Feast or famine: Role of TRPML in preventing cellular amino acid starvation

Lysosomal storage diseases are metabolic disorders characterized by the accumulation of acidic vacuoles, and are usually the consequence of the deficiency of an enzyme responsible for the metabolism of vesicular lipids, proteins or carbohydrates. In contrast, mucolipidosis type IV (MLIV), results fr...

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Detalles Bibliográficos
Autores principales: Venkatachalam, Kartik, Wong, Ching-On, Montell, Craig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Autophagic Punctum
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542223/
https://www.ncbi.nlm.nih.gov/pubmed/23047439
http://dx.doi.org/10.4161/auto.22260

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542223/
https://www.ncbi.nlm.nih.gov/pubmed/23047439
http://dx.doi.org/10.4161/auto.22260

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