Distal spinal and bulbar muscular atrophy caused by dynactin mutation-Reference-Cited by-同舟云学术

Distal spinal and bulbar muscular atrophy caused by dynactin mutation

Published:2005 Issue:5 Volume:57 Page:687-694
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Puls Imke,Oh Shin J.,Sumner Charlotte J.,Wallace Karen E.,Floeter Mary Kay,Mann Eric A.,Kennedy William R.,Wendelschafer-Crabb Gwen,Vortmeyer Alexander,Powers Richard,Finnegan Kimberly,Holzbaur Erika L. F.,Fischbeck Kenneth H.,Ludlow Christy L.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference40 articles.

1. Retarded Axonal Transport of R406W Mutant Tau in Transgenic Mice with a Neurodegenerative Tauopathy

2. Neuropathogenic Forms of Huntingtin and Androgen Receptor Inhibit Fast Axonal Transport

3. Disruption of Axonal Transport by Loss of Huntingtin or Expression of Pathogenic PolyQ Proteins in Drosophila

4. Slowing of axonal transport is a very early event in the toxicity of ALS–linked SOD1 mutants to motor neurons

5. Neurofilaments and Orthograde Transport Are Reduced in Ventral Root Axons of Transgenic Mice that Express Human SOD1 with a G93A Mutation

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