A disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motifs: the ADAMTS family
about
ADAMTS10 protein interacts with fibrillin-1 and promotes its deposition in extracellular matrix of cultured fibroblasts.Regulated expression of ADAMTS-12 in human trophoblastic cells: a role for ADAMTS-12 in epithelial cell invasion?Negative effects of ADAMTS-7 and ADAMTS-12 on endplate cartilage differentiationCell-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 proteinADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-beta bioavailability regulationADAMTS10 mutations in autosomal recessive Weill-Marchesani syndromeCurrent concepts in thrombotic thrombocytopenic purpuraFunctional 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.Genetic and functional linkage between ADAMTS superfamily proteins and fibrillin-1: a novel mechanism influencing microfibril assembly and functionThe 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 superfamilyADAMTS7B, the full-length product of the ADAMTS7 gene, is a chondroitin sulfate proteoglycan containing a mucin domainThe secreted metalloprotease ADAMTS20 is required for melanoblast survivalA case of Weill-Marchesani syndrome with inversion of chromosome 15.Systematic data-querying of large pediatric biorepository identifies novel Ehlers-Danlos Syndrome variantIdentification and characterization of human archaemetzincin-1 and -2, two novel members of a family of metalloproteases widely distributed in Archaea.The evolution of the vertebrate metzincins; insights from Ciona intestinalis and Danio rerio.Cloning, expression and functional characterization of the full-length murine ADAMTS13.Enzymatically active ADAMTS13 variants are not inhibited by anti-ADAMTS13 autoantibodies: a novel therapeutic strategy?An IAP retrotransposon in the mouse ADAMTS13 gene creates ADAMTS13 variant proteins that are less effective in cleaving von Willebrand factor multimers.Thrombotic thrombocytopenic purpura: a thrombotic disorder caused by ADAMTS13 deficiencyThe kidney in thrombotic thrombocytopenic purpura.ADAMTS13 and von Willebrand factor interactions.ADAMTS9 is a cell-autonomously acting, anti-angiogenic metalloprotease expressed by microvascular endothelial cells.Genome-wide association study of high-altitude pulmonary edema in a Han Chinese population.Tumor-specific urinary matrix metalloproteinase fingerprinting: identification of high molecular weight urinary matrix metalloproteinase species.Metabolism of cartilage proteoglycans in health and diseaseGranulin-epithelin precursor binds directly to ADAMTS-7 and ADAMTS-12 and inhibits their degradation of cartilage oligomeric matrix proteinGonadal steroids regulate the expression of aggrecanases in human endometrial stromal cells in vitro.Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process.Regulation of thrombospondin1 by extracellular proteases.ADAMTS proteoglycanases in the physiological and pathological central nervous systemDiminished bone formation during diabetic fracture healing is related to the premature resorption of cartilage associated with increased osteoclast activityWhy Do We Need ADAMTS13?N-glycoproteome analysis of the secretome of human metastatic hepatocellular carcinoma cell lines combining hydrazide chemistry, HILIC enrichment and mass spectrometryADAMTS1 mediates the release of antiangiogenic polypeptides from TSP1 and 2
P2860
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P2860
A disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motifs: the ADAMTS family
description
2004 nî lūn-bûn
@nan
2004 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
A disintegrin-like and metallo ...... pe 1 motifs: the ADAMTS family
@ast
A disintegrin-like and metallo ...... pe 1 motifs: the ADAMTS family
@en
A disintegrin-like and metallo ...... pe 1 motifs: the ADAMTS family
@nl
type
label
A disintegrin-like and metallo ...... pe 1 motifs: the ADAMTS family
@ast
A disintegrin-like and metallo ...... pe 1 motifs: the ADAMTS family
@en
A disintegrin-like and metallo ...... pe 1 motifs: the ADAMTS family
@nl
prefLabel
A disintegrin-like and metallo ...... pe 1 motifs: the ADAMTS family
@ast
A disintegrin-like and metallo ...... pe 1 motifs: the ADAMTS family
@en
A disintegrin-like and metallo ...... pe 1 motifs: the ADAMTS family
@nl
P3181
P1476
A disintegrin-like and metallo ...... pe 1 motifs: the ADAMTS family
@en
P2093
Suneel S Apte
P3181
P356
10.1016/J.BIOCEL.2004.01.014
P407
P577
2004-06-01T00:00:00Z