E Premkumar Reddy
Affiliations: | Molecular Biology and Genetics | Temple University, Philadelphia, PA, United States |
Area:
Molecular BiologyGoogle:
"E Reddy"Children
Sign in to add traineeAtul Kumar | grad student | 2001 | Temple University |
Anita L. Korapati | grad student | 2002 | Temple University |
Quang D. Nguyen | grad student | 2003 | Temple University |
Rachel B. Sumerson | grad student | 2003 | Temple University |
James K. Mangan | grad student | 2005 | Temple University |
Yen K. Lieu | grad student | 2006 | Temple University |
Zahidur R. Abedin | grad student | 2008 | Temple University |
Rachna Chawla | grad student | 2008 | Temple University |
Haritha K. DLReddy | grad student | 2008 | Temple University |
James J. Yi | grad student | 2008 | Temple University |
Amol A. Padgaonkar | grad student | 2014 | Temple University |
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Publications
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Sato K, Padgaonkar A, Cosenza S, et al. (2020) Abstract P5-05-04: A novel inhibitor of cancer stem cells overcomes chemotherapy resistance of triple negative breast cancers Cancer Research |
Padgaonkar A, Rechkoblit O, Vasquez-Del Carpio R, et al. (2018) Targeting protein kinase CK2 and CDK4/6 pathways with a multi-kinase inhibitor ON108110 suppresses pro-survival signaling and growth in mantle cell lymphoma and T-acute lymphoblastic leukemia. Oncotarget. 9: 37753-37765 |
Perumal D, Kuo PY, Leshchenko VV, et al. (2016) Dual Targeting of CDK4 and ARK5 Using a Novel Kinase Inhibitor ON123300 Exerts Potent Anticancer Activity against Multiple Myeloma. Cancer Research |
Reddy MV, Akula B, Jatiani S, et al. (2015) Discovery of 2-(1H-indol-5-ylamino)-6-(2,4-difluorophenylsulfonyl)-8-methylpyrido[2,3-d]pyrimidin-7(8H)-one (7ao) as a potent selective inhibitor of Polo like kinase 2 (PLK2). Bioorganic & Medicinal Chemistry |
Eachkoti R, Reddy MV, Lieu YK, et al. (2014) Identification and characterisation of a novel heat shock protein 90 inhibitor ONO4140. European Journal of Cancer (Oxford, England : 1990). 50: 1982-92 |
Baker SJ, Ma'ayan A, Lieu YK, et al. (2014) B-myb is an essential regulator of hematopoietic stem cell and myeloid progenitor cell development. Proceedings of the National Academy of Sciences of the United States of America. 111: 3122-7 |
Reddy MV, Akula B, Cosenza SC, et al. (2014) Discovery of 8-cyclopentyl-2-[4-(4-methyl-piperazin-1-yl)-phenylamino]-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carbonitrile (7x) as a potent inhibitor of cyclin-dependent kinase 4 (CDK4) and AMPK-related kinase 5 (ARK5). Journal of Medicinal Chemistry. 57: 578-99 |
Perumal D, Leshchenko VV, Kuo P, et al. (2014) Weighted Gene Co-Expression Network Analysis (WGCNA) Identifies Highly Proliferative Myeloma Subgroup Responsive to CDK4/ARK5 Inhibition Blood. 124: 3445-3445 |
Reddy MV, Mallireddigari MR, Pallela VR, et al. (2013) Design, synthesis, and biological evaluation of (E)-N-aryl-2-arylethenesulfonamide analogues as potent and orally bioavailable microtubule-targeted anticancer agents. Journal of Medicinal Chemistry. 56: 5562-86 |
Baker SJ, Reddy EP. (2012) CDK4: A Key Player in the Cell Cycle, Development, and Cancer. Genes & Cancer. 3: 658-69 |