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1. TTF1 control of LncRNA synthesis delineates a tumor suppressor pathway directly regulating the ribosomal RNA genes.

2. Senescence-associated ribosome biogenesis defects contributes to cell cycle arrest through the Rb pathway

7. EPH receptor tyrosine kinases phosphorylate the PAR-3 scaffold protein to modulate downstream signaling networks

9. Ribosomal DNA promoter recognition is determined in vivo by cooperation between UBTF1 and SL1 and is compromised in the UBTF-E210K neuroregression syndrome

10. Cellular Senescence limits Translational Readthrough

11. A hydride transfer complex reprograms NAD metabolism and bypasses senescence

12. The Short N-Terminal Repeats of Transcription Termination Factor 1 Contain Semi-Redundant Nucleolar Localization Signals and P19-ARF Tumor Suppressor Binding Sites

13. Bidirectional cooperation between Ubtf1 and SL1 determines RNA Polymerase I promoter recognition in cell and is negatively affected in the UBTF-E210K neuroregression syndrome

15. Proximity-dependent Mapping of the Androgen Receptor Identifies Kruppel-like Factor 4 as a Functional Partner

19. EPH Receptor Tyrosine Kinases Regulate Epithelial Morphogenesis and Phosphorylate the PAR-3 Scaffold Protein to Modulate Downstream Signaling Networks

20. A Hydride Transfer Complex Reprograms NAD Metabolism Preventing Senescence

24. Phosphorylation of SOCS1 Inhibits the SOCS1–p53 Tumor Suppressor Axis

25. Ribosomal protein RPL22/eL22 regulates the cell cycle by acting as an inhibitor of the CDK4-cyclin D complex

29. Abstract 2154: ERK/MAPK pathway inhibits tumorigenesis and cellular reprogramming of pancreatic cancer cells

38. Tumor suppressor activity of the ERK/MAPK pathway by promoting selective protein degradation

39. Abstract 4166: Tumor suppressor activity of the ERK/MAPK pathway by promoting selective protein degradation

43. SOCS1: phosphorylation, dimerization and tumor suppression.

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