Literature DB >> 7864685

Genetic aspects of familial osteoarthritis.

S A Jimenez1, R M Dharmavaram.   

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Year:  1994        PMID： 7864685      PMCID： PMC1005472          DOI： 10.1136/ard.53.12.789

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN： 0003-4967            Impact factor:   19.103


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  43 in total

1.  A limited association of generalized osteoarthritis with alleles at the type II collagen locus: COL2A1.

Authors:  L Priestley; C Fergusson; D Ogilvie; P Wordsworth; R Smith; M Pattrick; M Doherty; B Sykes
Journal:  Br J Rheumatol       Date:  1991-08

2.  Genetic linkage of a polymorphism in the type II procollagen gene (COL2A1) to primary osteoarthritis associated with mild chondrodysplasia.

Authors:  R G Knowlton; P L Katzenstein; R W Moskowitz; E J Weaver; C J Malemud; M N Pathria; S A Jimenez; D J Prockop
Journal:  N Engl J Med       Date:  1990-02-22       Impact factor: 91.245

3.  Tandem duplication within a type II collagen gene (COL2A1) exon in an individual with spondyloepiphyseal dysplasia.

Authors:  G E Tiller; D L Rimoin; L W Murray; D H Cohn
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

4.  Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy).

Authors:  N N Ahmad; L Ala-Kokko; R G Knowlton; S A Jimenez; E J Weaver; J I Maguire; W Tasman; D J Prockop
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-01       Impact factor: 11.205

Review 5.  A second mutation in the type II procollagen gene (COL2AI) causing stickler syndrome (arthro-ophthalmopathy) is also a premature termination codon.

Authors:  N N Ahmad; D M McDonald-McGinn; E H Zackai; R G Knowlton; D LaRossa; J DiMascio; D J Prockop
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

6.  Characterization of a type II collagen gene (COL2A1) mutation identified in cultured chondrocytes from human hypochondrogenesis.

Authors:  W A Horton; M A Machado; J Ellard; D Campbell; J Bartley; F Ramirez; E Vitale; B Lee
Journal:  Proc Natl Acad Sci U S A       Date:  1992-05-15       Impact factor: 11.205

7.  SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasia.

Authors:  W A Sweetman; B Rash; B Sykes; P Beighton; J T Hecht; B Zabel; J T Thomas; R Boot-Handford; M E Grant; G A Wallis
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

8.  An amino acid substitution (Gly853-->Glu) in the collagen alpha 1(II) chain produces hypochondrogenesis.

Authors:  R Bogaert; G E Tiller; M A Weis; H E Gruber; D L Rimoin; D H Cohn; D R Eyre
Journal:  J Biol Chem       Date:  1992-11-05       Impact factor: 5.157

9.  Low basal transcription of genes for tissue-specific collagens by fibroblasts and lymphoblastoid cells. Application to the characterization of a glycine 997 to serine substitution in alpha 1(II) collagen chains of a patient with spondyloepiphyseal dysplasia.

Authors:  D Chan; W G Cole
Journal:  J Biol Chem       Date:  1991-07-05       Impact factor: 5.157

10.  Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia.

Authors:  L Ala-Kokko; C T Baldwin; R W Moskowitz; D J Prockop
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205
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  2 in total

1.  Epidemiology of peripheral joint osteoarthritis.

Authors:  M Doherty; P Lanyon
Journal:  Ann Rheum Dis       Date:  1996-09       Impact factor: 19.103

Review 2.  Mechanisms of joint destruction, pain and disability in osteoarthritis.

Authors:  R S Pinals
Journal:  Drugs       Date:  1996       Impact factor: 9.546
  2 in total

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