Genomic imprinting and its relevance to genetic diseases
Genomic imprinting and its relevance to genetic diseases
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基因组印记及其与遗传疾病的相关性
DOI：
10.1007/bf01876325
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发表时间：
1996
期刊：
影响因子：
--
通讯作者：
N. Niikawa
中科院分区：
文献类型：
--
作者：
N. Niikawa
基因组印记是一种生物学现象，由进化获得的潜在系统决定，可能控制哺乳动物的和谐发育和生长。本文综述了印迹的生物学证据、小鼠和人类印迹基因的特征以及人类印迹疾病的研究结果和发生机制。
SummaryGenomic imprinting is a biological phenomenon determined by an evolutionally acquired, underlying system that may control harmonious development and growth in mammals. It is also relevant to some genetic disorders in man. In this article, lines of biological evidence of imprinting, characteristics of the mouse and human imprinted genes, and findings and mechanisms on the occurrence of several human imprinting disorders are reviewed.
普瑞德-威利综合征区域一个新的父系表达基因的鉴定。
影响因子：
3.5
作者：
Wevrick,R;Kerns,JA;Francke,U
通讯作者：
Francke,U