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The gene encoding subunit IV of cytochrome c oxidase maps to mouse chromosome 8.

作者信息

Makris G J, Samuelson L C, Lomax M I

机构信息

Department of Anatomy and Cell Biology, University of Michigan Medical School, 5724 Medical Science II, Box 0616, Ann Arbor, Michigan 48109-0616, USA.

出版信息

Mamm Genome. 1996 Oct;7(10):789-90. doi: 10.1007/s003359900299.

DOI:10.1007/s003359900299
PMID:8854875
Abstract
摘要

相似文献

1
The gene encoding subunit IV of cytochrome c oxidase maps to mouse chromosome 8.
Mamm Genome. 1996 Oct;7(10):789-90. doi: 10.1007/s003359900299.
2
The gene encoding the heart/muscle isoform of cytochrome c oxidase subunit VIII maps to mouse chromosome 7.
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Assignment of the gene coding for human cytochrome c oxidase subunit VIb to chromosome 19, band q13.1, by fluorescence in situ hybridisation.通过荧光原位杂交将编码人细胞色素c氧化酶亚基VIb的基因定位于19号染色体q13.1带。
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The OXA1L gene that controls cytochrome oxidase assembly maps to the 14q11.2 region of the human genome.控制细胞色素氧化酶组装的OXA1L基因定位于人类基因组的14q11.2区域。
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[Characterization of a yeast nuclear gene involved in the maturation of mitochondrial pre-messenger RNA of cytochrome c oxidase (author's transl)].[参与细胞色素c氧化酶线粒体前体信使核糖核酸成熟的酵母核基因的特性分析(作者译)]
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Structure of the human gene (COX6A2) for the heart/muscle isoform of cytochrome c oxidase subunit VIa and its chromosomal location in humans, mice, and cattle.细胞色素c氧化酶亚基VIa心脏/肌肉同工型的人类基因(COX6A2)的结构及其在人类、小鼠和牛中的染色体定位。
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引用本文的文献

1
The gene encoding the heart/muscle isoform of cytochrome c oxidase subunit VIII maps to mouse chromosome 7.
Mamm Genome. 1997 Jun;8(6):453-4. doi: 10.1007/s003359900470.

本文引用的文献

1
Mitochondrial encephalomyopathies: clinical and molecular analysis.线粒体脑肌病:临床与分子分析
J Bioenerg Biomembr. 1994 Jun;26(3):291-9. doi: 10.1007/BF00763100.
2
Molecular basis of mitochondrial DNA disease.线粒体DNA疾病的分子基础。
J Bioenerg Biomembr. 1994 Jun;26(3):273-89. doi: 10.1007/BF00763099.
3
Maps from two interspecific backcross DNA panels available as a community genetic mapping resource.来自两个种间回交DNA面板的图谱可作为社区遗传图谱资源使用。
Mamm Genome. 1994 May;5(5):253-74. doi: 10.1007/BF00389540.
4
Mitochondrial mutations and human disease.
Environ Mol Mutagen. 1995;25 Suppl 26:30-7. doi: 10.1002/em.2850250607.
5
Mouse alpha 1- and beta 2-syntrophin gene structure, chromosome localization, and homology with a discs large domain.
J Biol Chem. 1995 Oct 27;270(43):25859-65. doi: 10.1074/jbc.270.43.25859.
6
"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。附录
Anal Biochem. 1984 Feb;137(1):266-7. doi: 10.1016/0003-2697(84)90381-6.
7
The mitochondrial electron transport and oxidative phosphorylation system.线粒体电子传递与氧化磷酸化系统。
Annu Rev Biochem. 1985;54:1015-69. doi: 10.1146/annurev.bi.54.070185.005055.
8
Tissue-specific genes for respiratory proteins.
Trends Biochem Sci. 1989 Dec;14(12):501-3. doi: 10.1016/0968-0004(89)90185-0.
9
Nucleotide sequence of a mouse cDNA for subunit IV of cytochrome c oxidase.细胞色素c氧化酶亚基IV的小鼠cDNA核苷酸序列。
Nucleic Acids Res. 1990 Nov 11;18(21):6454. doi: 10.1093/nar/18.21.6454.
10
Structure and function of cytochrome c oxidase.
Annu Rev Biochem. 1990;59:569-96. doi: 10.1146/annurev.bi.59.070190.003033.