HeLa细胞线粒体翻译产物的高分辨率电泳分离及部分特性分析 - Suppr

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High-resolution electrophoretic fractionation and partial characterization of the mitochondrial translation products from HeLa cells.

作者信息

Ching E, Attardi G

出版信息

Biochemistry. 1982 Jun 22;21(13):3188-95. doi: 10.1021/bi00256a024.

DOI:10.1021/bi00256a024

PMID:6285960

Abstract

摘要

相似文献

High-resolution electrophoretic fractionation and partial characterization of the mitochondrial translation products from HeLa cells.HeLa细胞线粒体翻译产物的高分辨率电泳分离及部分特性分析

Biochemistry. 1982 Jun 22;21(13):3188-95. doi: 10.1021/bi00256a024.

Identification of discrete electrophoretic components among the products of mitochondrial protein synthesis in HeLa cells.在HeLa细胞线粒体蛋白质合成产物中鉴定离散的电泳成分。

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Antibodies against synthetic peptides reveal that the unidentified reading frame A6L, overlapping the ATPase 6 gene, is expressed in human mitochondria.针对合成肽的抗体表明，与ATPase 6基因重叠的未鉴定读码框A6L在人线粒体中表达。

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In vivo labeling and analysis of human mitochondrial translation products.人线粒体翻译产物的体内标记与分析

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Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.将与疾病相关的线粒体DNA缺失导入缺乏线粒体DNA的HeLa细胞会导致线粒体功能障碍。

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The biosynthesis of mitochondrial cytochromes.线粒体细胞色素的生物合成。

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Biogenesis of mitochondrial proteins in HeLa cells.

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Ribosome recycling defects modify the balance between the synthesis and assembly of specific subunits of the oxidative phosphorylation complexes in yeast mitochondria.核糖体循环缺陷改变了酵母线粒体中氧化磷酸化复合物特定亚基的合成与组装之间的平衡。

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Polymorphic sites and the mechanism of evolution in human mitochondrial DNA.人类线粒体DNA中的多态性位点与进化机制。

Genetics. 1984 Mar;106(3):479-99. doi: 10.1093/genetics/106.3.479.

Identification of the polypeptides encoded in the ATPase 6 gene and in the unassigned reading frames 1 and 3 of human mtDNA.鉴定人类线粒体DNA中ATPase 6基因以及未分配阅读框1和3所编码的多肽。

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Polymorphisms of mitochondrially encoded proteins.

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Transcription and translation of mitochondrial DNA in interspecific somatic cell hybrids.

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Identification of the polypeptides encoded in the unassigned reading frames 2, 4, 4L, and 5 of human mitochondrial DNA.人类线粒体DNA未分配阅读框2、4、4L和5中编码的多肽的鉴定。

Proc Natl Acad Sci U S A. 1986 Mar;83(6):1563-7. doi: 10.1073/pnas.83.6.1563.

Internal frameshifts within the mitochondrial genes for cytochrome oxidase subunit II and maxicircle unidentified reading frame 3 of Leishmania tarentolae are corrected by RNA editing: evidence for translation of the edited cytochrome oxidase subunit II mRNA.利什曼原虫细胞色素氧化酶亚基II和大环未知阅读框3的线粒体基因内的内部移码通过RNA编辑得到校正：编辑后的细胞色素氧化酶亚基II mRNA可翻译的证据。

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Familial mitochondrial complex I deficiency with an abnormal mitochondrial encoded protein.伴有异常线粒体编码蛋白的家族性线粒体复合体I缺乏症。

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