Ciliogenesis is regulated by a huntingtin-HAP1-PCM1 pathway and is altered in Huntington disease-Reference-Cited by-同舟云学术

Ciliogenesis is regulated by a huntingtin-HAP1-PCM1 pathway and is altered in Huntington disease

Published:2011-11-01 Issue:11 Volume:121 Page:4372-4382
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Keryer Guy,Pineda Jose R.,Liot Géraldine,Kim Jinho,Dietrich Paula,Benstaali Caroline,Smith Karen,Cordelières Fabrice P.,Spassky Nathalie,Ferrante Robert J.,Dragatsis Ioannis,Saudou Frédéric

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference37 articles.

1. Huntington’s disease: from huntingtin function and dysfunction to therapeutic strategies

2. Huntingtin facilitates dynein/dynactin-mediated vesicle transport

3. Huntingtin Controls Neurotrophic Support and Survival of Neurons by Enhancing BDNF Vesicular Transport along Microtubules

4. Huntingtin phosphorylation acts as a molecular switch for anterograde/retrograde transport in neurons

5. Huntingtin-associated protein 1 (HAP1) interacts with the p150Glued subunit of dynactin

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