Altered lipid metabolism in Drosophila model of Huntington’s disease

Huntington’s disease (HD) is late-onset, progressive neurodegenerative disorder caused by expansion of polyglutamine (polyQ) repeat within Huntingtin (Htt) protein. In HD patients, energy-related manifestations such as modulation of weight during entire course of disease with energy deficit at termi...

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Detalles Bibliográficos
Autores principales: Aditi, Kumari, Shakarad, Mallikarjun N., Agrawal, Namita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979013/
https://www.ncbi.nlm.nih.gov/pubmed/27506601
http://dx.doi.org/10.1038/srep31411

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979013/
https://www.ncbi.nlm.nih.gov/pubmed/27506601
http://dx.doi.org/10.1038/srep31411

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