{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,2]],"date-time":"2026-10-02T19:26:46Z","timestamp":1790969206386,"version":"4.1.0"},"reference-count":261,"publisher":"The Company of Biologists","issue":"1","license":[{"start":{"date-parts":[[2022,1,13]],"date-time":"2022-01-13T00:00:00Z","timestamp":1642032000000},"content-version":"vor","delay-in-days":12,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0"}],"funder":[{"DOI":"10.13039\/501100000268","name":"Biotechnology and Biological Sciences Research Council","doi-asserted-by":"crossref","award":["BB\/T001984\/1"],"award-info":[{"award-number":["BB\/T001984\/1"]}],"id":[{"id":"10.13039\/501100000268","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/501100000770","name":"University of Manchester","doi-asserted-by":"crossref","id":[{"id":"10.13039\/501100000770","id-type":"DOI","asserted-by":"crossref"}]},{"name":"Singapore A*Star Institute"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022,1,1]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>The biomechanical and biochemical properties of connective tissues are determined by the composition and quality of their extracellular matrix. This, in turn, is highly dependent on the function and organisation of the secretory pathway. The Golgi complex plays a vital role in directing matrix output by co-ordinating the post-translational modification and proteolytic processing of matrix components prior to their secretion. These modifications have broad impacts on the secretion and subsequent assembly of matrix components, as well as their function in the extracellular environment. In this Review, we highlight the role of the Golgi in the formation of an adaptable, healthy matrix, with a focus on proteoglycan and procollagen secretion as example cargoes. We then discuss the impact of Golgi dysfunction on connective tissue in the context of human disease and ageing.<\/jats:p>","DOI":"10.1242\/jcs.258879","type":"journal-article","created":{"date-parts":[[2022,1,13]],"date-time":"2022-01-13T05:52:38Z","timestamp":1642053158000},"source":"Crossref","is-referenced-by-count":32,"title":["Supply chain logistics \u2013 the role of the Golgi complex in extracellular matrix production and maintenance"],"prefix":"10.1242","volume":"135","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5533-273X","authenticated-orcid":false,"given":"John","family":"Hellicar","sequence":"first","affiliation":[{"name":"School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, The Michael Smith Building 1 , Oxford Road, Manchester, M13 9PT , UK"},{"name":"Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR) 2 , 61 Biopolis Drive, Proteos , Singapore, 138673"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8967-7277","authenticated-orcid":false,"given":"Nicola L.","family":"Stevenson","sequence":"additional","affiliation":[{"name":"School of Biochemistry, Faculty of Life Sciences, University Walk, University of Bristol 3 Cell Biology Laboratories , , Bristol, BS8 1TD , UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5297-3240","authenticated-orcid":false,"given":"David J.","family":"Stephens","sequence":"additional","affiliation":[{"name":"School of Biochemistry, Faculty of Life Sciences, University Walk, University of Bristol 3 Cell Biology Laboratories , , Bristol, BS8 1TD , UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9331-8143","authenticated-orcid":false,"given":"Martin","family":"Lowe","sequence":"additional","affiliation":[{"name":"School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, The Michael Smith Building 1 , Oxford Road, Manchester, M13 9PT , UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"237","published-online":{"date-parts":[[2022,1,13]]},"reference":[{"key":"2024061307214754500_JCS258879C1","doi-asserted-by":"publisher","first-page":"237","DOI":"10.1038\/79987","article-title":"Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene","volume":"26","author":"Akama","year":"2000","journal-title":"Nat. Genet."},{"key":"2024061307214754500_JCS258879C2","first-page":"238","article-title":"Anterior segment anomalies of the eye, clefting and skeletal abnormalities in two sibs of consanguineous parents: Michels syndrome or new syndrome?","volume":"3","author":"al Gazali","year":"1994","journal-title":"Clin. Dysmorphol."},{"key":"2024061307214754500_JCS258879C3","doi-asserted-by":"publisher","first-page":"1773","DOI":"10.1002\/ajmg.a.38244","article-title":"Endoplasmic reticulum retention of xylosyltransferase 1 (XYLT1) mutants underlying Desbuquois dysplasia type II","volume":"173","author":"Al-Jezawi","year":"2017","journal-title":"Am. J. Med. Genet. A"},{"key":"2024061307214754500_JCS258879C4","doi-asserted-by":"publisher","first-page":"jcs209890","DOI":"10.1242\/jcs.209890","article-title":"Formation of COPI-coated vesicles at a glance","volume":"131","author":"Arakel","year":"2018","journal-title":"J. Cell Sci."},{"key":"2024061307214754500_JCS258879C5","doi-asserted-by":"publisher","first-page":"3029","DOI":"10.1093\/hmg\/ddy213","article-title":"Integrating glycomics and genomics uncovers SLC10A7 as essential factor for bone mineralization by regulating post-Golgi protein transport and glycosylation","volume":"27","author":"Ashikov","year":"2018","journal-title":"Hum. Mol. Genet."},{"key":"2024061307214754500_JCS258879C6","doi-asserted-by":"publisher","first-page":"1125","DOI":"10.1002\/humu.21335","article-title":"Keratosis Follicularis Spinulosa Decalvans is caused by mutations in MBTPS2","volume":"31","author":"Aten","year":"2010","journal-title":"Hum. Mutat."},{"key":"2024061307214754500_JCS258879C7","doi-asserted-by":"publisher","first-page":"15","DOI":"10.1016\/j.ajhg.2011.05.021","article-title":"Faulty initiation of proteoglycan synthesis causes cardiac and joint defects","volume":"89","author":"Baasanjav","year":"2011","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C8","doi-asserted-by":"publisher","first-page":"2655","DOI":"10.1083\/jcb.105.6.2655","article-title":"Tyrosine sulfation is a trans-Golgi-specific protein modification","volume":"105","author":"Baeuerle","year":"1987","journal-title":"J. Cell Biol."},{"key":"2024061307214754500_JCS258879C9","doi-asserted-by":"publisher","first-page":"2415","DOI":"10.1002\/ajmg.a.38349","article-title":"MED resulting from recessively inherited mutations in the gene encoding calcium-activated nucleotidase CANT1","volume":"173","author":"Balasubramanian","year":"2017","journal-title":"Am. J. Med. Genet. A"},{"key":"2024061307214754500_JCS258879C10","doi-asserted-by":"publisher","first-page":"2701","DOI":"10.1016\/j.febslet.2009.07.032","article-title":"The COPI system: molecular mechanisms and function","volume":"583","author":"Beck","year":"2009","journal-title":"FEBS Lett."},{"key":"2024061307214754500_JCS258879C11","doi-asserted-by":"publisher","first-page":"46","DOI":"10.1016\/j.matbio.2015.04.001","article-title":"The procollagen N-proteinases ADAMTS2, 3 and 14 in pathophysiology","volume":"44-46","author":"Bekhouche","year":"2015","journal-title":"Matrix Biol."},{"key":"2024061307214754500_JCS258879C12","doi-asserted-by":"publisher","first-page":"1148","DOI":"10.1111\/cge.13236","article-title":"A B3GALT6 variant in patient originally described as Al-Gazali syndrome and implicating the endoplasmic reticulum quality control in the mechanism of some \u03b23GalT6-pathy mutations","volume":"93","author":"Ben-Mahmoud","year":"2018","journal-title":"Clin. Genet."},{"key":"2024061307214754500_JCS258879C13","doi-asserted-by":"publisher","first-page":"e82282","DOI":"10.1371\/journal.pone.0082282","article-title":"Oncogenic K-Ras and loss of Smad4 mediate invasion by activating an EGFR\/NF-\u03baB Axis that induces expression of MMP9 and uPA in human pancreas progenitor cells","volume":"8","author":"Bera","year":"2013","journal-title":"PLoS ONE"},{"key":"2024061307214754500_JCS258879C14","doi-asserted-by":"publisher","first-page":"2466","DOI":"10.1002\/1873-3468.13570","article-title":"Maintaining order: COG complex controls Golgi trafficking, processing, and sorting","volume":"593","author":"Blackburn","year":"2019","journal-title":"FEBS Lett."},{"key":"2024061307214754500_JCS258879C15","doi-asserted-by":"publisher","first-page":"993","DOI":"10.1016\/S0092-8674(00)81723-7","article-title":"Procollagen traverses the Golgi stack without leaving the lumen of cisternae: evidence for cisternal maturation","volume":"95","author":"Bonfanti","year":"1998","journal-title":"Cell"},{"key":"2024061307214754500_JCS258879C16","doi-asserted-by":"publisher","first-page":"249","DOI":"10.1007\/978-981-13-3681-2_10","article-title":"Skin Changes During Ageing","volume":"91","author":"Bont\u00e9","year":"2019","journal-title":"Subcell. Biochem."},{"key":"2024061307214754500_JCS258879C17","doi-asserted-by":"publisher","first-page":"298","DOI":"10.1007\/s002239900339","article-title":"Effects of bone CS-proteoglycans, DS-decorin, and DS-biglycan on hydroxyapatite formation in a gelatin gel","volume":"61","author":"Boskey","year":"1997","journal-title":"Calcif. Tissue Int."},{"key":"2024061307214754500_JCS258879C18","doi-asserted-by":"publisher","first-page":"382","DOI":"10.1038\/nrm3588","article-title":"Organization of the ER-Golgi interface for membrane traffic control","volume":"14","author":"Brandizzi","year":"2013","journal-title":"Nat. Rev. Mol. Cell Biol."},{"key":"2024061307214754500_JCS258879C19","doi-asserted-by":"publisher","first-page":"14219","DOI":"10.1073\/pnas.1305464110","article-title":"Metalloproteases meprin alpha and meprin beta are C- and N-procollagen proteinases important for collagen assembly and tensile strength","volume":"110","author":"Broder","year":"2013","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"2024061307214754500_JCS258879C20","doi-asserted-by":"publisher","first-page":"313","DOI":"10.1073\/pnas.76.1.313","article-title":"Procollagen segment-long-spacing crystallites: their role in collagen fibrillogenesis","volume":"76","author":"Bruns","year":"1979","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"2024061307214754500_JCS258879C21","doi-asserted-by":"publisher","first-page":"691","DOI":"10.1007\/s00439-015-1549-2","article-title":"Skeletal dysplasia in a consanguineous clan from the island of Nias\/Indonesia is caused by a novel mutation in B3GAT3","volume":"134","author":"Budde","year":"2015","journal-title":"Hum. Genet."},{"key":"2024061307214754500_JCS258879C22","doi-asserted-by":"publisher","first-page":"405","DOI":"10.1016\/j.ajhg.2014.01.020","article-title":"XYLT1 mutations in Desbuquois dysplasia type 2","volume":"94","author":"Bui","year":"2014","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C23","doi-asserted-by":"publisher","first-page":"5820","DOI":"10.1038\/s41467-020-19505-2","article-title":"The once and future gene therapy","volume":"11","author":"Bulaklak","year":"2020","journal-title":"Nat. Commun."},{"key":"2024061307214754500_JCS258879C24","doi-asserted-by":"publisher","first-page":"114","DOI":"10.1186\/s12967-021-02779-5","article-title":"MBTPS2, a membrane bound protease, underlying several distinct skin and bone disorders","volume":"19","author":"Caengprasath","year":"2021","journal-title":"J. Transl. Med."},{"key":"2024061307214754500_JCS258879C25","doi-asserted-by":"publisher","first-page":"22764","DOI":"10.1016\/S0021-9258(17)31711-8","article-title":"Differential effects of brefeldin A on chondroitin sulfate and hyaluronan synthesis in rat chondrosarcoma cells","volume":"269","author":"Calabro","year":"1994","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C26","doi-asserted-by":"publisher","first-page":"2070","DOI":"10.3390\/cells9092070","article-title":"Dynamic high-sensitivity quantitation of procollagen-i by endogenous CRISPR-Cas9 NanoLuciferase tagging","volume":"9","author":"Calverley","year":"2020","journal-title":"Cells"},{"key":"2024061307214754500_JCS258879C27","doi-asserted-by":"publisher","first-page":"685","DOI":"10.1146\/annurev-physiol-030212-183653","article-title":"Aging, cellular senescence, and cancer","volume":"75","author":"Campisi","year":"2013","journal-title":"Annu. Rev. Physiol."},{"key":"2024061307214754500_JCS258879C28","doi-asserted-by":"publisher","first-page":"1341","DOI":"10.1242\/jcs.01731","article-title":"Procollagen trafficking, processing and fibrillogenesis","volume":"118","author":"Canty","year":"2005","journal-title":"J. Cell Sci."},{"key":"2024061307214754500_JCS258879C29","doi-asserted-by":"publisher","first-page":"707","DOI":"10.1042\/BJ20111379","article-title":"Stepwise proteolytic activation of type I procollagen to collagen within the secretory pathway of tendon fibroblasts in situ","volume":"441","author":"Canty-Laird","year":"2012","journal-title":"Biochem. J."},{"key":"2024061307214754500_JCS258879C30","doi-asserted-by":"publisher","first-page":"3","DOI":"10.1016\/j.abb.2014.05.003","article-title":"Osteoblast and osteocyte: games without frontiers","volume":"561","author":"Capulli","year":"2014","journal-title":"Arch. Biochem. Biophys."},{"key":"2024061307214754500_JCS258879C31","doi-asserted-by":"publisher","first-page":"555","DOI":"10.1146\/annurev-cellbio-111315-125227","article-title":"Cellular and molecular mechanisms of MT1-MMP-dependent cancer cell invasion","volume":"32","author":"Castro-Castro","year":"2016","journal-title":"Annu. Rev. Cell Dev. Biol."},{"key":"2024061307214754500_JCS258879C32","doi-asserted-by":"publisher","first-page":"e1007242","DOI":"10.1371\/journal.pgen.1007242","article-title":"Impaired proteoglycan glycosylation, elevated TGF-\u03b2 signaling, and abnormal osteoblast differentiation as the basis for bone fragility in a mouse model for gerodermia osteodysplastica","volume":"14","author":"Chan","year":"2018","journal-title":"PLoS Genet."},{"key":"2024061307214754500_JCS258879C33","doi-asserted-by":"publisher","first-page":"74","DOI":"10.1038\/s41556-019-0441-z","article-title":"Circadian control of the secretory pathway maintains collagen homeostasis","volume":"22","author":"Chang","year":"2020","journal-title":"Nat. Cell Biol."},{"key":"2024061307214754500_JCS258879C34","doi-asserted-by":"publisher","first-page":"2120","DOI":"10.1111\/febs.12136","article-title":"The regulatory roles of small leucine-rich proteoglycans in extracellular matrix assembly","volume":"280","author":"Chen","year":"2013","journal-title":"FEBS J."},{"key":"2024061307214754500_JCS258879C35","doi-asserted-by":"publisher","first-page":"e108528","DOI":"10.1371\/journal.pone.0108528","article-title":"Sustained induction of collagen synthesis by TGF-\u03b2 requires regulated intramembrane proteolysis of CREB3L1","volume":"9","author":"Chen","year":"2014","journal-title":"PLoS ONE"},{"key":"2024061307214754500_JCS258879C36","doi-asserted-by":"publisher","first-page":"e01828","DOI":"10.7554\/eLife.01828","article-title":"ERK8 is a negative regulator of O-GalNAc glycosylation and cell migration","volume":"3","author":"Chia","year":"2014","journal-title":"Elife"},{"key":"2024061307214754500_JCS258879C37","doi-asserted-by":"publisher","first-page":"785","DOI":"10.1016\/j.cellsig.2011.01.001","article-title":"Alteration of Golgi structure in senescent cells and its regulation by a G protein \u03b3 subunit","volume":"23","author":"Cho","year":"2011","journal-title":"Cell. Signal."},{"key":"2024061307214754500_JCS258879C38","first-page":"71","article-title":"GBF1: A novel Golgi-associated BFA-resistant guanine nucleotide exchange factor that displays specificity for ADP-ribosylation factor 5","volume":"146","author":"Claude","year":"1999","journal-title":"J. Cell Biol."},{"key":"2024061307214754500_JCS258879C39","doi-asserted-by":"publisher","first-page":"2853","DOI":"10.1371\/journal.pbio.0060301","article-title":"Senescence-associated secretory phenotypes reveal cell-nonautonomous functions of oncogenic RAS and the p53 tumor suppressor","volume":"6","author":"Copp\u00e9","year":"2008","journal-title":"PLoS Biol."},{"key":"2024061307214754500_JCS258879C40","doi-asserted-by":"publisher","first-page":"217","DOI":"10.1038\/s41568-020-00329-7","article-title":"The matrix in cancer","volume":"21","author":"Cox","year":"2021","journal-title":"Nat. Rev. Cancer"},{"key":"2024061307214754500_JCS258879C41","doi-asserted-by":"publisher","first-page":"5195","DOI":"10.1074\/jbc.M611048200","article-title":"Biosynthesis of chondroitin and heparan sulfate in chinese hamster ovary cells depends on xylosyltransferase II","volume":"282","author":"Cuellar","year":"2007","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C42","doi-asserted-by":"publisher","first-page":"420","DOI":"10.1086\/321290","article-title":"A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes disease","volume":"69","author":"Dagenais","year":"2001","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C43","doi-asserted-by":"publisher","first-page":"269","DOI":"10.1016\/S0736-0266(00)00032-2","article-title":"Proteoglycans and glycosaminoglycan fine structure in the mouse tail tendon fascicle","volume":"19","author":"Derwin","year":"2001","journal-title":"J. Orthop. Res."},{"key":"2024061307214754500_JCS258879C44","doi-asserted-by":"publisher","first-page":"922","DOI":"10.1111\/exd.13886","article-title":"Replicative senescence of human dermal fibroblasts affects structural and functional aspects of the Golgi apparatus","volume":"28","author":"Despres","year":"2019","journal-title":"Exp. Dermatol."},{"key":"2024061307214754500_JCS258879C45","doi-asserted-by":"publisher","first-page":"926","DOI":"10.1369\/0022155412461256","article-title":"Proteoglycan synthesis and Golgi organization in polarized epithelial cells","volume":"60","author":"Dick","year":"2012","journal-title":"J. Histochem. Cytochem."},{"key":"2024061307214754500_JCS258879C46","doi-asserted-by":"publisher","first-page":"75","DOI":"10.1038\/s41580-020-00314-w","article-title":"Cellular senescence in ageing: from mechanisms to therapeutic opportunities","volume":"22","author":"Di Micco","year":"2021","journal-title":"Nat. Rev. Mol. Cell Biol."},{"key":"2024061307214754500_JCS258879C47","doi-asserted-by":"publisher","first-page":"440","DOI":"10.1093\/hmg\/ddn371","article-title":"The gene responsible for Dyggve-Melchior-Clausen syndrome encodes a novel peripheral membrane protein dynamically associated with the Golgi apparatus","volume":"18","author":"Dimitrov","year":"2009","journal-title":"Hum. Mol. Genet."},{"key":"2024061307214754500_JCS258879C48","doi-asserted-by":"publisher","first-page":"4836","DOI":"10.1093\/hmg\/ddx362","article-title":"Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly","volume":"26","author":"DiStasio","year":"2017","journal-title":"Hum. Mol. Genet."},{"key":"2024061307214754500_JCS258879C49","doi-asserted-by":"publisher","first-page":"3087","DOI":"10.1038\/s41467-018-05191-8","article-title":"SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects","volume":"9","author":"Dubail","year":"2018","journal-title":"Nat. Commun."},{"key":"2024061307214754500_JCS258879C50","doi-asserted-by":"publisher","first-page":"873","DOI":"10.1016\/j.ajhg.2009.11.010","article-title":"Loss of dermatan-4-sulfotransferase 1 function results in adducted thumb-clubfoot syndrome","volume":"85","author":"D\u00fcndar","year":"2009","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C51","doi-asserted-by":"publisher","first-page":"8235","DOI":"10.18632\/oncotarget.1632","article-title":"Activation of EGFR, HER2 and HER3 by neurotensin\/neurotensin receptor 1 renders breast tumors aggressive yet highly responsive to lapatinib and metformin in mice","volume":"5","author":"Dupouy","year":"2014","journal-title":"Oncotarget"},{"key":"2024061307214754500_JCS258879C52","doi-asserted-by":"publisher","first-page":"283","DOI":"10.1002\/humu.22235","article-title":"A novel RAB33B mutation in Smith-McCort dysplasia","volume":"34","author":"Dupuis","year":"2013","journal-title":"Hum. Mutat."},{"key":"2024061307214754500_JCS258879C53","doi-asserted-by":"publisher","first-page":"400","DOI":"10.1016\/j.ydbio.2010.02.035","article-title":"UDP xylose synthase 1 is required for morphogenesis and histogenesis of the craniofacial skeleton","volume":"341","author":"Eames","year":"2010","journal-title":"Dev. Biol."},{"key":"2024061307214754500_JCS258879C54","doi-asserted-by":"publisher","first-page":"31319","DOI":"10.1074\/jbc.M114.608182","article-title":"Golgi Phosphoprotein 3 Triggers Signal-mediated Incorporation of Glycosyltransferases into Coatomer-coated (COPI) Vesicles","volume":"289","author":"Eckert","year":"2014","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C55","doi-asserted-by":"publisher","first-page":"733","DOI":"10.1136\/jmedgenet-2013-101753","article-title":"Mutations in SLC35A3 cause autism spectrum disorder, epilepsy and arthrogryposis","volume":"50","author":"Edvardson","year":"2013","journal-title":"J. Med. Genet."},{"key":"2024061307214754500_JCS258879C56","doi-asserted-by":"publisher","first-page":"697","DOI":"10.1016\/j.ceb.2010.08.015","article-title":"Dynamic interplay between the collagen scaffold and tumor evolution","volume":"22","author":"Egeblad","year":"2010","journal-title":"Curr. Opin. Cell Biol."},{"key":"2024061307214754500_JCS258879C57","doi-asserted-by":"publisher","first-page":"20414","DOI":"10.1074\/jbc.272.33.20414","article-title":"Localization of a binding site for the proteoglycan decorin on collagen XIV (undulin)","volume":"272","author":"Ehnis","year":"1997","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C58","doi-asserted-by":"publisher","first-page":"357","DOI":"10.1093\/hmg\/ddg029","article-title":"Mutations in a novel gene Dymeclin (FLJ20071) are responsible for Dyggve-Melchior-Clausen syndrome","volume":"12","author":"Ghouzzi","year":"2003","journal-title":"Hum. Mol. Genet."},{"key":"2024061307214754500_JCS258879C59","doi-asserted-by":"publisher","first-page":"41928","DOI":"10.1074\/jbc.M404506200","article-title":"Inhibition by the soluble syndecan-1 ectodomains delays wound repair in mice overexpressing syndecan-1","volume":"279","author":"Elenius","year":"2004","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C60","doi-asserted-by":"publisher","first-page":"935","DOI":"10.1126\/science.abb5390","article-title":"A human tissue screen identifies a regulator of ER secretion as a brain-size determinant","volume":"370","author":"Esk","year":"2020","journal-title":"Science"},{"key":"2024061307214754500_JCS258879C61","doi-asserted-by":"publisher","first-page":"266","DOI":"10.1159\/000504295","article-title":"The Matrisome during aging and longevity: a systems-level approach toward defining matreotypes promoting healthy aging","volume":"66","author":"Ewald","year":"2020","journal-title":"Gerontology"},{"key":"2024061307214754500_JCS258879C62","doi-asserted-by":"publisher","first-page":"1157","DOI":"10.1002\/ajmg.a.33404","article-title":"Mutation of CANT1 causes Desbuquois dysplasia","volume":"152a","author":"Faden","year":"2010","journal-title":"Am. J. Med. Genet. A"},{"key":"2024061307214754500_JCS258879C63","doi-asserted-by":"publisher","first-page":"39","DOI":"10.1002\/ajmg.a.30005","article-title":"A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers\u2013Danlos syndrome resembling the progeroid type","volume":"128A","author":"Faiyaz-Ul-Haque","year":"2004","journal-title":"Am. J. Med. Genet. A"},{"key":"2024061307214754500_JCS258879C64","doi-asserted-by":"publisher","first-page":"121","DOI":"10.1016\/j.bone.2019.01.015","article-title":"Cellular senescence in bone","volume":"121","author":"Farr","year":"2019","journal-title":"Bone"},{"key":"2024061307214754500_JCS258879C65","doi-asserted-by":"publisher","first-page":"215","DOI":"10.1002\/jcp.1041510202","article-title":"Age-related changes in hyaluronan, proteoglycan, collagen, and osteonectin synthesis by human bone cells","volume":"151","author":"Fedarko","year":"1992","journal-title":"J. Cell. Physiol."},{"key":"2024061307214754500_JCS258879C66","doi-asserted-by":"publisher","first-page":"e14332","DOI":"10.15252\/emmm.202114332","article-title":"A spoonful of L-fucose-an efficient therapy for GFUS-CDG, a new glycosylation disorder","volume":"13","author":"Feichtinger","year":"2021","journal-title":"EMBO Mol. Med."},{"key":"2024061307214754500_JCS258879C67","doi-asserted-by":"publisher","first-page":"553","DOI":"10.1016\/j.ajhg.2018.09.003","article-title":"A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation","volume":"103","author":"Ferreira","year":"2018","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C68","doi-asserted-by":"publisher","first-page":"1231","DOI":"10.1016\/j.celrep.2019.03.107","article-title":"Modeling glycan processing reveals golgi-enzyme homeostasis upon trafficking defects and cellular differentiation","volume":"27","author":"Fisher","year":"2019","journal-title":"Cell Rep."},{"key":"2024061307214754500_JCS258879C69","doi-asserted-by":"publisher","first-page":"421746","DOI":"10.1155\/2015\/421746","article-title":"Biology of bone tissue: structure, function, and factors that influence bone cells","volume":"2015","author":"Florencio-Silva","year":"2015","journal-title":"Biomed. Res. Int."},{"key":"2024061307214754500_JCS258879C70","doi-asserted-by":"publisher","first-page":"25015","DOI":"10.1016\/S0021-9258(19)74565-7","article-title":"Binding of collagen XIV with the dermatan sulfate side chain of decorin","volume":"268","author":"Font","year":"1993","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C71","doi-asserted-by":"publisher","first-page":"341","DOI":"10.1016\/S0945-053X(96)90137-7","article-title":"Characterization of the interactions of type XII collagen with two small proteoglycans from fetal bovine tendon, decorin and fibromodulin","volume":"15","author":"Font","year":"1996","journal-title":"Matrix Biol."},{"key":"2024061307214754500_JCS258879C72","doi-asserted-by":"publisher","first-page":"3764","DOI":"10.1073\/pnas.0507685103","article-title":"Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II","volume":"103","author":"Foulquier","year":"2006","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"2024061307214754500_JCS258879C73","doi-asserted-by":"publisher","first-page":"15","DOI":"10.1016\/j.ajhg.2012.05.002","article-title":"TMEM165 deficiency causes a congenital disorder of glycosylation","volume":"91","author":"Foulquier","year":"2012","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C74","doi-asserted-by":"publisher","first-page":"244","DOI":"10.1111\/j.1749-6632.2000.tb06651.x","article-title":"Inflamm-aging. An evolutionary perspective on immunosenescence","volume":"908","author":"Franceschi","year":"2000","journal-title":"Ann. N. Y. Acad. Sci."},{"key":"2024061307214754500_JCS258879C75","doi-asserted-by":"publisher","first-page":"4195","DOI":"10.1242\/jcs.023820","article-title":"The extracellular matrix at a glance","volume":"123","author":"Frantz","year":"2010","journal-title":"J. Cell Sci."},{"key":"2024061307214754500_JCS258879C76","doi-asserted-by":"publisher","first-page":"537","DOI":"10.1038\/nrg1894","article-title":"Genetic defects in the human glycome","volume":"7","author":"Freeze","year":"2006","journal-title":"Nat. Rev. Genet."},{"key":"2024061307214754500_JCS258879C77","doi-asserted-by":"publisher","first-page":"a005371","DOI":"10.1101\/cshperspect.a005371","article-title":"Golgi glycosylation and human inherited diseases","volume":"3","author":"Freeze","year":"2011","journal-title":"Cold Spring Harb. Perspect Biol."},{"key":"2024061307214754500_JCS258879C78","doi-asserted-by":"publisher","first-page":"107","DOI":"10.1242\/jeb.203.1.107","article-title":"Luminal acidification of diverse organelles by V-ATPase in animal cells","volume":"203","author":"Futai","year":"2000","journal-title":"J. Exp. Biol."},{"key":"2024061307214754500_JCS258879C79","doi-asserted-by":"publisher","first-page":"843","DOI":"10.1083\/jcb.201003055","article-title":"Regulation of O-glycosylation through Golgi-to-ER relocation of initiation enzymes","volume":"189","author":"Gill","year":"2010","journal-title":"J. Cell Biol."},{"key":"2024061307214754500_JCS258879C80","doi-asserted-by":"publisher","first-page":"399","DOI":"10.1016\/j.tcb.2016.02.005","article-title":"Finding the Golgi: Golgin Coiled-Coil Proteins Show the Way","volume":"26","author":"Gillingham","year":"2016","journal-title":"Trends Cell Biol."},{"key":"2024061307214754500_JCS258879C81","doi-asserted-by":"publisher","first-page":"113","DOI":"10.1146\/annurev.cellbio.24.110707.175421","article-title":"Membrane traffic within the Golgi apparatus","volume":"25","author":"Glick","year":"2009","journal-title":"Annu. Rev. Cell Dev. Biol."},{"key":"2024061307214754500_JCS258879C82","doi-asserted-by":"publisher","first-page":"65","DOI":"10.1007\/s10528-005-1068-2","article-title":"Defective glycosaminoglycan substitution of decorin in a patient with progeroid syndrome is a direct consequence of two point mutations in the galactosyltransferase I (beta4GalT-7) gene","volume":"43","author":"G\u00f6tte","year":"2005","journal-title":"Biochem. Genet."},{"key":"2024061307214754500_JCS258879C83","doi-asserted-by":"publisher","first-page":"517","DOI":"10.1042\/BJ20081179","article-title":"Neutralization of endomembrane compartments in epithelial MDCK cells affects proteoglycan synthesis in the apical secretory pathway","volume":"418","author":"Grondahl","year":"2009","journal-title":"Biochem. J."},{"key":"2024061307214754500_JCS258879C84","doi-asserted-by":"publisher","first-page":"43638","DOI":"10.1074\/jbc.M202124200","article-title":"Age-related changes in human bone proteoglycan structure. Impact of osteogenesis imperfecta","volume":"277","author":"Grzesik","year":"2002","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C85","doi-asserted-by":"publisher","first-page":"903","DOI":"10.1016\/j.bbadis.2008.12.009","article-title":"Vacuolar H+-ATPase meets glycosylation in patients with cutis laxa","volume":"1792","author":"Guillard","year":"2009","journal-title":"Biochim. Biophys. Acta"},{"key":"2024061307214754500_JCS258879C86","doi-asserted-by":"publisher","first-page":"169","DOI":"10.1146\/annurev-cellbio-100913-013012","article-title":"Protein sorting at the trans-Golgi network","volume":"30","author":"Guo","year":"2014","journal-title":"Annu. Rev. Cell Dev. Biol."},{"key":"2024061307214754500_JCS258879C87","doi-asserted-by":"publisher","first-page":"571","DOI":"10.1038\/jid.2012.289","article-title":"A missense mutation in the MBTPS2 gene underlies the X-linked form of Olmsted syndrome","volume":"133","author":"Haghighi","year":"2013","journal-title":"J. Invest. Dermatol."},{"key":"2024061307214754500_JCS258879C88","first-page":"1454","article-title":"Scyl1 scaffolds class II Arfs to specific subcomplexes of coatomer through the \u03b3-COP appendage domain","volume":"127","author":"Hamlin","year":"2014","journal-title":"J. Cell Sci."},{"key":"2024061307214754500_JCS258879C89","doi-asserted-by":"publisher","first-page":"3600","DOI":"10.1016\/S0021-9258(17)35689-2","article-title":"Ammonium chloride interferes with a distinct step in the biosynthesis and cell surface expression of human melanoma-type chondroitin sulfate proteoglycan","volume":"261","author":"Harper","year":"1986","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C90","doi-asserted-by":"publisher","first-page":"135","DOI":"10.1002\/ar.1091980202","article-title":"Ultrastructure of the chondrocytes and extracellular matrix of the swarm rat chondrosarcoma","volume":"198","author":"Hascall","year":"1980","journal-title":"Anat. Rec."},{"key":"2024061307214754500_JCS258879C91","first-page":"80","article-title":"Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies","volume":"60","author":"Hecht","year":"1997","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C92","doi-asserted-by":"publisher","first-page":"555","DOI":"10.1038\/s41586-020-2938-9","article-title":"Fibrosis: from mechanisms to medicines","volume":"587","author":"Henderson","year":"2020","journal-title":"Nature"},{"key":"2024061307214754500_JCS258879C93","doi-asserted-by":"publisher","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."},{"key":"2024061307214754500_JCS258879C94","doi-asserted-by":"publisher","first-page":"1368","DOI":"10.1016\/j.ajhg.2008.05.006","article-title":"Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis","volume":"82","author":"Hermanns","year":"2008","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C95","doi-asserted-by":"publisher","first-page":"527","DOI":"10.1042\/bj3020527","article-title":"Interaction of the small interstitial proteoglycans biglycan, decorin and fibromodulin with transforming growth factor beta","volume":"302","author":"Hildebrand","year":"1994","journal-title":"Biochem. J."},{"key":"2024061307214754500_JCS258879C96","doi-asserted-by":"publisher","first-page":"13810","DOI":"10.1074\/jbc.M113.543322","article-title":"Master regulator for chondrogenesis, Sox9, regulates transcriptional activation of the endoplasmic reticulum stress transducer BBF2H7\/CREB3L2 in chondrocytes","volume":"289","author":"Hino","year":"2014","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C97","doi-asserted-by":"publisher","first-page":"623","DOI":"10.1016\/j.bbagen.2018.12.006","article-title":"Structural alteration of glycosaminoglycan side chains and spatial disorganization of collagen networks in the skin of patients with mcEDS-CHST14","volume":"1863","author":"Hirose","year":"2019","journal-title":"Biochim. Biophys. Acta Gen. Subj."},{"key":"2024061307214754500_JCS258879C98","doi-asserted-by":"publisher","first-page":"63","DOI":"10.1146\/annurev.bi.56.070187.000431","article-title":"Topography of glycosylation in the rough endoplasmic reticulum and Golgi apparatus","volume":"56","author":"Hirschberg","year":"1987","journal-title":"Annu. Rev. Biochem."},{"key":"2024061307214754500_JCS258879C99","doi-asserted-by":"publisher","first-page":"36","DOI":"10.1111\/febs.15453","article-title":"Rab family of small GTPases: an updated view on their regulation and functions","volume":"288","author":"Homma","year":"2021","journal-title":"FEBS J."},{"key":"2024061307214754500_JCS258879C100","doi-asserted-by":"publisher","first-page":"91","DOI":"10.1111\/j.1432-1033.1985.tb09167.x","article-title":"Influence of monensin on biosynthesis, processing and secretion of proteodermatan sulfate by skin fibroblasts","volume":"152","author":"Hoppe","year":"1985","journal-title":"Eur. J. Biochem."},{"key":"2024061307214754500_JCS258879C101","doi-asserted-by":"publisher","first-page":"706","DOI":"10.1016\/j.ajhg.2009.10.001","article-title":"Identification of CANT1 mutations in Desbuquois dysplasia","volume":"85","author":"Huber","year":"2009","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C102","doi-asserted-by":"publisher","first-page":"2149","DOI":"10.1093\/hmg\/ddp148","article-title":"Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival","volume":"18","author":"Hucthagowder","year":"2009","journal-title":"Hum. Mol. Genet."},{"key":"2024061307214754500_JCS258879C103","doi-asserted-by":"publisher","first-page":"12129","DOI":"10.1074\/jbc.M708198200","article-title":"Active negative control of collagen fibrillogenesis in vivo. Intracellular cleavage of the type I procollagen propeptides in tendon fibroblasts without intracellular fibrils","volume":"283","author":"Humphries","year":"2008","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C104","doi-asserted-by":"publisher","first-page":"11","DOI":"10.1016\/j.matbio.2015.02.003","article-title":"Proteoglycan form and function: A comprehensive nomenclature of proteoglycans","volume":"42","author":"Iozzo","year":"2015","journal-title":"Matrix Biol."},{"key":"2024061307214754500_JCS258879C105","doi-asserted-by":"publisher","first-page":"2010","DOI":"10.1038\/jid.2012.103","article-title":"BBF2H7-mediated Sec23A pathway is required for endoplasmic reticulum-to-Golgi trafficking in dermal fibroblasts to promote collagen synthesis","volume":"132","author":"Ishikura-Kinoshita","year":"2012","journal-title":"J. Invest. Dermatol."},{"key":"2024061307214754500_JCS258879C106","doi-asserted-by":"publisher","first-page":"451","DOI":"10.1016\/j.ajhg.2016.06.011","article-title":"ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects","volume":"99","author":"Izumi","year":"2016","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C107","doi-asserted-by":"publisher","first-page":"e49573","DOI":"10.7554\/eLife.49573","article-title":"Golgi compartments enable controlled biomolecular assembly using promiscuous enzymes","volume":"9","author":"Jaiman","year":"2020","journal-title":"Elife"},{"key":"2024061307214754500_JCS258879C108","doi-asserted-by":"publisher","first-page":"2691","DOI":"10.1002\/ajmg.a.37209","article-title":"A homozygous B3GAT3 mutation causes a severe syndrome with multiple fractures, expanding the phenotype of linkeropathy syndromes","volume":"167a","author":"Jones","year":"2015","journal-title":"Am. J. Med. Genet. A"},{"key":"2024061307214754500_JCS258879C109","doi-asserted-by":"publisher","first-page":"21415","DOI":"10.1074\/jbc.M210977200","article-title":"Initiation of the decorin glycosaminoglycan chain in the endoplasmic reticulum-Golgi intermediate compartment","volume":"278","author":"Jonsson","year":"2003","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C110","doi-asserted-by":"publisher","first-page":"312","DOI":"10.1034\/j.1600-0838.2000.010006312.x","article-title":"Structure of the tendon connective tissue","volume":"10","author":"Kannus","year":"2000","journal-title":"Scand. J. Med. Sci. Sports"},{"key":"2024061307214754500_JCS258879C111","doi-asserted-by":"publisher","DOI":"10.1111\/febs.15776","article-title":"A guide to the composition and functions of the extracellular matrix","author":"Karamanos","year":"2021","journal-title":"FEBS J."},{"key":"2024061307214754500_JCS258879C112","doi-asserted-by":"publisher","first-page":"7477","DOI":"10.1021\/bi00244a016","article-title":"Initiation of chondroitin sulfate biosynthesis: a kinetic analysis of UDP-D-xylose: core protein beta-D-xylosyltransferase","volume":"30","author":"Kearns","year":"1991","journal-title":"Biochemistry"},{"key":"2024061307214754500_JCS258879C113","doi-asserted-by":"publisher","first-page":"11097","DOI":"10.1016\/S0021-9258(18)82097-X","article-title":"Topography of glycosylation and UDP-xylose production","volume":"268","author":"Kearns","year":"1993","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C114","doi-asserted-by":"publisher","first-page":"19","DOI":"10.1038\/sj.cr.7290106","article-title":"Structure and function of aggrecan","volume":"12","author":"Kiani","year":"2002","journal-title":"Cell Res."},{"key":"2024061307214754500_JCS258879C115","doi-asserted-by":"publisher","first-page":"e121596","DOI":"10.1172\/jci.insight.121596","article-title":"Site-1 protease deficiency causes human skeletal dysplasia due to defective inter-organelle protein trafficking","volume":"3","author":"Kondo","year":"2018","journal-title":"JCI Insight"},{"key":"2024061307214754500_JCS258879C116","doi-asserted-by":"publisher","first-page":"32","DOI":"10.1038\/ng.2007.45","article-title":"Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2","volume":"40","author":"Kornak","year":"2008","journal-title":"Nat. Genet."},{"key":"2024061307214754500_JCS258879C117","first-page":"436","article-title":"Glycosaminoglycan-free small proteoglycan core protein is secreted by fibroblasts from a patient with a syndrome resembling progeroid","volume":"41","author":"Kresse","year":"1987","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C118","doi-asserted-by":"publisher","first-page":"287","DOI":"10.3109\/03008209709160228","article-title":"Increased diameters of collagen fibrils precipitated in vitro in the presence of decorin from various connective tissues","volume":"36","author":"Kuc","year":"1997","journal-title":"Connect. Tissue Res."},{"key":"2024061307214754500_JCS258879C119","doi-asserted-by":"publisher","first-page":"1133","DOI":"10.1038\/ejhg.2011.101","article-title":"Desbuquois dysplasia type I and fetal hydrops due to novel mutations in the CANT1 gene","volume":"19","author":"Laccone","year":"2011","journal-title":"Eur. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C120","doi-asserted-by":"publisher","first-page":"504","DOI":"10.3389\/fgene.2019.00504","article-title":"A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta","volume":"10","author":"Laugel-Haushalter","year":"2019","journal-title":"Front. Genet."},{"key":"2024061307214754500_JCS258879C121","doi-asserted-by":"publisher","first-page":"123","DOI":"10.1002\/ar.1092240204","article-title":"Synthesis and secretion of collagen by cells of connective tissue, bone, and dentin","volume":"224","author":"Leblond","year":"1989","journal-title":"Anat. Rec."},{"key":"2024061307214754500_JCS258879C122","doi-asserted-by":"publisher","first-page":"14304","DOI":"10.1016\/S0021-9258(19)49712-3","article-title":"Activation of human furin precursor processing endoprotease occurs by an intramolecular autoproteolytic cleavage","volume":"267","author":"Leduc","year":"1992","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C123","doi-asserted-by":"publisher","first-page":"174","DOI":"10.1016\/j.jdermsci.2016.05.016","article-title":"Glycosaminoglycan and proteoglycan in skin aging","volume":"83","author":"Lee","year":"2016","journal-title":"J. Dermatol. Sci."},{"key":"2024061307214754500_JCS258879C124","doi-asserted-by":"publisher","first-page":"2636","DOI":"10.1111\/febs.15282","article-title":"The ECM path of senescence in aging: components and modifiers","volume":"287","author":"Levi","year":"2020","journal-title":"FEBS J."},{"key":"2024061307214754500_JCS258879C125","first-page":"3691","article-title":"Golgi phosphoprotein 3 regulates metastasis of prostate cancer via matrix metalloproteinase 9","volume":"8","author":"Li","year":"2015","journal-title":"Int J Clin Exp Pathol"},{"key":"2024061307214754500_JCS258879C126","doi-asserted-by":"publisher","first-page":"2422","DOI":"10.1038\/srep02422","article-title":"Age-dependent alterations of decorin glycosaminoglycans in human skin","volume":"3","author":"Li","year":"2013","journal-title":"Sci. Rep."},{"key":"2024061307214754500_JCS258879C127","doi-asserted-by":"publisher","first-page":"11920","DOI":"10.1038\/ncomms11920","article-title":"MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta","volume":"7","author":"Lindert","year":"2016","journal-title":"Nat. Commun."},{"key":"2024061307214754500_JCS258879C128","doi-asserted-by":"publisher","first-page":"801","DOI":"10.1016\/0092-8674(89)90685-5","article-title":"Rapid redistribution of Golgi proteins into the ER in cells treated with brefeldin A: evidence for membrane cycling from Golgi to ER","volume":"56","author":"Lippincott-Schwartz","year":"1989","journal-title":"Cell"},{"key":"2024061307214754500_JCS258879C129","doi-asserted-by":"publisher","first-page":"18775","DOI":"10.1016\/S0021-9258(18)51534-9","article-title":"Xylosyl transfer to the core protein precursor of the rat chondrosarcoma proteoglycan","volume":"264","author":"Lohmander","year":"1989","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C130","doi-asserted-by":"publisher","first-page":"5517","DOI":"10.1128\/MCB.00430-09","article-title":"Dermatan sulfate epimerase 1-deficient mice have reduced content and changed distribution of iduronic acids in dermatan sulfate and an altered collagen structure in skin","volume":"29","author":"Maccarana","year":"2009","journal-title":"Mol. Cell. Biol."},{"key":"2024061307214754500_JCS258879C131","doi-asserted-by":"publisher","first-page":"1233","DOI":"10.1002\/humu.21355","article-title":"Musculocontractural Ehlers-Danlos Syndrome (former EDS type VIB) and adducted thumb clubfoot syndrome (ATCS) represent a single clinical entity caused by mutations in the dermatan-4-sulfotransferase 1 encoding CHST14 gene","volume":"31","author":"Malfait","year":"2010","journal-title":"Hum. Mutat."},{"key":"2024061307214754500_JCS258879C132","doi-asserted-by":"publisher","first-page":"935","DOI":"10.1016\/j.ajhg.2013.04.016","article-title":"Defective initiation of glycosaminoglycan synthesis due to B3GALT6 mutations causes a pleiotropic Ehlers-Danlos-syndrome-like connective tissue disorder","volume":"92","author":"Malfait","year":"2013","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C133","doi-asserted-by":"publisher","first-page":"1705","DOI":"10.1083\/jcb.98.5.1705","article-title":"Radioautographic characterization of successive compartments along the rough endoplasmic reticulum-Golgi pathway of collagen precursors in foot pad fibroblasts of [3H]proline-injected rats","volume":"98","author":"Marchi","year":"1984","journal-title":"J. Cell Biol."},{"key":"2024061307214754500_JCS258879C134","doi-asserted-by":"publisher","first-page":"1710","DOI":"10.1016\/j.ajhg.2021.08.002","article-title":"COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay","volume":"108","author":"Marom","year":"2021","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C135","doi-asserted-by":"publisher","first-page":"940","DOI":"10.1016\/j.tcb.2019.08.007","article-title":"ER-to-Golgi Transport: A Sizeable Problem","volume":"29","author":"McCaughey","year":"2019","journal-title":"Trends Cell Biol."},{"key":"2024061307214754500_JCS258879C136","doi-asserted-by":"publisher","first-page":"1648","DOI":"10.1016\/j.celrep.2016.04.062","article-title":"TFG Promotes Organization of Transitional ER and Efficient Collagen Secretion","volume":"15","author":"McCaughey","year":"2016","journal-title":"Cell Rep"},{"key":"2024061307214754500_JCS258879C137","doi-asserted-by":"publisher","first-page":"jcs259075","DOI":"10.1242\/jcs.259075","article-title":"A general role for TANGO1, encoded by MIA3, in secretory pathway organization and function","volume":"134","author":"McCaughey","year":"2021","journal-title":"J. Cell Sci."},{"key":"2024061307214754500_JCS258879C138","doi-asserted-by":"publisher","first-page":"83","DOI":"10.1007\/s12551-009-0011-x","article-title":"Corneal collagen-its role in maintaining corneal shape and transparency","volume":"1","author":"Meek","year":"2009","journal-title":"Biophys Rev"},{"key":"2024061307214754500_JCS258879C139","doi-asserted-by":"publisher","first-page":"446","DOI":"10.1016\/j.bone.2019.07.016","article-title":"Biallelic CSGALNACT1-mutations cause a mild skeletal dysplasia","volume":"127","author":"Meyer","year":"2019","journal-title":"Bone"},{"key":"2024061307214754500_JCS258879C140","doi-asserted-by":"publisher","first-page":"19","DOI":"10.1080\/03008207.2019.1669577","article-title":"Evidence of biglycan structure-function in bone homeostasis and aging","volume":"61","author":"Miguez","year":"2020","journal-title":"Connect. Tissue Res."},{"key":"2024061307214754500_JCS258879C141","doi-asserted-by":"publisher","first-page":"4719","DOI":"10.1016\/j.bbagen.2013.06.006","article-title":"Biosynthesis and function of chondroitin sulfate","volume":"1830","author":"Mikami","year":"2013","journal-title":"Biochim. Biophys. Acta"},{"key":"2024061307214754500_JCS258879C142","doi-asserted-by":"publisher","first-page":"1225","DOI":"10.1083\/jcb.200108073","article-title":"Small cargo proteins and large aggregates can traverse the Golgi by a common mechanism without leaving the lumen of cisternae","volume":"155","author":"Mironov","year":"2001","journal-title":"J. Cell Biol."},{"key":"2024061307214754500_JCS258879C143","doi-asserted-by":"publisher","first-page":"9891","DOI":"10.1016\/S0021-9258(17)42783-9","article-title":"Formation of collagen fibrils by enzymic cleavage of precursors of type I collagen in vitro","volume":"259","author":"Miyahara","year":"1984","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C144","doi-asserted-by":"publisher","first-page":"966","DOI":"10.1002\/humu.21300","article-title":"Loss-of-function mutations of CHST14 in a new type of Ehlers-Danlos syndrome","volume":"31","author":"Miyake","year":"2010","journal-title":"Hum. Mutat."},{"key":"2024061307214754500_JCS258879C145","doi-asserted-by":"publisher","first-page":"10953","DOI":"10.1074\/jbc.R112.437038","article-title":"Human genetic disorders caused by mutations in genes encoding biosynthetic enzymes for sulfated glycosaminoglycans","volume":"288","author":"Mizumoto","year":"2013","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C146","doi-asserted-by":"publisher","first-page":"655","DOI":"10.1002\/humu.23952","article-title":"CSGALNACT1-congenital disorder of glycosylation: a mild skeletal dysplasia with advanced bone age","volume":"41","author":"Mizumoto","year":"2020","journal-title":"Hum. Mutat."},{"key":"2024061307214754500_JCS258879C147","doi-asserted-by":"publisher","first-page":"861752","DOI":"10.1155\/2015\/861752","article-title":"Mutations in biosynthetic enzymes for the protein linker region of chondroitin\/dermatan\/heparan sulfate cause skeletal and skin dysplasias","volume":"2015","author":"Mizumoto","year":"2015","journal-title":"Biomed. Res. Int."},{"key":"2024061307214754500_JCS258879C148","doi-asserted-by":"publisher","first-page":"e14814","DOI":"10.7554\/eLife.14814","article-title":"Golgi self-correction generates bioequivalent glycans to preserve cellular homeostasis","volume":"5","author":"Mkhikian","year":"2016","journal-title":"Elife"},{"key":"2024061307214754500_JCS258879C149","doi-asserted-by":"publisher","first-page":"84","DOI":"10.1002\/humu.20190","article-title":"Identification and analysis of 21 novel disease-causing amino acid substitutions in the conserved part of ATP7A","volume":"26","author":"M\u00f8ller","year":"2005","journal-title":"Hum. Mutat."},{"key":"2024061307214754500_JCS258879C150","doi-asserted-by":"publisher","first-page":"448","DOI":"10.1038\/nrm3383","article-title":"Vertebrate protein glycosylation: diversity, synthesis and function","volume":"13","author":"Moremen","year":"2012","journal-title":"Nat. Rev. Mol. Cell Biol."},{"key":"2024061307214754500_JCS258879C151","doi-asserted-by":"publisher","first-page":"16968","DOI":"10.1074\/jbc.M109316200","article-title":"UDP-glucuronate decarboxylase, a key enzyme in proteoglycan synthesis: cloning, characterization, and localization","volume":"277","author":"Moriarity","year":"2002","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C152","doi-asserted-by":"publisher","first-page":"3761","DOI":"10.1093\/hmg\/ddt227","article-title":"Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural Ehlers-Danlos syndrome","volume":"22","author":"M\u00fcller","year":"2013","journal-title":"Hum. Mol. Genet."},{"key":"2024061307214754500_JCS258879C153","doi-asserted-by":"publisher","first-page":"971","DOI":"10.1016\/j.ajhg.2015.04.017","article-title":"Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects","volume":"96","author":"Munns","year":"2015","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C154","doi-asserted-by":"publisher","first-page":"4695","DOI":"10.1002\/j.1460-2075.1995.tb00151.x","article-title":"An investigation of the role of transmembrane domains in Golgi protein retention","volume":"14","author":"Munro","year":"1995","journal-title":"EMBO J."},{"key":"2024061307214754500_JCS258879C155","doi-asserted-by":"publisher","first-page":"1205","DOI":"10.1038\/ncb1963","article-title":"Signalling mediated by the endoplasmic reticulum stress transducer OASIS is involved in bone formation","volume":"11","author":"Murakami","year":"2009","journal-title":"Nat. Cell Biol."},{"key":"2024061307214754500_JCS258879C156","doi-asserted-by":"publisher","first-page":"927","DOI":"10.1016\/j.ajhg.2013.04.003","article-title":"Mutations in B3GALT6, which encodes a glycosaminoglycan linker region enzyme, cause a spectrum of skeletal and connective tissue disorders","volume":"92","author":"Nakajima","year":"2013","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C157","doi-asserted-by":"publisher","first-page":"11","DOI":"10.1002\/(SICI)1096-8628(19971003)72:1&lt;11::AID-AJMG3&gt;3.0.CO;2-Y","article-title":"Dyggve-Melchior-Clausen syndrome without mental retardation (Smith-McCort dysplasia): morphological findings in the growth plate of the iliac crest","volume":"72","author":"Nakamura","year":"1997","journal-title":"Am. J. Med. Genet."},{"key":"2024061307214754500_JCS258879C158","doi-asserted-by":"publisher","first-page":"467","DOI":"10.1016\/j.ceb.2012.05.009","article-title":"Modular organization of the mammalian Golgi apparatus","volume":"24","author":"Nakamura","year":"2012","journal-title":"Curr. Opin. Cell Biol."},{"key":"2024061307214754500_JCS258879C159","doi-asserted-by":"publisher","first-page":"3389","DOI":"10.1111\/j.1432-1033.2004.04273.x","article-title":"Differential interactions of decorin and decorin mutants with type I and type VI collagens","volume":"271","author":"Nareyeck","year":"2004","journal-title":"Eur. J. Biochem."},{"key":"2024061307214754500_JCS258879C160","doi-asserted-by":"publisher","first-page":"jcs250100","DOI":"10.1242\/jcs.250100","article-title":"Molecular basis for KDEL-mediated retrieval of escaped ER-resident proteins - SWEET talking the COPs","volume":"133","author":"Newstead","year":"2020","journal-title":"J. Cell Sci."},{"key":"2024061307214754500_JCS258879C161","doi-asserted-by":"publisher","first-page":"639","DOI":"10.1016\/j.ccell.2017.10.001","article-title":"Organelle specific O-glycosylation drives MMP14 activation, tumor growth, and metastasis","volume":"32","author":"Nguyen","year":"2017","journal-title":"Cancer Cell"},{"key":"2024061307214754500_JCS258879C162","doi-asserted-by":"publisher","first-page":"2949","DOI":"10.1167\/iovs.02-0740","article-title":"Truncating mutations in the carbohydrate sulfotransferase 6 gene (CHST6) result in macular corneal dystrophy","volume":"44","author":"Niel","year":"2003","journal-title":"Invest. Ophthalmol. Vis. Sci."},{"key":"2024061307214754500_JCS258879C163","doi-asserted-by":"publisher","first-page":"12936","DOI":"10.1016\/S0021-9258(18)69252-X","article-title":"Xylosylation and glucuronosylation reactions in rat liver Golgi apparatus and endoplasmic reticulum","volume":"261","author":"Nuwayhid","year":"1986","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C164","doi-asserted-by":"publisher","first-page":"459","DOI":"10.1016\/j.ajhg.2009.03.014","article-title":"IFAP syndrome is caused by deficiency in MBTPS2, an intramembrane zinc metalloprotease essential for cholesterol homeostasis and ER stress response","volume":"84","author":"Oeffner","year":"2009","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C165","doi-asserted-by":"publisher","first-page":"28841","DOI":"10.1074\/jbc.274.41.28841","article-title":"Molecular basis for the progeroid variant of Ehlers-Danlos syndrome. Identification and characterization of two mutations in galactosyltransferase I gene","volume":"274","author":"Okajima","year":"1999","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C166","doi-asserted-by":"publisher","first-page":"216","DOI":"10.1016\/S0014-5793(00)01857-3","article-title":"A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome)","volume":"478","author":"Orrico","year":"2000","journal-title":"FEBS Lett."},{"key":"2024061307214754500_JCS258879C167","doi-asserted-by":"publisher","first-page":"281","DOI":"10.1016\/j.ajhg.2017.01.013","article-title":"Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome","volume":"100","author":"Oud","year":"2017","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C168","doi-asserted-by":"publisher","first-page":"3008","DOI":"10.1111\/febs.14984","article-title":"Bone and connective tissue disorders caused by defects in glycosaminoglycan biosynthesis: a panoramic view","volume":"286","author":"Paganini","year":"2019","journal-title":"FEBS J."},{"key":"2024061307214754500_JCS258879C169","doi-asserted-by":"publisher","first-page":"205","DOI":"10.1007\/s00439-016-1747-6","article-title":"Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract","volume":"136","author":"Patel","year":"2017","journal-title":"Hum. Genet."},{"key":"2024061307214754500_JCS258879C170","doi-asserted-by":"publisher","first-page":"643","DOI":"10.1016\/j.ejmg.2017.10.012","article-title":"Congenital disorders of glycosylation (CDG): Quo vadis?","volume":"61","author":"P\u00e9anne","year":"2018","journal-title":"Eur. J. Med. Genet."},{"key":"2024061307214754500_JCS258879C171","doi-asserted-by":"publisher","first-page":"34580","DOI":"10.1074\/jbc.M007399200","article-title":"Heparan\/chondroitin sulfate biosynthesis. Structure and mechanism of human glucuronyltransferase I","volume":"275","author":"Pedersen","year":"2000","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C172","doi-asserted-by":"publisher","first-page":"520","DOI":"10.1086\/515505","article-title":"Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses","volume":"61","author":"Philippe","year":"1997","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C173","doi-asserted-by":"publisher","first-page":"2406","DOI":"10.1242\/jcs.026849","article-title":"In migrating cells, the Golgi complex and the position of the centrosome depend on geometrical constraints of the substratum","volume":"121","author":"Pouthas","year":"2008","journal-title":"J. Cell Sci."},{"key":"2024061307214754500_JCS258879C174","doi-asserted-by":"publisher","first-page":"2003","DOI":"10.3390\/biom5032003","article-title":"Determinants of Glycosaminoglycan (GAG) Structure","volume":"5","author":"Prydz","year":"2015","journal-title":"Biomolecules"},{"key":"2024061307214754500_JCS258879C175","doi-asserted-by":"publisher","first-page":"42129","DOI":"10.1074\/jbc.M112.414565","article-title":"Ric1-Rgp1 complex is a guanine nucleotide exchange factor for the late Golgi Rab6A GTPase and an effector of the medial Golgi Rab33B GTPase","volume":"287","author":"Pusapati","year":"2012","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C176","doi-asserted-by":"publisher","first-page":"267","DOI":"10.1016\/j.chembiol.2004.11.020","article-title":"Structural insights into biological roles of protein-glycosaminoglycan interactions","volume":"12","author":"Raman","year":"2005","journal-title":"Chem. Biol."},{"key":"2024061307214754500_JCS258879C177","doi-asserted-by":"publisher","first-page":"1132","DOI":"10.1002\/1873-3468.13715","article-title":"Liquid\u2013liquid phase separation of the Golgi matrix protein GM130","volume":"594","author":"Rebane","year":"2020","journal-title":"FEBS Lett."},{"key":"2024061307214754500_JCS258879C178","doi-asserted-by":"publisher","first-page":"346","DOI":"10.1038\/s41581-019-0129-4","article-title":"Glycosylation in health and disease","volume":"15","author":"Reily","year":"2019","journal-title":"Nat. Rev. Nephrol."},{"key":"2024061307214754500_JCS258879C179","doi-asserted-by":"publisher","first-page":"631","DOI":"10.3390\/genes10090631","article-title":"Further defining the phenotypic spectrum of B3GAT3 mutations and literature review on linkeropathy syndromes","volume":"10","author":"Ritelli","year":"2019","journal-title":"Genes (Basel)"},{"key":"2024061307214754500_JCS258879C180","doi-asserted-by":"publisher","first-page":"e107238","DOI":"10.15252\/embj.2020107238","article-title":"Golgi maturation-dependent glycoenzyme recycling controls glycosphingolipid biosynthesis and cell growth via GOLPH3","volume":"40","author":"Rizzo","year":"2021","journal-title":"EMBO J."},{"key":"2024061307214754500_JCS258879C181","doi-asserted-by":"publisher","first-page":"46","DOI":"10.1016\/j.cellimm.2018.03.007","article-title":"Glycosylation in cancer: Selected roles in tumour progression, immune modulation and metastasis","volume":"333","author":"Rodrigues","year":"2018","journal-title":"Cell. Immunol."},{"key":"2024061307214754500_JCS258879C182","doi-asserted-by":"publisher","first-page":"463","DOI":"10.1111\/j.1432-1033.1985.tb08862.x","article-title":"Two N-acetylgalactosaminyltransferase are involved in the biosynthesis of chondroitin sulfate","volume":"148","author":"Rohrmann","year":"1985","journal-title":"Eur. J. Biochem."},{"key":"2024061307214754500_JCS258879C183","doi-asserted-by":"publisher","first-page":"338","DOI":"10.1038\/s41556-018-0270-5","article-title":"Extracellular matrix mechanical cues regulate lipid metabolism through Lipin-1 and SREBP","volume":"21","author":"Romani","year":"2019","journal-title":"Nat. Cell Biol."},{"key":"2024061307214754500_JCS258879C184","doi-asserted-by":"publisher","first-page":"233","DOI":"10.1016\/S0002-9297(07)64297-9","article-title":"A C2055T transition in exon 8 of the ATP7A gene is associated with exon skipping in an occipital horn syndrome family","volume":"61","author":"Ronce","year":"1997","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C185","doi-asserted-by":"publisher","first-page":"1371","DOI":"10.1038\/s41556-020-00590-w","article-title":"ER-resident oxidoreductases are glycosylated and trafficked to the cell surface to promote matrix degradation by tumour cells","volume":"22","author":"Ros","year":"2020","journal-title":"Nat. Cell Biol."},{"key":"2024061307214754500_JCS258879C186","doi-asserted-by":"publisher","first-page":"2914","DOI":"10.1093\/hmg\/ddt146","article-title":"Impact of disease-causing mutations on TMEM165 subcellular localization, a recently identified protein involved in CDG-II","volume":"22","author":"Rosnoblet","year":"2013","journal-title":"Hum. Mol. Genet."},{"key":"2024061307214754500_JCS258879C187","doi-asserted-by":"publisher","first-page":"2701","DOI":"10.1002\/1873-3468.13609","article-title":"Jim's View: Is the Golgi stack a phase-separated liquid crystal?","volume":"593","author":"Rothman","year":"2019","journal-title":"FEBS Lett."},{"key":"2024061307214754500_JCS258879C188","doi-asserted-by":"publisher","first-page":"4246","DOI":"10.1111\/j.1742-4658.2007.05951.x","article-title":"The glycosaminoglycan chain of decorin plays an important role in collagen fibril formation at the early stages of fibrillogenesis","volume":"274","author":"Ruhland","year":"2007","journal-title":"FEBS J."},{"key":"2024061307214754500_JCS258879C189","doi-asserted-by":"publisher","first-page":"1197","DOI":"10.1038\/ncb1962","article-title":"Regulation of endoplasmic reticulum stress response by a BBF2H7-mediated Sec23a pathway is essential for chondrogenesis","volume":"11","author":"Saito","year":"2009","journal-title":"Nat. Cell Biol."},{"key":"2024061307214754500_JCS258879C190","doi-asserted-by":"publisher","first-page":"891","DOI":"10.1016\/j.cell.2008.12.025","article-title":"TANGO1 facilitates cargo loading at endoplasmic reticulum exit sites","volume":"136","author":"Saito","year":"2009","journal-title":"Cell"},{"key":"2024061307214754500_JCS258879C191","doi-asserted-by":"publisher","first-page":"2301","DOI":"10.1091\/mbc.e11-02-0143","article-title":"cTAGE5 mediates collagen secretion through interaction with TANGO1 at endoplasmic reticulum exit sites","volume":"22","author":"Saito","year":"2011","journal-title":"Mol. Biol. Cell"},{"key":"2024061307214754500_JCS258879C192","doi-asserted-by":"publisher","first-page":"41","DOI":"10.1097\/MCD.0b013e32831868ea","article-title":"Portuguese case of Smith-McCort syndrome caused by a new mutation in the Dymeclin (FLJ20071) gene","volume":"18","author":"Santos","year":"2009","journal-title":"Clin. Dysmorphol."},{"key":"2024061307214754500_JCS258879C193","doi-asserted-by":"publisher","first-page":"3063","DOI":"10.1074\/jbc.M208886200","article-title":"Differential roles of two N-acetylgalactosaminyltransferases, CSGalNAcT-1, and a novel enzyme, CSGalNAcT-2. Initiation and elongation in synthesis of chondroitin sulfate","volume":"278","author":"Sato","year":"2003","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C194","doi-asserted-by":"publisher","first-page":"729","DOI":"10.1038\/s41580-020-00294-x","article-title":"Global view of human protein glycosylation pathways and functions","volume":"21","author":"Schjoldager","year":"2020","journal-title":"Nat. Rev. Mol. Cell Biol."},{"key":"2024061307214754500_JCS258879C195","doi-asserted-by":"publisher","first-page":"1044","DOI":"10.1016\/j.ajhg.2020.10.007","article-title":"Bi-allelic pathogenic variants in HS2ST1 cause a syndrome characterized by developmental delay and corpus callosum, skeletal, and renal abnormalities","volume":"107","author":"Schneeberger","year":"2020","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C196","doi-asserted-by":"publisher","first-page":"2776","DOI":"10.1074\/jbc.270.6.2776","article-title":"Interaction of biglycan with type I collagen","volume":"270","author":"Schonherr","year":"1995","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C197","doi-asserted-by":"publisher","first-page":"29","DOI":"10.1007\/s00439-013-1351-y","article-title":"The missing \u201clink\u201d: an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation","volume":"133","author":"Schreml","year":"2014","journal-title":"Hum. Genet."},{"key":"2024061307214754500_JCS258879C198","doi-asserted-by":"publisher","first-page":"D649","DOI":"10.2741\/A540","article-title":"Biosynthesis and regulation of expression of proteoglycans","volume":"5","author":"Schwartz","year":"2000","journal-title":"Front. Biosci."},{"key":"2024061307214754500_JCS258879C199","doi-asserted-by":"publisher","first-page":"869","DOI":"10.1038\/sj.ejhg.5200553","article-title":"Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome","volume":"8","author":"Schwartz","year":"2000","journal-title":"Eur. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C200","doi-asserted-by":"publisher","first-page":"933","DOI":"10.3390\/ijms21030933","article-title":"Oncogenic roles of GOLPH3 in the physiopathology of Cancer","volume":"21","author":"Sechi","year":"2020","journal-title":"Int. J. Mol. Sci."},{"key":"2024061307214754500_JCS258879C201","doi-asserted-by":"publisher","first-page":"21473","DOI":"10.1074\/jbc.R113.481549","article-title":"The multifaceted proprotein convertases: their unique, redundant, complementary, and opposite functions","volume":"288","author":"Seidah","year":"2013","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C202","doi-asserted-by":"publisher","first-page":"583","DOI":"10.1007\/s00109-006-0046-4","article-title":"Defective glycosylation of decorin and biglycan, altered collagen structure, and abnormal phenotype of the skin fibroblasts of an Ehlers\u2013Danlos syndrome patient carrying the novel Arg270Cys substitution in galactosyltransferase I (\u03b24GalT-7)","volume":"84","author":"Seidler","year":"2006","journal-title":"J. Mol. Med."},{"key":"2024061307214754500_JCS258879C203","doi-asserted-by":"publisher","first-page":"84","DOI":"10.1016\/j.spen.2014.04.007","article-title":"A newborn with complex skeletal abnormalities, joint contractures, and bilateral corneal clouding with sclerocornea","volume":"21","author":"Sellars","year":"2014","journal-title":"Semin. Pediatr. Neurol."},{"key":"2024061307214754500_JCS258879C204","doi-asserted-by":"publisher","first-page":"489","DOI":"10.1136\/jmedgenet-2017-105003","article-title":"Homozygous CHST11 mutation in chondrodysplasia, brachydactyly, overriding digits, clino-symphalangism and synpolydactyly","volume":"55","author":"Shabbir","year":"2018","journal-title":"J. Med. Genet."},{"key":"2024061307214754500_JCS258879C205","doi-asserted-by":"publisher","first-page":"D1136","DOI":"10.1093\/nar\/gkz849","article-title":"MatrisomeDB: the ECM-protein knowledge database","volume":"48","author":"Shao","year":"2020","journal-title":"Nucleic Acids Res."},{"key":"2024061307214754500_JCS258879C206","doi-asserted-by":"publisher","first-page":"158","DOI":"10.1016\/j.cell.2010.05.037","article-title":"A comprehensive comparison of transmembrane domains reveals organelle-specific properties","volume":"142","author":"Sharpe","year":"2010","journal-title":"Cell"},{"key":"2024061307214754500_JCS258879C207","doi-asserted-by":"publisher","first-page":"177","DOI":"10.1080\/15216540214923","article-title":"Biosynthesis of chondroitin\/dermatan sulfate","volume":"54","author":"Silbert","year":"2002","journal-title":"IUBMB Life"},{"key":"2024061307214754500_JCS258879C208","doi-asserted-by":"publisher","first-page":"757","DOI":"10.1038\/s41598-017-00618-6","article-title":"Characterization of ATP7A missense mutants suggests a correlation between intracellular trafficking and severity of Menkes disease","volume":"7","author":"Skj\u00f8rringe","year":"2017","journal-title":"Sci. Rep."},{"key":"2024061307214754500_JCS258879C209","doi-asserted-by":"publisher","first-page":"206","DOI":"10.1056\/NEJMoa0900158","article-title":"Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210","volume":"362","author":"Smits","year":"2010","journal-title":"N. Engl. J. Med."},{"key":"2024061307214754500_JCS258879C210","doi-asserted-by":"publisher","first-page":"1463","DOI":"10.1083\/jcb.115.5.1463","article-title":"Uncoupling of chondroitin sulfate glycosaminoglycan synthesis by brefeldin A","volume":"115","author":"Spiro","year":"1991","journal-title":"J. Cell Biol."},{"key":"2024061307214754500_JCS258879C211","doi-asserted-by":"publisher","first-page":"1198","DOI":"10.1126\/science.6729450","article-title":"T and Tn, general carcinoma autoantigens","volume":"224","author":"Springer","year":"1984","journal-title":"Science"},{"key":"2024061307214754500_JCS258879C212","doi-asserted-by":"crossref","first-page":"4132","DOI":"10.1242\/jcs.212308","article-title":"Giantin-knockout models reveal a feedback loop between Golgi function and glycosyltransferase expression","volume":"130","author":"Stevenson","year":"2017","journal-title":"J. Cell Sci."},{"key":"2024061307214754500_JCS258879C213","doi-asserted-by":"publisher","first-page":"e202005166","DOI":"10.1083\/jcb.202005166","article-title":"Giantin is required for intracellular N-terminal processing of type I procollagen","volume":"220","author":"Stevenson","year":"2021","journal-title":"J. Cell Biol."},{"key":"2024061307214754500_JCS258879C214","doi-asserted-by":"publisher","first-page":"18284","DOI":"10.1016\/S0021-9258(17)44750-8","article-title":"Relationship of sulfation to ongoing chondroitin polymerization during biosynthesis of chondroitin 4-sulfate by microsomal preparations from cultured mouse mastocytoma cells","volume":"265","author":"Sugumaran","year":"1990","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C215","doi-asserted-by":"publisher","first-page":"9565","DOI":"10.1016\/S0021-9258(18)92857-7","article-title":"Subfractionation of chick embryo epiphyseal cartilage Golgi. Localization of enzymes involved in the synthesis of the polysaccharide portion of proteochondroitin sulfate","volume":"266","author":"Sugumaran","year":"1991","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C216","doi-asserted-by":"publisher","first-page":"8802","DOI":"10.1016\/S0021-9258(19)50350-7","article-title":"Effects of brefeldin A on the localization of chondroitin sulfate-synthesizing enzymes. Activities in subfractions of the Golgi from chick embryo epiphyseal cartilage","volume":"267","author":"Sugumaran","year":"1992","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C217","doi-asserted-by":"publisher","first-page":"1249","DOI":"10.1091\/mbc.E18-12-0820","article-title":"ARF GTPases and their GEFs and GAPs: concepts and challenges","volume":"30","author":"Sztul","year":"2019","journal-title":"Mol. Biol. Cell"},{"key":"2024061307214754500_JCS258879C218","doi-asserted-by":"publisher","first-page":"41","DOI":"10.1177\/39.1.1898498","article-title":"Biochemical and immunocytochemical characterization of mineral binding proteoglycans in rat bone","volume":"39","author":"Takagi","year":"1991","journal-title":"J. Histochem. Cytochem."},{"key":"2024061307214754500_JCS258879C219","doi-asserted-by":"publisher","first-page":"15","DOI":"10.1042\/bj2660015","article-title":"Isolation and characterization of proteoglycans synthesized by mouse osteoblastic cells in culture during the mineralization process","volume":"266","author":"Takeuchi","year":"1990","journal-title":"Biochem. J."},{"key":"2024061307214754500_JCS258879C220","doi-asserted-by":"publisher","first-page":"711","DOI":"10.1097\/01.gim.0000245578.94312.1e","article-title":"Functional copper transport explains neurologic sparing in occipital horn syndrome","volume":"8","author":"Tang","year":"2006","journal-title":"Genet. Med."},{"key":"2024061307214754500_JCS258879C221","doi-asserted-by":"publisher","first-page":"19771","DOI":"10.1073\/pnas.0609267103","article-title":"Anisotropy of cell adhesive microenvironment governs cell internal organization and orientation of polarity","volume":"103","author":"Thery","year":"2006","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"2024061307214754500_JCS258879C222","doi-asserted-by":"publisher","first-page":"10155","DOI":"10.1073\/pnas.0400334101","article-title":"Loss of chondroitin 6-O-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvement","volume":"101","author":"Thiele","year":"2004","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"2024061307214754500_JCS258879C223","doi-asserted-by":"publisher","first-page":"e41301","DOI":"10.7554\/eLife.41301","article-title":"The spatial separation of processing and transport functions to the interior and periphery of the Golgi stack","volume":"7","author":"Tie","year":"2018","journal-title":"Elife"},{"key":"2024061307214754500_JCS258879C224","doi-asserted-by":"publisher","first-page":"228","DOI":"10.1016\/0012-1606(79)90166-0","article-title":"Tendon collagen fibrillogenesis: intracellular subassemblies and cell surface changes associated with fibril growth","volume":"71","author":"Trelstad","year":"1979","journal-title":"Dev. Biol."},{"key":"2024061307214754500_JCS258879C225","doi-asserted-by":"publisher","first-page":"1071","DOI":"10.1038\/ncb1180","article-title":"Secretory traffic triggers the formation of tubular continuities across Golgi sub-compartments","volume":"6","author":"Trucco","year":"2004","journal-title":"Nat. Cell Biol."},{"key":"2024061307214754500_JCS258879C226","doi-asserted-by":"publisher","first-page":"404","DOI":"10.1126\/science.1159411","article-title":"Signal-Mediated Dynamic Retention of Glycosyltransferases in the Golgi","volume":"321","author":"Tu","year":"2008","journal-title":"Science"},{"key":"2024061307214754500_JCS258879C227","first-page":"63","article-title":"Identification of point mutations in 41 unrelated patients affected with Menkes disease","volume":"60","author":"T\u00fcmer","year":"1997","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C228","doi-asserted-by":"publisher","first-page":"31020","DOI":"10.1074\/jbc.M301179200","article-title":"Localized cdc42 activation, detected using a novel assay, mediates microtubule organizing center positioning in endothelial cells in response to fluid shear stress","volume":"278","author":"Tzima","year":"2003","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C229","doi-asserted-by":"publisher","first-page":"17342","DOI":"10.1038\/srep17342","article-title":"Impaired ATP6V0A2 expression contributes to Golgi dispersion and glycosylation changes in senescent cells","volume":"5","author":"Udono","year":"2015","journal-title":"Sci. Rep."},{"key":"2024061307214754500_JCS258879C230","doi-asserted-by":"publisher","first-page":"3200","DOI":"10.1074\/jbc.272.6.3200","article-title":"Mouse mastocytoma cells synthesize undersulfated heparin and chondroitin sulfate in the presence of brefeldin A","volume":"272","author":"Uhlin-Hansen","year":"1997","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C231","doi-asserted-by":"publisher","first-page":"98","DOI":"10.1038\/s41591-019-0705-y","article-title":"Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies","volume":"26","author":"Unlu","year":"2020","journal-title":"Nat. Med."},{"key":"2024061307214754500_JCS258879C232","doi-asserted-by":"publisher","first-page":"e47318","DOI":"10.7554\/eLife.47318","article-title":"A minimal self-organisation model of the Golgi apparatus","volume":"9","author":"Vagne","year":"2020","journal-title":"Elife"},{"key":"2024061307214754500_JCS258879C233","doi-asserted-by":"publisher","first-page":"216","DOI":"10.1016\/j.ajhg.2016.12.010","article-title":"Mutations in ATP6V1E1 or ATP6V1A cause autosomal-recessive cutis laxa","volume":"100","author":"Van Damme","year":"2017","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C234","doi-asserted-by":"publisher","first-page":"3475","DOI":"10.1093\/hmg\/ddy234","article-title":"Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome","volume":"27","author":"Van Damme","year":"2018","journal-title":"Hum. Mol. Genet."},{"key":"2024061307214754500_JCS258879C235","doi-asserted-by":"publisher","first-page":"11105","DOI":"10.1016\/S0021-9258(18)82098-1","article-title":"Xylosylation is an endoplasmic reticulum to Golgi event","volume":"268","author":"Vertel","year":"1993","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C236","doi-asserted-by":"publisher","first-page":"608","DOI":"10.1016\/j.ajhg.2011.04.002","article-title":"Chondrodysplasia and abnormal joint development associated with mutations in IMPAD1, encoding the Golgi-resident nucleotide phosphatase, gPAPP","volume":"88","author":"Vissers","year":"2011","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C237","doi-asserted-by":"publisher","first-page":"34","DOI":"10.1002\/humu.23070","article-title":"Chondroitin Sulfate N-acetylgalactosaminyltransferase-1 (CSGalNAcT-1) deficiency results in a mild skeletal dysplasia and joint laxity","volume":"38","author":"Vodopiutz","year":"2017","journal-title":"Hum. Mutat."},{"key":"2024061307214754500_JCS258879C238","doi-asserted-by":"publisher","first-page":"623","DOI":"10.1084\/jem.20161525","article-title":"EXTL3 mutations cause skeletal dysplasia, immune deficiency, and developmental delay","volume":"214","author":"Volpi","year":"2017","journal-title":"J. Exp. Med."},{"key":"2024061307214754500_JCS258879C239","doi-asserted-by":"publisher","first-page":"1580","DOI":"10.1002\/ajmg.a.36487","article-title":"Skeletal dysplasia, global developmental delay, and multiple congenital anomalies in a 5-year-old boy-report of the second family with B3GAT3 mutation and expansion of the phenotype","volume":"164a","author":"von Oettingen","year":"2014","journal-title":"Am. J. Med. Genet. A"},{"key":"2024061307214754500_JCS258879C240","doi-asserted-by":"publisher","first-page":"492","DOI":"10.1111\/cge.12413","article-title":"Spondyloepimetaphyseal dysplasia with joint laxity (Beighton type); mutation analysis in eight affected South African families","volume":"87","author":"Vorster","year":"2015","journal-title":"Clin. Genet."},{"key":"2024061307214754500_JCS258879C241","doi-asserted-by":"publisher","first-page":"12","DOI":"10.22203\/eCM.v006a02","article-title":"Differential roles for small leucine-rich proteoglycans in bone formation","volume":"6","author":"Waddington","year":"2003","journal-title":"Eur. Cell Mater."},{"key":"2024061307214754500_JCS258879C242","doi-asserted-by":"publisher","first-page":"dev175596","DOI":"10.1242\/dev.175596","article-title":"The extracellular matrix in development","volume":"147","author":"Walma","year":"2020","journal-title":"Development"},{"key":"2024061307214754500_JCS258879C243","doi-asserted-by":"publisher","first-page":"767","DOI":"10.1111\/tra.12524","article-title":"SNARE proteins in membrane trafficking","volume":"18","author":"Wang","year":"2017","journal-title":"Traffic"},{"key":"2024061307214754500_JCS258879C244","doi-asserted-by":"publisher","first-page":"19549","DOI":"10.1074\/jbc.M300767200","article-title":"Transforming growth factor-beta induces secretion of activated ADAMTS-2. A procollagen III N-proteinase","volume":"278","author":"Wang","year":"2003","journal-title":"J. Biol. Chem."},{"key":"2024061307214754500_JCS258879C245","doi-asserted-by":"publisher","first-page":"164","DOI":"10.1002\/jbm4.10030","article-title":"Age-related deterioration of bone toughness is related to diminishing amount of matrix glycosaminoglycans (GAGS)","volume":"2","author":"Wang","year":"2018","journal-title":"JBMR Plus"},{"key":"2024061307214754500_JCS258879C246","doi-asserted-by":"publisher","first-page":"e124701","DOI":"10.1172\/jci.insight.124701","article-title":"Hypomorphic mutations of TRIP11 cause odontochondrodysplasia","volume":"4","author":"Wehrle","year":"2019","journal-title":"JCI Insight"},{"key":"2024061307214754500_JCS258879C247","doi-asserted-by":"publisher","first-page":"2452","DOI":"10.1002\/1873-3468.13553","article-title":"A tale of short tails, through thick and thin: investigating the sorting mechanisms of Golgi enzymes","volume":"593","author":"Welch","year":"2019","journal-title":"FEBS Lett."},{"key":"2024061307214754500_JCS258879C248","doi-asserted-by":"publisher","first-page":"e202106115","DOI":"10.1083\/jcb.202106115","article-title":"GOLPH3 and GOLPH3L are broad-spectrum COPI adaptors for sorting into intra-Golgi transport vesicles","volume":"220","author":"Welch","year":"2021","journal-title":"J. Cell Biol."},{"key":"2024061307214754500_JCS258879C249","doi-asserted-by":"publisher","first-page":"G950","DOI":"10.1152\/ajpgi.00132.2011","article-title":"The extracellular matrix: an active or passive player in fibrosis?","volume":"301","author":"Wight","year":"2011","journal-title":"Am. J. Physiol. Gastrointest. Liver Physiol."},{"key":"2024061307214754500_JCS258879C250","doi-asserted-by":"publisher","first-page":"5120","DOI":"10.1038\/s41467-020-18794-x","article-title":"Concepts of extracellular matrix remodelling in tumour progression and metastasis","volume":"11","author":"Winkler","year":"2020","journal-title":"Nat. Commun."},{"key":"2024061307214754500_JCS258879C251","first-page":"86","article-title":"The Golgin family of coiled-coil tethering proteins","volume":"3","author":"Witkos","year":"2015","journal-title":"Front. Cell Dev. Biol."},{"key":"2024061307214754500_JCS258879C252","doi-asserted-by":"publisher","first-page":"16","DOI":"10.1016\/j.ceb.2017.02.003","article-title":"Recognition and tethering of transport vesicles at the Golgi apparatus","volume":"47","author":"Witkos","year":"2017","journal-title":"Curr. Opin. Cell Biol."},{"key":"2024061307214754500_JCS258879C253","doi-asserted-by":"publisher","first-page":"127","DOI":"10.1038\/s41467-018-08044-6","article-title":"GORAB scaffolds COPI at the trans-Golgi for efficient enzyme recycling and correct protein glycosylation","volume":"10","author":"Witkos","year":"2019","journal-title":"Nat. Commun."},{"key":"2024061307214754500_JCS258879C254","doi-asserted-by":"publisher","first-page":"550","DOI":"10.1038\/ncb2225","article-title":"TFG-1 function in protein secretion and oncogenesis","volume":"13","author":"Witte","year":"2011","journal-title":"Nat. Cell Biol."},{"key":"2024061307214754500_JCS258879C255","doi-asserted-by":"publisher","first-page":"518","DOI":"10.1038\/nm1041","article-title":"Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder","volume":"10","author":"Wu","year":"2004","journal-title":"Nat. Med."},{"key":"2024061307214754500_JCS258879C256","doi-asserted-by":"publisher","first-page":"346","DOI":"10.1086\/301726","article-title":"Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses","volume":"62","author":"Wuyts","year":"1998","journal-title":"Am. J. Hum. Genet."},{"key":"2024061307214754500_JCS258879C257","doi-asserted-by":"publisher","first-page":"608","DOI":"10.1161\/ATVBAHA.110.220749","article-title":"Decorin GAG synthesis and TGF-beta signaling mediate Ox-LDL-induced mineralization of human vascular smooth muscle cells","volume":"31","author":"Yan","year":"2011","journal-title":"Arterioscler. Thromb. Vasc. Biol."},{"key":"2024061307214754500_JCS258879C258","doi-asserted-by":"publisher","first-page":"2138","DOI":"10.3390\/molecules20022138","article-title":"Tyrosine sulfation as a protein post-translational modification","volume":"20","author":"Yang","year":"2015","journal-title":"Molecules"},{"key":"2024061307214754500_JCS258879C259","doi-asserted-by":"publisher","first-page":"1075","DOI":"10.3892\/ijmm.2012.1091","article-title":"Glycosaminoglycan chains of biglycan promote bone morphogenetic protein-4-induced osteoblast differentiation","volume":"30","author":"Ye","year":"2012","journal-title":"Int. J. Mol. Med."},{"key":"2024061307214754500_JCS258879C260","doi-asserted-by":"publisher","first-page":"145","DOI":"10.1007\/8904_2012_172","article-title":"Bone dysplasia as a key feature in three patients with a novel congenital disorder of glycosylation (CDG) Type II due to a deep intronic splice mutation in TMEM165","volume":"8","author":"Zeevaert","year":"2013","journal-title":"JIMD Rep"},{"key":"2024061307214754500_JCS258879C261","doi-asserted-by":"publisher","first-page":"880","DOI":"10.1177\/154405910408301111","article-title":"Chondroitin sulfate in palatal wound healing","volume":"83","author":"Zou","year":"2004","journal-title":"J. Dent. Res."}],"container-title":["Journal of Cell Science"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.biologists.com\/jcs\/article-pdf\/doi\/10.1242\/jcs.258879\/3489275\/jcs258879.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/journals.biologists.com\/jcs\/article-pdf\/doi\/10.1242\/jcs.258879\/3489275\/jcs258879.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,6,13]],"date-time":"2024-06-13T03:22:29Z","timestamp":1718248949000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.biologists.com\/jcs\/article\/135\/1\/jcs258879\/273996\/Supply-chain-logistics-the-role-of-the-Golgi"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,1,1]]},"references-count":261,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2022,1,1]]}},"URL":"https:\/\/doi.org\/10.1242\/jcs.258879","relation":{},"ISSN":["0021-9533","1477-9137"],"issn-type":[{"value":"0021-9533","type":"print"},{"value":"1477-9137","type":"electronic"}],"subject":[],"published":{"date-parts":[[2022,1,1]]},"article-number":"jcs258879"}}