Mitochondrial copper in human genetic disorders-Reference-Cited by-同舟云学术

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Mitochondrial copper in human genetic disorders

Published:2023-01 Issue:1 Volume:34 Page:21-33
ISSN:1043-2760
Container-title:Trends in Endocrinology & Metabolism
language:en
Short-container-title:Trends in Endocrinology & Metabolism

Author:

Garza Natalie M.,Swaminathan Abhinav B.,Maremanda Krishna P.,Zulkifli Mohammad,Gohil Vishal M.

Funder

National Institutes of Health

National Institute of General Medical Sciences

Texas A and M University

Publisher

Elsevier BV

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference111 articles.

1. Evolution of copper transporting ATPases in eukaryotic organisms;Gupta;Curr. Genomics,2012

2. Mechanisms for copper acquisition, distribution and regulation;Kim;Nat. Chem. Biol.,2008

3. An exposure-response curve for copper excess and deficiency;Chambers;J. Toxicol. Environ. Health B Crit. Rev.,2010

4. Ctr1 drives intestinal copper absorption and is essential for growth, iron metabolism, and neonatal cardiac function;Nose;Cell Metab.,2006

5. Characterization of a cytochrome b558 ferric/cupric reductase from rabbit duodenal brush border membranes;Knöpfel;Biochem. Biophys. Res. Commun.,2002

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