关注
Gary G. Chiang
Gary G. Chiang
eFFECTOR Therapeutics
在 effector.com 的电子邮件经过验证
标题
引用次数
引用次数
年份
Regulation of hypoxia-inducible factor 1α expression and function by the mammalian target of rapamycin
CC Hudson, M Liu, GG Chiang, DM Otterness, DC Loomis, F Kaper, ...
Molecular and cellular biology 22 (20), 7004-7014, 2002
15352002
Phosphorylation of Mammalian Target of Rapamycin (mTOR) at Ser-2448 IsMediated by p70S6 Kinase
GG Chiang, RT Abraham
Journal of Biological Chemistry 280 (27), 25485-25490, 2005
6622005
Discovery of a selective catalytic p300/CBP inhibitor that targets lineage-specific tumours
LM Lasko, CG Jakob, RP Edalji, W Qiu, D Montgomery, EL Digiammarino, ...
Nature 550 (7674), 128-132, 2017
6032017
Targeting the mTOR signaling network in cancer
GG Chiang, RT Abraham
Trends in molecular medicine 13 (10), 433-442, 2007
4272007
Comparative metabolic flux profiling of melanoma cell lines: beyond the Warburg effect
DA Scott, AD Richardson, FV Filipp, CA Knutzen, GG Chiang, AR Ze'ev, ...
Journal of Biological Chemistry 286 (49), 42626-42634, 2011
3982011
Genotoxic stress targets human Chk1 for degradation by the ubiquitin-proteasome pathway
YW Zhang, DM Otterness, GG Chiang, W Xie, YC Liu, F Mercurio, ...
Molecular cell 19 (5), 607-618, 2005
3152005
Differential effects of rapamycin on mammalian target of rapamycin signaling functions in mammalian cells
AL Edinger, CM Linardic, GG Chiang, CB Thompson, RT Abraham
Cancer research 63 (23), 8451-8460, 2003
2192003
The EED protein–protein interaction inhibitor A-395 inactivates the PRC2 complex
Y He, S Selvaraju, ML Curtin, CG Jakob, H Zhu, KM Comess, B Shaw, ...
Nature chemical biology 13 (4), 389-395, 2017
2102017
Isoform-specific phosphoinositide 3-kinase inhibitors from an arylmorpholine scaffold
ZA Knight, GG Chiang, PJ Alaimo, DM Kenski, CB Ho, K Coan, ...
Bioorganic & medicinal chemistry 12 (17), 4749-4759, 2004
2032004
Specific dephosphorylation of the Lck tyrosine protein kinase at Tyr-394 by the SHP-1 protein-tyrosine phosphatase
GG Chiang, BM Sefton
Journal of Biological Chemistry 276 (25), 23173-23178, 2001
1982001
The phosphatidylinositol 3-kinase inhibitor, PX-866, is a potent inhibitor of cancer cell motility and growth in three-dimensional cultures
AL Howes, GG Chiang, ES Lang, CB Ho, G Powis, K Vuori, RT Abraham
Molecular cancer therapeutics 6 (9), 2505-2514, 2007
1902007
Discovery and development of potent and selective inhibitors of histone methyltransferase g9a
RF Sweis, M Pliushchev, PJ Brown, J Guo, F Li, D Maag, AM Petros, ...
ACS medicinal chemistry letters 5 (2), 205-209, 2014
1892014
REDD1, an inhibitor of mTOR signalling, is regulated by the CUL4A–DDB1 ubiquitin ligase
S Katiyar, E Liu, CA Knutzen, ES Lang, CR Lombardo, S Sankar, JI Toth, ...
EMBO reports 10 (8), 866-872, 2009
1662009
Structure-based design of pyridone–aminal eFT508 targeting dysregulated translation by selective mitogen-activated protein kinase interacting kinases 1 and 2 (MNK1/2) inhibition
SH Reich, PA Sprengeler, GG Chiang, JR Appleman, J Chen, J Clarine, ...
Journal of medicinal chemistry 61 (8), 3516-3540, 2018
1362018
The SUV4-20 inhibitor A-196 verifies a role for epigenetics in genomic integrity
KD Bromberg, TRH Mitchell, AK Upadhyay, CG Jakob, MA Jhala, ...
Nature chemical biology 13 (3), 317-324, 2017
1122017
Control of mTORC1 signaling by the Opitz syndrome protein MID1
E Liu, CA Knutzen, S Krauss, S Schweiger, GG Chiang
Proceedings of the National Academy of Sciences 108 (21), 8680-8685, 2011
1092011
Synthesis and biological evaluation of synthetic viridins derived from C (20)-heteroalkylation of the steroidal PI-3-kinase inhibitor wortmannin
P Wipf, DJ Minion, RJ Halter, MI Berggren, CB Ho, GG Chiang, ...
Organic & biomolecular chemistry 2 (13), 1911-1920, 2004
1062004
Design of development candidate eFT226, a first in class inhibitor of eukaryotic initiation factor 4A RNA helicase
JT Ernst, PA Thompson, C Nilewski, PA Sprengeler, S Sperry, G Packard, ...
Journal of medicinal chemistry 63 (11), 5879-5955, 2020
972020
Mammalian target of rapamycin activator RHEB is frequently overexpressed in human carcinomas and is critical and sufficient for skin epithelial carcinogenesis
ZH Lu, MB Shvartsman, AY Lee, JM Shao, MM Murray, RD Kladney, ...
Cancer research 70 (8), 3287-3298, 2010
952010
The histone methyltransferase inhibitor A-366 uncovers a role for G9a/GLP in the epigenetics of leukemia
WN Pappano, J Guo, Y He, D Ferguson, S Jagadeeswaran, DJ Osterling, ...
PloS one 10 (7), e0131716, 2015
932015
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