Genomic organization and full-length cDNA sequence of human collagen X

Genomic organization and full-length cDNA sequence of human collagen X

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http://www.wikidata.org/entity/Q28190180
Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasiaAmino acid substitutions of conserved residues in the carboxyl-terminal domain of the alpha 1(X) chain of type X collagen occur in two unrelated families with metaphyseal chondrodysplasia type SchmidSelf-assembly and supramolecular organization of EMILINEMILIN, a component of the elastic fiber and a new member of the C1q/tumor necrosis factor superfamily of proteinsIdentification of conformation-dependent epitopes and V gene selection in the B cell response to type II collagen in the DA rat.The cDNA sequence of human endothelial cell multimerin. A unique protein with RGDS, coiled-coil, and epidermal growth factor-like domains and a carboxyl terminus similar to the globular domain of complement C1q and collagens type VIII and X.A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasiaThe EMILIN/Multimerin family.Collagen X chains harboring Schmid metaphyseal chondrodysplasia NC1 domain mutations are selectively retained and degraded in stably transfected cells.Coexpression of alpha and beta subunits of prolyl 4-hydroxylase stabilizes the triple helix of recombinant human type X collagen.Raf signaling stimulates and represses the human collagen X promoter through distinguishable elements.Characterization of human type X procollagen and its NC-1 domain expressed as recombinant proteins in HEK293 cells.Localization of silencer and enhancer elements in the human type X collagen gene.Transcriptional regulation of the human type X collagen gene expression.Site-directed mutagenesis of human type X collagen. Expression of alpha1(X) NC1, NC2, and helical mutations in vitro and in transfected cells.Beta-sheet secondary structure of the trimeric globular domain of C1q of complement and collagen types VIII and X by Fourier-transform infrared spectroscopy and averaged structure predictions.Intron-exon structure, alternative use of promoter and expression of the mouse collagen X gene, Col10a-1.
P2860

Genomic organization and full-length cDNA sequence of human collagen X

Item
http://www.wikidata.org/entity/Q28190180
description
1992 nî lūn-bûn
@nan
1992 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Genomic organization and full-length cDNA sequence of human collagen X
@ast
Genomic organization and full-length cDNA sequence of human collagen X
@en
Genomic organization and full-length cDNA sequence of human collagen X
@nl
type
label
Genomic organization and full-length cDNA sequence of human collagen X
@ast
Genomic organization and full-length cDNA sequence of human collagen X
@en
Genomic organization and full-length cDNA sequence of human collagen X
@nl
prefLabel
Genomic organization and full-length cDNA sequence of human collagen X
@ast
Genomic organization and full-length cDNA sequence of human collagen X
@en
Genomic organization and full-length cDNA sequence of human collagen X
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P5875
P698
P356
P1433
P1476
Genomic organization and full-length cDNA sequence of human collagen X
@en
P2093
P2860
P304
P31
P356
10.1016/0014-5793(92)81126-7
P407
P433
P478
P50
P577
P5875
P698