טוען...
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...
שמור ב:
| הוצא לאור ב: | PLoS One |
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| Main Authors: | , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Public Library of Science
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7173924/ https://ncbi.nlm.nih.gov/pubmed/32315313 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0230874 |
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