Sequence 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 termi
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150-kD von Willebrand factor binding protein extracted from human vascular subendothelium is type VI collagenMore von Willebrand factor type A domains? Sequence similarities with malaria thrombospondin-related anonymous protein, dihydropyridine-sensitive calcium channel and inter-alpha-trypsin inhibitorMosaic 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 inhibitorsUllrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VIExpression of NG2 proteoglycan causes retention of type VI collagen on the cell surfaceA mouse model for dominant collagen VI disorders: heterozygous deletion of Col6a3 Exon 16Molecular, biochemical and functional characterizations of C1q/TNF family members: adipose-tissue-selective expression patterns, regulation by PPAR-gamma agonist, cysteine-mediated oligomerizations, combinatorial associations and metabolic functionsMultiple forms of chicken alpha 3(VI) collagen chain generated by alternative splicing in type A repeated domainsRecessive COL6A2 C-globular missense mutations in Ullrich congenital muscular dystrophy: role of the C2a splice variant.Allele-specific Gene Silencing of Mutant mRNA Restores Cellular Function in Ullrich Congenital Muscular Dystrophy Fibroblasts.New 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.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 dystrophyThe expanded collagen VI family: new chains and new questionsWARP interacts with collagen VI-containing microfibrils in the pericellular matrix of human chondrocytes.Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report.Molecular cloning of the rat integrin alpha 1-subunit: a receptor for laminin and collagenColVI myopathies: where do we stand, where do we go?Position of glycine substitutions in the triple helix of COL6A1, COL6A2, and COL6A3 is correlated with severity and mode of inheritance in collagen VI myopathies.The promoter of the chicken alpha 2(VI) collagen gene has features characteristic of house-keeping genes and of proto-oncogenes.Characterization of an intronless collagen gene family in the marine sponge Microciona prolifera.Extracellular matrix in the trabecular meshwork.Cloning of alpha 2 chain of type VI collagen and expression during mouse development.Cloning and sequence analysis of cDNAs encoding the alpha 1, alpha 2 and alpha 3 chains of mouse collagen VICOL6A3 protein deficiency in mice leads to muscle and tendon defects similar to human collagen VI congenital muscular dystrophy.Identification and characterization of CTRP9, a novel secreted glycoprotein, from adipose tissue that reduces serum glucose in mice and forms heterotrimers with adiponectinLarge genomic deletions: a novel cause of Ullrich congenital muscular dystrophyDefining the hierarchical organisation of collagen VI microfibrils at nanometre to micrometre length scales.Collagen VI, conformation of A-domain arrays and microfibril architecture.Tenascin variants: differential binding to fibronectin and distinct distribution in cell cultures and tissues.Type VI collagen microfibrils: evidence for a structural association with hyaluronan.Molecular composition of type VI collagen. Evidence for chain heterogeneity in mammalian tissues and cultured cells.
P2860
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P2860
Sequence 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 termi
description
1989 nî lūn-bûn
@nan
1989 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Sequence analysis of alpha 1(V ...... at differ in the carboxy termi
@en
Sequence analysis of alpha 1(V ...... at differ in the carboxy termi
@nl
type
label
Sequence analysis of alpha 1(V ...... at differ in the carboxy termi
@en
Sequence analysis of alpha 1(V ...... at differ in the carboxy termi
@nl
prefLabel
Sequence analysis of alpha 1(V ...... at differ in the carboxy termi
@en
Sequence analysis of alpha 1(V ...... at differ in the carboxy termi
@nl
P2093
P2860
P1433
P1476
Sequence analysis of alpha 1(V ...... differ in the carboxy terminus
@en
P2093
R Deutzmann
R W Glanville
P2860
P304
P356
10.1002/J.1460-2075.1989.TB03598.X
P407
P577
1989-07-01T00:00:00Z