MYSM1 maintains ribosomal protein gene expression in hematopoietic stem cells to prevent hematopoietic dysfunction

Ribosomopathies are congenital disorders caused by mutations in the genes encoding ribosomal and other functionally related proteins. They are characterized by anemia, other hematopoietic and developmental abnormalities, and p53 activation. Ribosome assembly requires coordinated expression of many r...

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Bibliografiset tiedot
Julkaisussa:JCI Insight
Päätekijät: Belle, Jad I., Wang, HanChen, Fiore, Amanda, Petrov, Jessica C., Lin, Yun Hsiao, Feng, Chu-Han, Nguyen, Thi Tuyet Mai, Tung, Jacky, Campeau, Philippe M., Behrends, Uta, Brunet, Theresa, Leszinski, Gloria Sarah, Gros, Philippe, Langlais, David, Nijnik, Anastasia
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Society for Clinical Investigation 2020
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7406308/
https://ncbi.nlm.nih.gov/pubmed/32641579
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/jci.insight.125690
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