A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1

MAGEL2 encodes the L2 member of the MAGE (melanoma antigen) protein family. Protein truncating mutations in MAGEL2 cause Schaaf-Yang syndrome, and MAGEL2 is one of a small set of genes deleted in Prader-Willi syndrome. Excessive daytime sleepiness, night-time or early morning waking, and narcoleptic...

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Detalles Bibliográficos
Autores principales: Carias, K. Vanessa, Zoeteman, Mercedes, Seewald, Abigail, Sanderson, Matthea R., Bischof, Jocelyn M., Wevrick, Rachel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173924/
https://www.ncbi.nlm.nih.gov/pubmed/32315313
http://dx.doi.org/10.1371/journal.pone.0230874

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173924/
https://www.ncbi.nlm.nih.gov/pubmed/32315313
http://dx.doi.org/10.1371/journal.pone.0230874

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