D
David W. Crabb
Researcher at Indiana University
Publications - 217
Citations - 13218
David W. Crabb is an academic researcher from Indiana University. The author has contributed to research in topics: Alcohol dehydrogenase & Aldehyde dehydrogenase. The author has an hindex of 53, co-authored 216 publications receiving 12209 citations. Previous affiliations of David W. Crabb include University of Groningen & Regenstrief Institute.
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Journal Article
Alcohol and aldehyde dehydrogenase genotypes and alcoholism in Chinese men.
Holly R. Thomasson,Howard J. Edenberg,David W. Crabb,Xiao Ling Mai,Ronald E. Jerome,Ting-Kai Li,Shiou Ping Wang,Yu Tsai Lin,Ru Band Lu,Shin Jiun Yin +9 more
TL;DR: The genotypes of the ADH2, ADH3, and ALDH2 loci of alcoholic and nonalcoholic Chinese men living in Taiwan are determined using leukocyte DNA amplified by the PCR and allele-specific oligonucleotides, suggesting that genetic variation in both ADH and AL DH, by modulating the rate of metabolism of ethanol and acetaldehyde, influences drinking behavior and the risk of developing alcoholism.
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Genotypes for aldehyde dehydrogenase deficiency and alcohol sensitivity. The inactive ALDH2(2) allele is dominant.
TL;DR: The polymerase chain reaction is used to determine the genotypes of 24 livers from Japanese individuals and it is concluded that the allele (ALDH2(2)) encoding the abnormal subunit is dominant.
Genotypes for Aldehyde Dehydrogenase Deficiency and Alcohol Sensitivity
TL;DR: This article used the polymerase chain reaction to determine the genotype of 24 livers from Japanese individuals and found that the allele (ALDH22) encoding the abnormal subunit is dominant.
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Ethanol induces fatty acid synthesis pathways by activation of sterol regulatory element-binding protein (SREBP).
TL;DR: It is suggested that metabolism of ethanol increased hepatic lipogenesis by activating SREBP-1 and that this effect of ethanol may contribute to the development of alcoholic fatty liver.
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Overview of the role of alcohol dehydrogenase and aldehyde dehydrogenase and their variants in the genesis of alcohol-related pathology
TL;DR: The strongest correlations found to date have been those between the ALDH2*2 allele and cancers of the oro-pharynx and oesophagus, and it will be important to replicate other interesting associations between these variants and other cancers and heart disease, and to determine the biochemical mechanisms underlying the associations.