Huntington’s disease: Neural dysfunction linked to inositol polyphosphate multikinase

Huntington’s disease (HD) is a progressive neurodegenerative disease caused by a glutamine repeat expansion in mutant huntingtin (mHtt). Despite the known genetic cause of HD, the pathophysiology of this disease remains to be elucidated. Inositol polyphosphate multikinase (IPMK) is an enzyme that di...

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Bibliografiska uppgifter
I publikationen:Proc Natl Acad Sci U S A
Huvudupphovsmän: Ahmed, Ishrat, Sbodio, Juan I., Harraz, Maged M., Tyagi, Richa, Grima, Jonathan C., Albacarys, Lauren K., Hubbi, Maimon E., Xu, Risheng, Kim, Seyun, Paul, Bindu D., Snyder, Solomon H.
Materialtyp: Artigo
Språk:Inglês
Publicerad: National Academy of Sciences 2015
Ämnen:
Biological Sciences
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4534278/
https://ncbi.nlm.nih.gov/pubmed/26195796
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1511810112
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