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Novel septin 9 repeat motifs altered in neuralgic amyotrophy bind and bundle microtubules
Septin 9 (SEPT9) interacts with microtubules (MTs) and is mutated in hereditary neuralgic amyotrophy (HNA), an autosomal-dominant neuropathy. The mechanism of SEPT9 interaction with MTs and the molecular basis of HNA are unknown. Here, we show that the N-terminal domain of SEPT9 contains the novel r...
Autores principales: | Bai, Xiaobo, Bowen, Jonathan R., Knox, Tara K., Zhou, Kaifeng, Pendziwiat, Manuela, Kuhlenbäumer, Gregor, Sindelar, Charles V., Spiliotis, Elias T. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871440/ https://www.ncbi.nlm.nih.gov/pubmed/24344182 http://dx.doi.org/10.1083/jcb.201308068 |
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