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线粒体疾病:基因型与表型

Mitochondrial diseases: genotype versus phenotype.

作者信息

Wallace D C

机构信息

Department of Genetics and Molecular Medicine, Emory University Medical School, Atlanta, GA 30322.

出版信息

Trends Genet. 1993 Apr;9(4):128-33. doi: 10.1016/0168-9525(93)90207-x.

Abstract

Recently, a variety of degenerative diseases have been attributed to mutations in mitochondrial DNA. Even though these mutations are inherited and present throughout the body, they frequently cause late-onset, tissue-specific disease. This may be explained by a combination of the tissue-specific accumulation of somatic mtDNA mutations with age and the variation between tissues in the expression of nuclear genes that encode mitochondrial functions.

摘要

最近,多种退行性疾病被归因于线粒体DNA的突变。尽管这些突变是遗传性的且遍布全身,但它们经常导致迟发性的、组织特异性疾病。这可能是由于随着年龄增长体细胞线粒体DNA突变在组织中的特异性积累,以及编码线粒体功能的核基因在不同组织中表达的差异共同作用的结果。

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