Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference24 articles.
1. Hereditary spastic paraplegia: The pace quickens
2. Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease
3. Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60
4. A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10)
5. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
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1. A novel truncated variant in SPAST results in spastin accumulation and defects in microtubule dynamics;BMC Medical Genomics;2023-12-08
2. Human atlastins are sufficient to drive the fusion of liposomes with a physiological lipid composition;Journal of Cell Biology;2023-02-09
3. Rab3A interacts with spastin to regulate neurite outgrowth in hippocampal neurons;Biochemical and Biophysical Research Communications;2023-02
4. The interconnection of endoplasmic reticulum and microtubule and its implication in Hereditary Spastic Paraplegia;Computational and Structural Biotechnology Journal;2023
5. Structural Diversity within the Endoplasmic Reticulum—From the Microscale to the Nanoscale;Cold Spring Harbor Perspectives in Biology;2022-09-19
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