-
1
-
-
84856394571
-
Bromodomains as therapeutic targets
-
Muller, S.; Filippakopoulos, P.; Knapp, S. Bromodomains as therapeutic targets Expert Rev. Mol. Med. 2011, 13, e29
-
(2011)
Expert Rev. Mol. Med.
, vol.13
, pp. e29
-
-
Muller, S.1
Filippakopoulos, P.2
Knapp, S.3
-
2
-
-
84899973908
-
Targeting bromodomains: epigenetic readers of lysine acetylation
-
Filippakopoulos, P.; Knapp, S. Targeting bromodomains: epigenetic readers of lysine acetylation Nature Rev. Drug Discovery 2014, 13, 337-356
-
(2014)
Nature Rev. Drug Discovery
, vol.13
, pp. 337-356
-
-
Filippakopoulos, P.1
Knapp, S.2
-
3
-
-
78650847770
-
Selective inhibition of BET bromodomains
-
Filippakopoulos, P.; Qi, J.; Picaud, S.; Shen, Y.; Smith, W. B.; Fedorov, O.; Morse, E. M.; Keates, T.; Hickman, T. T.; Felletar, I.; Philpott, M.; Munro, S.; McKeown, M. R.; Wang, Y.; Christie, A. L.; West, N.; Cameron, M. J.; Schwartz, B.; Heightman, T. D.; La Thangue, N.; French, C. A.; Wiest, O.; Kung, A. L.; Knapp, S.; Bradner, J. E. Selective inhibition of BET bromodomains Nature 2010, 468, 1067-1073
-
(2010)
Nature
, vol.468
, pp. 1067-1073
-
-
Filippakopoulos, P.1
Qi, J.2
Picaud, S.3
Shen, Y.4
Smith, W.B.5
Fedorov, O.6
Morse, E.M.7
Keates, T.8
Hickman, T.T.9
Felletar, I.10
Philpott, M.11
Munro, S.12
McKeown, M.R.13
Wang, Y.14
Christie, A.L.15
West, N.16
Cameron, M.J.17
Schwartz, B.18
Heightman, T.D.19
La Thangue, N.20
French, C.A.21
Wiest, O.22
Kung, A.L.23
Knapp, S.24
Bradner, J.E.25
more..
-
4
-
-
80054984945
-
Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia
-
Dawson, M. A.; Prinjha, R. K.; Dittmann, A.; Giotopoulos, G.; Bantscheff, M.; Chan, W. I.; Robson, S. C.; Chung, C. W.; Hopf, C.; Savitski, M. M.; Huthmacher, C.; Gudgin, E.; Lugo, D.; Beinke, S.; Chapman, T. D.; Roberts, E. J.; Soden, P. E.; Auger, K. R.; Mirguet, O.; Doehner, K.; Delwel, R.; Burnett, A. K.; Jeffrey, P.; Drewes, G.; Lee, K.; Huntly, B. J.; Kouzarides, T. Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia Nature 2011, 478, 529-533
-
(2011)
Nature
, vol.478
, pp. 529-533
-
-
Dawson, M.A.1
Prinjha, R.K.2
Dittmann, A.3
Giotopoulos, G.4
Bantscheff, M.5
Chan, W.I.6
Robson, S.C.7
Chung, C.W.8
Hopf, C.9
Savitski, M.M.10
Huthmacher, C.11
Gudgin, E.12
Lugo, D.13
Beinke, S.14
Chapman, T.D.15
Roberts, E.J.16
Soden, P.E.17
Auger, K.R.18
Mirguet, O.19
Doehner, K.20
Delwel, R.21
Burnett, A.K.22
Jeffrey, P.23
Drewes, G.24
Lee, K.25
Huntly, B.J.26
Kouzarides, T.27
more..
-
5
-
-
80052955256
-
BET bromodomain inhibition as a therapeutic strategy to target c-Myc
-
Delmore, J. E.; Issa, G. C.; Lemieux, M. E.; Rahl, P. B.; Shi, J.; Jacobs, H. M.; Kastritis, E.; Gilpatrick, T.; Paranal, R. M.; Qi, J.; Chesi, M.; Schinzel, A. C.; McKeown, M. R.; Heffernan, T. P.; Vakoc, C. R.; Bergsagel, P. L.; Ghobrial, I. M.; Richardson, P. G.; Young, R. A.; Hahn, W. C.; Anderson, K. C.; Kung, A. L.; Bradner, J. E.; Mitsiades, C. S. BET bromodomain inhibition as a therapeutic strategy to target c-Myc Cell 2011, 146, 904-917
-
(2011)
Cell
, vol.146
, pp. 904-917
-
-
Delmore, J.E.1
Issa, G.C.2
Lemieux, M.E.3
Rahl, P.B.4
Shi, J.5
Jacobs, H.M.6
Kastritis, E.7
Gilpatrick, T.8
Paranal, R.M.9
Qi, J.10
Chesi, M.11
Schinzel, A.C.12
McKeown, M.R.13
Heffernan, T.P.14
Vakoc, C.R.15
Bergsagel, P.L.16
Ghobrial, I.M.17
Richardson, P.G.18
Young, R.A.19
Hahn, W.C.20
Anderson, K.C.21
Kung, A.L.22
Bradner, J.E.23
Mitsiades, C.S.24
more..
-
6
-
-
84878565710
-
PFI-1, a highly selective protein interaction inhibitor, targeting BET Bromodomains
-
Picaud, S.; Da Costa, D.; Thanasopoulou, A.; Filippakopoulos, P.; Fish, P. V.; Philpott, M.; Fedorov, O.; Brennan, P.; Bunnage, M. E.; Owen, D. R.; Bradner, J. E.; Taniere, P.; O'Sullivan, B.; Muller, S.; Schwaller, J.; Stankovic, T.; Knapp, S. PFI-1, a highly selective protein interaction inhibitor, targeting BET Bromodomains Cancer Res. 2013, 73, 3336-3346
-
(2013)
Cancer Res.
, vol.73
, pp. 3336-3346
-
-
Picaud, S.1
Da Costa, D.2
Thanasopoulou, A.3
Filippakopoulos, P.4
Fish, P.V.5
Philpott, M.6
Fedorov, O.7
Brennan, P.8
Bunnage, M.E.9
Owen, D.R.10
Bradner, J.E.11
Taniere, P.12
O'Sullivan, B.13
Muller, S.14
Schwaller, J.15
Stankovic, T.16
Knapp, S.17
-
7
-
-
84877097843
-
Inhibition of BET bromodomain targets genetically diverse glioblastoma
-
Cheng, Z.; Gong, Y.; Ma, Y.; Lu, K.; Lu, X.; Pierce, L. A.; Thompson, R. C.; Muller, S.; Knapp, S.; Wang, J. Inhibition of BET bromodomain targets genetically diverse glioblastoma Clin. Cancer Res. 2013, 19, 1748-1759
-
(2013)
Clin. Cancer Res.
, vol.19
, pp. 1748-1759
-
-
Cheng, Z.1
Gong, Y.2
Ma, Y.3
Lu, K.4
Lu, X.5
Pierce, L.A.6
Thompson, R.C.7
Muller, S.8
Knapp, S.9
Wang, J.10
-
8
-
-
78650806593
-
Suppression of inflammation by a synthetic histone mimic
-
Nicodeme, E.; Jeffrey, K. L.; Schaefer, U.; Beinke, S.; Dewell, S.; Chung, C. W.; Chandwani, R.; Marazzi, I.; Wilson, P.; Coste, H.; White, J.; Kirilovsky, J.; Rice, C. M.; Lora, J. M.; Prinjha, R. K.; Lee, K.; Tarakhovsky, A. Suppression of inflammation by a synthetic histone mimic Nature 2010, 468, 1119-1123
-
(2010)
Nature
, vol.468
, pp. 1119-1123
-
-
Nicodeme, E.1
Jeffrey, K.L.2
Schaefer, U.3
Beinke, S.4
Dewell, S.5
Chung, C.W.6
Chandwani, R.7
Marazzi, I.8
Wilson, P.9
Coste, H.10
White, J.11
Kirilovsky, J.12
Rice, C.M.13
Lora, J.M.14
Prinjha, R.K.15
Lee, K.16
Tarakhovsky, A.17
-
9
-
-
84903739739
-
Discovery and optimization of small-molecule ligands for the CBP/p300 bromodomains
-
Hay, D. A.; Fedorov, O.; Martin, S.; Singleton, D. C.; Tallant, C.; Wells, C.; Picaud, S.; Philpott, M.; Monteiro, O. P.; Rogers, C. M.; Conway, S. J.; Rooney, T. P.; Tumber, A.; Yapp, C.; Filippakopoulos, P.; Bunnage, M. E.; Muller, S.; Knapp, S.; Schofield, C. J.; Brennan, P. E. Discovery and optimization of small-molecule ligands for the CBP/p300 bromodomains J. Am. Chem. Soc. 2014, 136, 9308-9319
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 9308-9319
-
-
Hay, D.A.1
Fedorov, O.2
Martin, S.3
Singleton, D.C.4
Tallant, C.5
Wells, C.6
Picaud, S.7
Philpott, M.8
Monteiro, O.P.9
Rogers, C.M.10
Conway, S.J.11
Rooney, T.P.12
Tumber, A.13
Yapp, C.14
Filippakopoulos, P.15
Bunnage, M.E.16
Muller, S.17
Knapp, S.18
Schofield, C.J.19
Brennan, P.E.20
more..
-
10
-
-
84893130847
-
[1,2,4]Triazolo[4,3-a]phthalazines: inhibitors of diverse bromodomains
-
Fedorov, O.; Lingard, H.; Wells, C.; Monteiro, O. P.; Picaud, S.; Keates, T.; Yapp, C.; Philpott, M.; Martin, S. J.; Felletar, I.; Marsden, B. D.; Filippakopoulos, P.; Muller, S.; Knapp, S.; Brennan, P. E. [1,2,4]Triazolo[4,3-a]phthalazines: inhibitors of diverse bromodomains J. Med. Chem. 2014, 57, 462-476
-
(2014)
J. Med. Chem.
, vol.57
, pp. 462-476
-
-
Fedorov, O.1
Lingard, H.2
Wells, C.3
Monteiro, O.P.4
Picaud, S.5
Keates, T.6
Yapp, C.7
Philpott, M.8
Martin, S.J.9
Felletar, I.10
Marsden, B.D.11
Filippakopoulos, P.12
Muller, S.13
Knapp, S.14
Brennan, P.E.15
-
11
-
-
84921309148
-
1,3-Dimethyl Benzimidazolones Are Potent, Selective Inhibitors of the BRPF1 Bromodomain
-
Demont, E. H.; Bamborough, P.; Chung, C. W.; Craggs, P. D.; Fallon, D.; Gordon, L. J.; Grandi, P.; Hobbs, C. I.; Hussain, J.; Jones, E. J.; Le Gall, A.; Michon, A. M.; Mitchell, D. J.; Prinjha, R. K.; Roberts, A. D.; Sheppard, R. J.; Watson, R. J. 1,3-Dimethyl Benzimidazolones Are Potent, Selective Inhibitors of the BRPF1 Bromodomain ACS Med. Chem. Lett. 2014, 5, 1190-1195
-
(2014)
ACS Med. Chem. Lett.
, vol.5
, pp. 1190-1195
-
-
Demont, E.H.1
Bamborough, P.2
Chung, C.W.3
Craggs, P.D.4
Fallon, D.5
Gordon, L.J.6
Grandi, P.7
Hobbs, C.I.8
Hussain, J.9
Jones, E.J.10
Le Gall, A.11
Michon, A.M.12
Mitchell, D.J.13
Prinjha, R.K.14
Roberts, A.D.15
Sheppard, R.J.16
Watson, R.J.17
-
12
-
-
84902096046
-
A series of potent CREBBP bromodomain ligands reveals an induced-fit pocket stabilized by a cation-pi interaction
-
Rooney, T. P.; Filippakopoulos, P.; Fedorov, O.; Picaud, S.; Cortopassi, W. A.; Hay, D. A.; Martin, S.; Tumber, A.; Rogers, C. M.; Philpott, M.; Wang, M.; Thompson, A. L.; Heightman, T. D.; Pryde, D. C.; Cook, A.; Paton, R. S.; Muller, S.; Knapp, S.; Brennan, P. E.; Conway, S. J. A series of potent CREBBP bromodomain ligands reveals an induced-fit pocket stabilized by a cation-pi interaction Angew. Chem., Int. Ed. Engl. 2014, 53, 6126-6130
-
(2014)
Angew. Chem., Int. Ed. Engl.
, vol.53
, pp. 6126-6130
-
-
Rooney, T.P.1
Filippakopoulos, P.2
Fedorov, O.3
Picaud, S.4
Cortopassi, W.A.5
Hay, D.A.6
Martin, S.7
Tumber, A.8
Rogers, C.M.9
Philpott, M.10
Wang, M.11
Thompson, A.L.12
Heightman, T.D.13
Pryde, D.C.14
Cook, A.15
Paton, R.S.16
Muller, S.17
Knapp, S.18
Brennan, P.E.19
Conway, S.J.20
more..
-
13
-
-
84866338076
-
Druggability analysis and structural classification of bromodomain acetyl-lysine binding sites
-
Vidler, L. R.; Brown, N.; Knapp, S.; Hoelder, S. Druggability analysis and structural classification of bromodomain acetyl-lysine binding sites J. Med. Chem. 2012, 55, 7346-7359
-
(2012)
J. Med. Chem.
, vol.55
, pp. 7346-7359
-
-
Vidler, L.R.1
Brown, N.2
Knapp, S.3
Hoelder, S.4
-
14
-
-
84859181036
-
Histone recognition and large-scale structural analysis of the human bromodomain family
-
Filippakopoulos, P.; Picaud, S.; Mangos, M.; Keates, T.; Lambert, J. P.; Barsyte-Lovejoy, D.; Felletar, I.; Volkmer, R.; Muller, S.; Pawson, T.; Gingras, A. C.; Arrowsmith, C. H.; Knapp, S. Histone recognition and large-scale structural analysis of the human bromodomain family Cell 2012, 149, 214-231
-
(2012)
Cell
, vol.149
, pp. 214-231
-
-
Filippakopoulos, P.1
Picaud, S.2
Mangos, M.3
Keates, T.4
Lambert, J.P.5
Barsyte-Lovejoy, D.6
Felletar, I.7
Volkmer, R.8
Muller, S.9
Pawson, T.10
Gingras, A.C.11
Arrowsmith, C.H.12
Knapp, S.13
-
15
-
-
84864578590
-
The bromodomain interaction module
-
Filippakopoulos, P.; Knapp, S. The bromodomain interaction module FEBS Lett. 2012, 586, 2692-2704
-
(2012)
FEBS Lett.
, vol.586
, pp. 2692-2704
-
-
Filippakopoulos, P.1
Knapp, S.2
-
16
-
-
84886504602
-
Discovery of novel small-molecule inhibitors of BRD4 using structure-based virtual screening
-
Vidler, L. R.; Filippakopoulos, P.; Fedorov, O.; Picaud, S.; Martin, S.; Tomsett, M.; Woodward, H.; Brown, N.; Knapp, S.; Hoelder, S. Discovery of novel small-molecule inhibitors of BRD4 using structure-based virtual screening J. Med. Chem. 2013, 56, 8073-8088
-
(2013)
J. Med. Chem.
, vol.56
, pp. 8073-8088
-
-
Vidler, L.R.1
Filippakopoulos, P.2
Fedorov, O.3
Picaud, S.4
Martin, S.5
Tomsett, M.6
Woodward, H.7
Brown, N.8
Knapp, S.9
Hoelder, S.10
-
17
-
-
84896611007
-
Dual kinase-bromodomain inhibitors for rationally designed polypharmacology
-
Ciceri, P.; Muller, S.; O'Mahony, A.; Fedorov, O.; Filippakopoulos, P.; Hunt, J. P.; Lasater, E. A.; Pallares, G.; Picaud, S.; Wells, C.; Martin, S.; Wodicka, L. M.; Shah, N. P.; Treiber, D. K.; Knapp, S. Dual kinase-bromodomain inhibitors for rationally designed polypharmacology Nature Chem. Biol. 2014, 10, 305-312
-
(2014)
Nature Chem. Biol.
, vol.10
, pp. 305-312
-
-
Ciceri, P.1
Muller, S.2
O'Mahony, A.3
Fedorov, O.4
Filippakopoulos, P.5
Hunt, J.P.6
Lasater, E.A.7
Pallares, G.8
Picaud, S.9
Wells, C.10
Martin, S.11
Wodicka, L.M.12
Shah, N.P.13
Treiber, D.K.14
Knapp, S.15
-
18
-
-
84899936534
-
Acetyl-lysine binding site of bromodomain-containing protein 4 (BRD4) interacts with diverse kinase inhibitors
-
Ember, S. W.; Zhu, J. Y.; Olesen, S. H.; Martin, M. P.; Becker, A.; Berndt, N.; Georg, G. I.; Schonbrunn, E. Acetyl-lysine binding site of bromodomain-containing protein 4 (BRD4) interacts with diverse kinase inhibitors ACS Chem. Biol. 2014, 9, 1160-1171
-
(2014)
ACS Chem. Biol.
, vol.9
, pp. 1160-1171
-
-
Ember, S.W.1
Zhu, J.Y.2
Olesen, S.H.3
Martin, M.P.4
Becker, A.5
Berndt, N.6
Georg, G.I.7
Schonbrunn, E.8
-
19
-
-
78650353481
-
TRIM24 links a non-canonical histone signature to breast cancer
-
Tsai, W. W.; Wang, Z.; Yiu, T. T.; Akdemir, K. C.; Xia, W.; Winter, S.; Tsai, C. Y.; Shi, X.; Schwarzer, D.; Plunkett, W.; Aronow, B.; Gozani, O.; Fischle, W.; Hung, M. C.; Patel, D. J.; Barton, M. C. TRIM24 links a non-canonical histone signature to breast cancer Nature 2010, 468, 927-932
-
(2010)
Nature
, vol.468
, pp. 927-932
-
-
Tsai, W.W.1
Wang, Z.2
Yiu, T.T.3
Akdemir, K.C.4
Xia, W.5
Winter, S.6
Tsai, C.Y.7
Shi, X.8
Schwarzer, D.9
Plunkett, W.10
Aronow, B.11
Gozani, O.12
Fischle, W.13
Hung, M.C.14
Patel, D.J.15
Barton, M.C.16
-
20
-
-
85028219982
-
TRIM24 promotes glioma progression and enhances chemoresistance through activation of the PI3K/Akt signaling pathway
-
Zhang, L. H.; Yin, A. A.; Cheng, J. X.; Huang, H. Y.; Li, X. M.; Zhang, Y. Q.; Han, N.; Zhang, X. TRIM24 promotes glioma progression and enhances chemoresistance through activation of the PI3K/Akt signaling pathway Oncogene 2015, 34, 600-610
-
(2015)
Oncogene
, vol.34
, pp. 600-610
-
-
Zhang, L.H.1
Yin, A.A.2
Cheng, J.X.3
Huang, H.Y.4
Li, X.M.5
Zhang, Y.Q.6
Han, N.7
Zhang, X.8
-
21
-
-
84897002465
-
Overexpression of TRIM24 is associated with the onset and progress of human hepatocellular carcinoma
-
Liu, X.; Huang, Y.; Yang, D.; Li, X.; Liang, J.; Lin, L.; Zhang, M.; Zhong, K.; Liang, B.; Li, J. Overexpression of TRIM24 is associated with the onset and progress of human hepatocellular carcinoma PLoS One 2014, 9, e85462
-
(2014)
PLoS One
, vol.9
-
-
Liu, X.1
Huang, Y.2
Yang, D.3
Li, X.4
Liang, J.5
Lin, L.6
Zhang, M.7
Zhong, K.8
Liang, B.9
Li, J.10
-
22
-
-
84937511212
-
TRIM24 is upregulated in human gastric cancer and promotes gastric cancer cell growth and chemoresistance
-
Miao, Z. F.; Wang, Z. N.; Zhao, T. T.; Xu, Y. Y.; Wu, J. H.; Liu, X. Y.; Xu, H.; You, Y.; Xu, H. M. TRIM24 is upregulated in human gastric cancer and promotes gastric cancer cell growth and chemoresistance Virchows Arch. 2015, 466, 525-532
-
(2015)
Virchows Arch.
, vol.466
, pp. 525-532
-
-
Miao, Z.F.1
Wang, Z.N.2
Zhao, T.T.3
Xu, Y.Y.4
Wu, J.H.5
Liu, X.Y.6
Xu, H.7
You, Y.8
Xu, H.M.9
-
23
-
-
84861650468
-
Overexpression of TRIM24 correlates with tumor progression in non-small cell lung cancer
-
Li, H.; Sun, L.; Tang, Z.; Fu, L.; Xu, Y.; Li, Z.; Luo, W.; Qiu, X.; Wang, E. Overexpression of TRIM24 correlates with tumor progression in non-small cell lung cancer PLoS One 2012, 7, e37657
-
(2012)
PLoS One
, vol.7
-
-
Li, H.1
Sun, L.2
Tang, Z.3
Fu, L.4
Xu, Y.5
Li, Z.6
Luo, W.7
Qiu, X.8
Wang, E.9
-
24
-
-
84878025828
-
TRIM24 overexpression is common in locally advanced head and neck squamous cell carcinoma and correlates with aggressive malignant phenotypes
-
Cui, Z.; Cao, W.; Li, J.; Song, X.; Mao, L.; Chen, W. TRIM24 overexpression is common in locally advanced head and neck squamous cell carcinoma and correlates with aggressive malignant phenotypes PLoS One 2013, 8, e63887
-
(2013)
PLoS One
, vol.8
-
-
Cui, Z.1
Cao, W.2
Li, J.3
Song, X.4
Mao, L.5
Chen, W.6
-
25
-
-
84907485595
-
Prostate cancer. Ubiquitylome analysis identifies dysregulation of effector substrates in SPOP-mutant prostate cancer
-
Theurillat, J. P.; Udeshi, N. D.; Errington, W. J.; Svinkina, T.; Baca, S. C.; Pop, M.; Wild, P. J.; Blattner, M.; Groner, A. C.; Rubin, M. A.; Moch, H.; Prive, G. G.; Carr, S. A.; Garraway, L. A. Prostate cancer. Ubiquitylome analysis identifies dysregulation of effector substrates in SPOP-mutant prostate cancer Science 2014, 346, 85-89
-
(2014)
Science
, vol.346
, pp. 85-89
-
-
Theurillat, J.P.1
Udeshi, N.D.2
Errington, W.J.3
Svinkina, T.4
Baca, S.C.5
Pop, M.6
Wild, P.J.7
Blattner, M.8
Groner, A.C.9
Rubin, M.A.10
Moch, H.11
Prive, G.G.12
Carr, S.A.13
Garraway, L.A.14
-
26
-
-
67650895889
-
Trim24 targets endogenous p53 for degradation
-
Allton, K.; Jain, A. K.; Herz, H. M.; Tsai, W. W.; Jung, S. Y.; Qin, J.; Bergmann, A.; Johnson, R. L.; Barton, M. C. Trim24 targets endogenous p53 for degradation Proc. Natl. Acad. Sci. U. S. A. 2009, 106, 11612-11616
-
(2009)
Proc. Natl. Acad. Sci. U. S. A.
, vol.106
, pp. 11612-11616
-
-
Allton, K.1
Jain, A.K.2
Herz, H.M.3
Tsai, W.W.4
Jung, S.Y.5
Qin, J.6
Bergmann, A.7
Johnson, R.L.8
Barton, M.C.9
-
27
-
-
0029841744
-
A possible involvement of TIF1 alpha and TIF1 beta in the epigenetic control of transcription by nuclear receptors
-
Le Douarin, B.; Nielsen, A. L.; Garnier, J. M.; Ichinose, H.; Jeanmougin, F.; Losson, R.; Chambon, P. A possible involvement of TIF1 alpha and TIF1 beta in the epigenetic control of transcription by nuclear receptors EMBO J. 1996, 15, 6701-6715
-
(1996)
EMBO J.
, vol.15
, pp. 6701-6715
-
-
Le Douarin, B.1
Nielsen, A.L.2
Garnier, J.M.3
Ichinose, H.4
Jeanmougin, F.5
Losson, R.6
Chambon, P.7
-
28
-
-
84911120313
-
Knockdown of tripartite motif containing 24 by lentivirus suppresses cell growth and induces apoptosis in human colorectal cancer cells
-
Wang, J.; Zhu, J.; Dong, M.; Yu, H.; Dai, X.; Li, K. Knockdown of tripartite motif containing 24 by lentivirus suppresses cell growth and induces apoptosis in human colorectal cancer cells Oncol. Res. 2014, 22, 39-45
-
(2014)
Oncol. Res.
, vol.22
, pp. 39-45
-
-
Wang, J.1
Zhu, J.2
Dong, M.3
Yu, H.4
Dai, X.5
Li, K.6
-
29
-
-
84930089331
-
TRIM24 links glucose metabolism with transformation of human mammary epithelial cells
-
Pathiraja, T. N.; Thakkar, K. N.; Jiang, S.; Stratton, S.; Liu, Z.; Gagea, M.; Shi, X.; Shah, P. K.; Phan, L.; Lee, M. H.; Andersen, J.; Stampfer, M.; Barton, M. C. TRIM24 links glucose metabolism with transformation of human mammary epithelial cells Oncogene 2014, 10.1038/onc.2014.220
-
(2014)
Oncogene
-
-
Pathiraja, T.N.1
Thakkar, K.N.2
Jiang, S.3
Stratton, S.4
Liu, Z.5
Gagea, M.6
Shi, X.7
Shah, P.K.8
Phan, L.9
Lee, M.H.10
Andersen, J.11
Stampfer, M.12
Barton, M.C.13
-
30
-
-
36549086517
-
Loss of Trim24 (Tif1alpha) gene function confers oncogenic activity to retinoic acid receptor alpha
-
Khetchoumian, K.; Teletin, M.; Tisserand, J.; Mark, M.; Herquel, B.; Ignat, M.; Zucman-Rossi, J.; Cammas, F.; Lerouge, T.; Thibault, C.; Metzger, D.; Chambon, P.; Losson, R. Loss of Trim24 (Tif1alpha) gene function confers oncogenic activity to retinoic acid receptor alpha Nature Genet. 2007, 39, 1500-1506
-
(2007)
Nature Genet.
, vol.39
, pp. 1500-1506
-
-
Khetchoumian, K.1
Teletin, M.2
Tisserand, J.3
Mark, M.4
Herquel, B.5
Ignat, M.6
Zucman-Rossi, J.7
Cammas, F.8
Lerouge, T.9
Thibault, C.10
Metzger, D.11
Chambon, P.12
Losson, R.13
-
31
-
-
80555135984
-
Kinase inhibitor selectivity profiling using differential scanning fluorimetry
-
Fedorov, O.; Niesen, F. H.; Knapp, S. Kinase inhibitor selectivity profiling using differential scanning fluorimetry Methods Mol. Biol. 2012, 795, 109-118
-
(2012)
Methods Mol. Biol.
, vol.795
, pp. 109-118
-
-
Fedorov, O.1
Niesen, F.H.2
Knapp, S.3
-
32
-
-
84924674529
-
Structure Enabled Design of BAZ2-ICR, A Chemical Probe Targeting the Bromodomains of BAZ2A and BAZ2B
-
Drouin, L.; McGrath, S.; Vidler, L. R.; Chaikuad, A.; Monteiro, O.; Tallant, C.; Philpott, M.; Rogers, C.; Fedorov, O.; Liu, M.; Akhtar, W.; Hayes, A.; Raynaud, F.; Muller, S.; Knapp, S.; Hoelder, S. Structure Enabled Design of BAZ2-ICR, A Chemical Probe Targeting the Bromodomains of BAZ2A and BAZ2B J. Med. Chem. 2015, 58, 2553-2559
-
(2015)
J. Med. Chem.
, vol.58
, pp. 2553-2559
-
-
Drouin, L.1
McGrath, S.2
Vidler, L.R.3
Chaikuad, A.4
Monteiro, O.5
Tallant, C.6
Philpott, M.7
Rogers, C.8
Fedorov, O.9
Liu, M.10
Akhtar, W.11
Hayes, A.12
Raynaud, F.13
Muller, S.14
Knapp, S.15
Hoelder, S.16
-
33
-
-
84904082319
-
Assessing cellular efficacy of bromodomain inhibitors using fluorescence recovery after photobleaching
-
Philpott, M.; Rogers, C. M.; Yapp, C.; Wells, C.; Lambert, J. P.; Strain-Damerell, C.; Burgess-Brown, N. A.; Gingras, A. C.; Knapp, S.; Muller, S. Assessing cellular efficacy of bromodomain inhibitors using fluorescence recovery after photobleaching Epigenetics Chromatin 2014, 7, 14
-
(2014)
Epigenetics Chromatin
, vol.7
, pp. 14
-
-
Philpott, M.1
Rogers, C.M.2
Yapp, C.3
Wells, C.4
Lambert, J.P.5
Strain-Damerell, C.6
Burgess-Brown, N.A.7
Gingras, A.C.8
Knapp, S.9
Muller, S.10
-
34
-
-
84897107879
-
Molecular insights into the recognition of N-terminal histone modifications by the BRPF1 bromodomain
-
Poplawski, A.; Hu, K.; Lee, W.; Natesan, S.; Peng, D.; Carlson, S.; Shi, X.; Balaz, S.; Markley, J. L.; Glass, K. C. Molecular insights into the recognition of N-terminal histone modifications by the BRPF1 bromodomain J. Mol. Biol. 2014, 426, 1661-1676
-
(2014)
J. Mol. Biol.
, vol.426
, pp. 1661-1676
-
-
Poplawski, A.1
Hu, K.2
Lee, W.3
Natesan, S.4
Peng, D.5
Carlson, S.6
Shi, X.7
Balaz, S.8
Markley, J.L.9
Glass, K.C.10
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