-
1
-
-
0025270737
-
Nuclear receptor that identifies a novel retinoic acid response pathway
-
Mangelsdorf DJ, Ong ES, Dyck JA, Evans RM. Nuclear receptor that identifies a novel retinoic acid response pathway. Nature 1990;345:224-9.
-
(1990)
Nature
, vol.345
, pp. 224-229
-
-
Mangelsdorf, D.J.1
Ong, E.S.2
Dyck, J.A.3
Evans, R.M.4
-
2
-
-
12844252576
-
Retinoid X receptors: X-ploring their (patho)physiological functions
-
Szanto A, Narkar V, Shen Q, Uray IP, Davies PJ, Nagy L. Retinoid X receptors: X-ploring their (patho)physiological functions. Cell Death Differ 2004;11:S126-43.
-
(2004)
Cell Death Differ
, vol.11
-
-
Szanto, A.1
Narkar, V.2
Shen, Q.3
Uray, I.P.4
Davies, P.J.5
Nagy, L.6
-
3
-
-
0029562554
-
The RXR heterodimers and orphan receptors
-
DOI 10.1016/0092-8674(95)90200-7
-
Mangelsdorf DJ, Evans RM. The RXR heterodimers and orphan receptors. Cell 1995;83:841-50. (Pubitemid 26006526)
-
(1995)
Cell
, vol.83
, Issue.6
, pp. 841-850
-
-
Mangelsdorf, D.J.1
Evans, R.M.2
-
4
-
-
33846094038
-
Is 9-cis-retinoic acid the endogenous ligand for the retinoic acid-X receptor?
-
Wolf G. Is 9-cis-retinoic acid the endogenous ligand for the retinoic acid-X receptor? Nutr Rev 2006;64:532-8.
-
(2006)
Nutr Rev
, vol.64
, pp. 532-538
-
-
Wolf, G.1
-
5
-
-
33751533155
-
LXIII. Retinoid X receptors
-
International Union of Pharmacology
-
Germain P, Chambon P, Eichele G, Evans RM, Lazar MA, Leid M, et al. International Union of Pharmacology. LXIII. Retinoid X receptors. Pharmacol Rev 2006;58:760-72.
-
(2006)
Pharmacol Rev
, vol.58
, pp. 760-772
-
-
Germain, P.1
Chambon, P.2
Eichele, G.3
Evans, R.M.4
Lazar, M.A.5
Leid, M.6
-
6
-
-
0027982042
-
Prevention of breast cancer in the rat with 9-cis-retinoic acid as a single agent and in combination with tamoxifen
-
Anzano MA, Byers SW, Smith JM, Peer CW, Mullen LT, Brown CC, et al. Prevention of breast cancer in the rat with 9-cis-retinoic acid as a single agent and in combination with tamoxifen. Cancer Res 1994;54:4614-7. (Pubitemid 24276483)
-
(1994)
Cancer Research
, vol.54
, Issue.17
, pp. 4614-4617
-
-
Anzano, M.A.1
Byers, S.W.2
Smith, J.M.3
Peer, C.W.4
Mullen, L.T.5
Brown, C.C.6
Roberts, A.B.7
Sporn, M.B.8
-
7
-
-
0036794975
-
Prevention and treatment of experimental breast cancer with the combination of a new selective estrogen receptor modulator, arzoxifene, and a new rexinoid, LG 100268
-
Suh N, Lamph WW, Glasebrook AL, Grese TA, Palkowitz AD, Williams CR, et al. Prevention and treatment of experimental breast cancer with the combination of a new selective estrogen receptor modulator, arzoxifene, and a new rexinoid, LG 100268. Clin Cancer Res 2002;8:3270-5. (Pubitemid 35155040)
-
(2002)
Clinical Cancer Research
, vol.8
, Issue.10
, pp. 3270-3275
-
-
Suh, N.1
Lamph, W.W.2
Glasebrook, A.L.3
Grese, T.A.4
Palkowitz, A.D.5
Williams, C.R.6
Risingsong, R.7
Farris, M.R.8
Heyman, R.A.9
Sporn, M.B.10
-
8
-
-
0029731340
-
Chemoprevention of mammary carcinoma by LGD1069 (Targretin): An RXR- Selective ligand
-
Gottardis MM, Bischoff ED, Shirley MA, Wagoner MA, Lamph WW, Heyman RA. Chemoprevention of mammary carcinoma by LGD1069 (Targretin): an RXR-selective ligand. Cancer Res 1996;56:5566-70. (Pubitemid 26422151)
-
(1996)
Cancer Research
, vol.56
, Issue.24
, pp. 5566-5570
-
-
Gottardis, M.M.1
Bischoff, E.D.2
Shirley, M.A.3
Wagoner, M.A.4
Lamph, W.W.5
Heyman, R.A.6
-
9
-
-
2442707861
-
Management of AIDS-related Kaposi sarcoma: Advances in target discovery and treatment
-
Dezube BJ, Pantanowitz L, Aboulafia DM. Management of AIDS-related Kaposi sarcoma: advances in target discovery and treatment. AIDS Read 2004;14:236-8, 243-4, 251-3.
-
(2004)
AIDS Read
, vol.14
-
-
Dezube, B.J.1
Pantanowitz, L.2
Aboulafia, D.M.3
-
10
-
-
33646571880
-
Bexarotene in the treatment of cutaneous T-cell lymphoma
-
Querfeld C, Nagelli LV, Rosen ST, Kuzel TM, Guitart J. Bexarotene in the treatment of cutaneous T-cell lymphoma. Expert Opin Pharmacother 2006;7:907-15.
-
(2006)
Expert Opin Pharmacother
, vol.7
, pp. 907-915
-
-
Querfeld, C.1
Nagelli, L.V.2
Rosen, S.T.3
Kuzel, T.M.4
Guitart, J.5
-
11
-
-
34548504314
-
Optimization of the indenone ring of indenoisoquinoline topoisomerase I inhibitors
-
DOI 10.1021/jm070307+
-
Morrell A, Placzek M, Parmley S, Grella B, Antony S, Pommier Y, et al. Optimization of the indenone ring of indenoisoquinoline topoisomerase I inhibitors. J Med Chem 2007;50:4388-404. (Pubitemid 47378837)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.18
, pp. 4388-4404
-
-
Morrell, A.1
Placzek, M.2
Parmley, S.3
Grella, B.4
Antony, S.5
Pommier, Y.6
Cushman, M.7
-
12
-
-
34548510839
-
Nitrated indenoisoquinolines as topoisomerase I inhibitors: A systematic study and optimization
-
DOI 10.1021/jm070361q
-
Morrell A, Placzek M, Parmley S, Antony S, Dexheimer TS, Pommier Y, et al. Nitrated indenoisoquinolines as topoisomerase I inhibitors: a systematic study and optimization. J Med Chem 2007;50:4419-30. (Pubitemid 47378839)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.18
, pp. 4419-4430
-
-
Morrell, A.1
Placzek, M.2
Parmley, S.3
Antony, S.4
Dexheimer, T.S.5
Pommier, Y.6
Cushman, M.7
-
13
-
-
0034609859
-
Synthesis of new Indeno[1,2-c]isoquinolines: Cytotoxic non-camptothecin topoisomerase I inhibitors
-
Cushman M, Jayaraman M, Vroman JA, Fukunaga AK, Fox BM, Kohlhagen G, et al. Synthesis of new Indeno[1,2-c]isoquinolines: cytotoxic non-camptothecin topoisomerase I inhibitors. J Med Chem 2000;43:3688-98.
-
(2000)
J Med Chem
, vol.43
, pp. 3688-3698
-
-
Cushman, M.1
Jayaraman, M.2
Vroman, J.A.3
Fukunaga, A.K.4
Fox, B.M.5
Kohlhagen, G.6
-
14
-
-
33144472888
-
Synthesis of benz[d]indeno[1,2-b]pyran-5,11-diones: Versatile intermediates for the design and synthesis of topoisomerase I inhibitors
-
Morrell A, Antony S, Kohlhagen G, Pommier Y, Cushman M. Synthesis of benz[d]indeno[1,2-b]pyran-5,11-diones: versatile intermediates for the design and synthesis of topoisomerase I inhibitors. Bioorg Med Chem Lett 2006;16:1846-49.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 1846-1849
-
-
Morrell, A.1
Antony, S.2
Kohlhagen, G.3
Pommier, Y.4
Cushman, M.5
-
15
-
-
33845955224
-
A systematic study of nitrated indenoisoquinolines reveals a potent topoisomerase I inhibitor
-
DOI 10.1021/jm060974n
-
Morrell A, Antony S, Kohlhagen G, Pommier Y, Cushman M. Systematic study of nitrated indenoisoquinolines reveals a potent topoisomerase I inhibitor. J Med Chem 2006;49:7740-53. (Pubitemid 46033665)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.26
, pp. 7740-7753
-
-
Morrell, A.1
Antony, S.2
Kohlhagen, G.3
Pommier, Y.4
Cushman, M.5
-
16
-
-
0025341331
-
New colorimetric cytotoxicity assay for anticancer-drug screening
-
Skehan P, Storeng R, Scudiero D, Monks A, McMahon J, Vistica D, et al. New colorimetric cytotoxicity assay for anticancer-drug screening. J Natl Cancer Inst 1990;82:1107-12. (Pubitemid 20213250)
-
(1990)
Journal of the National Cancer Institute
, vol.82
, Issue.13
, pp. 1107-1112
-
-
Skehan, P.1
Storeng, R.2
Scudiero, D.3
Monks, A.4
McMahon, J.5
Vistica, D.6
Warren, J.T.7
Bokesch, H.8
Kenney, S.9
Boyd, M.R.10
-
17
-
-
16544361997
-
Flow cytometric analysis of electronic nuclear volume and DNA content in normal mouse tissues
-
Krishan A, Cabana R. Flow cytometric analysis of electronic nuclear volume and DNA content in normal mouse tissues. Cell Cycle 2004;3:380-3. (Pubitemid 41359090)
-
(2004)
Cell Cycle
, vol.3
, Issue.3
, pp. 380-383
-
-
Krishan, A.1
Cabana, R.2
-
18
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
-
Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976;72:248-54.
-
(1976)
Anal Biochem
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
19
-
-
0023277545
-
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
-
DOI 10.1006/abio.1987.9999
-
Chomczynski P, Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 1987;162:156-9. (Pubitemid 17064313)
-
(1987)
Analytical Biochemistry
, vol.162
, Issue.1
, pp. 156-159
-
-
Chomczynski, P.1
Sacchi, N.2
-
20
-
-
0035710746
-
-DeltaDeltaCT method
-
DOI 10.1006/meth.2001.1262
-
Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods 2001;25:402-8. (Pubitemid 34164012)
-
(2001)
Methods
, vol.25
, Issue.4
, pp. 402-408
-
-
Livak, K.J.1
Schmittgen, T.D.2
-
21
-
-
38749106953
-
In vitro metabolism of isoliquiritigenin by human liver microsomes
-
Guo J, Liu D, Nikolic D, Zhu D, Pezzuto JM, van Breemen RB. In vitro metabolism of isoliquiritigenin by human liver microsomes. Drug Metab Dispos 2008;36:461-8.
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 461-468
-
-
Guo, J.1
Liu, D.2
Nikolic, D.3
Zhu, D.4
Pezzuto, J.M.5
Van Breemen, R.B.6
-
22
-
-
0347512122
-
Increasing the Throughput and Productivity of Caco-2 Cell Permeability Assays Using Liquid Chromatography-Mass Spectrometry: Application to Resveratrol Absorption and Metabolism
-
Li Y, Shin YG, Yu C, Kosmeder JW, Hirschelman WH, Pezzuto JM, et al. Increasing the throughput and productivity of Caco-2 cell permeability assays using liquid chromatography-mass spectrometry: application to resveratrol absorption and metabolism. Comb Chem High Throughput Screen 2003;6:757-67. (Pubitemid 38017483)
-
(2003)
Combinatorial Chemistry and High Throughput Screening
, vol.6
, Issue.8
, pp. 757-767
-
-
Li, Y.1
Shin, Y.G.2
Yu, C.3
Kosmeder, J.W.4
Hirschelman, W.H.5
Pezzuto, J.M.6
Van Breemen, R.B.7
-
23
-
-
12244285648
-
Human, rat, and mouse metabolism of resveratrol
-
DOI 10.1023/A:1021414129280
-
Yu C, Shin YG, Chow A, Li Y, Kosmeder JW, Lee YS, et al. Human, rat, and mouse metabolism of resveratrol. Pharm Res 2002;19:1907-14. (Pubitemid 36016041)
-
(2002)
Pharmaceutical Research
, vol.19
, Issue.12
, pp. 1907-1914
-
-
Yu, C.1
Geun, S.Y.2
Chow, A.3
Li, Y.4
Kosmeder, J.W.5
Sup, L.Y.6
Hirschelman, W.H.7
Pezzuto, J.M.8
Mehta, R.G.9
Van Breemen, R.B.10
-
24
-
-
42249091885
-
Effects of gefitinib (Iressa) on mammary cancers: Preventive studies with varied dosages, combinations with vorozole or targretin, and biomarker changes
-
DOI 10.1158/1535-7163.MCT-07-2141
-
Lubet RA, Szabo E, Christov K, Bode AM, Ericson ME, Steele VE, et al. Effects of gefitinib (Iressa) on mammary cancers: preventive studies with varied dosages, combinations with vorozole or targretin, and biomarker studies. Mol Cancer Ther 2008;7:972-79. (Pubitemid 351551051)
-
(2008)
Molecular Cancer Therapeutics
, vol.7
, Issue.4
, pp. 972-979
-
-
Lubet, R.A.1
Szabo, E.2
Christov, K.3
Bode, A.M.4
Ericson, M.E.5
Steele, V.E.6
Juliana, M.M.7
Grubbs, C.J.8
-
25
-
-
0031838157
-
Induction of apoptosis in MCF-7 breast carcinoma cell line by RAR and RXR selective retinoids
-
Toma S, Isnardi L, Riccardi L, Bollag W. Induction of apoptosis in MCF-7 breast carcinoma cell line by RAR and RXR selective retinoids. Anticancer Res 1998;18:935-42. (Pubitemid 28239619)
-
(1998)
Anticancer Research
, vol.18
, Issue.2 A
, pp. 935-942
-
-
Toma, S.1
Isnardi, L.2
Riccardi, L.3
Bollag, W.4
-
26
-
-
0032500615
-
Overexpressed activated retinoid X receptors can mediate growth inhibitory effects of retinoids in human carcinoma cells
-
DOI 10.1074/jbc.273.41.26915
-
Wan H, Dawson MI, Hong WK, Lotan R. Overexpressed activated retinoid X receptors can mediate growth inhibitory effects of retinoids in human carcinoma cells. J Biol Chem 1998;273:26915-22. (Pubitemid 28471712)
-
(1998)
Journal of Biological Chemistry
, vol.273
, Issue.41
, pp. 26915-26922
-
-
Wan, H.1
Dawson, M.I.2
Hong, W.K.3
Lotan, R.4
-
27
-
-
0033305351
-
P120 Acts as a specific coactivator for 9-cis-retinoic acid receptor (RXR) on peroxisome proliferator-activated receptor-γ/RXR heterodimers
-
Monden T, Kishi M, Hosoya T, Satoh T, Wondisford FE, Hollenberg AN, et al. p120 acts as a specific coactivator for 9-cis-retinoic acid receptor (RXR) on peroxisome proliferator-activated receptor-γ/RXR heterodimers. Mol Endocrinol 1999;13:1695-703. (Pubitemid 30645274)
-
(1999)
Molecular Endocrinology
, vol.13
, Issue.10
, pp. 1695-1703
-
-
Monden, T.1
Kishi, M.2
Hosoya, T.3
Satoh, T.4
Wondisford, F.E.5
Hollenberg, A.N.6
Yamada, M.7
Mori, M.8
-
28
-
-
0007565558
-
Stereoselective oxidation by thionyl chloride leading to the indeno[1,2-c]isoquinoline system
-
Cushman M, Cheng L. Stereoselective oxidation by thionyl chloride leading to the indeno[1,2-c]isoquinoline system. J Org Chem 1978;43:3781-3.
-
(1978)
J Org Chem
, vol.43
, pp. 3781-3783
-
-
Cushman, M.1
Cheng, L.2
-
29
-
-
35948968756
-
Novel indenoisoquinolines NSC 725776 and NSC 724998 produce persistent topoisomerase I cleavage complexes and overcome multidrug resistance
-
DOI 10.1158/0008-5472.CAN-07-0938
-
Antony S, Agama KK, Miao ZH, Takagi K, Wright MH, Robles AI, et al. Novel indenoisoquinolines NSC 725776 and NSC 724998 produce persistent topoisomerase I cleavage complexes and overcome multi-drug resistance. Cancer Res 2007;67:10397-405. (Pubitemid 350070815)
-
(2007)
Cancer Research
, vol.67
, Issue.21
, pp. 10397-10405
-
-
Antony, S.1
Agama, K.K.2
Miao, Z.-H.3
Takagi, K.4
Wright, M.H.5
Robles, A.I.6
Varticovski, L.7
Nagarajan, M.8
Morrell, A.9
Cushman, M.10
Pommier, Y.11
-
30
-
-
33747600400
-
Bisindenoisoquinoline bis-1,3-{(5,6-dihydro-5,11-diketo- 11H-indeno[1,2-c]isoquinoline)-6-propylamino}propane bis(trifluoroacetate) (NSC 727357), a DNA intercalator and topoisomerase inhibitor with antitumor activity
-
Antony S, Agama KK, Miao ZH, Hollingshead M , Holbeck SL , Wright MH , et al. Bisindenoisoquinoline bis-1,3-{(5,6-dihydro-5,11-diketo- 11H-indeno[1,2-c]isoquinoline)-6-propylamino}propane bis(trifluoroacetate) (NSC 727357), a DNA intercalator and topoisomerase inhibitor with antitumor activity. Mol Pharmacol 2006;70:1109-20.
-
(2006)
Mol Pharmacol
, vol.70
, pp. 1109-1120
-
-
Antony, S.1
Agama, K.K.2
Miao, Z.H.3
Hollingshead, M.4
Holbeck, S.L.5
Wright, M.H.6
-
31
-
-
38849090062
-
Indeno[1,2- c]isoquinolines as enhancing agents on all-trans retinoic acid-mediated differentiation of human myeloid leukemia cells
-
Kim SH, Oh SM, Song JH, Cho D, Le QM, Lee SH, et al. Indeno[1,2- c]isoquinolines as enhancing agents on all-trans retinoic acid-mediated differentiation of human myeloid leukemia cells. Bioorg Med Chem 2008;16:1125-32.
-
(2008)
Bioorg Med Chem
, vol.16
, pp. 1125-1132
-
-
Kim, S.H.1
Oh, S.M.2
Song, J.H.3
Cho, D.4
Le, Q.M.5
Lee, S.H.6
-
32
-
-
34848834842
-
RAR and RXR modulation in cancer and metabolic disease
-
DOI 10.1038/nrd2397, PII NRD2397
-
Altucci L, Leibowitz MD, Ogilvie KM, de Lera AR, Gronemeyer H. RAR and RXR modulation in cancer and metabolic disease. Nat Rev Drug Discov 2007;6:793-810. (Pubitemid 47504871)
-
(2007)
Nature Reviews Drug Discovery
, vol.6
, Issue.10
, pp. 793-810
-
-
Altucci, L.1
Leibowitz, M.D.2
Ogilvie, K.M.3
De Lera, A.R.4
Gronemeyer, H.5
-
33
-
-
34848862778
-
Design of selective nuclear receptor modulators: RAR and RXR as a case study
-
DOI 10.1038/nrd2398, PII NRD2398
-
de Lera AR, Bourguet W, Altucci L, Gronemeyer H. Design of selective nuclear receptor modulators: RAR and RXR as a case study. Nat Rev Drug Discov 2007;6:811-20. (Pubitemid 47504872)
-
(2007)
Nature Reviews Drug Discovery
, vol.6
, Issue.10
, pp. 811-820
-
-
De Lera, A.R.1
Bourguet, W.2
Altucci, L.3
Gronemeyer, H.4
-
34
-
-
9544242711
-
Conformationally defined 6-S-trans-retinoic acid analogs. 3. Structure-activity relationships for nuclear receptor binding, transcriptional activity, and cancer chemopreventive activity
-
Muccio DD, Brouillette WJ, Alam M, Vaezi MF, Sani BP, Venepally P, et al. Conformationally defined 6-S-trans-retinoic acid analogs. 3. Structure-activity relationships for nuclear receptor binding, transcriptional activity, and cancer chemopreventive activity. J Med Chem 1996;39:3625-35.
-
(1996)
J Med Chem
, vol.39
, pp. 3625-3635
-
-
Muccio, D.D.1
Brouillette, W.J.2
Alam, M.3
Vaezi, M.F.4
Sani, B.P.5
Venepally, P.6
-
35
-
-
0036252668
-
Changes in BRCA1 and BRCA2 expression produced by chemotherapeutic agents in human breast cancer cells
-
DOI 10.1016/S1357-2725(02)00016-X, PII S135727250200016X
-
Su J, Ciftci K. Changes in BRCA1 and BRCA2 expression produced by chemotherapeutic agents in human breast cancer cells. Int J Biochem Cell Biol 2002;34:950-7. (Pubitemid 34499593)
-
(2002)
International Journal of Biochemistry and Cell Biology
, vol.34
, Issue.8
, pp. 950-957
-
-
Su, J.1
Ciftci, K.2
-
36
-
-
0031472370
-
Association of BRCA1 with Rad51 in mitotic and meiotic cells
-
DOI 10.1016/S0092-8674(00)81847-4
-
Scully R, Chen J, Plug A, Xiao Y, Weaver D, Feunteun J, et al. Association of BRCA1 with Rad51 in mitotic and meiotic cells. Cell 1997;88:265-75. (Pubitemid 28015875)
-
(1997)
Cell
, vol.88
, Issue.2
, pp. 265-275
-
-
Scully, R.1
Chen, J.2
Plug, A.3
Xiao, Y.4
Weaver, D.5
Feunteun, J.6
Ashley, T.7
Livingston, D.M.8
-
37
-
-
27244443082
-
Proliferation marker Ki-67 in early breast cancer
-
Urruticoechea A, Smith IE, Dowsett M. Proliferation marker Ki-67 in early breast cancer. J Clin Oncol 2005;23:7212-20.
-
(2005)
J Clin Oncol
, vol.23
, pp. 7212-7220
-
-
Urruticoechea, A.1
Smith, I.E.2
Dowsett, M.3
-
38
-
-
35648954161
-
WAF1/CIP1 is a common transcriptional target of retinoid receptors: Pleiotropic regulatory mechanism through retinoic acid receptor (RAR)/retinoid X receptor (RXR) heterodimer and RXR/RXR homodimer
-
WAF1/CIP1 is a common transcriptional target of retinoid receptors: pleiotropic regulatory mechanism through retinoic acid receptor (RAR)/retinoid X receptor (RXR) heterodimer and RXR/RXR homodimer. J Biol Chem 2007;282:29987-97.
-
(2007)
J Biol Chem
, vol.282
, pp. 29987-29997
-
-
Tanaka, T.1
Suh, K.S.2
Lo, A.M.3
De Luca, L.M.4
-
40
-
-
3042820298
-
Induction of S-phase arrest and p21 overexpression by a small molecule 2[[3-(2,3-dichlorophenoxy)propyl] amino]ethanol in correlation with activation of ERK
-
DOI 10.1038/sj.onc.1207645
-
Zhu H, Zhang L, Wu S, Teraishi F, Davis JJ, Jacob D, et al. Induction of S-phase arrest and p21 overexpression by a small molecule 2{[3-(2,3- dichlorophenoxy)propyl] amino}ethanol in correlation with activation of ERK. Oncogene 2004;23:4984-92. (Pubitemid 38938731)
-
(2004)
Oncogene
, vol.23
, Issue.29
, pp. 4984-4992
-
-
Zhu, H.1
Zhang, L.2
Wu, S.3
Teraishi, F.4
Davis, J.J.5
Jacob, D.6
Fang, B.7
-
42
-
-
0034720447
-
Gadd45 family proteins are coactivators of nuclear hormone receptors
-
DOI 10.1006/bbrc.2000.2760
-
Yi YW, Kim D, Jung N, Hong SS, Lee HS, Bae I. Gadd45 family proteins are coactivators of nuclear hormone receptors. Biochem Biophys Res Commun 2000;272:193-8. (Pubitemid 30444921)
-
(2000)
Biochemical and Biophysical Research Communications
, vol.272
, Issue.1
, pp. 193-198
-
-
Yi, Y.-W.1
Kim, D.2
Jung, N.3
Hong, S.-S.4
Lee, H.-S.5
Bae, I.6
-
44
-
-
30344478870
-
A global map of p53 transcription-factor binding sites in the human genome
-
DOI 10.1016/j.cell.2005.10.043, PII S0092867405013991
-
Wei CL, Wu Q, Vega VB, Chiu KP, Ng P, Zhang T, et al. A global map of p53 transcription-factor binding sites in the human genome. Cell 2006;124:207-19. (Pubitemid 43069320)
-
(2006)
Cell
, vol.124
, Issue.1
, pp. 207-219
-
-
Wei, C.-L.1
Wu, Q.2
Vega, V.B.3
Chiu, K.P.4
Ng, P.5
Zhang, T.6
Shahab, A.7
Yong, H.C.8
Fu, Y.9
Weng, Z.10
Liu, J.11
Zhao, X.D.12
Chew, J.-L.13
Lee, Y.L.14
Kuznetsov, V.A.15
Sung, W.-K.16
Miller, L.D.17
Lim, B.18
Liu, E.T.19
Yu, Q.20
Ng, H.-H.21
Ruan, Y.22
more..
-
45
-
-
1642523688
-
HGTSE-1 Expression Stimulates Cytoplasmic Localization of p53
-
DOI 10.1074/jbc.M311123200
-
Monte M, Benetti R, Collavin L, Marchionni L, Del Sal G, Schneider C. hGTSE-1 expression stimulates cytoplasmic localization of p53. J Biol Chem 2004;279:11744-52. (Pubitemid 38401679)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.12
, pp. 11744-11752
-
-
Monte, M.1
Benetti, R.2
Collavin, L.3
Marchionni, L.4
Del, S.G.5
Schneider, C.6
-
46
-
-
0027496935
-
The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin- Dependent kinases
-
DOI 10.1016/0092-8674(93)90499-G
-
Harper JW, Adami GR, Wei N, Keyomarsi K, Elledge SJ. The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases. Cell 1993;75:805-16. (Pubitemid 23346377)
-
(1993)
Cell
, vol.75
, Issue.4
, pp. 805-816
-
-
Harper, J.W.1
Adami, G.R.2
Wei, N.3
Keyomarsi, K.4
Elledge, S.J.5
-
47
-
-
0041919542
-
Improved protein-ligand docking using GOLD
-
DOI 10.1002/prot.10465
-
Verdonk ML, Cole JC, Hartshorn MJ, Murray CW, Taylor RD. Improved protein-ligand docking using GOLD. Proteins 2003;52:609-23. (Pubitemid 37034158)
-
(2003)
Proteins: Structure, Function and Genetics
, vol.52
, Issue.4
, pp. 609-623
-
-
Verdonk, M.L.1
Cole, J.C.2
Hartshorn, M.J.3
Murray, C.W.4
Taylor, R.D.5
-
48
-
-
0034213831
-
Crystal structure of the human RXRa ligand-binding domain bound to its natural ligand: 9-cis retinoic acid
-
Egea PF, Mitschler A, Rochel N, Ruff M, Chambon P, Moras D. Crystal. structure of the human RXRa ligand-binding domain bound to its natural ligand: 9-cis retinoic acid. EMBO J 2000;19:2592-601. (Pubitemid 30323548)
-
(2000)
EMBO Journal
, vol.19
, Issue.11
, pp. 2592-2601
-
-
Egea, P.F.1
Mitschler, A.2
Rochel, N.3
Ruff, M.4
Chambon, P.5
Moras, D.6
-
49
-
-
0016318441
-
Cellular tumorigenicity in nude mice: Correlation with cell growth in semi-solid medium
-
Freedman VH, Shin SI. Cellular tumorigenicity in nude mice: correlation with cell growth in semi-solid medium. Cell 1974;3:355-9.
-
(1974)
Cell
, vol.3
, pp. 355-359
-
-
Freedman, V.H.1
Shin, S.I.2
-
50
-
-
0027527396
-
Cancer chemoprevention: Principles and prospects
-
Morse MA, Stoner GD. Cancer chemoprevention: principles and prospects. Carcinogenesis 1993;14:1737-46. (Pubitemid 23290882)
-
(1993)
Carcinogenesis
, vol.14
, Issue.9
, pp. 1737-1746
-
-
Morse, M.A.1
Stoner, G.D.2
-
51
-
-
33645696402
-
Retinoic acid-induced CD38 expression in HL-60 myeloblastic leukemia cells regulates cell differentiation or viability depending on expression levels
-
Lamkin TJ, Chin V, Varvayanis S, Smith JL, Sramkoski RM, Jacobberger JW, et al. Retinoic acid-induced CD38 expression in HL-60 myeloblastic leukemia cells regulates cell differentiation or viability depending on expression levels. J Cell Biochem 2006;97:1328-38.
-
(2006)
J Cell Biochem
, vol.97
, pp. 1328-1338
-
-
Lamkin, T.J.1
Chin, V.2
Varvayanis, S.3
Smith, J.L.4
Sramkoski, R.M.5
Jacobberger, J.W.6
-
52
-
-
33846672898
-
Retinoic acid therapy served by ligands cross linking and masking CD38
-
DOI 10.1016/j.leukres.2006.07.003, PII S0145212606002645
-
Yen A. Retinoic acid therapy served by ligands cross linking and masking CD38. Leuk Res 2007;31:423-5. (Pubitemid 46198936)
-
(2007)
Leukemia Research
, vol.31
, Issue.4
, pp. 423-425
-
-
Yen, A.1
|