Literature DB >> 3893465

Molecular genetic analysis of human alcohol dehydrogenase.

G Duester, G W Hatfield, M Smith.   

Abstract

Human alcohol dehydrogenase (ADH) consists of a complex group of isozymes encoded by at least five non-identical genes, two of which have previously been shown through enzymatic analysis to possess polymorphic variants. Using a cDNA probe the ADH2 gene encoding the beta subunit of human ADH was mapped to human chromosome 4. The cDNA probe for ADH2 was also used to detect a restriction fragment length polymorphism present in human populations. This polymorphism may help establish whether certain ADH allelic variants are linked with certain types of altered alcohol tolerance observed in various individuals. The restriction fragment length polymorphism may also be of use in genetic linkage studies of other genes located near ADH on human chromosome 4.

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Year:  1985        PMID: 3893465     DOI: 10.1016/0741-8329(85)90015-1

Source DB:  PubMed          Journal:  Alcohol        ISSN: 0741-8329            Impact factor:   2.405


  5 in total

1.  ADH single nucleotide polymorphism associations with alcohol metabolism in vivo.

Authors:  Andrew J Birley; Michael R James; Peter A Dickson; Grant W Montgomery; Andrew C Heath; Nicholas G Martin; John B Whitfield
Journal:  Hum Mol Genet       Date:  2009-02-04       Impact factor: 6.150

2.  Research on alcohol metabolism among Asians and its implications for understanding causes of alcoholism.

Authors:  R F Suddendorf
Journal:  Public Health Rep       Date:  1989 Nov-Dec       Impact factor: 2.792

3.  Mammalian alcohol dehydrogenases of separate classes: intermediates between different enzymes and intraclass isozymes.

Authors:  H Jörnvall; J O Höög; H von Bahr-Lindström; B L Vallee
Journal:  Proc Natl Acad Sci U S A       Date:  1987-05       Impact factor: 11.205

4.  Alcohol dehydrogenase genes: restriction fragment length polymorphisms for ADH4 (pi-ADH) and ADH5 (chi-ADH) and construction of haplotypes among different ADH classes.

Authors:  K Edman; W Maret
Journal:  Hum Genet       Date:  1992-12       Impact factor: 4.132

5.  Genetic variants associated with Fabry disease progression despite enzyme replacement therapy.

Authors:  Francesca Scionti; Maria Teresa Di Martino; Simona Sestito; Angela Nicoletti; Francesca Falvo; Katia Roppa; Mariamena Arbitrio; Pietro Hiram Guzzi; Giuseppe Agapito; Antonio Pisani; Eleonora Riccio; Daniela Concolino; Licia Pensabene
Journal:  Oncotarget       Date:  2017-11-18
  5 in total

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