Golgi-Dependent Copper Homeostasis Sustains Synaptic Development and Mitochondrial Content

Rare genetic diseases preponderantly affect the nervous system causing neurodegeneration to neurodevelopmental disorders. This is the case for both Menkes and Wilson disease, arising from mutations in ATP7A and ATP7B, respectively. The ATP7A and ATP7B proteins localize to the Golgi and regulate copp...

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Detalhes bibliográficos
Publicado no:J Neurosci
Main Authors: Hartwig, Cortnie, Méndez, Gretchen Macías, Bhattacharjee, Shatabdi, Vrailas-Mortimer, Alysia D., Zlatic, Stephanie A., Freeman, Amanda A. H., Gokhale, Avanti, Concilli, Mafalda, Werner, Erica, Sapp Savas, Christie, Rudin-Rush, Samantha, Palmer, Laura, Shearing, Nicole, Margewich, Lindsey, McArthy, Jacob, Taylor, Savanah, Roberts, Blaine, Lupashin, Vladimir, Polishchuk, Roman S., Cox, Daniel N., Jorquera, Ramon A., Faundez, Victor
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2021
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7810662/
https://ncbi.nlm.nih.gov/pubmed/33208468
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.1284-20.2020
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