Electron-microscopical approach to a structural model of intima collagen
about
Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrilsSequence analysis of alpha 1(VI) and alpha 2(VI) chains of human type VI collagen reveals internal triplication of globular domains similar to the A domains of von Willebrand factor and two alpha 2(VI) chain variants that differ in the carboxy termiThe membrane-spanning proteoglycan NG2 binds to collagens V and VI through the central nonglobular domain of its core proteinThree novel collagen VI chains, alpha4(VI), alpha5(VI), and alpha6(VI)150-kD von Willebrand factor binding protein extracted from human vascular subendothelium is type VI collagenMosaic structure of globular domains in the human type VI collagen alpha 3 chain: similarity to von Willebrand factor, fibronectin, actin, salivary proteins and aprotinin type protease inhibitorsMutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophyChromosomal assignments of the genes coding for human types II, III, and IV collagen: a dispersed gene familyIdentification and characterization of the human type II collagen gene (COL2A1)Partial characterization of a low molecular weight human collagen that undergoes alternative splicingCollagen VI related muscle disordersRegulation of corneal stroma extracellular matrix assemblyA TALEN-Exon Skipping Design for a Bethlem Myopathy Model in ZebrafishStructural basis of type VI collagen dimer formation.Microfibril-associated glycoprotein-1 (MAGP-1) binds to the pepsin-resistant domain of the alpha3(VI) chain of type VI collagenRecombinant expression and structural and binding properties of alpha 1(VI) and alpha 2(VI) chains of human collagen type VIBinding of the NG2 proteoglycan to type VI collagen and other extracellular matrix moleculesCharacterization of three constituent chains of collagen type VI by peptide sequences and cDNA clonesDysfunction of mitochondria and sarcoplasmic reticulum in the pathogenesis of collagen VI muscular dystrophiesThe C5 domain of the collagen VI alpha3(VI) chain is critical for extracellular microfibril formation and is present in the extracellular matrix of cultured cellsA structure of a collagen VI VWA domain displays N and C termini at opposite sides of the protein.Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy.Ultrastructure of type VI collagen in human skin and cartilage suggests an anchoring function for this filamentous networkType VI collagen in extracellular, 100-nm periodic filaments and fibrils: identification by immunoelectron microscopy.Biglycan and decorin bind close to the n-terminal region of the collagen VI triple helix.Biglycan organizes collagen VI into hexagonal-like networks resembling tissue structures.Multiple forms of chicken alpha 3(VI) collagen chain generated by alternative splicing in type A repeated domainsThe globular domains of type VI collagen are related to the collagen-binding domains of cartilage matrix protein and von Willebrand factorThree-dimensional architecture of collagen type VI in the human trabecular meshworkPolymorphism of DNA sequence in the human pro alpha 2(I) collagen geneCollagen genes and proteins in osteogenesis imperfecta.Endotrophin triggers adipose tissue fibrosis and metabolic dysfunctionType VI collagen is composed of a 200 kd subunit and two 140 kd subunitsNew molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.Structure of recombinant N-terminal globule of type VI collagen alpha 3 chain and its binding to heparin and hyaluronan.The collagen VI-related myopathies Ullrich congenital muscular dystrophy and Bethlem myopathy.Substrate-dependent morphology of supramolecular assemblies: fibrillin and type-VI collagen microfibrils.Collagen VI microfibril formation is abolished by an {alpha}2(VI) von Willebrand factor type A domain mutation in a patient with Ullrich congenital muscular dystrophyMitochondrial dysfunction and defective autophagy in the pathogenesis of collagen VI muscular dystrophies.The expanded collagen VI family: new chains and new questions
P2860
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P2860
Electron-microscopical approach to a structural model of intima collagen
description
1983 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1983 թվականի մայիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1983
@ast
im Mai 1983 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1983/05/01)
@sk
vědecký článek publikovaný v roce 1983
@cs
wetenschappelijk artikel (gepubliceerd op 1983/05/01)
@nl
наукова стаття, опублікована в травні 1983
@uk
مقالة علمية (نشرت في مايو 1983)
@ar
name
Electron-microscopical approach to a structural model of intima collagen
@ast
Electron-microscopical approach to a structural model of intima collagen
@en
Electron-microscopical approach to a structural model of intima collagen
@nl
type
label
Electron-microscopical approach to a structural model of intima collagen
@ast
Electron-microscopical approach to a structural model of intima collagen
@en
Electron-microscopical approach to a structural model of intima collagen
@nl
prefLabel
Electron-microscopical approach to a structural model of intima collagen
@ast
Electron-microscopical approach to a structural model of intima collagen
@en
Electron-microscopical approach to a structural model of intima collagen
@nl
P2093
P2860
P356
P1433
P1476
Electron-microscopical approach to a structural model of intima collagen
@en
P2093
E. Odermatt
H. Furthmayr
H. Wiedemann
P2860
P304
P356
10.1042/BJ2110303
P407
P577
1983-05-01T00:00:00Z