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yin198716新虫 (正式写手)
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| Mutations of the Jagged1and Notch3 genes in humans lead to the autosomal dominantdisorders Alagille syndrome and cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy,respectively, both of which exhibit severe vascular defects .Mice deficient for a variety of components of the Notch path-way display embryonic lethality with severe vascular abnormalities |
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yin198716: 金币+5, 翻译EPI+1, ★有帮助 2013-03-31 15:33:04
yin198716: 金币+5, 翻译EPI+1, ★有帮助 2013-03-31 15:33:04
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Mutations of the Jagged1and Notch3 genes in humans lead to the autosomal dominantdisorders Alagille syndrome and cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy,respectively, both of which exhibit severe vascular defects . 人类的Jagged1和Notch3基因突变会导致 常染色体显性异常艾欧吉勒综合征 和 常染色体显性遗传脑动脉病（伴有皮层下梗死和脑白质病变），它们表现出严重的血管缺乏。 Mice deficient for a variety of components of the Notch path-way display embryonic lethality with severe vascular abnormalities Notch信号通路中各种组分缺失型的的小鼠，会出现血管严重异常性胚胎死亡。  |
2楼2013-03-29 14:30:38