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Wilms Tumor Suppressor, WT1, Cooperates with MicroRNA-26a and MicroRNA-101 to Suppress Translation of the Polycomb Protein, EZH2, in Mesenchymal Stem Cells

Hereditary forms of Wilms arise from developmentally arrested clones of renal progenitor cells with biallelic mutations of WT1; recently, it has been found that Wilms tumors may also be associated with biallelic mutations in DICER1 or DROSHA, crucial for miRNA biogenesis. We have previously shown th...

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Détails bibliographiques
Publié dans:J Biol Chem
Auteurs principaux: Akpa, Murielle M., Iglesias, Diana, Chu, LeeLee, Thiébaut, Antonin, Jentoft, Ida, Hammond, Leah, Torban, Elena, Goodyer, Paul R.
Format: Artigo
Langue:Inglês
Publié: American Society for Biochemistry and Molecular Biology 2016
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Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4759161/
https://ncbi.nlm.nih.gov/pubmed/26655220
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M115.678029
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