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人红细胞乙二醛酶II的基因多态性

Genetic polymorphism of human erythrocyte glyoxalase II.

作者信息

Board P G

出版信息

Am J Hum Genet. 1980 Sep;32(5):690-4.

Abstract

A new method for the detection of glyoxalase II (hydroxyacylglutathione hydrolase) after starch gel electrophoresis is described. A survey of Asian-Pacific populations indicates that genetic polymorphism of glyoxalase II is extremely rare. Polymorphism was observed only in a Micronesian population from the island of Nauru, in which the frequency of the new variant allele HAGH2 was found to be .016. The electrophoretic pattern in heterozygotes was a double band, suggesting that the structure of glyoxalase II is monomeric.

摘要

本文描述了一种在淀粉凝胶电泳后检测乙二醛酶II(羟酰谷胱甘肽水解酶)的新方法。对亚太地区人群的调查表明,乙二醛酶II的基因多态性极为罕见。仅在来自瑙鲁岛的密克罗尼西亚人群中观察到多态性,其中新变异等位基因HAGH2的频率为0.016。杂合子的电泳图谱为两条带,表明乙二醛酶II的结构是单体的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/975c/1686103/993f1120e4aa/ajhg00191-0055-a.jpg

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