The human collagen X gene. Complete primary translated sequence and chromosomal localization
about
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 SchmidGenomic organization and full-length cDNA sequence of human collagen XAssociation analysis of single nucleotide polymorphisms in cartilage-specific collagen genes with knee and hip osteoarthritis in the Japanese populationCloning of the human and mouse type X collagen genes and mapping of the mouse type X collagen gene to chromosome 10A type X collagen mutation causes Schmid metaphyseal chondrodysplasiaConcentration of mutations causing Schmid metaphyseal chondrodysplasia in the C-terminal noncollagenous domain of type X collagenC1q/tumor necrosis factor-related protein 11 (CTRP11), a novel adipose stroma-derived regulator of adipogenesisPartial characterization of cell-type X collagen interactions.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.Mutation of the type X collagen gene (COL10A1) causes spondylometaphyseal dysplasia.SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasia.Characterization of an intronless collagen gene family in the marine sponge Microciona prolifera.The mouse collagen X gene: complete nucleotide sequence, exon structure and expression patternFrom collagen chemistry towards cell therapy - a personal journey.Academic and molecular matrices: a study of the transformations of connective tissue research at the University of Manchester (1947-1996).A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasiaC1q/TNF-related protein 4 (CTRP4) is a unique secreted protein with two tandem C1q domains that functions in the hypothalamus to modulate food intake and body weight.Metabolic function of the CTRP family of hormones.The EMILIN/Multimerin family.Collagen X chains harboring Schmid metaphyseal chondrodysplasia NC1 domain mutations are selectively retained and degraded in stably transfected cells.Chondrocyte phenotype and cell survival are regulated by culture conditions and by specific cytokines through the expression of Sox-9 transcription factor.Autoimmune recognition of cartilage collagens.The chondrocyte, architect of cartilage. Biomechanics, structure, function and molecular biology of cartilage matrix macromolecules.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.Site-directed mutagenesis of human type X collagen. Expression of alpha1(X) NC1, NC2, and helical mutations in vitro and in transfected cells.Cartilage collagens: strategies for the study of their organisation and expression in the extracellular matrix.Reconstitution of the folding pathway of collagen in a cell-free system: formation of correctly aligned and hydroxylated triple helices.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.Partial characterization of the C-terminal non-collagenous domain (NC1) of collagen type X.Deletions in the COL10A1 gene are not associated with skeletal changes in dogs.Metaphyseal chondrodysplasia type Schmid mutations are predicted to occur in two distinct three-dimensional clusters within type X collagen NC1 domains that retain the ability to trimerize.Schmid type of metaphyseal chondrodysplasia and COL10A1 mutations--findings in 10 patients.New nucleotide sequence data on the EMBL File ServerNew nucleotide sequence data on the EMBL File Server
P2860
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P2860
The human collagen X gene. Complete primary translated sequence and chromosomal localization
description
1991 nî lūn-bûn
@nan
1991 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
The human collagen X gene. Com ...... e and chromosomal localization
@ast
The human collagen X gene. Com ...... e and chromosomal localization
@en
The human collagen X gene. Com ...... e and chromosomal localization
@en-gb
The human collagen X gene. Com ...... e and chromosomal localization
@nl
type
label
The human collagen X gene. Com ...... e and chromosomal localization
@ast
The human collagen X gene. Com ...... e and chromosomal localization
@en
The human collagen X gene. Com ...... e and chromosomal localization
@en-gb
The human collagen X gene. Com ...... e and chromosomal localization
@nl
prefLabel
The human collagen X gene. Com ...... e and chromosomal localization
@ast
The human collagen X gene. Com ...... e and chromosomal localization
@en
The human collagen X gene. Com ...... e and chromosomal localization
@en-gb
The human collagen X gene. Com ...... e and chromosomal localization
@nl
P2093
P2860
P356
P1433
P1476
The human collagen X gene. Com ...... e and chromosomal localization
@en
P2093
C J Cresswell
J T Thomas
R P Boot-Handford
P2860
P304
P356
10.1042/BJ2800617
P407
P478
280 ( Pt 3)
P577
1991-12-15T00:00:00Z