Protein-Arginine N-Methyltransferases
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Subject Areas on Research
- A PRMT5-RNF168-SMURF2 Axis Controls H2AX Proteostasis.
- A monitor for bud emergence in the yeast morphogenesis checkpoint.
- A role for the Pkc1p/Mpk1p kinase cascade in the morphogenesis checkpoint.
- CARM1-expressing ovarian cancer depends on the histone methyltransferase EZH2 activity.
- Cell-cycle checkpoints that ensure coordination between nuclear and cytoplasmic events in Saccharomyces cerevisiae.
- DNA replication checkpoint control of Wee1 stability by vertebrate Hsl7.
- Determinants of Swe1p degradation in Saccharomyces cerevisiae.
- Effects of a novel arginine methyltransferase inhibitor on T-helper cell cytokine production.
- Epigenetic Regulation of Fanconi Anemia Genes Implicates PRMT5 Blockage as a Strategy for Tumor Chemosensitization.
- Feedback control of Swe1p degradation in the yeast morphogenesis checkpoint.
- Methed-up FOXOs can't in-Akt-ivate.
- Molecular dissection of the checkpoint kinase Hsl1p.
- NIP45 controls the magnitude of the type 2 T helper cell response.
- Protein Arginine Methyltransferase 5 Promotes pICln-Dependent Androgen Receptor Transcription in Castration-Resistant Prostate Cancer.
- Roles of Hsl1p and Hsl7p in Swe1p degradation: beyond septin tethering.
- Sensing a bud in the yeast morphogenesis checkpoint: a role for Elm1.
- Septin-dependent assembly of a cell cycle-regulatory module in Saccharomyces cerevisiae.
- Targeting Protein Arginine Methyltransferase 5 Suppresses Radiation-induced Neuroendocrine Differentiation and Sensitizes Prostate Cancer Cells to Radiation.
- The expression and function of androgen receptor coactivator p44 and protein arginine methyltransferase 5 in the developing testis and testicular tumors.
- The morphogenesis checkpoint in Saccharomyces cerevisiae: cell cycle control of Swe1p degradation by Hsl1p and Hsl7p.
- Toxoplasma gondii Arginine Methyltransferase 1 (PRMT1) Is Necessary for Centrosome Dynamics during Tachyzoite Cell Division.
- Wnt activation promotes memory T cell polyfunctionality via epigenetic regulator PRMT1.