Spastic Paraplegia Mutation N256S in the Neuronal Microtubule Motor KIF5A Disrupts Axonal Transport in a Drosophila HSP Model
Published 2012 View Full Article
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Title
Spastic Paraplegia Mutation N256S in the Neuronal Microtubule Motor KIF5A Disrupts Axonal Transport in a Drosophila HSP Model
Authors
Keywords
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Journal
PLoS Genetics
Volume 8, Issue 11, Pages e1003066
Publisher
Public Library of Science (PLoS)
Online
2012-11-30
DOI
10.1371/journal.pgen.1003066
References
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Note: Only part of the references are listed.- Kinesin Heavy Chain Function in Drosophila Glial Cells Controls Neuronal Activity
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- Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients
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- Tight Functional Coupling of Kinesin-1A and Dynein Motors in the Bidirectional Transport of Neurofilaments
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- Effect of spastic paraplegia mutations in KIF5A kinesin on transport activity
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- Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10
- (2008) Cyril Goizet et al. HUMAN MUTATION
- SPG10 is a rare cause of spastic paraplegia in European families
- (2008) R Schule et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- A Presynaptic Giant Ankyrin Stabilizes the NMJ through Regulation of Presynaptic Microtubules and Transsynaptic Cell Adhesion
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- The Parallel Worm Tracker: A Platform for Measuring Average Speed and Drug-Induced Paralysis in Nematodes
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- Tug-of-war as a cooperative mechanism for bidirectional cargo transport by molecular motors
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