(Q47675169)

4 February 2018

review article

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title

Phenotypic and biochemical consequences of collagen X mutations in mice and humans (English)

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4 February 2018

author name string

Chan D

series ordinal

1

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4 February 2018

Jacenko O

series ordinal

2

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4 February 2018

publication date

1 July 1998

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4 February 2018

published in

Matrix Biology

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4 February 2018

volume

17

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4 February 2018

issue

3

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4 February 2018

page(s)

169-184

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4 February 2018

Collagens of the chicken eggshell membranes

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7 January 2021

Abnormal type I collagen metabolism by cultured fibroblasts in lethal perinatal osteogenesis imperfecta

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7 January 2021

Mutations in three subdomains of the carboxy-terminal region of collagen type X account for most of the Schmid metaphyseal dysplasias

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7 January 2021

The fibrillar collagens, collagen VIII, collagen X and the C1q complement proteins share a similar domain in their C-terminal non-collagenous regions

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7 January 2021

The avian eggshell extracellular matrix as a model for biomineralization

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7 January 2021

Type X collagen multimer assembly in vitro is prevented by a Gly618 to Val mutation in the alpha 1(X) NC1 domain resulting in Schmid metaphyseal chondrodysplasia

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7 January 2021

Type X collagen NC1 mutations produced by site-directed mutagenesis prevent in vitro assembly

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7 January 2021

A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasia

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7 January 2021

Site-directed mutagenesis of human type X collagen. Expression of alpha1(X) NC1, NC2, and helical mutations in vitro and in transfected cells

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7 January 2021

Domains of type X collagen: alteration of cartilage matrix by fibril association and proteoglycan accumulation

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7 January 2021

Craniofacial abnormalities in mice carrying a dominant interference mutation in type X collagen

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7 January 2021

Identification of a mutation in type X collagen in a family with Schmid metaphyseal chondrodysplasia

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7 January 2021

The mouse collagen X gene: complete nucleotide sequence, exon structure and expression pattern

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7 January 2021

Mouse models of human genetic disease: which mouse is more like a man?

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7 January 2021

Cellular turnover at the chondro-osseous junction of growth plate cartilage: analysis by serial sections at the light microscopical level

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7 January 2021

Condensation of hypertrophic chondrocytes at the chondro-osseous junction of growth plate cartilage in Yucatan swine: relationship to long bone growth

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7 January 2021

Effects of matrix macromolecules on chondrocyte gene expression: synthesis of a low molecular weight collagen species by cells cultured within collagen gels

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7 January 2021

Ruthenium hexammine trichloride (RHT)-mediated interaction between plasmalemmal components and pericellular matrix proteoglycans is responsible for the preservation of chondrocytic plasma membranes in situ during cartilage fixation

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7 January 2021

Physiological mechanisms adopted by chondrocytes in regulating longitudinal bone growth in rats

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7 January 2021

Skeletal and hematopoietic defects in mice transgenic for collagen X

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7 January 2021

Spondylometaphyseal dysplasia in mice carrying a dominant negative mutation in a matrix protein specific for cartilage-to-bone transition

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7 January 2021

Annexin V-mediated calcium flux across membranes is dependent on the lipid composition: implications for cartilage mineralization

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7 January 2021

Regulated production of mineralization-competent matrix vesicles in hypertrophic chondrocytes

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7 January 2021

Ca2+binding properties of type X collagen

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7 January 2021

Intron-exon structure, alternative use of promoter and expression of the mouse collagen X gene, Col10a-1.

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7 January 2021

Macromolecular organization of chicken type X collagen in vitro

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7 January 2021

Abnormal compartmentalization of cartilage matrix components in mice lacking collagen X: implications for function

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7 January 2021

Intracellular avian type X collagen in situ and determination of its thermal stability using a conformation-dependent monoclonal antibody

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7 January 2021

Multiple negative elements in a gene that codes for an extracellular matrix protein, collagen X, restrict expression to hypertrophic chondrocytes

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7 January 2021

A recurrent 1992delCT mutation of the type X collagen gene in a Japanese patient with Schmid metaphyseal chondrodysplasia

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7 January 2021

Concentration of mutations causing Schmid metaphyseal chondrodysplasia in the C-terminal noncollagenous domain of type X collagen

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7 January 2021

Additional mutations of type X collagen confirm COL10A1 as the Schmid metaphyseal chondrodysplasia locus

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7 January 2021

Immunochemical and immunocytochemical identification of matrix vesicle proteins

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7 January 2021

Type X collagen isolated from the hypertrophic cartilage of embryonic chick tibiae contains both hydroxylysyl- and lysylpyridinoline cross-links

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7 January 2021

Fourier transform infrared microspectroscopic analysis identifies alterations in mineral properties in bones from mice transgenic for type X collagen

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7 January 2021

A novel mutation substituting tryptophan with arginine in the carboxyl-terminal, non-collagenous domain of collagen X in a case of Schmid metaphyseal chondrodysplasia

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7 January 2021

Immunoelectron microscopic studies of type X collagen in endochondral ossification

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7 January 2021

Effects of calcium deficiency on chondrocyte hypertrophy and type X collagen expression in chick embryonic sternum

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7 January 2021

In situ hybridization studies on the expression of type X collagen in fetal human cartilage

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7 January 2021

Normal long bone growth and development in type X collagen-null mice

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7 January 2021

Identification of lysine-derived crosslinks in porcine collagen type X from growth plate and newly mineralized bone

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7 January 2021

Characterization of the collagen in the hexagonal lattice of Descemet's membrane: its relation to type VIII collagen

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7 January 2021

Immunoelectron microscopy of type X collagen: supramolecular forms within embryonic chick cartilage

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7 January 2021

Dideoxyfingerprinting (ddF) analysis of the type X collagen gene (COL10A1) and identification of a novel mutation (S671P) in a kindred with Schmid metaphyseal chondrodysplasia

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7 January 2021

The human collagen X gene. Complete primary translated sequence and chromosomal localization

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7 January 2021

Here today, bone tomorrow

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7 January 2021

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 chondrodysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2898%2990056-7

7 January 2021

A type X collagen mutation causes Schmid metaphyseal chondrodysplasia

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https://api.crossref.org/works/10.1016%2FS0945-053X%2898%2990056-7

7 January 2021

Evidence for specific interaction between matrix vesicle proteins and the connective tissue matrix

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https://api.crossref.org/works/10.1016%2FS0945-053X%2898%2990056-7

7 January 2021

10.1016/S0945-053X(98)90056-7

Identifiers

DOI

1 reference

4 February 2018

1 reference

4 February 2018