نتائج البحث - "Justin L. Tan"

المساهمون: Harvard Stem Cell Institute [Cambridge, USA] (HSCI), Harvard University, Howard Hughes Medical Institute [Boston] (HHMI), Howard Hughes Medical Institute (HHMI)-Harvard Medical School [Boston] (HMS), Boston Children's Hospital, Harvard Medical School [Boston] (HMS), Dana-Farber Cancer Institute [Boston], Center for Personal Dynamic Regulomes [Stanford] (CPDR), Stanford Medicine, Stanford University-Stanford University, Whitehead Institute, Massachusetts Institute of Technology (MIT), Department of Biology [MIT Cambridge, USA], Brigham & Women’s Hospital [Boston] (BWH), University of California [San Francisco] (UC San Francisco), University of California (UC), Yale School of Medicine [New Haven, Connecticut] (YSM), University of Texas at Dallas [Richardson] (UT Dallas), Beth Israel Deaconess Medical Center [Boston] (BIDMC), Cancer Research Institute [Boston, USA], Harvard Medical School [Boston] (HMS)-Harvard Medical School [Boston] (HMS), University of Iowa [Iowa City], Genome Institute of Singapore (GIS), Memorial Sloane Kettering Cancer Center [New York], Weill Medical College of Cornell University [New York], This work was supported by the Howard Hughes Medical Institute and the National Cancer Institute (NIH) R01CA103846 (to L.I.Z.). L.I.Z. is a founder and stockholder of Fate, Inc., Scholar Rock, and a scientific advisor for Stemgent. J.L.T. is an Agency for Science, Technology & Research, Singapore National Science Scholarship recipient. C.B.G. is a PhRMA Foundation predoctoral fellow. R.A.Y. is a founder and stockholder of Syros Pharmaceuticals. This work was partially supported by NIH grants 2P01CA120964 (to J.M.A.), 5P30CA006516 (to J.M.A.), R01CA140485 (to T.H.K.), R21AI107067 (to T.H.K.), R01-ES023168 (to H.Y.C), and R01-HG004361 (to H.Y.C), We thank Min Yuan for her help with the metabolomics studies and Dr. Telmo Henriques for his advice on RNA assays., Harvard University [Cambridge], University of California [San Francisco] (UCSF), University of California, Yale University School of Medicine, Massachusetts Institute of Technology. Department of Biology, Saint-André, Violaine, Fan, Zi Peng, Young, Richard A

المصدر: Molecular Cell
Molecular Cell, 2016, 62 (1), pp.34-46. ⟨10.1016/j.molcel.2016.03.013⟩
Molecular Cell, Elsevier, 2016, 62 (1), pp.34-46. ⟨10.1016/j.molcel.2016.03.013⟩
PMC
Molecular cell, vol 62, iss 1

مصطلحات موضوعية: 0301 basic medicine, Transcription, Genetic, [SDV]Life Sciences [q-bio], Melanoma, Experimental, MESH: Oncogene Proteins / genetics, Medical and Health Sciences, Transcription (biology), MESH: Melanoma / genetics, Gene expression, Transcriptional regulation, 2.1 Biological and endogenous factors, MESH: Melanoma / pathology, Positive Transcriptional Elongation Factor B, MESH: Animals, Aetiology, Zebrafish, Melanoma, Cancer, Regulation of gene expression, Oncogene Proteins, MESH: RNA-Binding Proteins / genetics, Gene knockdown, Tumor, biology, Kinase, RNA-Binding Proteins, MESH: Gene Expression Regulation, Neoplastic, Biological Sciences, 3. Good health, MESH: RNA-Binding Proteins / metabolism, Gene Expression Regulation, Neoplastic, MESH: Melanoma, Experimental, MESH: Tumor Suppressor Proteins / genetics, Transcription, Biotechnology, MESH: Cell Line, Tumor, MESH: Zebrafish Proteins / metabolism, [SDV.CAN]Life Sciences [q-bio]/Cancer, Article, Cell Line, MESH: Zebrafish / genetics, 03 medical and health sciences, Experimental, Genetic, Cell Line, Tumor, medicine, Genetics, Animals, Humans, Molecular Biology, Neoplastic, MESH: Humans, Tumor Suppressor Proteins, MESH: Transcription, Genetic, Cell Biology, Zebrafish Proteins, biology.organism_classification, medicine.disease, MESH: Positive Transcriptional Elongation Factor B / genetics, 030104 developmental biology, Pyrimidines, Gene Expression Regulation, Cancer research, MESH: Pyrimidines / metabolism, MESH: Zebrafish Proteins / genetics, MESH: Melanoma / metabolism, Transcription Factors, Developmental Biology