A newly identified NES sequence present in spastin regulates its subcellular localization and microtubule severing activity
Author:
Funder
Japan Agency for Medical Research and Development
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology
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1. A novel variant (p.A524P) in Spastin is responsible for a Chinese family with hereditary spastic paraplegia;Molecular Biology Reports;2024-09-04
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3. Alu Retrotransposition Event in SPAST Gene as a Novel Cause of Hereditary Spastic Paraplegia;Movement Disorders;2023-07-02
4. Spastin is required for human immunodeficiency virus-1 efficient replication through cooperation with the endosomal sorting complex required for transport (ESCRT) protein;Virologica Sinica;2023-06
5. A novel truncating variant of SPAST associated with hereditary spastic paraplegia indicates a haploinsufficiency pathogenic mechanism;Frontiers in Neurology;2022-11-14
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