Atlastin-1 regulates endosomal tubulation and lysosomal proteolysis in human cortical neurons
Mutation of the ATL1 gene is one of the most common causes of hereditary spastic paraplegia (HSP), a group of genetic neurodegenerative conditions characterised by distal axonal degeneration of the corticospinal tract axons. Atlastin-1, the protein encoded by ATL1, is one of three mammalian atlastin...
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| Asıl Yazarlar: | , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Elsevier
2024-09-01
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| Seri Bilgileri: | Neurobiology of Disease |
| Konular: | |
| Online Erişim: | http://www.sciencedirect.com/science/article/pii/S0969996124001554 |
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