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Interaction between Sdo1p and Btn1p in the Saccharomyces cerevisiae model for Batten disease

Juvenile Batten disease is an autosomal recessive pediatric neurodegenerative disorder caused by mutations in the CLN3 gene. The CLN3 protein primarily resides in the lysosomal membrane, but its function is unknown. We demonstrate that CLN3 interacts with SBDS, the protein mutated in Shwachman–Bodia...

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Detalhes bibliográficos
Main Authors: Vitiello, Seasson Phillips, Benedict, Jared W., Padilla-Lopez, Sergio, Pearce, David A.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2816617/
https://ncbi.nlm.nih.gov/pubmed/20015955
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp560
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