hCTR1: A human gene for copper uptake identified by complementation in yeast
The molecular mechanisms responsible for the cellular uptake of copper in mammalian cells are unknown. We describe isolation of a human gene involved in this process by complementation of the yeast high-affinity copper uptake mutant, ctr1. Besides complementing ctr1 growth defect on nonfermentable m...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Proc Natl Acad Sci U S A |
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| Prif Awduron: | , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
National Academy of Sciences
1997
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC23847/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9207117/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.94.14.7481 |
| Tagiau: |
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