Literature DB >> 2998971

Allelic variation adjacent to the human insulin and apolipoprotein C-II genes in different ethnic groups.

L G Williams, N I Jowett, M A Vella, S Humphries, D J Galton.   

Abstract

We have used DNA probes for the human insulin gene and apolipoprotein C-II (apo C-II) gene to determine the extent of allelic variation in different ethnic groups. The distribution of an apo C-II DNA polymorphism revealed by the restriction endonuclease Taq I showed no significant variation amongst racial groups; in contrast, an insulin gene-related DNA polymorphism showed marked variability. In Japanese, Chinese, and Asian Indian groups there was an increased frequency of homozygosity for the class 1 allele compared to Caucasian groups (P less than 0.001, P less than 0.01, and P less than 0.05, respectively). In Caucasian, Japanese, Chinese, and Asian Indian groups no class 2 allele was observed; but in the Negroid populations (African and West Indian) the class 2 allele frequencies were 0.23 and 0.25 respectively. Possible reasons for this variation in allele distribution are considered in relation to disease associations.

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Year:  1985        PMID: 2998971     DOI: 10.1007/bf00284580

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  14 in total

1.  Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Authors:  E M Southern
Journal:  J Mol Biol       Date:  1975-11-05       Impact factor: 5.469

2.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

3.  The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences.

Authors:  G I Bell; M J Selby; W J Rutter
Journal:  Nature       Date:  1982-01-07       Impact factor: 49.962

4.  Polymorphisms in the 5'-flanking region of the insulin gene and non-insulin-dependent diabetes.

Authors:  G A Hitman; N I Jowett; L G Williams; S Humphries; R M Winter; D J Galton
Journal:  Clin Sci (Lond)       Date:  1984-04       Impact factor: 6.124

5.  DNA sequences flanking the insulin gene on chromosome 11 confer risk of atherosclerosis.

Authors:  T Mandrup-Poulsen; D Owerbach; S A Mortensen; K Johansen; H Meinertz; H Sørensen; J Nerup
Journal:  Lancet       Date:  1984-02-04       Impact factor: 79.321

6.  Diabetic hypertriglyceridaemia and related 5' flanking polymorphism of the human insulin gene.

Authors:  N I Jowett; L G Williams; G A Hitman; D J Galton
Journal:  Br Med J (Clin Res Ed)       Date:  1984-01-14

7.  A DNA polymorphism adjacent to the human apolipoprotein CII gene.

Authors:  S E Humphries; N I Jowett; L Williams; A Rees; M Vella; A Kessling; O Myklebost; A Lydon; M Seed; D J Galton
Journal:  Mol Biol Med       Date:  1983-12

8.  A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus.

Authors:  G I Bell; S Horita; J H Karam
Journal:  Diabetes       Date:  1984-02       Impact factor: 9.461

9.  Familial apolipoprotein CII deficiency: a preliminary analysis of the gene defect in two independent families.

Authors:  S E Humphries; L Williams; O Myklebost; A F Stalenhoef; P N Demacker; G Baggio; G Crepaldi; D J Galton; R Williamson
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  Lack of association of the polymorphic locus in the 5'-flanking region of the human insulin gene and diabetes in American blacks.

Authors:  S Elbein; P Rotwein; M A Permutt; G I Bell; N Sanz; J H Karam
Journal:  Diabetes       Date:  1985-05       Impact factor: 9.461

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  2 in total

1.  DNA polymorphic patterns and haplotype arrangements of the apo A-1, apo C-III, apo A-IV gene cluster in different ethnic groups.

Authors:  H Paul; D Galton; J Stocks
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132

2.  Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population.

Authors:  A E MacKenzie; H L MacLeod; A G Hunter; R G Korneluk
Journal:  Am J Hum Genet       Date:  1989-01       Impact factor: 11.025

  2 in total

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