Metal-dependent regulation of ATP7A and ATP7B in fibroblast cultures
Deficiency of one of the copper transporters ATP7A and ATP7B leads to the rare X-linked disorder Menkes Disease (MD) or the rare autosomal disorder Wilson disease (WD), respectively. In order to investigate whether the ATP7A and the ATP7B genes may be transcriptionally regulated, we measured the exp...
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| Auteurs principaux: | , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Frontiers Media S.A.
2016-08-01
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| Collection: | Frontiers in Molecular Neuroscience |
| Sujets: | |
| Accès en ligne: | http://journal.frontiersin.org/Journal/10.3389/fnmol.2016.00068/full |
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