Literature DB >> 7557978

A region of primer binding variation at the D6S265 locus associated with HLA-A25 and HLA-A26 antigens.

W Pyper1, M Burt, L Powell, S Webb, L Adès, J Halliday, E Jazwinska.   

Abstract

D6S265 is a polymorphic dinucleotide repeat, mapped within 70 kb centromeric of HLA-A, on chromosome 6p21.3. While genotyping families for genetic linkage analysis, allele non-amplification resulting in apparent non-Mendelian inheritance was observed at the D6S265 locus in 15 individuals, on chromosomes carrying the HLA-A25 and HLA-A26 antigens. The D6S265 locus was sequenced in a variant individual homozygous for allele non-amplification, and in a non-HLA-A25/-A26 individual, homozygous for D6S265 allele 1. Five base changes were identified in the reverse primer binding region of the variant individual, effectively preventing annealing of the 3' primer to the template.

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Year:  1995        PMID: 7557978     DOI: 10.1007/bf00191814

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


  12 in total

1.  Molecular definition of an elusive third HLA-A9 molecule: HLA-A9.3.

Authors:  A M Little; J A Madrigal; P Parham
Journal:  Immunogenetics       Date:  1992       Impact factor: 2.846

2.  Influence of aberrant observations on high-resolution linkage analysis outcomes.

Authors:  K H Buetow
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

3.  Genotyping errors with the polymerase chain reaction.

Authors:  F K Fujimura; H Northrup; A L Beaudet; W E O'Brien
Journal:  N Engl J Med       Date:  1990-01-04       Impact factor: 91.245

4.  Mapping of human chromosome 5 microsatellite DNA polymorphisms.

Authors:  J L Weber; M H Polymeropoulos; P E May; A E Kwitek; H Xiao; J D McPherson; J J Wasmuth
Journal:  Genomics       Date:  1991-11       Impact factor: 5.736

5.  Average heterozygosity per locus in man: an estimate based on the incidence of enzyme polymorphisms.

Authors:  H Harris; D A Hopkinson
Journal:  Ann Hum Genet       Date:  1972-07       Impact factor: 1.670

6.  Screening for carriers of genetic disease: points to consider.

Authors:  E A Haan
Journal:  Med J Aust       Date:  1993-03-15       Impact factor: 7.738

Review 7.  DNA diagnostic tests: presymptomatic and prenatal.

Authors:  L J Sheffield
Journal:  Med J Aust       Date:  1993-03-01       Impact factor: 7.738

8.  Allele non-amplification: a source of confusion in linkage studies employing microsatellite polymorphisms.

Authors:  D J Koorey; G A Bishop; G W McCaughan
Journal:  Hum Mol Genet       Date:  1993-03       Impact factor: 6.150

9.  Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene.

Authors:  L Grunebaum; J P Cazenave; G Camerino; C Kloepfer; J L Mandel; P Tolstoshev; M Jaye; H De la Salle; J P Lecocq
Journal:  J Clin Invest       Date:  1984-05       Impact factor: 14.808

10.  Cryptic simplicity in DNA is a major source of genetic variation.

Authors:  D Tautz; M Trick; G A Dover
Journal:  Nature       Date:  1986 Aug 14-20       Impact factor: 49.962

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