a role in cardiolipin metabolism.","volume":"278","author":"Vaz","year":"2003","journal-title":"J. Biol. Chem."},{"key":"B300","first-page":"45","article-title":"Non-bilayer structures in membrane fusion.","volume":"103","author":"Verkleij","year":"1984","journal-title":"Ciba Found. Symp."},{"key":"B301","doi-asserted-by":"publisher","first-page":"1056","DOI":"10.1016\/j.jhep.2014.06.038","article-title":"Individual exome analysis in diagnosis and management of paediatric liver failure of indeterminate aetiology.","volume":"61","author":"Vilarinho","year":"2014","journal-title":"J. Hepatol."},{"key":"B302","doi-asserted-by":"publisher","first-page":"237","DOI":"10.1083\/jcb.200605138","article-title":"Dynamic subcompartmentalization of the mitochondrial inner membrane.","volume":"175","author":"Vogel","year":"2006","journal-title":"J. Cell Biol."},{"key":"B303","doi-asserted-by":"publisher","first-page":"694","DOI":"10.1016\/j.devcel.2011.08.026","article-title":"Dual role of mitofilin in mitochondrial membrane organization and protein biogenesis.","volume":"21","author":"von der Malsburg","year":"2011","journal-title":"Dev. Cell"},{"key":"B304","doi-asserted-by":"publisher","first-page":"378","DOI":"10.1006\/bbrc.2000.3952","article-title":"Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome.","volume":"279","author":"Vreken","year":"2000","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"B305","doi-asserted-by":"publisher","first-page":"38228","DOI":"10.1074\/jbc.M405932200","article-title":"MuLK, a eukaryotic multi-substrate lipid kinase.","volume":"279","author":"Waggoner","year":"2004","journal-title":"J. Biol. Chem."},{"key":"B306","doi-asserted-by":"publisher","first-page":"1427","DOI":"10.1126\/science.3201231","article-title":"Mitochondrial DNA mutation associated with Leber\u00e2\u20ac\u2122s hereditary optic neuropathy.","volume":"242","author":"Wallace","year":"1988","journal-title":"Science"},{"key":"B307","doi-asserted-by":"publisher","first-page":"616","DOI":"10.1038\/nm.3545","article-title":"Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies.","volume":"20","author":"Wang","year":"2014a","journal-title":"Nat. Med."},{"key":"B308","doi-asserted-by":"publisher","DOI":"10.1002\/hep.27420","article-title":"ALCAT1 controls mitochondrial etiology of fatty liver diseases, linking defective mitophagy to hepatosteatosis.","author":"Wang","year":"2014b","journal-title":"Hepatology"},{"key":"B309","doi-asserted-by":"publisher","first-page":"347","DOI":"10.1016\/j.abb.2007.06.033","article-title":"Cloning and functional characterization of a novel mitochondrial N-ethylmaleimide-sensitive glycerol-3-phosphate acyltransferase (GPAT2).","volume":"465","author":"Wang","year":"2007","journal-title":"Arch. Biochem. Biophys."},{"key":"B310","doi-asserted-by":"publisher","first-page":"364","DOI":"10.1016\/j.devcel.2011.01.005","article-title":"MITOPLD is a mitochondrial protein essential for nuage formation and piRNA biogenesis in the mouse germline.","volume":"20","author":"Watanabe","year":"2011","journal-title":"Dev. Cell"},{"key":"B311","doi-asserted-by":"crossref","first-page":"1583","DOI":"10.1016\/S0022-2275(20)32186-6","article-title":"Docosahexaenoic acid accumulates in cardiolipin and enhances HT-29 cell oxidant production.","volume":"39","author":"Watkins","year":"1998","journal-title":"J. Lipid Res."},{"issue":"e63683","key":"B312","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0063683","article-title":"APOOL is a cardiolipin-binding constituent of the Mitofilin\/MINOS protein complex determining cristae morphology in mammalian mitochondria.","volume":"8","author":"Weber","year":"2013","journal-title":"PLoS ONE"},{"key":"B313","doi-asserted-by":"publisher","DOI":"10.1111\/nan.12190","article-title":"Tubular aggregates caused by serine active site containing 1 (SERAC1) mutations in a patient with a mitochondrial encephalopathy.","author":"Wedatilake","year":"2014","journal-title":"Neuropathol. Appl. Neurobiol."},{"key":"B314","doi-asserted-by":"crossref","first-page":"691","DOI":"10.1089\/dna.1997.16.691","article-title":"Cloning and expression of two human lysophosphatidic acid acyltransferase cDNAs that enhance cytokine-induced signaling responses in cells.","volume":"16","author":"West","year":"1997","journal-title":"DNA Cell Biol."},{"key":"B315","doi-asserted-by":"crossref","first-page":"4114","DOI":"10.1016\/S0021-9258(19)45047-3","article-title":"Enrichment of bis-(monoacylglyceryl) phosphate in lysosomes from rat liver.","volume":"247","author":"Wherrett","year":"1972","journal-title":"J. Biol. Chem."},{"key":"B316","doi-asserted-by":"publisher","first-page":"483","DOI":"10.1093\/hmg\/dds447","article-title":"Seven functional classes of Barth syndrome mutation.","volume":"22","author":"Whited","year":"2013","journal-title":"Hum. Mol. Genet."},{"key":"B317","doi-asserted-by":"publisher","first-page":"45","DOI":"10.1016\/j.mito.2006.11.025","article-title":"Diagnostic challenges of mitochondrial DNA disorders.","volume":"7","author":"Wong","year":"2007","journal-title":"Mitochondrion"},{"key":"B318","doi-asserted-by":"publisher","first-page":"47","DOI":"10.1016\/j.ymgme.2006.01.013","article-title":"Association of 3-methylglutaconic aciduria with sensori-neural deafness, encephalopathy, and Leigh-like syndrome (MEGDEL association) in four patients with a disorder of the oxidative phosphorylation.","volume":"88","author":"Wortmann","year":"2006","journal-title":"Mol. Genet. Metab."},{"key":"B319","doi-asserted-by":"publisher","first-page":"797","DOI":"10.1038\/ng.2325","article-title":"Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness.","volume":"44","author":"Wortmann","year":"2012","journal-title":"Nat. Genet."},{"key":"B320","doi-asserted-by":"publisher","first-page":"399","DOI":"10.1016\/0009-8981(76)90353-3","article-title":"3-Hydroxy-3-methylglutaric aciduria, combined with 3-methylglutaconic aciduria.","volume":"70","author":"Wysocki","year":"1976","journal-title":"Clin. Chim. Acta"},{"key":"B321","doi-asserted-by":"publisher","first-page":"11860","DOI":"10.1073\/pnas.1109290108","article-title":"Structural and functional analysis of PTPMT1, a phosphatase required for cardiolipin synthesis.","volume":"108","author":"Xiao","year":"2011","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B322","doi-asserted-by":"publisher","first-page":"11584","DOI":"10.1073\/pnas.0603242103","article-title":"A Drosophila model of Barth syndrome.","volume":"103","author":"Xu","year":"2006a","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B323","doi-asserted-by":"publisher","first-page":"39217","DOI":"10.1074\/jbc.M606100200","article-title":"The enzymatic function of tafazzin.","volume":"281","author":"Xu","year":"2006b","journal-title":"J. Biol. Chem."},{"key":"B324","doi-asserted-by":"publisher","first-page":"823","DOI":"10.1038\/labinvest.3700274","article-title":"Characterization of lymphoblast mitochondria from patients with Barth syndrome.","volume":"85","author":"Xu","year":"2005","journal-title":"Lab. Invest."},{"key":"B325","doi-asserted-by":"publisher","first-page":"29230","DOI":"10.1074\/jbc.M109.016642","article-title":"Characterization of tafazzin splice variants from humans and fruit flies.","volume":"284","author":"Xu","year":"2009","journal-title":"J. Biol. Chem."},{"key":"B326","doi-asserted-by":"publisher","first-page":"519","DOI":"10.1016\/S0092-8674(02)01053-X","article-title":"Tim50 is a subunit of the TIM23 complex that links protein translocation across the outer and inner mitochondrial membranes.","volume":"111","author":"Yamamoto","year":"2002","journal-title":"Cell"},{"key":"B327","doi-asserted-by":"publisher","first-page":"3114","DOI":"10.1074\/jbc.M113.529487","article-title":"Deletion of the cardiolipin-specific phospholipase Cld1 rescues growth and life span defects in the tafazzin mutant: implications for Barth syndrome.","volume":"289","author":"Ye","year":"2014a","journal-title":"J. Biol. Chem."},{"key":"B328","doi-asserted-by":"publisher","first-page":"10654","DOI":"10.1073\/pnas.1403521111","article-title":"Extensive pathogenicity of mitochondrial heteroplasmy in healthy human individuals.","volume":"111","author":"Ye","year":"2014b","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"B329","doi-asserted-by":"publisher","first-page":"9486","DOI":"10.1021\/bi00087a029","article-title":"Expression and identification of p90 as the murine mitochondrial glycerol-3-phosphate acyltransferase.","volume":"32","author":"Yet","year":"1993","journal-title":"Biochemistry"},{"key":"B330","doi-asserted-by":"publisher","first-page":"3003","DOI":"10.1194\/jlr.M008060","article-title":"Mitochondrial dysfunction and reduced prostaglandin synthesis in skeletal muscle of Group VIB Ca2+-independent phospholipase A2gamma-deficient mice.","volume":"51","author":"Yoda","year":"2010","journal-title":"J. Lipid Res."},{"key":"B331","doi-asserted-by":"publisher","first-page":"1436","DOI":"10.1091\/mbc.E05-08\u00e2\u20ac\u201c0740","article-title":"Proteomic analysis of the yeast mitochondrial outer membrane reveals accumulation of a subclass of preproteins.","volume":"17","author":"Zahedi","year":"2006","journal-title":"Mol. Biol. Cell"},{"key":"B332","doi-asserted-by":"publisher","first-page":"366","DOI":"10.1016\/j.bbrc.2014.05.133","article-title":"Increasing levels of cardiolipin differentially influence packing of phospholipids found in the mitochondrial inner membrane.","volume":"450","author":"Zeczycki","year":"2014","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"B333","doi-asserted-by":"publisher","first-page":"690","DOI":"10.1016\/j.cmet.2011.04.007","article-title":"Mitochondrial phosphatase PTPMT1 is essential for cardiolipin biosynthesis.","volume":"13","author":"Zhang","year":"2011","journal-title":"Cell Metab."},{"key":"B334","doi-asserted-by":"publisher","first-page":"43553","DOI":"10.1074\/jbc.C200551200","article-title":"Gluing the respiratory chain together. Cardiolipin is required for supercomplex formation in the inner mitochondrial membrane.","volume":"277","author":"Zhang","year":"2002","journal-title":"J. Biol. Chem."},{"key":"B335","doi-asserted-by":"publisher","first-page":"945","DOI":"10.1194\/jlr.M800567-JLR200","article-title":"The microsomal cardiolipin remodeling enzyme acyl-CoA lysocardiolipin acyltransferase is an acyltransferase of multiple anionic lysophospholipids.","volume":"50","author":"Zhao","year":"2009","journal-title":"J. Lipid Res."},{"key":"B336","doi-asserted-by":"publisher","first-page":"2356","DOI":"10.1021\/bi972625o","article-title":"Identity of a conserved motif in phospholipid scramblase that is required for Ca2+-accelerated transbilayer movement of membrane phospholipids.","volume":"37","author":"Zhou","year":"1998","journal-title":"Biochemistry"},{"key":"B337","doi-asserted-by":"publisher","first-page":"493","DOI":"10.1002\/yea.320110602","article-title":"Isolation and biochemical characterization of organelles from the yeast, Saccharomyces cerevisiae.","volume":"11","author":"Zinser","year":"1995","journal-title":"Yeast"},{"key":"B338","doi-asserted-by":"crossref","first-page":"2026","DOI":"10.1128\/jb.173.6.2026-2034.1991","article-title":"Phospholipid synthesis and lipid composition of subcellular membranes in the unicellular eukaryote Saccharomyces cerevisiae.","volume":"173","author":"Zinser","year":"1991","journal-title":"J. Bacteriol."}],"container-title":["Frontiers in Genetics"],"original-title":[],"deposited":{"date-parts":[[2022,4,28]],"date-time":"2022-04-28T10:59:46Z","timestamp":1651143586000},"score":1,"resource":{"primary":{"URL":"http:\/\/journal.frontiersin.org\/Article\/10.3389\/fgene.2015.00003\/abstract"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,2,3]]},"references-count":338,"URL":"https:\/\/doi.org\/10.3389\/fgene.2015.00003","relation":{},"ISSN":["1664-8021"],"issn-type":[{"value":"1664-8021","type":"electronic"}],"subject":[],"published":{"date-parts":[[2015,2,3]]}}}