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ESCRT-III-associated proteins and spastin inhibit protrudin-dependent polarised membrane traffic
Mutations in the gene encoding the microtubule severing ATPase spastin are the most frequent cause of hereditary spastic paraplegia, a genetic condition characterised by length-dependent axonal degeneration. Here, we show that HeLa cells lacking spastin and embryonic fibroblasts from a spastin knock...
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| Publicado no: | Cell Mol Life Sci |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer International Publishing
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7320071/ https://ncbi.nlm.nih.gov/pubmed/31587092 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00018-019-03313-z |
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