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Friedreich's ataxia reveals a mechanism for coordinate regulation of oxidative metabolism via feedback inhibition of the SIRT3 deacetylase

Friedreich's ataxia (FRDA) is the most common inherited human ataxia and is caused by a deficiency in the mitochondrial protein frataxin. Clinically, patients suffer from progressive spinocerebellar degeneration, diabetes and a fatal cardiomyopathy, associated with mitochondrial respiratory cha...

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Detalhes bibliográficos
Main Authors: Wagner, Gregory R., Pride, P. Melanie, Babbey, Clifford M., Payne, R. Mark
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3363336/
https://ncbi.nlm.nih.gov/pubmed/22394676
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds095
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