Characterization of Human SCO1 and COX17 Genes in Mitochondrial Cytochrome-c-Oxidase Deficiency-Reference-Cited by-同舟云学术

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Characterization of Human SCO1 and COX17 Genes in Mitochondrial Cytochrome-c-Oxidase Deficiency

Published:2000-09 Issue:2 Volume:276 Page:530-533
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Horvath Rita,Lochmüller Hanns,Stucka Rolf,Yao Jianbo,Shoubridge Eric A.,Kim Sang-Ho,Gerbitz Klaus-Dieter,Jaksch Michaela

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference27 articles.

1. Localization of Cu and hema a on cytochrome c oxidase polypeptides;Gutteridge;Biochem. Biophys. Res. Commun.,1977

2. Structure and function of cytochrome c oxidase;Capaldi;Arch. Biochem. Biophys.,1990

3. Human cytochrome c oxidase: Structure, function, and deficiency;Taanman;J. Bioenerg. Biomembr.,1997

4. The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 A;Tsukihara;Science,1996

5. Molecular analysis of cytochrome c oxidase deficiency in Leigh's Syndrome;Adams;Ann. Neurol.,1977

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3. Regulation of COX Assembly and Function by Twin CX9C Proteins—Implications for Human Disease;Cells;2021-01-20

4. Mitochondrial Chaperones in the Brain: Safeguarding Brain Health and Metabolism?;Frontiers in Endocrinology;2018-04-26

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