Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene
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Ehlers-Danlos syndrome type IVEhlers-danlos syndrome, hypermobility type: an underdiagnosed hereditary connective tissue disorder with mucocutaneous, articular, and systemic manifestationsIdentification, characterization, and intracellular processing of ADAM-TS12, a novel human disintegrin with a complex structural organization involving multiple thrombospondin-1 repeatsProcollagen II amino propeptide processing by ADAMTS-3. Insights on dermatosparaxisStructure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpuraBinding of ADAMTS13 to von Willebrand factorCell-surface processing of pro-ADAMTS9 by furinInhibition of ADAMTS-7 and ADAMTS-12 degradation of cartilage oligomeric matrix protein by alpha-2-macroglobulinADAMTS-12 associates with and degrades cartilage oligomeric matrix proteinCharacterization of ADAMTS-9 and ADAMTS-20 as a distinct ADAMTS subfamily related to Caenorhabditis elegans GON-1ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndromeClassical Ehlers-Danlos syndrome caused by a mutation in type I collagen.A disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif (ADAMTS) superfamily: functions and mechanismsFunctional evolution of ADAMTS genes: evidence from analyses of phylogeny and gene organizationADAMTS proteinases: a multi-domain, multi-functional family with roles in extracellular matrix turnover and arthritis.Pathophysiological Function of ADAMTS Enzymes on Molecular Mechanism of Alzheimer's DiseaseThe Function and Roles of ADAMTS-7 in Inflammatory DiseasesProteolytic processing of von Willebrand factor by adamts13 and leukocyte proteasesTransforming growth factor-beta induces secretion of activated ADAMTS-2. A procollagen III N-proteinase.Cloning and characterization of ADAMTS-14, a novel ADAMTS displaying high homology with ADAMTS-2 and ADAMTS-3The ADAMTS(L) family and human genetic disordersDiscovery and characterization of a novel, widely expressed metalloprotease, ADAMTS10, and its proteolytic activationO-fucosylation of thrombospondin type 1 repeats in ADAMTS-like-1/punctin-1 regulates secretion: implications for the ADAMTS superfamilyTransgenic mice with inactive alleles for procollagen N-proteinase (ADAMTS-2) develop fragile skin and male sterilityADAMTS7B, the full-length product of the ADAMTS7 gene, is a chondroitin sulfate proteoglycan containing a mucin domainThe secreted metalloprotease ADAMTS20 is required for melanoblast survivalIdentification and characterization of ADAMTS-20 defines a novel subfamily of metalloproteinases-disintegrins with multiple thrombospondin-1 repeats and a unique GON domainThe ADAMTS metalloproteinasesIdentification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta.Systematic data-querying of large pediatric biorepository identifies novel Ehlers-Danlos Syndrome variantMutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.ADAMTS9 is a cell-autonomously acting, anti-angiogenic metalloprotease expressed by microvascular endothelial cells.Granulin-epithelin precursor binds directly to ADAMTS-7 and ADAMTS-12 and inhibits their degradation of cartilage oligomeric matrix proteinCollagens and collagen-related diseases.Biosynthetic processing of the Pro-alpha1(V)Pro-alpha2(V)Pro-alpha3(V) procollagen heterotrimer.First mouse model for combined osteogenesis imperfecta and Ehlers-Danlos syndrome.The genetics of eye disorders in the dogADAMTS-7: a metalloproteinase that directly binds to and degrades cartilage oligomeric matrix proteinC. elegans ADAMTS ADT-2 regulates body size by modulating TGFβ signaling and cuticle collagen organization.Treatment of periodontal disease in a patient with Ehlers-Danlos syndrome. A case report and literature review.
P2860
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P2860
Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene
description
1999 nî lūn-bûn
@nan
1999 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@ast
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@en
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@en-gb
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@nl
type
label
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@ast
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@en
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@en-gb
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@nl
prefLabel
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@ast
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@en
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@en-gb
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@nl
P2093
P2860
P921
P3181
P356
P1476
Human Ehlers-Danlos syndrome t ...... rocollagen I N-proteinase gene
@en
P2093
B V Nusgens
C M Lapière
D J Prockop
U Schwarze
P2860
P304
P3181
P356
10.1086/302504
P407
P577
1999-08-01T00:00:00Z