Ali Fattaey

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Phase 1 first-in-human trial of MTB-9655, the first oral inhibitor of ACSS2, in patients with advanced solid tumors von Perets, Ruth, Geva, Ravit, McKean, Meredith, Goutopoulos, Andreas, Erez, Omri, Phadnis, Monica, Youssoufian, Hagop, Schwartz, Brian E., Kansra, Vikram, Fattaey, Ali

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Inhibition of E2F-1 transactivation by direct binding of the retinoblastoma protein von HELIN, K, HARLOW, E, FATTAEY, A

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New functional activities for the p21 family of CDK inhibitors von LaBaer, J, Garrett, M D, Stevenson, L F, Slingerland, J M, Sandhu, C, Chou, H S, Fattaey, A, Harlow, E

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The Combination of Venetoclax and CUDC-907 Exhibits Synergistic Activity in Venetoclax-Refractory DLBCL von Sun, Kaiming, Atoyan, Ruzanna, Borek, Mylissa A, Dellarocca, Steven, Rhyasen, Garrett, Fattaey, Ali, Tuck, David P

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Abstract 2326: Preclinical characterization of MTB-9655, a first-in-class, clinical stage ACSS2 inhibitor von Goutopoulos, Andreas, Amanati, Iris, Fattaey, Ali, Hay-Koren, Avital, Nakache, Philippe, Erez, Omri, Kovalerchik, Dimitri, Paz, Dikla, Botti, Simone, Oppenheimer, Hannah, Fainer, Irit

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Abstract 1397: A phenotypic-based drug discovery approach against tumors with MTAP loss von Goutopoulos, Andreas, Amanati, Iris, Hay-Koren, Avital, Fattaey, Ali, Nakache, Philippe, Kovalerchik, Dimitri, Paz, Dikla, Botti, Simone, Oppenheimer, Hanna, Erez, Omri, Fainer, Irit

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Abstract 4634: Novel dual HDAC & PI3K inhibitor, CUDC-907, for MYC-driven malignancies von Sun, Kaiming, Atoyan, Ruzanna, Borek, Mylissa A., Dellarocca, Steven, Samson, Maria E., Ma, Anna W., Xu, Guangxin, Patterson, Troy, Tuck, David P., Viner, Jaye L., Fattaey, Ali, Wang, Jing

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Reverse Two-Hybrid and One-Hybrid Systems to Detect Dissociation of Protein-Protein and DNA-Protein Interactions von Vidal, Marc, Brachmann, Rainer K., Fattaey, Ali, Harlow, Ed, Boeke, Jef D.

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Heterodimerization of the transcription factors E2F-1 and DP-1 leads to cooperative trans-activation von HELIN, K, CHIN-LEE WU, FATTAEY, A. R, LEES, J. A, DYNLACHT, B. D, CHIDI NGWU, HARLOW, E

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Pyrido[2,3-d]pyrimidin-7-one Inhibitors of Cyclin-Dependent Kinases von Barvian, Mark, Boschelli, Diane H, Cossrow, Jennifer, Dobrusin, Ellen, Fattaey, Ali, Fritsch, Alex, Fry, David, Harvey, Patricia, Keller, Paul, Garrett, Michelle, La, Frances, Leopold, Wilbur, McNamara, Dennis, Quin, Maire, Trumpp-Kallmeyer, Susanne, Toogood, Peter, Wu, Zhipei, Zhang, Erli

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Human Myt1 Is a Cell Cycle-regulated Kinase That Inhibits Cdc2 but Not Cdk2 Activity von Booher, Robert N., Holman, Patricia S., Fattaey, Ali

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Inhibition of cell proliferation by p107, a relative of the retinoblastoma protein von LIANG ZHU, VAN DEN HEUVEL, S, HELIN, K, ALI FATTAEY, EWEN, M, LIVINGSTON, D, DYSON, N, HARLOW, E

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Analyses of Single-Amino-Acid Substitution Mutants of Adenovirus Type 5 E1B-55K Protein von Shen, Y, Kitzes, G, Nye, J A, Fattaey, A, Hermiston, T

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CDK inhibition and cancer therapy von Garrett, Michelle D, Fattaey, Ali

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Independent regions of adenovirus E1A are required for binding to and dissociation of E2F-protein complexes von FATTAEY, A. R, HARLOW, E, HELIN, K

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A First-In-Man Phase 1 Study Of CUDC-907, a First-In-Class Chemically-Designed Dual Inhibitor Of PI3K and HDAC In Patients With Refractory Or Relapsed Lymphoma and Multiple Myeloma von Younes, Anas, Flinn, Ian W., Oki, Yasuhiro, Copland, Amanda, Fattaey, Ali, Lai, Cheng-Jung, Laliberte, Robert, Voi, Maurizio, Berdeja, Jesus G

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Pharmacokinetic and pharmacodynamic analysis of gastric cancer patients treated with telatinib von Burd, A., Castillo, J., Whiteside, M., White, M., Ajani, J. A., Fattaey, A., Kunkel, L. A.

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ACTB-1003: An oral kinase inhibitor targeting cancer mutations (FGFR), angiogenesis (VEGFR2, TEK), and induction of apoptosis (RSK and p70S6K) von Patel, K., Fattaey, A., Burd, A.

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Direct interaction of human TFIID with the HIV-1 transactivator Tat von Kashanchi, Fatah, Piras, Graziella, Radonovich, Michael F, Duvall, Janet F, Fattaey, Ali, Chiang, Cheng-Ming, Roeder, Robert G, Brady, John N

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