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NTIS 바로가기Bulletin of the Korean chemical society, v.41 no.5, 2020년, pp.567 - 569
Ali, Imran (Therapeutics and Biotechnology Division Korea Research Institute of Chemical Technology Daejeon 34114 Korea) , Park, Sangjun (Therapeutics and Biotechnology Division Korea Research Institute of Chemical Technology Daejeon 34114 Korea) , Jung, Myoung Eun (Therapeutics and Biotechnology Division Korea Research Institute of Chemical Technology Daejeon 34114 Korea) , Lee, Nari (Therapeutics and Biotechnology Division Korea Research Institute of Chemical Technology Daejeon 34114 Korea) , Bibi, Maimoona (Therapeutics and Biotechnology Division Korea Research Institute of Chemical Technology Daejeon 34114 Korea) , Chae, Chong Hak (Therapeutics and Biotechnology Division Korea Research Institute of Chemical Technology Daejeon 34114 Korea) , Yang, Kyung‐Min (Precision Medicine Research Center, Advanced Institutes of Convergence Technology Seoul National University Suwon 16229 Korea) , Kim, Seong‐Jin (Precision Medicine Research Center, Advanced Institutes of Convergence Technology Seoul National University Suwon 16229 Korea) , Choi, Gildon (Therapeutics and Biotechnology Division Korea Research Institute of Chemical Technol) , Lee, Kwangho
초록이 없습니다.
Sanjo, Hideki, Kawai, Taro, Akira, Shizuo. DRAKs, Novel Serine/Threonine Kinases Related to Death-associated Protein Kinase That Trigger Apoptosis. The Journal of biological chemistry, vol.273, no.44, 29066-29071.
Shiloh, Ruth, Bialik, Shani, Kimchi, Adi. The DAPK family: a structure-function analysis. Apoptosis : an international journal on programmed cell death, vol.19, no.2, 286-297.
Kögel, Donat, Prehn, Jochen H.M., Scheidtmann, Karl Heinz. The DAP kinase family of pro-apoptotic proteins: novel players in the apoptotic game. BioEssays, vol.23, no.4, 352-358.
Kuwahara, Hiroshi, Nakamura, Norihiro, Kanazawa, Hiroshi. Nuclear Localization of the Serine/Threonine Kinase DRAK2 Is Involved in UV-Induced Apoptosis. Biological & pharmaceutical bulletin, vol.29, no.2, 225-233.
Yang, K.M., Kim, W., Bae, E., Gim, J., Weist, Brian M., Jung, Y., Hyun, J.S., Hernandez, Jennifer B., Leem, S.H., Park, T., Jeong, J., Walsh, Craig M., Kim, S.J.. DRAK2 Participates in a Negative Feedback Loop to Control TGF-β/Smads Signaling by Binding to Type I TGF-β Receptor. Cell reports, vol.2, no.5, 1286-1299.
Wang, S., Xu, L., Lu, Y.T., Liu, Y.F., Han, B., Liu, T., Tang, J., Li, J., Wu, J., Li, J.Y., Yu, L.F., Yang, F.. Discovery of benzofuran-3(2H)-one derivatives as novel DRAK2 inhibitors that protect islet β-cells from apoptosis. European journal of medicinal chemistry, vol.130, 195-208.
Gao, Ling-Jie, Kovackova, Sona, Šála, Michal, Ramadori, Anna Teresa, De Jonghe, Steven, Herdewijn, Piet. Discovery of Dual Death-Associated Protein Related Apoptosis Inducing Protein Kinase 1 and 2 Inhibitors by a Scaffold Hopping Approach. Journal of medicinal chemistry, vol.57, no.18, 7624-7643.
Jung, M.E., Byun, B.J., Kim, H.M., Lee, J.Y., Park, J.H., Lee, N., Son, Y.H., Choi, S.U., Yang, K.M., Kim, S.J., Lee, K., Kim, Y.C., Choi, G.. Discovery of indirubin derivatives as new class of DRAK2 inhibitors from high throughput screening. Bioorganic & medicinal chemistry letters, vol.26, no.11, 2719-2723.
Statsuk, Alexander V., Maly, Dustin J., Seeliger, Markus A., Fabian, Miles A., Biggs, William H., Lockhart, David J., Zarrinkar, Patrick P., Kuriyan, John, Shokat, Kevan M.. Tuning a Three-Component Reaction For Trapping Kinase Substrate Complexes. Journal of the American Chemical Society, vol.130, no.51, 17568-17574.
Getlik, M., Grutter, C., Simard, J.R., Nguyen, H.D., Robubi, A., Aust, B., van Otterlo, W.A.L., Rauh, D.. Structure-based design, synthesis and biological evaluation of N-pyrazole, N'-thiazole urea inhibitors of MAP kinase p38α. European journal of medicinal chemistry, vol.48, 1-15.
Choe, Hyeonjeong, Jeon, Byeong Uk, Jung, Myoung Eun, Jeon, Moon‐Kook, Shin, Inji, Cho, Byoung Chul, Choi, Gildon, Chae, Chong Hak, Lee, Kwangho. Structure-Activity Relationship Study of 2,4‐Dianilinopyrimidine Containing Methanesulfonamide (TRE‐069) as Potent and Selective Epidermal Growth Factor Receptor T790M/C797S Mutant Inhibitor for Anticancer Treatment. Bulletin of the Korean chemical society, vol.38, no.11, 1353-1357.
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