Type VI collagen anchors endothelial basement membranes by interacting with type IV collagen
about
Perlecan protein core interacts with extracellular matrix protein 1 (ECM1), a glycoprotein involved in bone formation and angiogenesisMatrix metalloproteinase-11/stromelysin-3 exhibits collagenolytic function against collagen VI under normal and malignant conditionsThe first draft of the endostatin interaction networkMutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophyA mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathyCollagen VI related muscle disordersHemorrhage Caused by Snake Venom Metalloproteinases: A Journey of Discovery and UnderstandingA TALEN-Exon Skipping Design for a Bethlem Myopathy Model in ZebrafishA collagen VI-dependent pathogenic mechanism for Hirschsprung's disease.Fibrillins in TendonA Comprehensive View of the Structural and Functional Alterations of Extracellular Matrix by Snake Venom Metalloproteinases (SVMPs): Novel Perspectives on the Pathophysiology of EnvenomingSelf-assembly and supramolecular organization of EMILINFibroblast growth factor-binding protein is a novel partner for perlecan protein coreThe protein core of the proteoglycan perlecan binds specifically to fibroblast growth factor-7Evidence for a direct interaction between the tumor suppressor serpin, maspin, and types I and III collagenIdentification of a major microfibril-associated glycoprotein-1-binding domain in fibrillin-2Congenital muscular dystrophies: a brief reviewTranscriptome Analysis of Ullrich Congenital Muscular Dystrophy Fibroblasts Reveals a Disease Extracellular Matrix Signature and Key Molecular RegulatorsMMP mediated degradation of type VI collagen is highly associated with liver fibrosis--identification and validation of a novel biochemical marker assayMice lacking the extracellular matrix protein WARP develop normally but have compromised peripheral nerve structure and functionWARP is a new member of the von Willebrand factor A-domain superfamily of extracellular matrix proteinsRole of collagens and perlecan in microvascular stability: exploring the mechanism of capillary vessel damage by snake venom metalloproteinases.Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy.Biglycan and decorin bind close to the n-terminal region of the collagen VI triple helix.Characterization of EHD4, an EH domain-containing protein expressed in the extracellular matrix.Biglycan organizes collagen VI into hexagonal-like networks resembling tissue structures.Microfibril-associated glycoprotein-2 interacts with fibrillin-1 and fibrillin-2 suggesting a role for MAGP-2 in elastic fiber assembly.ADAMTS1 interacts with, cleaves, and modifies the extracellular location of the matrix inhibitor tissue factor pathway inhibitor-2.Three-dimensional architecture of collagen type VI in the human trabecular meshworkCMG2/ANTXR2 regulates extracellular collagen VI which accumulates in hyaline fibromatosis syndromePneumothoraces in collagen VI-related dystrophy: a case series and recommendations for management.New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.Distinct mitral valve proteomic profiles in rheumatic heart disease and myxomatous degeneration.The collagen VI-related myopathies Ullrich congenital muscular dystrophy and Bethlem myopathy.Mitochondrial dysfunction and defective autophagy in the pathogenesis of collagen VI muscular dystrophies.Overexpression of type VI collagen in neoplastic lung tissues.Proteomics of Fuchs' endothelial corneal dystrophy support that the extracellular matrix of Descemet's membrane is disorderedWARP interacts with collagen VI-containing microfibrils in the pericellular matrix of human chondrocytes.Melanocytes from Patients Affected by Ullrich Congenital Muscular Dystrophy and Bethlem Myopathy have Dysfunctional Mitochondria That Can be Rescued with Cyclophilin Inhibitors.Basement membranes: cell scaffoldings and signaling platforms.
P2860
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P2860
Type VI collagen anchors endothelial basement membranes by interacting with type IV collagen
description
1997 nî lūn-bûn
@nan
1997 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Type VI collagen anchors endot ...... eracting with type IV collagen
@ast
Type VI collagen anchors endot ...... eracting with type IV collagen
@en
Type VI collagen anchors endot ...... eracting with type IV collagen
@nl
type
label
Type VI collagen anchors endot ...... eracting with type IV collagen
@ast
Type VI collagen anchors endot ...... eracting with type IV collagen
@en
Type VI collagen anchors endot ...... eracting with type IV collagen
@nl
prefLabel
Type VI collagen anchors endot ...... eracting with type IV collagen
@ast
Type VI collagen anchors endot ...... eracting with type IV collagen
@en
Type VI collagen anchors endot ...... eracting with type IV collagen
@nl
P2093
P3181
P356
P1476
Type VI collagen anchors endot ...... eracting with type IV collagen
@en
P2093
C L Maslen
R W Glanville
P304
P3181
P356
10.1074/JBC.272.42.26522
P407
P577
1997-10-17T00:00:00Z