The mutations in mtDNA encoded NADH dehydrogenase subunit genes as common causes of MELAS

Ji K.; Yan C.

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The mutations in mtDNA encoded NADH dehydrogenase subunit genes as common causes of MELAS

机译：MTDNA编码NADH脱氢酶亚基基因的突变作为Melas的常见原因

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《Neuromuscular disorders: NMD》 |2019年第1期|共1页
作者
Ji K.; Yan C.;
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Qilu Hosp Jinan Shandong Peoples R China;

Qilu Hosp Jinan Shandong Peoples R China;

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正文语种 eng
中图分类神经病学;
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1. The mutations in mtDNA encoded NADH dehydrogenase subunit genes as common causes of MELAS [J] . Ji K., Yan C. Neuromuscular disorders: NMD . 2019,第Suppla1期

机译：MTDNA编码NADH脱氢酶亚基基因的突变作为Melas的常见原因
2. A Missense Mutation in Mitochondrially Encoded NADH Dehydrogenase Subunit-5 Gene Associates with Chicken Fetal Growth under Hypoxia Condition [J] . H.G. Bao, J.Y. Li Journal of animal and veterinary advances . 2011,第15期

机译：缺氧条件下线粒体编码的NADH脱氢酶亚基5基因的错义突变与鸡的胎儿生长。
3. Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia. [J] . A S Jun, I A Trounce, M D Brown, Molecular and Cellular Biology . 1996,第3期

机译：使用线粒体杂合体将复杂的I缺陷分配给核苷酸对14459处的线粒体DNA编码的NADH脱氢酶亚基6基因突变，导致Leber遗传性视神经病变和肌张力障碍。
4. Nucleotide Variation in the NADH Dehydrogenase Subunit-2 Gene Sequences of Lorikeet (Genus Trichoglossus) Birds from Sulawesi Island [C] . Dwi Astuti, Siti Nuramaliati Prijono International Conference on Biological Science . 2016

机译：苏拉威西岛纳迪脱氢酶亚甲基脱氢酶亚基-2基因序列的核苷酸变异
5. Organization and expression of mitochondrial genes for ribosomal proteins and NADH dehydrogenase subunits from a liverwort, Marchantia polymoropha [D] . Takemura, Miho 1995

机译：地衣麦（Marchentia polymoropha）核糖体蛋白和NADH脱氢酶亚基的线粒体基因的组织和表达
6. The mtDNA-encoded ND6 subunit of mitochondrial NADH dehydrogenase is essential for the assembly of the membrane arm and the respiratory function of the enzyme. [O] . Y Bai, G Attardi 1998

机译：线粒体NADH脱氢酶的mtDNA编码的ND6亚基对于膜臂的组装和该酶的呼吸功能至关重要。
7. Lack of complex I activity in human cells carrying a mutation in MtDNA-encoded ND4 subunit is corrected by the Saccharomyces cerevisiae NADH-quinone oxidoreductase (NDI1) gene [O] . Bai Yidong, Hájek Petr, Chomyn Anne, 2001

机译：通过酿酒酵母NADH-醌氧化还原酶（NDI1）基因纠正了携带MtDNA编码的ND4亚基突变的人类细胞中缺乏复杂的I活性。

The mutations in mtDNA encoded NADH dehydrogenase subunit genes as common causes of MELAS

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