Literature DB >> 8957963

Human heat shock protein gene polymorphisms and sudden infant death syndrome.

R A Rahim1, P A Boyd, W J Ainslie Patrick, R H Burdon.   

Abstract

Comparison of the frequency of occurrence of restriction fragment length polymorphisms in control human DNAs and DNAs from infants dying from sudden infant death syndrome has indicated no significant difference in the case of restriction fragment length polymorphisms associated with the heat shock protein genes hsp70 and hsp90. A highly significant difference was detected, however, in the case of the specific restriction fragment length polymorphisms detected by an hsp60 gene probe in MspI digests.

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Year:  1996        PMID: 8957963      PMCID: PMC1511788          DOI: 10.1136/adc.75.5.451

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  5 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.  Hydrogen peroxide and sequence-specific DNA damage in human cells.

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3.  Strategies for detecting and characterizing restriction fragment length polymorphisms (RFLP's).

Authors:  M H Skolnick; R White
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4.  Brown adipose tissue activity in pyrexial cases of cot death.

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5.  Localization of a human heat-shock HSP 70 gene sequence to chromosome 6 and detection of two other loci by somatic-cell hybrid and restriction fragment length polymorphism analysis.

Authors:  A M Goate; D N Cooper; C Hall; T K Leung; E Solomon; L Lim
Journal:  Hum Genet       Date:  1987-02       Impact factor: 4.132

  5 in total
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Review 5.  Systems-level perspective of sudden infant death syndrome.

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7.  Genetic variation in heat shock protein 60 gene and coronary heart disease in China: tagging-SNP haplotype analysis in a case-control study.

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  8 in total

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