טוען...
Disruption of Rab11 activity in a knock-in mouse model of Huntington's Disease
The Huntington's disease (HD) mutation causes polyglutamine expansion in huntingtin (Htt) and neurodegeneration. Htt interacts with a complex containing Rab11GDP and is involved in activation of Rab11, which functions in endosomal recycling and neurite growth and long-term potentiation. Like ot...
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| Main Authors: | , , , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2009
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2798579/ https://ncbi.nlm.nih.gov/pubmed/19699304 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2009.08.003 |
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