Copper Transporting P-Type ATPases and Human Disease
- 1 January 2002
- journal article
- review article
- Published by Springer Nature in Journal of Bioenergetics and Biomembranes
- Vol. 34 (5) , 333-338
- https://doi.org/10.1023/a:1021293818125
Abstract
Copper transporting P-type ATPases, designated ATP7A and ATP7B, play an essential role in mammalian copper balance. Impaired intestinal transport of copper, resulting from mutations in the ATP7A...Keywords
This publication has 59 references indexed in Scilit:
- Expression in Mouse Kidney of Membrane Copper Transporters Atp7a and Atp7bNephron, 2002
- Localization of the Wilson's disease protein in human liverGastroenterology, 1999
- Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13- p16Human Molecular Genetics, 1999
- Functional Characterization of Missense Mutations in ATP7B: Wilson Disease Mutation or Normal Variant?American Journal of Human Genetics, 1998
- Manifestations of copper excessThe American Journal of Clinical Nutrition, 1998
- Metal Ion Chaperone Function of the Soluble Cu(I) Receptor Atx1Science, 1997
- Failure of Copper Incorporation into Ceruloplasmin in the Golgi Apparatus of LEC Rat HepatocytesBiochemical and Biophysical Research Communications, 1995
- The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake.Proceedings of the National Academy of Sciences, 1995
- Copper pumping ATPases: Common concepts in bacteria and manFEBS Letters, 1994
- Metallothionein Messenger RNA Levels in the Macular Mutant Mouse: An Animal Model of Menkes’ Kinky-Hair DiseaseNeonatology, 1991