{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,27]],"date-time":"2026-09-27T13:42:43Z","timestamp":1790516563574,"version":"4.1.0"},"reference-count":62,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2019,9,1]],"date-time":"2019-09-01T00:00:00Z","timestamp":1567296000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,9,1]],"date-time":"2019-09-01T00:00:00Z","timestamp":1567296000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2019,9,1]],"date-time":"2019-09-01T00:00:00Z","timestamp":1567296000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2019,9,1]],"date-time":"2019-09-01T00:00:00Z","timestamp":1567296000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2019,9,1]],"date-time":"2019-09-01T00:00:00Z","timestamp":1567296000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2019,9,1]],"date-time":"2019-09-01T00:00:00Z","timestamp":1567296000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2019,9,1]],"date-time":"2019-09-01T00:00:00Z","timestamp":1567296000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"funder":[{"DOI":"10.13039\/100000009","name":"Foundation for the National Institutes of Health","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000009","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100008582","name":"McGill University","doi-asserted-by":"publisher","award":["1S10RR026820-01"],"award-info":[{"award-number":["1S10RR026820-01"]}],"id":[{"id":"10.13039\/100008582","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["AR070748"],"award-info":[{"award-number":["AR070748"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["AR44745"],"award-info":[{"award-number":["AR44745"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["AR53890"],"award-info":[{"award-number":["AR53890"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Matrix Biology"],"published-print":{"date-parts":[[2019,9]]},"DOI":"10.1016\/j.matbio.2019.02.001","type":"journal-article","created":{"date-parts":[[2019,2,10]],"date-time":"2019-02-10T05:29:09Z","timestamp":1549776549000},"page":"38-53","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":33,"special_numbering":"C","title":["Limb- and tendon-specific Adamtsl2 deletion identifies a role for ADAMTSL2 in tendon growth in a mouse model for geleophysic dysplasia"],"prefix":"10.1016","volume":"82","author":[{"given":"Dirk","family":"Hubmacher","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nandaraj","family":"Taye","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zerina","family":"Balic","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Stetson","family":"Thacker","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sheila M.","family":"Adams","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4865-9088","authenticated-orcid":false,"given":"David E.","family":"Birk","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ronen","family":"Schweitzer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Suneel S.","family":"Apte","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.matbio.2019.02.001_bb0005","doi-asserted-by":"crossref","first-page":"1119","DOI":"10.1038\/ng.199","article-title":"ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-beta bioavailability regulation","volume":"40","author":"Le Goff","year":"2008","journal-title":"Nat. Genet."},{"key":"10.1016\/j.matbio.2019.02.001_bb0010","doi-asserted-by":"crossref","first-page":"417","DOI":"10.1136\/jmg.2010.087544","article-title":"Molecular screening of ADAMTSL2 gene in 33 patients reveals the genetic heterogeneity of geleophysic dysplasia","volume":"48","author":"Allali","year":"2011","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.matbio.2019.02.001_bb0015","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1016\/j.ajhg.2011.05.012","article-title":"Mutations in the TGFbeta binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias","volume":"89","author":"Le Goff","year":"2011","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.matbio.2019.02.001_bb0020","first-page":"418","article-title":"Genetic and molecular aspects of acromelic dysplasia","volume":"6","author":"Le Goff","year":"2009","journal-title":"Pediatr. Endocrinol. Rev."},{"key":"10.1016\/j.matbio.2019.02.001_bb0025","doi-asserted-by":"crossref","first-page":"161","DOI":"10.1179\/146532808X302206","article-title":"Clinical and morphological phenotype of geleophysic dysplasia","volume":"28","author":"Giray","year":"2008","journal-title":"Ann. Trop. Paediatr."},{"key":"10.1016\/j.matbio.2019.02.001_bb0030","doi-asserted-by":"crossref","first-page":"818","DOI":"10.1080\/01443610500336058","article-title":"Geleophysic dysplasia: a patient with a severe form of the disorder","volume":"25","author":"Panagopoulos","year":"2005","journal-title":"J. Obstet. Gynaecol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0035","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1002\/(SICI)1096-8628(19971003)72:1<85::AID-AJMG18>3.0.CO;2-Q","article-title":"Patients with geleophysic dysplasia are not always geleophysic","volume":"72","author":"Santolaya","year":"1997","journal-title":"Am. J. Med. Genet."},{"key":"10.1016\/j.matbio.2019.02.001_bb0040","doi-asserted-by":"crossref","first-page":"50","DOI":"10.1002\/(SICI)1096-8628(19960503)63:1<50::AID-AJMG11>3.0.CO;2-T","article-title":"Clinical and ultrastructural findings in three patients with geleophysic dysplasia","volume":"63","author":"Pontz","year":"1996","journal-title":"Am. J. Med. Genet."},{"key":"10.1016\/j.matbio.2019.02.001_bb0045","doi-asserted-by":"crossref","first-page":"227","DOI":"10.1016\/S0022-3476(05)80534-7","article-title":"Geleophysic dysplasia: a storage disorder affecting the skin, bone, liver, heart, and trachea","volume":"117","author":"Shohat","year":"1990","journal-title":"J. Pediatr."},{"key":"10.1016\/j.matbio.2019.02.001_bb0050","article-title":"Fibrillin protein pleiotropy: acromelic dysplasias","author":"Sakai","year":"2018","journal-title":"Matrix Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0055","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0012817","article-title":"An ADAMTSL2 founder mutation causes Musladin-Lueke Syndrome, a heritable disorder of beagle dogs, featuring stiff skin and joint contractures","volume":"5","author":"Bader","year":"2010","journal-title":"PLoS One"},{"key":"10.1016\/j.matbio.2019.02.001_bb0060","doi-asserted-by":"crossref","first-page":"532","DOI":"10.1111\/jvim.14654","article-title":"Clinical phenotype of Musladin-Lueke syndrome in 2 beagles","volume":"31","author":"Packer","year":"2017","journal-title":"J. Vet. Intern. Med."},{"key":"10.1016\/j.matbio.2019.02.001_bb0065","doi-asserted-by":"crossref","first-page":"31493","DOI":"10.1074\/jbc.R109.052340","article-title":"A disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif (ADAMTS) superfamily: functions and mechanisms","volume":"284","author":"Apte","year":"2009","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.matbio.2019.02.001_bb0070","doi-asserted-by":"crossref","first-page":"431","DOI":"10.1016\/j.matbio.2007.03.003","article-title":"ADAMTS-like 2 (ADAMTSL2) is a secreted glycoprotein that is widely expressed during mouse embryogenesis and is regulated during skeletal myogenesis","volume":"26","author":"Koo","year":"2007","journal-title":"Matrix Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0075","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1016\/j.matbio.2018.06.002","article-title":"ADAMTS proteins in human disorders","volume":"71\u201372","author":"Mead","year":"2018","journal-title":"Matrix Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0080","doi-asserted-by":"crossref","first-page":"24","DOI":"10.1016\/j.matbio.2015.03.001","article-title":"Insights on ADAMTS proteases and ADAMTS-like proteins from mammalian genetics","volume":"44\u201346","author":"Dubail","year":"2015","journal-title":"Matrix Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0085","doi-asserted-by":"crossref","first-page":"34","DOI":"10.1016\/j.matbio.2015.05.004","article-title":"ADAMTS proteins as modulators of microfibril formation and function","volume":"47","author":"Hubmacher","year":"2015","journal-title":"Matrix Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0090","doi-asserted-by":"crossref","first-page":"1079","DOI":"10.1016\/j.biocel.2003.12.010","article-title":"Papilin, a novel component of basement membranes, in relation to ADAMTS metalloproteases and ECM development","volume":"36","author":"Fessler","year":"2004","journal-title":"Int. J. Biochem. Cell Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0095","doi-asserted-by":"crossref","first-page":"558","DOI":"10.1016\/j.ajhg.2009.09.011","article-title":"Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature","volume":"85","author":"Morales","year":"2009","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.matbio.2019.02.001_bb0100","doi-asserted-by":"crossref","first-page":"1425","DOI":"10.1002\/humu.20797","article-title":"Functional analysis of an ADAMTS10 signal peptide mutation in Weill-Marchesani syndrome demonstrates a long-range effect on secretion of the full-length enzyme","volume":"29","author":"Kutz","year":"2008","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.matbio.2019.02.001_bb0105","doi-asserted-by":"crossref","first-page":"34","DOI":"10.1136\/jmg.40.1.34","article-title":"In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome","volume":"40","author":"Faivre","year":"2003","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.matbio.2019.02.001_bb0110","doi-asserted-by":"crossref","first-page":"801","DOI":"10.1086\/425231","article-title":"ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndrome","volume":"75","author":"Dagoneau","year":"2004","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.matbio.2019.02.001_bb0115","doi-asserted-by":"crossref","first-page":"2305","DOI":"10.1002\/ajmg.a.36044","article-title":"Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndrome","volume":"161A","author":"Cecchi","year":"2013","journal-title":"Am. J. Med. Genet. A"},{"key":"10.1016\/j.matbio.2019.02.001_bb0120","series-title":"The Extracellular Matrix; An Overview","first-page":"233","author":"Hubmacher","year":"2011"},{"key":"10.1016\/j.matbio.2019.02.001_bb0125","doi-asserted-by":"crossref","first-page":"13874","DOI":"10.1074\/jbc.M707820200","article-title":"Targeting of bone morphogenetic protein growth factor complexes to fibrillin","volume":"283","author":"Sengle","year":"2008","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.matbio.2019.02.001_bb0130","doi-asserted-by":"crossref","first-page":"5087","DOI":"10.1074\/jbc.M110.188615","article-title":"Prodomains of transforming growth factor beta (TGFbeta) superfamily members specify different functions: extracellular matrix interactions and growth factor bioavailability","volume":"286","author":"Sengle","year":"2011","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.matbio.2019.02.001_bb0135","doi-asserted-by":"crossref","first-page":"410","DOI":"10.1002\/jcb.23385","article-title":"LTBPs, more than just an escort service","volume":"113","author":"Todorovic","year":"2012","journal-title":"J. Cell. Biochem."},{"key":"10.1016\/j.matbio.2019.02.001_bb0140","doi-asserted-by":"crossref","first-page":"82","DOI":"10.1016\/j.matbio.2017.07.004","article-title":"Marfan syndrome; a connective tissue disease at the crossroads of mechanotransduction, TGFbeta signaling and cell stemness","volume":"71\u201372","author":"Ramirez","year":"2018","journal-title":"Matrix Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0145","doi-asserted-by":"crossref","first-page":"487","DOI":"10.1242\/dmm.017046","article-title":"Adamtsl2 deletion results in bronchial fibrillin microfibril accumulation and bronchial epithelial dysplasia-a novel mouse model providing insights into geleophysic dysplasia","volume":"8","author":"Hubmacher","year":"2015","journal-title":"Dis. Model. Mech."},{"key":"10.1016\/j.matbio.2019.02.001_bb0150","doi-asserted-by":"crossref","first-page":"87","DOI":"10.3109\/03008209509028396","article-title":"Fibrillin-1 and fibrillin-2 show temporal and tissue-specific regulation of expression in developing elastic tissues","volume":"31","author":"Mariencheck","year":"1995","journal-title":"Connect. Tissue Res."},{"key":"10.1016\/j.matbio.2019.02.001_bb0155","doi-asserted-by":"crossref","first-page":"1165","DOI":"10.1083\/jcb.129.4.1165","article-title":"Developmental expression of fibrillin genes suggests heterogeneity of extracellular microfibrils","volume":"129","author":"Zhang","year":"1995","journal-title":"J. Cell Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0160","doi-asserted-by":"crossref","first-page":"43","DOI":"10.1016\/j.matbio.2010.10.003","article-title":"Fibrillin-3 expression in human development","volume":"30","author":"Sabatier","year":"2011","journal-title":"Matrix Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0165","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1002\/gene.10092","article-title":"Expression of Cre recombinase in the developing mouse limb bud driven by a Prxl enhancer","volume":"33","author":"Logan","year":"2002","journal-title":"Genesis (New York, N.Y.: 2000)"},{"key":"10.1016\/j.matbio.2019.02.001_bb0170","doi-asserted-by":"crossref","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":"10.1016\/j.matbio.2019.02.001_bb0175","doi-asserted-by":"crossref","first-page":"9636","DOI":"10.1074\/jbc.274.14.9636","article-title":"Fibromodulin-null mice have abnormal collagen fibrils, tissue organization, and altered lumican deposition in tendon","volume":"274","author":"Svensson","year":"1999","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.matbio.2019.02.001_bb0180","doi-asserted-by":"crossref","first-page":"729","DOI":"10.1083\/jcb.136.3.729","article-title":"Targeted disruption of decorin leads to abnormal collagen fibril morphology and skin fragility","volume":"136","author":"Danielson","year":"1997","journal-title":"J. Cell Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0185","doi-asserted-by":"crossref","first-page":"673","DOI":"10.1096\/fj.01-0848com","article-title":"Abnormal collagen fibrils in tendons of biglycan\/fibromodulin-deficient mice lead to gait impairment, ectopic ossification, and osteoarthritis","volume":"16","author":"Ameye","year":"2002","journal-title":"FASEB J."},{"key":"10.1016\/j.matbio.2019.02.001_bb0190","doi-asserted-by":"crossref","first-page":"846","DOI":"10.1091\/mbc.e08-08-0830","article-title":"Fibrillin assembly requires fibronectin","volume":"20","author":"Sabatier","year":"2009","journal-title":"Mol. Biol. Cell"},{"key":"10.1016\/j.matbio.2019.02.001_bb0195","doi-asserted-by":"crossref","first-page":"8337","DOI":"10.1167\/iovs.13-13121","article-title":"Nonselective assembly of fibrillin 1 and fibrillin 2 in the rodent ocular zonule and in cultured cells: implications for Marfan syndrome","volume":"54","author":"Beene","year":"2013","journal-title":"Invest. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.matbio.2019.02.001_bb0200","doi-asserted-by":"crossref","first-page":"50795","DOI":"10.1074\/jbc.M210611200","article-title":"Homo- and heterotypic fibrillin-1 and -2 interactions constitute the basis for the assembly of microfibrils","volume":"277","author":"Lin","year":"2002","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.matbio.2019.02.001_bb0205","doi-asserted-by":"crossref","first-page":"8","DOI":"10.6065\/apem.2015.20.1.8","article-title":"Pubertal growth and epiphyseal fusion","volume":"20","author":"Shim","year":"2015","journal-title":"Ann. Pediatr. Endocrinol. Metab."},{"key":"10.1016\/j.matbio.2019.02.001_bb0210","doi-asserted-by":"crossref","first-page":"T1","DOI":"10.1530\/JME-14-0022","article-title":"Recent research on the growth plate: recent insights into the regulation of the growth plate","volume":"53","author":"Lui","year":"2014","journal-title":"J. Mol. Endocrinol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0215","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1016\/j.semcdb.2016.05.007","article-title":"Signaling pathways effecting crosstalk between cartilage and adjacent tissues: seminars in cell and developmental biology: the biology and pathology of cartilage","volume":"62","author":"Maes","year":"2017","journal-title":"Semin. Cell Dev. Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0220","doi-asserted-by":"crossref","first-page":"334","DOI":"10.1002\/humu.20854","article-title":"Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature","volume":"30","author":"Callewaert","year":"2009","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.matbio.2019.02.001_bb0225","doi-asserted-by":"crossref","first-page":"276","DOI":"10.1111\/j.1399-0004.2009.01204.x","article-title":"Lethal cutis laxa with contractural arachnodactyly, overgrowth and soft tissue bleeding due to a novel homozygous fibulin-4 gene mutation","volume":"76","author":"Hoyer","year":"2009","journal-title":"Clin. Genet."},{"key":"10.1016\/j.matbio.2019.02.001_bb0230","doi-asserted-by":"crossref","first-page":"456","DOI":"10.1038\/ng1295-456","article-title":"Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly","volume":"11","author":"Putnam","year":"1995","journal-title":"Nat. Genet."},{"key":"10.1016\/j.matbio.2019.02.001_bb0235","doi-asserted-by":"crossref","first-page":"250","DOI":"10.1002\/dvdy.10160","article-title":"Multiple mechanisms of perichondrial regulation of cartilage growth","volume":"225","author":"Di Nino","year":"2002","journal-title":"Dev. Dyn."},{"key":"10.1016\/j.matbio.2019.02.001_bb0240","doi-asserted-by":"crossref","first-page":"1067","DOI":"10.1242\/dev.125.6.1067","article-title":"Regulation of growth region cartilage proliferation and differentiation by perichondrium","volume":"125","author":"Long","year":"1998","journal-title":"Development"},{"key":"10.1016\/j.matbio.2019.02.001_bb0245","doi-asserted-by":"crossref","first-page":"1179","DOI":"10.1016\/S0969-2126(03)00181-3","article-title":"Tendon cell array isolation reveals a previously unknown fibrillin-2-containing macromolecular assembly","volume":"11","author":"Ritty","year":"2003","journal-title":"Structure"},{"key":"10.1016\/j.matbio.2019.02.001_bb0250","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1002\/ajpa.20155","article-title":"The aging of Wolff's \u201claw\u201d: ontogeny and responses to mechanical loading in cortical bone","volume":"39","author":"Pearson","year":"2004","journal-title":"Am. J. Phys. Anthropol. Suppl."},{"key":"10.1016\/j.matbio.2019.02.001_bb0255","doi-asserted-by":"crossref","first-page":"2707","DOI":"10.1096\/fj.201800753RR","article-title":"Impairment of chondrogenesis and microfibrillar network in Adamtsl2 deficiency","volume":"33","author":"Delhon","year":"2019","journal-title":"FASEB J."},{"key":"10.1016\/j.matbio.2019.02.001_bb0265","doi-asserted-by":"crossref","first-page":"17156","DOI":"10.1074\/jbc.M111.231571","article-title":"ADAMTS10 protein interacts with fibrillin-1 and promotes its deposition in extracellular matrix of cultured fibroblasts","volume":"286","author":"Kutz","year":"2011","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.matbio.2019.02.001_bb0270","article-title":"Adamts10 inactivation in mice leads to persistence of ocular microfibrils subsequent to reduced fibrillin-2 cleavage","author":"Wang","year":"2018","journal-title":"Matrix Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0275","doi-asserted-by":"crossref","first-page":"4454","DOI":"10.1093\/hmg\/ddv181","article-title":"A microfibril assembly assay identifies different mechanisms of dominance underlying Marfan syndrome, stiff skin syndrome and acromelic dysplasias","volume":"24","author":"Jensen","year":"2015","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.matbio.2019.02.001_bb0280","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0048634","article-title":"Fibrillin-1 mutations causing Weill-Marchesani syndrome and acromicric and geleophysic dysplasias disrupt heparan sulfate interactions","volume":"7","author":"Cain","year":"2012","journal-title":"PLoS One"},{"key":"10.1016\/j.matbio.2019.02.001_bb0285","doi-asserted-by":"crossref","first-page":"36035","DOI":"10.1074\/jbc.M104985200","article-title":"Interactions of fibrillin-1 with heparin\/heparan sulfate, implications for microfibrillar assembly","volume":"276","author":"Tiedemann","year":"2001","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.matbio.2019.02.001_bb0290","doi-asserted-by":"crossref","first-page":"861","DOI":"10.1016\/j.devcel.2009.10.010","article-title":"Bone ridge patterning during musculoskeletal assembly is mediated through SCX regulation of Bmp4 at the tendon-skeleton junction","volume":"17","author":"Blitz","year":"2009","journal-title":"Dev. Cell"},{"key":"10.1016\/j.matbio.2019.02.001_bb0295","doi-asserted-by":"crossref","first-page":"687","DOI":"10.1016\/j.devcel.2009.09.008","article-title":"ADAMTS metalloproteases generate active versican fragments that regulate interdigital web regression","volume":"17","author":"McCulloch","year":"2009","journal-title":"Dev. Cell"},{"key":"10.1016\/j.matbio.2019.02.001_bb0300","doi-asserted-by":"crossref","first-page":"231","DOI":"10.1016\/S0945-053X(96)90114-6","article-title":"Immunolocalization of type X collagen in normal fetal and adult osteoarthritic cartilage with monoclonal antibodies","volume":"15","author":"Girkontaite","year":"1996","journal-title":"Matrix Biol."},{"key":"10.1016\/j.matbio.2019.02.001_bb0305","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0042522","article-title":"Nuclear morphometric analysis (NMA): screening of senescence, apoptosis and nuclear irregularities","volume":"7","author":"Filippi-Chiela","year":"2012","journal-title":"PLoS One"},{"key":"10.1016\/j.matbio.2019.02.001_bb0310","doi-asserted-by":"crossref","first-page":"41871","DOI":"10.1038\/srep41871","article-title":"Unusual life cycle and impact on microfibril assembly of ADAMTS17, a secreted metalloprotease mutated in genetic eye disease","volume":"7","author":"Hubmacher","year":"2017","journal-title":"Sci. Rep."},{"key":"10.1016\/j.matbio.2019.02.001_bb0315","doi-asserted-by":"crossref","first-page":"25533","DOI":"10.1074\/jbc.M709962200","article-title":"Deficiency in microfibril-associated glycoprotein-1 leads to complex phenotypes in multiple organ systems","volume":"283","author":"Weinbaum","year":"2008","journal-title":"J. Biol. Chem."}],"container-title":["Matrix Biology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0945053X1830372X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0945053X1830372X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,15]],"date-time":"2025-10-15T18:58:25Z","timestamp":1760554705000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0945053X1830372X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,9]]},"references-count":62,"alternative-id":["S0945053X1830372X"],"URL":"https:\/\/doi.org\/10.1016\/j.matbio.2019.02.001","relation":{},"ISSN":["0945-053X"],"issn-type":[{"value":"0945-053X","type":"print"}],"subject":[],"published":{"date-parts":[[2019,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Limb- and tendon-specific Adamtsl2 deletion identifies a role for ADAMTSL2 in tendon growth in a mouse model for geleophysic dysplasia","name":"articletitle","label":"Article Title"},{"value":"Matrix Biology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.matbio.2019.02.001","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2019 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}