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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Bibliografiset tiedot
Julkaisussa:J Neurosci
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Society for Neuroscience 2021
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Research Articles
Linkit: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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