Genetic linkage analysis of 14 candidate gene loci in a family with autosomal dominant osteoarthritis without dysplasia. - sprookjes - yvandenbroek - TriplyDB

Genetic linkage analysis of 14 candidate gene loci in a family with autosomal dominant osteoarthritis without dysplasia.

Genetic linkage analysis of 14 candidate gene loci in a family with autosomal dominant osteoarthritis without dysplasia.

http://www.wikidata.org/entity/Q33679916

about

The role of structural genes in the pathogenesis of osteoarthritic disorders Genetic markers of osteoarticular disorders: facts and hopes TUFT1, a novel candidate gene for metatarsophalangeal osteoarthritis, plays a role in chondrogenesis on a calcium-related pathway A gain of function mutation in TNFRSF11B encoding osteoprotegerin causes osteoarthritis with chondrocalcinosis.Strong linkage on 2q33.3 to familial early-onset generalized osteoarthritis and a consideration of two positional candidate genes.Del1 Knockout Mice Developed More Severe Osteoarthritis Associated with Increased Susceptibility of Chondrocytes to Apoptosis The genetics of osteoarthritis.

P2860

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P2860

Genetic linkage analysis of 14 candidate gene loci in a family with autosomal dominant osteoarthritis without dysplasia.

http://www.wikidata.org/entity/Q33679916

description

1997 nî lūn-bûn

@nan

1997 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1997 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

1997年の論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年论文

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name

Genetic linkage analysis of 14 ...... eoarthritis without dysplasia.

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Genetic linkage analysis of 14 ...... eoarthritis without dysplasia.

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type

label

Genetic linkage analysis of 14 ...... eoarthritis without dysplasia.

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Genetic linkage analysis of 14 ...... eoarthritis without dysplasia.

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prefLabel

Genetic linkage analysis of 14 ...... eoarthritis without dysplasia.

@ast

Genetic linkage analysis of 14 ...... eoarthritis without dysplasia.

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Genetic linkage analysis of 14 ...... teoarthritis without dysplasia

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P2860

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valine in alpha 1 (XI) collagen

Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene

Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen gene

Linkage of early-onset osteoarthritis and chondrocalcinosis to human chromosome 8q

Molecular cloning of the alpha 3 chain of human type IX collagen: linkage of the gene COL9A3 to chromosome 20q13.3

A polymorphic microsatellite repeat is located close to the promoter region of the c-fgr proto-oncogene (FGR) at chromosome 1p36.2-p36.1

A restriction fragment length polymorphism results in a nonconservative amino acid substitution encoded within the first exon of the human lysyl oxidase gene

Physical and linkage mapping of the human and murine genes for the alpha 1 chain of type IX collagen (COL9A1)

The human alpha 2(XI) collagen gene (COL11A2) maps to the centromeric border of the major histocompatibility complex on chromosome 6

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1024-1027

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12

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Ingrid Meulenbelt

Pieternella E Slagboom

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13801575

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1051158

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