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Neuronal Tsc1/2 complex controls autophagy through AMPK-dependent regulation of ULK1
Tuberous sclerosis complex (TSC) is a disorder arising from mutation in the TSC1 or TSC2 gene, characterized by the development of hamartomas in various organs and neurological manifestations including epilepsy, intellectual disability and autism. TSC1/2 protein complex negatively regulates the mamm...
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| Huvudupphovsmän: | , , , , , , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Oxford University Press
2014
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4065158/ https://ncbi.nlm.nih.gov/pubmed/24599401 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu101 |
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