-
1
-
-
77950349016
-
Th17 and regulatory T cells in mediating and restraining inflammation
-
D.R. Littman, and A.Y. Rudensky Th17 and regulatory T cells in mediating and restraining inflammation Cell 140 2010 845 858
-
(2010)
Cell
, vol.140
, pp. 845-858
-
-
Littman, D.R.1
Rudensky, A.Y.2
-
2
-
-
39449101603
-
Transcriptional regulation of Th17 cell differentiation
-
I.I. Ivanov, L. Zhou, and D.R. Littman Transcriptional regulation of Th17 cell differentiation Seminars in Immunology 19 2007 409 417
-
(2007)
Seminars in Immunology
, vol.19
, pp. 409-417
-
-
Ivanov, I.I.1
Zhou, L.2
Littman, D.R.3
-
3
-
-
46749138596
-
Molecular antagonism and plasticity of regulatory and inflammatory T cell programs
-
X.O. Yang, R. Nurieva, G.J. Martinez, H.S. Kang, Y. Chung, B.P. Pappu, B. Shah, S.H. Chang, K.S. Schluns, S.S. Watowich, X.H. Feng, A.M. Jetten, and C. Dong Molecular antagonism and plasticity of regulatory and inflammatory T cell programs Immunity 29 2008 44 56
-
(2008)
Immunity
, vol.29
, pp. 44-56
-
-
Yang, X.O.1
Nurieva, R.2
Martinez, G.J.3
Kang, H.S.4
Chung, Y.5
Pappu, B.P.6
Shah, B.7
Chang, S.H.8
Schluns, K.S.9
Watowich, S.S.10
Feng, X.H.11
Jetten, A.M.12
Dong, C.13
-
5
-
-
74549224652
-
The benzenesulfoamide T0901317 [N-(2,2,2-trifluoroethyl)-N-[4-[2,2,2- trifluoro-1-hydroxy-1-(trifluoromethyl)ethy l]phenyl]-benzenesulfonamide] is a novel retinoic acid receptor-related orphan receptor-alpha/gamma inverse agonist
-
N. Kumar, L.A. Solt, J.J. Conkright, Y. Wang, M.A. Istrate, S.A. Busby, R.D. Garcia-Ordonez, T.P. Burris, and P.R. Griffin The benzenesulfoamide T0901317 [N-(2,2,2-trifluoroethyl)-N-[4-[2,2,2-trifluoro-1-hydroxy-1- (trifluoromethyl)ethy l]phenyl]-benzenesulfonamide] is a novel retinoic acid receptor-related orphan receptor-alpha/gamma inverse agonist Molecular Pharmacology 77 2010 228 236
-
(2010)
Molecular Pharmacology
, vol.77
, pp. 228-236
-
-
Kumar, N.1
Solt, L.A.2
Conkright, J.J.3
Wang, Y.4
Istrate, M.A.5
Busby, S.A.6
Garcia-Ordonez, R.D.7
Burris, T.P.8
Griffin, P.R.9
-
6
-
-
84877283659
-
Synthetic modulators of the retinoic acid receptor-related orphan receptors
-
T.M. Kamenecka, B. Lyda, M.R. Chang, and P.R. Griffin Synthetic modulators of the retinoic acid receptor-related orphan receptors MedChemComm 4 2013 764 776
-
(2013)
MedChemComm
, vol.4
, pp. 764-776
-
-
Kamenecka, T.M.1
Lyda, B.2
Chang, M.R.3
Griffin, P.R.4
-
7
-
-
84865772592
-
Small molecule inhibitors of RORgammat: Targeting Th17 cells and other applications
-
J.R. Huh, and D.R. Littman Small molecule inhibitors of RORgammat: targeting Th17 cells and other applications European Journal of Immunology 42 2012 2232 2237
-
(2012)
European Journal of Immunology
, vol.42
, pp. 2232-2237
-
-
Huh, J.R.1
Littman, D.R.2
-
8
-
-
79955538365
-
Digoxin and its derivatives suppress TH17 cell differentiation by antagonizing RORgammat activity
-
J.R. Huh, M.W. Leung, P. Huang, D.A. Ryan, M.R. Krout, R.R. Malapaka, J. Chow, N. Manel, M. Ciofani, S.V. Kim, A. Cuesta, F.R. Santori, J.J. Lafaille, H.E. Xu, D.Y. Gin, F. Rastinejad, and D.R. Littman Digoxin and its derivatives suppress TH17 cell differentiation by antagonizing RORgammat activity Nature 472 2011 486 490
-
(2011)
Nature
, vol.472
, pp. 486-490
-
-
Huh, J.R.1
Leung, M.W.2
Huang, P.3
Ryan, D.A.4
Krout, M.R.5
Malapaka, R.R.6
Chow, J.7
Manel, N.8
Ciofani, M.9
Kim, S.V.10
Cuesta, A.11
Santori, F.R.12
Lafaille, J.J.13
Xu, H.E.14
Gin, D.Y.15
Rastinejad, F.16
Littman, D.R.17
-
9
-
-
80052423903
-
Structural basis of digoxin that antagonizes RORgamma t receptor activity and suppresses Th17 cell differentiation and interleukin (IL)-17 production
-
S. Fujita-Sato, S. Ito, T. Isobe, T. Ohyama, K. Wakabayashi, K. Morishita, O. Ando, and F. Isono Structural basis of digoxin that antagonizes RORgamma t receptor activity and suppresses Th17 cell differentiation and interleukin (IL)-17 production Journal of Biological Chemistry 286 2011 31409 31417
-
(2011)
Journal of Biological Chemistry
, vol.286
, pp. 31409-31417
-
-
Fujita-Sato, S.1
Ito, S.2
Isobe, T.3
Ohyama, T.4
Wakabayashi, K.5
Morishita, K.6
Ando, O.7
Isono, F.8
-
10
-
-
79959538387
-
Ursolic acid suppresses interleukin-17 (IL-17) production by selectively antagonizing the function of RORgamma t protein
-
T. Xu, X. Wang, B. Zhong, R.I. Nurieva, S. Ding, and C. Dong Ursolic acid suppresses interleukin-17 (IL-17) production by selectively antagonizing the function of RORgamma t protein Journal of Biological Chemistry 286 2011 22707 22710
-
(2011)
Journal of Biological Chemistry
, vol.286
, pp. 22707-22710
-
-
Xu, T.1
Wang, X.2
Zhong, B.3
Nurieva, R.I.4
Ding, S.5
Dong, C.6
-
11
-
-
79955526989
-
Suppression of TH17 differentiation and autoimmunity by a synthetic ROR ligand
-
L.A. Solt, N. Kumar, P. Nuhant, Y. Wang, J.L. Lauer, J. Liu, M.A. Istrate, T.M. Kamenecka, W.R. Roush, D. Vidovic, S.C. Schurer, J. Xu, G. Wagoner, P.D. Drew, P.R. Griffin, and T.P. Burris Suppression of TH17 differentiation and autoimmunity by a synthetic ROR ligand Nature 472 2011 491 494
-
(2011)
Nature
, vol.472
, pp. 491-494
-
-
Solt, L.A.1
Kumar, N.2
Nuhant, P.3
Wang, Y.4
Lauer, J.L.5
Liu, J.6
Istrate, M.A.7
Kamenecka, T.M.8
Roush, W.R.9
Vidovic, D.10
Schurer, S.C.11
Xu, J.12
Wagoner, G.13
Drew, P.D.14
Griffin, P.R.15
Burris, T.P.16
-
12
-
-
84860176210
-
Identification of SR2211: A potent synthetic RORgamma-selective modulator
-
N. Kumar, B. Lyda, M.R. Chang, J.L. Lauer, L.A. Solt, T.P. Burris, T.M. Kamenecka, and P.R. Griffin Identification of SR2211: a potent synthetic RORgamma-selective modulator ACS Chemical Biology 7 2012 672 677
-
(2012)
ACS Chemical Biology
, vol.7
, pp. 672-677
-
-
Kumar, N.1
Lyda, B.2
Chang, M.R.3
Lauer, J.L.4
Solt, L.A.5
Burris, T.P.6
Kamenecka, T.M.7
Griffin, P.R.8
-
13
-
-
84868089340
-
Identification of a selective RORgamma ligand that suppresses T(H)17 cells and stimulates T regulatory cells
-
L.A. Solt, N. Kumar, Y. He, T.M. Kamenecka, P.R. Griffin, and T.P. Burris Identification of a selective RORgamma ligand that suppresses T(H)17 cells and stimulates T regulatory cells ACS Chemical Biology 7 2012 1515 1519
-
(2012)
ACS Chemical Biology
, vol.7
, pp. 1515-1519
-
-
Solt, L.A.1
Kumar, N.2
He, Y.3
Kamenecka, T.M.4
Griffin, P.R.5
Burris, T.P.6
-
14
-
-
84872281985
-
Identification of potent and selective diphenylpropanamide RORgamma inhibitors
-
J.R. Huh, E.E. Englund, H. Wang, R. Huang, P. Huang, F. Rastinejad, J. Inglese, C.P. Austin, R.L. Johnson, W. Huang, and D.R. Littman Identification of potent and selective diphenylpropanamide RORgamma inhibitors ACS Medicinal Chemistry Letters 4 2013 79 84
-
(2013)
ACS Medicinal Chemistry Letters
, vol.4
, pp. 79-84
-
-
Huh, J.R.1
Englund, E.E.2
Wang, H.3
Huang, R.4
Huang, P.5
Rastinejad, F.6
Inglese, J.7
Austin, C.P.8
Johnson, R.L.9
Huang, W.10
Littman, D.R.11
-
15
-
-
84888857603
-
Structure-based design of substituted hexafluoroisopropanol- arylsulfonamides as modulators of RORc
-
B.P. Fauber, G. de Leon Boenig, B. Burton, C. Eidenschenk, C. Everett, A. Gobbi, S.G. Hymowitz, A.R. Johnson, M. Liimatta, P. Lockey, M. Norman, W. Ouyang, O. Rene, and H. Wong Structure-based design of substituted hexafluoroisopropanol-arylsulfonamides as modulators of RORc Bioorganic & Medicinal Chemistry Letters 23 2013 6604 6609
-
(2013)
Bioorganic & Medicinal Chemistry Letters
, vol.23
, pp. 6604-6609
-
-
Fauber, B.P.1
De Leon Boenig, G.2
Burton, B.3
Eidenschenk, C.4
Everett, C.5
Gobbi, A.6
Hymowitz, S.G.7
Johnson, A.R.8
Liimatta, M.9
Lockey, P.10
Norman, M.11
Ouyang, W.12
Rene, O.13
Wong, H.14
-
16
-
-
84892366573
-
Discovery of novel N-(5-(arylcarbonyl)thiazol-2-yl)amides and N-(5-(arylcarbonyl)thiophen-2-yl)amides as potent RORgammat inhibitors
-
Y. Wang, W. Cai, G. Zhang, T. Yang, Q. Liu, Y. Cheng, L. Zhou, Y. Ma, Z. Cheng, S. Lu, Y.G. Zhao, W. Zhang, Z. Xiang, S. Wang, L. Yang, Q. Wu, L.A. Orband-Miller, Y. Xu, J. Zhang, R. Gao, M. Huxdorf, J.N. Xiang, Z. Zhong, J.D. Elliott, S. Leung, and X. Lin Discovery of novel N-(5-(arylcarbonyl)thiazol-2- yl)amides and N-(5-(arylcarbonyl)thiophen-2-yl)amides as potent RORgammat inhibitors Bioorganic & Medicinal Chemistry 22 2014 692 702
-
(2014)
Bioorganic & Medicinal Chemistry
, vol.22
, pp. 692-702
-
-
Wang, Y.1
Cai, W.2
Zhang, G.3
Yang, T.4
Liu, Q.5
Cheng, Y.6
Zhou, L.7
Ma, Y.8
Cheng, Z.9
Lu, S.10
Zhao, Y.G.11
Zhang, W.12
Xiang, Z.13
Wang, S.14
Yang, L.15
Wu, Q.16
Orband-Miller, L.A.17
Xu, Y.18
Zhang, J.19
Gao, R.20
Huxdorf, M.21
Xiang, J.N.22
Zhong, Z.23
Elliott, J.D.24
Leung, S.25
Lin, X.26
more..
-
17
-
-
84892608180
-
Discovery of tertiary amine and indole derivatives as potent RORγt inverse agonists
-
T. Yang, Q. Liu, Y. Cheng, W. Cai, Y. Ma, L. Yang, Q. Wu, L.A. Orband-Miller, L. Zhou, Z. Xiang, M. Huxdorf, W. Zhang, J. Zhang, J.-N. Xiang, S. Leung, Y. Qiu, Z. Zhong, J.D. Elliott, X. Lin, and Y. Wang Discovery of tertiary amine and indole derivatives as potent RORγt inverse agonists ACS Medicinal Chemistry Letters 22 2014 692 702
-
(2014)
ACS Medicinal Chemistry Letters
, vol.22
, pp. 692-702
-
-
Yang, T.1
Liu, Q.2
Cheng, Y.3
Cai, W.4
Ma, Y.5
Yang, L.6
Wu, Q.7
Orband-Miller, L.A.8
Zhou, L.9
Xiang, Z.10
Huxdorf, M.11
Zhang, W.12
Zhang, J.13
Xiang, J.-N.14
Leung, S.15
Qiu, Y.16
Zhong, Z.17
Elliott, J.D.18
Lin, X.19
Wang, Y.20
more..
-
18
-
-
84864416292
-
Discovery and structure-activity analysis of selective estrogen receptor modulators via similarity-based virtual screening
-
J. Shen, J. Jiang, G. Kuang, C. Tan, G. Liu, J. Huang, and Y. Tang Discovery and structure-activity analysis of selective estrogen receptor modulators via similarity-based virtual screening European Journal of Medicinal Chemistry 54 2012 188 196
-
(2012)
European Journal of Medicinal Chemistry
, vol.54
, pp. 188-196
-
-
Shen, J.1
Jiang, J.2
Kuang, G.3
Tan, C.4
Liu, G.5
Huang, J.6
Tang, Y.7
-
19
-
-
84867870692
-
Discovery of new non-steroidal FXR ligands via a virtual screening workflow based on phase shape and induced fit docking
-
J. Fu, P. Si, M. Zheng, L. Chen, X. Shen, Y. Tang, and W. Li Discovery of new non-steroidal FXR ligands via a virtual screening workflow based on phase shape and induced fit docking Bioorganic & Medicinal Chemistry Letters 22 2012 6848 6853
-
(2012)
Bioorganic & Medicinal Chemistry Letters
, vol.22
, pp. 6848-6853
-
-
Fu, J.1
Si, P.2
Zheng, M.3
Chen, L.4
Shen, X.5
Tang, Y.6
Li, W.7
-
20
-
-
84866903943
-
Discovery and optimization of 1,3,4-trisubstituted-pyrazolone derivatives as novel, potent, and nonsteroidal farnesoid X receptor (FXR) selective antagonists
-
H. Huang, Y. Yu, Z. Gao, Y. Zhang, C. Li, X. Xu, H. Jin, W. Yan, R. Ma, J. Zhu, X. Shen, H. Jiang, L. Chen, and J. Li Discovery and optimization of 1,3,4-trisubstituted-pyrazolone derivatives as novel, potent, and nonsteroidal farnesoid X receptor (FXR) selective antagonists Journal of Medicinal Chemistry 55 2012 7037 7053
-
(2012)
Journal of Medicinal Chemistry
, vol.55
, pp. 7037-7053
-
-
Huang, H.1
Yu, Y.2
Gao, Z.3
Zhang, Y.4
Li, C.5
Xu, X.6
Jin, H.7
Yan, W.8
Ma, R.9
Zhu, J.10
Shen, X.11
Jiang, H.12
Chen, L.13
Li, J.14
-
21
-
-
78951492767
-
The orphan nuclear receptor TR4 is a vitamin A-activated nuclear receptor
-
X.E. Zhou, K.M. Suino-Powell, Y. Xu, C.W. Chan, O. Tanabe, S.W. Kruse, R. Reynolds, J.D. Engel, and H.E. Xu The orphan nuclear receptor TR4 is a vitamin A-activated nuclear receptor Journal of Biological Chemistry 286 2011 2877 2885
-
(2011)
Journal of Biological Chemistry
, vol.286
, pp. 2877-2885
-
-
Zhou, X.E.1
Suino-Powell, K.M.2
Xu, Y.3
Chan, C.W.4
Tanabe, O.5
Kruse, S.W.6
Reynolds, R.7
Engel, J.D.8
Xu, H.E.9
-
22
-
-
40349098064
-
Doubling the size of the glucocorticoid receptor ligand binding pocket by deacylcortivazol
-
K. Suino-Powell, Y. Xu, C. Zhang, Y.G. Tao, W.D. Tolbert, S.S. Simons Jr., and H.E. Xu Doubling the size of the glucocorticoid receptor ligand binding pocket by deacylcortivazol Molecular and Cellular Biology 28 2008 1915 1923
-
(2008)
Molecular and Cellular Biology
, vol.28
, pp. 1915-1923
-
-
Suino-Powell, K.1
Xu, Y.2
Zhang, C.3
Tao, Y.G.4
Tolbert, W.D.5
Simons, Jr.S.S.6
Xu, H.E.7
-
23
-
-
77954844606
-
Structural basis for hydroxycholesterols as natural ligands of orphan nuclear receptor RORgamma
-
L. Jin, D. Martynowski, S. Zheng, T. Wada, W. Xie, and Y. Li Structural basis for hydroxycholesterols as natural ligands of orphan nuclear receptor RORgamma Molecular Endocrinology 24 2010 923 929
-
(2010)
Molecular Endocrinology
, vol.24
, pp. 923-929
-
-
Jin, L.1
Martynowski, D.2
Zheng, S.3
Wada, T.4
Xie, W.5
Li, Y.6
-
24
-
-
77956345169
-
Identification and mechanism of ABA receptor antagonism
-
K. Melcher, Y. Xu, L.M. Ng, X.E. Zhou, F.F. Soon, V. Chinnusamy, K.M. Suino-Powell, A. Kovach, F.S. Tham, S.R. Cutler, J. Li, E.L. Yong, J.K. Zhu, and H.E. Xu Identification and mechanism of ABA receptor antagonism Nature Structural & Molecular Biology 17 2010 1102 1108
-
(2010)
Nature Structural & Molecular Biology
, vol.17
, pp. 1102-1108
-
-
Melcher, K.1
Xu, Y.2
Ng, L.M.3
Zhou, X.E.4
Soon, F.F.5
Chinnusamy, V.6
Suino-Powell, K.M.7
Kovach, A.8
Tham, F.S.9
Cutler, S.R.10
Li, J.11
Yong, E.L.12
Zhu, J.K.13
Xu, H.E.14
-
25
-
-
84881187701
-
An ABA-mimicking ligand that reduces water loss and promotes drought resistance in plants
-
M. Cao, X. Liu, Y. Zhang, X. Xue, X.E. Zhou, K. Melcher, P. Gao, F. Wang, L. Zeng, Y. Zhao, Y. Zhao, P. Deng, D. Zhong, J.K. Zhu, H.E. Xu, and Y. Xu An ABA-mimicking ligand that reduces water loss and promotes drought resistance in plants Cell Research 23 2013 1043 1054
-
(2013)
Cell Research
, vol.23
, pp. 1043-1054
-
-
Cao, M.1
Liu, X.2
Zhang, Y.3
Xue, X.4
Zhou, X.E.5
Melcher, K.6
Gao, P.7
Wang, F.8
Zeng, L.9
Zhao, Y.10
Zhao, Y.11
Deng, P.12
Zhong, D.13
Zhu, J.K.14
Xu, H.E.15
Xu, Y.16
|