Identification of the Drosophila Ortholog of HSPB8: IMPLICATION OF HSPB8 LOSS OF FUNCTION IN PROTEIN FOLDING DISEASES

Protein aggregation is a hallmark of many neuronal disorders, including the polyglutamine disorder spinocerebellar ataxia 3 and peripheral neuropathies associated with the K141E and K141N mutations in the small heat shock protein HSPB8. In cells, HSPB8 cooperates with BAG3 to stimulate autophagy in...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Carra, Serena, Boncoraglio, Alessandra, Kanon, Bart, Brunsting, Jeanette F., Minoia, Melania, Rana, Anil, Vos, Michel J., Seidel, Kay, Sibon, Ody C. M., Kampinga, Harm H.
Format: Artigo
Idioma:Inglês
Publicat: American Society for Biochemistry and Molecular Biology 2010
Matèries:
Protein Synthesis and Degradation
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2988385/
https://ncbi.nlm.nih.gov/pubmed/20858900
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M110.127498
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars