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Res."},{"issue":"1","key":"10.1016\/j.lfs.2024.122489_bb0345","doi-asserted-by":"crossref","DOI":"10.1038\/ncomms15098","article-title":"Lamin B1 is required for mature neuron-specific gene expression during olfactory sensory neuron differentiation","volume":"8","author":"Gigante","year":"2017","journal-title":"Nat. Commun."},{"issue":"5","key":"10.1016\/j.lfs.2024.122489_bb0350","doi-asserted-by":"crossref","first-page":"913","DOI":"10.1083\/jcb.147.5.913","article-title":"Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy","volume":"147","author":"Sullivan","year":"1999","journal-title":"J. Cell Biol."},{"issue":"8","key":"10.1016\/j.lfs.2024.122489_bb0355","doi-asserted-by":"crossref","first-page":"2115","DOI":"10.1172\/JCI28968","article-title":"A farnesyltransferase inhibitor improves disease phenotypes in mice with a Hutchinson-Gilford progeria syndrome mutation","volume":"116","author":"Yang","year":"2006","journal-title":"J. Clin. Invest."},{"issue":"2","key":"10.1016\/j.lfs.2024.122489_bb0360","doi-asserted-by":"crossref","first-page":"420","DOI":"10.1016\/j.bbrc.2003.12.109","article-title":"Differentiation of human adipose tissue stem cells using extracts of rat cardiomyocytes","volume":"314","author":"Gaustad","year":"2004","journal-title":"Biochem. Biophys. Res. Commun."},{"issue":"May","key":"10.1016\/j.lfs.2024.122489_bb0365","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1016\/j.semcdb.2014.03.021","article-title":"Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective","volume":"29","author":"Cau","year":"2014","journal-title":"Semin. Cell Dev. Biol."},{"issue":"5628","key":"10.1016\/j.lfs.2024.122489_bb0370","doi-asserted-by":"crossref","first-page":"2055","DOI":"10.1126\/science.1084125","article-title":"Lamin a truncation in Hutchinson-Gilford progeria","volume":"300","author":"De Sandre-Giovannoli","year":"2003","journal-title":"Science (New York, N.Y.)"},{"issue":"24","key":"10.1016\/j.lfs.2024.122489_bb0375","doi-asserted-by":"crossref","first-page":"8963","DOI":"10.1073\/pnas.0402943101","article-title":"Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome","volume":"101","author":"Goldman","year":"2004","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"issue":"4","key":"10.1016\/j.lfs.2024.122489_bb0380","doi-asserted-by":"crossref","first-page":"440","DOI":"10.1038\/nm1204","article-title":"Reversal of the cellular phenotype in the premature aging disease Hutchinson-Gilford progeria syndrome","volume":"11","author":"Scaffidi","year":"2005","journal-title":"Nat. Med."},{"issue":"5776","key":"10.1016\/j.lfs.2024.122489_bb0385","doi-asserted-by":"crossref","first-page":"1059","DOI":"10.1126\/science.1127168","article-title":"Lamin A-dependent nuclear defects in human aging","volume":"312","author":"Scaffidi","year":"2006","journal-title":"Science (New York, N.Y.)"},{"issue":"3","key":"10.1016\/j.lfs.2024.122489_bb0390","first-page":"H1451","article-title":"Age-related changes in lamin A\/C expression in cardiomyocytes","volume":"293","author":"Afilalo","year":"2007","journal-title":"Am. J. Phys. Heart Circ. 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Res."},{"key":"10.1016\/j.lfs.2024.122489_bb0410","doi-asserted-by":"crossref","first-page":"788","DOI":"10.3389\/fphys.2017.00788","article-title":"mTOR as a key regulator in maintaining skeletal muscle mass","volume":"8","author":"Yoon","year":"2017","journal-title":"Front. Physiol."},{"issue":"144","key":"10.1016\/j.lfs.2024.122489_bb0415","doi-asserted-by":"crossref","DOI":"10.1126\/scitranslmed.3003802","article-title":"Rapamycin reverses elevated mTORC1 signaling in lamin A\/C-deficient mice, rescues cardiac and skeletal muscle function, and extends survival","volume":"4","author":"Ramos","year":"2012","journal-title":"Sci. Transl. Med."},{"issue":"144","key":"10.1016\/j.lfs.2024.122489_bb0420","doi-asserted-by":"crossref","DOI":"10.1126\/scitranslmed.3003875","article-title":"Temsirolimus activates autophagy and ameliorates cardiomyopathy caused by lamin A\/C gene mutation","volume":"4","author":"Choi","year":"2012","journal-title":"Sci. Transl. Med."},{"issue":"48","key":"10.1016\/j.lfs.2024.122489_bb0425","doi-asserted-by":"crossref","first-page":"40513","DOI":"10.1074\/jbc.M112.404541","article-title":"Dual specificity phosphatase 4 mediates cardiomyopathy caused by lamin A\/C (LMNA) gene mutation","volume":"287","author":"Choi","year":"2012","journal-title":"J. Biol. Chem."},{"issue":"2","key":"10.1016\/j.lfs.2024.122489_bb0430","doi-asserted-by":"crossref","first-page":"176","DOI":"10.4161\/auto.5269","article-title":"Promoting basal levels of autophagy in the nervous system enhances longevity and oxidant resistance in adult Drosophila","volume":"4","author":"Simonsen","year":"2008","journal-title":"Autophagy"},{"issue":"11","key":"10.1016\/j.lfs.2024.122489_bb0435","doi-asserted-by":"crossref","first-page":"1305","DOI":"10.1038\/ncb1975","article-title":"Induction of autophagy by spermidine promotes longevity","volume":"11","author":"Eisenberg","year":"2009","journal-title":"Nat. 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Mutat."},{"issue":"12","key":"10.1016\/j.lfs.2024.122489_bb0480","doi-asserted-by":"crossref","first-page":"3002","DOI":"10.1002\/ajmg.a.34336","article-title":"Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A","volume":"0","author":"Hisama","year":"2011","journal-title":"Am. J. Med. Genet. A"},{"issue":"1","key":"10.1016\/j.lfs.2024.122489_bb0485","doi-asserted-by":"crossref","first-page":"66","DOI":"10.1002\/ajmg.a.30663","article-title":"Somatic and gonadal mosaicism in Hutchinson-Gilford progeria","volume":"135","author":"Wuyts","year":"2005","journal-title":"Am. J. Med. Genet. A"},{"issue":"4","key":"10.1016\/j.lfs.2024.122489_bb0490","doi-asserted-by":"crossref","first-page":"406","DOI":"10.1016\/j.mjafi.2013.01.001","article-title":"A rare case of acrogeria","volume":"69","author":"Sanghi","year":"2013","journal-title":"Med. J. Armed Forces India"},{"key":"10.1016\/j.lfs.2024.122489_bb0495","series-title":"GeneReviews\u00ae","article-title":"Berardinelli-Seip congenital lipodystrophy","author":"Van Maldergem","year":"1993"},{"key":"10.1016\/j.lfs.2024.122489_bb0500","series-title":"GeneReviews\u00ae","article-title":"Cockayne syndrome","author":"Laugel","year":"1993"},{"issue":"10","key":"10.1016\/j.lfs.2024.122489_bb0505","doi-asserted-by":"crossref","first-page":"2519","DOI":"10.1002\/ajmg.a.36128","article-title":"Redefining the progeroid form of Ehlers-Danlos syndrome: report of the fourth patient with B4GALT7 deficiency and review of the literature","volume":"161","author":"Guo","year":"2013","journal-title":"Am. J. Med. Genet. A"},{"issue":"12","key":"10.1016\/j.lfs.2024.122489_bb0510","doi-asserted-by":"crossref","first-page":"1410","DOI":"10.1038\/ng.252","article-title":"Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin","volume":"40","author":"Hennies","year":"2008","journal-title":"Nat. Genet."},{"issue":"4","key":"10.1016\/j.lfs.2024.122489_bb0515","first-page":"331","article-title":"Hallermann-Streiff syndrome: case report and literature review","volume":"42","author":"Robotta","year":"2011","journal-title":"Quintessence International (Berlin, Germany: 1985)"},{"issue":"March","key":"10.1016\/j.lfs.2024.122489_bb0520","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.arr.2017.12.001","article-title":"Mandibuloacral dysplasia: a premature ageing disease with aspects of physiological ageing","volume":"42","author":"Cenni","year":"2018","journal-title":"Ageing Res. 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Chem."},{"issue":"11","key":"10.1016\/j.lfs.2024.122489_bb0620","doi-asserted-by":"crossref","first-page":"848","DOI":"10.1038\/nrm950","article-title":"Lamins: building blocks or regulators of gene expression?","volume":"3","author":"Hutchison","year":"2002","journal-title":"Nat. Rev. Mol. Cell Biol."},{"issue":"7450","key":"10.1016\/j.lfs.2024.122489_bb0625","doi-asserted-by":"crossref","first-page":"507","DOI":"10.1038\/nature12105","article-title":"Lamin A\/C and emerin regulate MKL1-SRF activity by modulating actin dynamics","volume":"497","author":"Ho","year":"2013","journal-title":"Nature"},{"issue":"5","key":"10.1016\/j.lfs.2024.122489_bb0630","doi-asserted-by":"crossref","first-page":"1282","DOI":"10.1172\/JCI29042","article-title":"Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy","volume":"117","author":"Muchir","year":"2007","journal-title":"J. Clin. Invest."},{"issue":"47","key":"10.1016\/j.lfs.2024.122489_bb0635","doi-asserted-by":"crossref","first-page":"28092","DOI":"10.1074\/jbc.270.47.28092","article-title":"The mitogen-activated protein kinase kinase MEK1 stimulates a pattern of gene expression typical of the hypertrophic phenotype in rat ventricular cardiomyocytes (*)","volume":"270","author":"Gillespie-Brown","year":"1995","journal-title":"J. Biol. Chem."},{"issue":"15","key":"10.1016\/j.lfs.2024.122489_bb0640","doi-asserted-by":"crossref","first-page":"1884","DOI":"10.1093\/hmg\/ddm137","article-title":"Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery\u2013Dreifuss muscular dystrophy","volume":"16","author":"Muchir","year":"2007","journal-title":"Hum. Mol. Genet."},{"issue":"5","key":"10.1016\/j.lfs.2024.122489_bb0645","doi-asserted-by":"crossref","first-page":"353","DOI":"10.1038\/nrm2890","article-title":"Linking actin dynamics and gene transcription to drive cellular motile functions","volume":"11","author":"Olson","year":"2010","journal-title":"Nat. Rev. Mol. Cell Biol."},{"issue":"20","key":"10.1016\/j.lfs.2024.122489_bb0650","doi-asserted-by":"crossref","first-page":"3448","DOI":"10.1038\/emboj.2010.216","article-title":"An actin-regulated importin \u03b1\/\u03b2-dependent extended bipartite NLS directs nuclear import of MRTF-A","volume":"29","author":"Paw\u0142owski","year":"2010","journal-title":"EMBO J."},{"issue":"3","key":"10.1016\/j.lfs.2024.122489_bb0655","doi-asserted-by":"crossref","first-page":"370","DOI":"10.1172\/JCI200419670","article-title":"Lamin A\/C deficiency causes defective nuclear mechanics and mechanotransduction","volume":"113","author":"Lammerding","year":"2004","journal-title":"J. Clin. Invest."},{"issue":"12","key":"10.1016\/j.lfs.2024.122489_bb0660","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0015167","article-title":"LMNA E82K mutation activates FAS and mitochondrial pathways of apoptosis in heart tissue specific transgenic mice","volume":"5","author":"Lu","year":"2010","journal-title":"PloS One"},{"issue":"1","key":"10.1016\/j.lfs.2024.122489_bb0665","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1161\/CIRCIMAGING.110.960740","article-title":"Cardiac involvement in patients with muscular dystrophies: magnetic resonance imaging phenotype and genotypic considerations","volume":"4","author":"Verhaert","year":"2011","journal-title":"Circ. Cardiovasc. 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Med."},{"issue":"1","key":"10.1016\/j.lfs.2024.122489_bb0860","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1111\/j.1752-8062.2008.00017.x","article-title":"Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy","volume":"1","author":"Hershberger","year":"2008","journal-title":"Clin. Transl. Sci."},{"issue":"2","key":"10.1016\/j.lfs.2024.122489_bb0865","doi-asserted-by":"crossref","first-page":"93","DOI":"10.1053\/euhj.1998.1145","article-title":"Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy","volume":"20","author":"Mestroni","year":"1999","journal-title":"Eur. 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