Palmitoyl-Protein Thioesterase 1 Deficiency in Drosophila melanogaster Causes Accumulation of Abnormal Storage Material and Reduced Life Span

Human neuronal ceroid lipofuscinoses (NCLs) are a group of genetic neurodegenerative diseases characterized by progressive death of neurons in the central nervous system (CNS) and accumulation of abnormal lysosomal storage material. Infantile NCL (INCL), the most severe form of NCL, is caused by mut...

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Bibliografske podrobnosti
Main Authors: Hickey, Anthony J., Chotkowski, Heather L., Singh, Navjot, Ault, Jeffrey G., Korey, Christopher A., MacDonald, Marcy E., Glaser, Robert L.
Format: Artigo
Jezik:Inglês
Izdano: Copyright © 2006 by the Genetics Society of America 2006
Teme:
Investigations
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1456391/
https://ncbi.nlm.nih.gov/pubmed/16452138
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.105.053306
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