Characterization of Drosophila Saposin-related mutants as a model for lysosomal sphingolipid storage diseases

Sphingolipidoses are inherited diseases belonging to the class of lysosomal storage diseases (LSDs), which are characterized by the accumulation of indigestible material in the lysosome caused by specific defects in the lysosomal degradation machinery. While some LSDs can be efficiently treated by e...

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Detalhes bibliográficos
Publicado no:Dis Model Mech
Principais autores: Sellin, Julia, Schulze, Heike, Paradis, Marie, Gosejacob, Dominic, Papan, Cyrus, Shevchenko, Andrej, Psathaki, Olympia Ekaterina, Paululat, Achim, Thielisch, Melanie, Sandhoff, Konrad, Hoch, Michael
Formato: Artigo
Idioma:Inglês
Publicado em: The Company of Biologists Ltd 2017
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5483003/
https://ncbi.nlm.nih.gov/pubmed/28389479
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.027953
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