-
1
-
-
77249176947
-
Toxicity, disulfiram
-
Aug. Available from, [cited 2009 Jul 6]
-
Soghoian, S.; Wiener, S. W.; Díaz-Alcalá, J. E. Toxicity, disulfiram. Emedicine, Medscape.com. 2008 Aug. Available from: http://emedicinemedscape.com/article/814525-overview. [cited 2009 Jul 6].
-
(2008)
Emedicine, Medscape.com
-
-
Soghoian, S.1
Wiener, S.W.2
Díaz-Alcalá, J.E.3
-
2
-
-
33644843388
-
Disulfiram, an old drug with new potential therapeutic uses for human cancers and fungal infections
-
Sauna, Z. E.; Shukla, S.; Ambudkar, S. V. Disulfiram, an old drug with new potential therapeutic uses for human cancers and fungal infections. Mol. BioSyst. 2005, 124-134.
-
(2005)
Mol. BioSyst
, pp. 124-134
-
-
Sauna, Z.E.1
Shukla, S.2
Ambudkar, S.V.3
-
4
-
-
0016686540
-
Inhibition of dimethylhydrazine-induced neoplasia of the large intestine by disulfiram
-
Wattenberg, L. W. Inhibition of dimethylhydrazine-induced neoplasia of the large intestine by disulfiram. J. Natl. Cancer Inst. 1975, 54, 1005-1006.
-
(1975)
J. Natl. Cancer Inst
, vol.54
, pp. 1005-1006
-
-
Wattenberg, L.W.1
-
5
-
-
0017065258
-
Inhibition of macromolecular binding of benzo(a)pyrene and inhibition of neoplasia by disulfiram in the mouse forestomach
-
Borchert, P.; Wattenberg, L. W. Inhibition of macromolecular binding of benzo(a)pyrene and inhibition of neoplasia by disulfiram in the mouse forestomach. J. Natl. Cancer Inst. 1976, 57, 173-179.
-
(1976)
J. Natl. Cancer Inst
, vol.57
, pp. 173-179
-
-
Borchert, P.1
Wattenberg, L.W.2
-
6
-
-
0021864126
-
Restoration of sensitivity to ox-azaphosphorines by inhibitors of aldehyde dehydrogenase activity in cultured oxazaphosphorine-resistant L1210 and cross-linking agent-resistant P388 cell lines
-
Sladek, N. E.; Landkamer, G. J. Restoration of sensitivity to ox-azaphosphorines by inhibitors of aldehyde dehydrogenase activity in cultured oxazaphosphorine-resistant L1210 and cross-linking agent-resistant P388 cell lines. Cancer Res. 1985, 45, 1549-1555.
-
(1985)
Cancer Res
, vol.45
, pp. 1549-1555
-
-
Sladek, N.E.1
Landkamer, G.J.2
-
7
-
-
0024317044
-
Potentiation of nitrogen mustard cytotoxicity by disulfiram, diethyldithiocarbamic acid, and diethylamine in mice
-
Valeriote, F.; Grates, H. E. Potentiation of nitrogen mustard cytotoxicity by disulfiram, diethyldithiocarbamic acid, and diethylamine in mice. Cancer Res. 1989, 49, 6658-6661.
-
(1989)
Cancer Res
, vol.49
, pp. 6658-6661
-
-
Valeriote, F.1
Grates, H.E.2
-
8
-
-
0022508021
-
Selective protection against cis-diamminedichloroplatinum(II)-induced toxicity in kidney, gut, and bone marrow by diethyldithio-carbamate
-
Bodenner, D. L.; Dedon, P. C.; Keng, P. C.; Katz, J. C.; Borch, R. F. Selective protection against cis-diamminedichloroplatinum(II)-induced toxicity in kidney, gut, and bone marrow by diethyldithio-carbamate. Cancer Res. 1986, 46, 2751-2755.
-
(1986)
Cancer Res
, vol.46
, pp. 2751-2755
-
-
Bodenner, D.L.1
Dedon, P.C.2
Keng, P.C.3
Katz, J.C.4
Borch, R.F.5
-
9
-
-
0021118703
-
Quantitative analysis of dose-effect relationships: The combined effects of multiple drugs or enzyme inhibitors
-
Chou, T. C.; Talalay, P. Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors. Adv. Enzyme Regul. 1984, 22, 27-55.
-
(1984)
Adv. Enzyme Regul
, vol.22
, pp. 27-55
-
-
Chou, T.C.1
Talalay, P.2
-
10
-
-
0023696927
-
Phase I clinical and pharmacokinetic study of diethyldithiocarbamate as a chemoprotector from toxic effects of cisplatin
-
Qazi, R.; Chang, A. Y.; Borch, R. F.; Montine, T.; Dedon, P.; Loughner, J.; Bennett, J. M. Phase I clinical and pharmacokinetic study of diethyldithiocarbamate as a chemoprotector from toxic effects of cisplatin. J. Natl. Cancer Inst. 1988, 80, 1486-1488.
-
(1988)
J. Natl. Cancer Inst
, vol.80
, pp. 1486-1488
-
-
Qazi, R.1
Chang, A.Y.2
Borch, R.F.3
Montine, T.4
Dedon, P.5
Loughner, J.6
Bennett, J.M.7
-
11
-
-
0025359391
-
A randomized phase II study of cisplatin alone versus cisplatin plus disulfiram
-
Verma, S.; Stewart, D. J.; Maroun, J. A.; Nair, R. C. A randomized phase II study of cisplatin alone versus cisplatin plus disulfiram. Am. J. Clin. Oncol. 1990, 13, 119-124.
-
(1990)
Am. J. Clin. Oncol
, vol.13
, pp. 119-124
-
-
Verma, S.1
Stewart, D.J.2
Maroun, J.A.3
Nair, R.C.4
-
12
-
-
0034616637
-
Blockage of drug resistance in vitro by disulfiram, a drug used to treat alcoholism
-
Loo, T. W.; Clarke, D. M. Blockage of drug resistance in vitro by disulfiram, a drug used to treat alcoholism. J. Natl. Cancer Inst. 2000, 92, 898-902.
-
(2000)
J. Natl. Cancer Inst
, vol.92
, pp. 898-902
-
-
Loo, T.W.1
Clarke, D.M.2
-
13
-
-
0031855760
-
Induction of apoptosis by thiuramdisulfides, the reactive metabolites of dithiocarbamates, through coordinative modulation of NFkappaB, c-fos/c-jun, and p53 proteins
-
Liu, G. Y.; Frank, N.; Bartsch, H.; Lin, J. K. Induction of apoptosis by thiuramdisulfides, the reactive metabolites of dithiocarbamates, through coordinative modulation of NFkappaB, c-fos/c-jun, and p53 proteins. Mol. Carcinog. 1998, 22, 235-246.
-
(1998)
Mol. Carcinog
, vol.22
, pp. 235-246
-
-
Liu, G.Y.1
Frank, N.2
Bartsch, H.3
Lin, J.K.4
-
14
-
-
79951686474
-
Disulfiram is a DNA demethylating agent and inhibits prostate cancer cell growth
-
Epub ahead of print
-
Lin, J.; Haffner, M. C.; Zhang, Y.; Kachhap, S.; Liu, J.; Yegnasubramanian, S.; Nelson, W. G.; Carducci, M. A. Disulfiram is a DNA demethylating agent and inhibits prostate cancer cell growth. Prostate 2010, Epub ahead of print.
-
(2010)
Prostate
-
-
Lin, J.1
Haffner, M.C.2
Zhang, Y.3
Kachhap, S.4
Liu, J.5
Yegnasubramanian, S.6
Nelson, W.G.7
Carducci, M.A.8
-
15
-
-
0142148099
-
Inhibition of invasion and angiogenesis by zinc-chelating agent disulfiram
-
Shian, S. G.; Kao, Y. R.; Wu, F. Y.; Wu, C. W. Inhibition of invasion and angiogenesis by zinc-chelating agent disulfiram. Mol. Pharmacol. 2003, 64, 1076-1084.
-
(2003)
Mol. Pharmacol
, vol.64
, pp. 1076-1084
-
-
Shian, S.G.1
Kao, Y.R.2
Wu, F.Y.3
Wu, C.W.4
-
16
-
-
0022993363
-
Chelating drugs and zinc
-
Weismann, K. Chelating drugs and zinc. Dan. Med. Bull. 1986 33, 208-211.
-
(1986)
Dan. Med. Bull
, vol.33
, pp. 208-211
-
-
Weismann, K.1
-
17
-
-
33644549964
-
Inhibition of proteasome activity, nuclear factor-KappaB translocation and cell survival by the anti-alcoholism drug disulfiram
-
Lövborg, H.; Oberg, F.; Rickardson, L.; Gullbo, J.; Nygren P.; Larsson, R. Inhibition of proteasome activity, nuclear factor-KappaB translocation and cell survival by the anti-alcoholism drug disulfiram. Int. J. Cancer 2006, 118, 1577-1580.
-
(2006)
Int. J. Cancer
, vol.118
, pp. 1577-1580
-
-
Lövborg, H.1
Oberg, F.2
Rickardson, L.3
Gullbo, J.4
Nygren, P.5
Larsson, R.6
-
18
-
-
33845304732
-
Pharmacological profiling of disulfiram using human tumor cell lines and human tumor cells from patients
-
Wickström, M.; Danielsson, K.; Rickardson, L.; Gullbo, J.; Nygren, P.; Isaksson, A.; Larsson, R.; Lövborg, H. Pharmacological profiling of disulfiram using human tumor cell lines and human tumor cells from patients. Biochem. Pharmacol. 2007, 73, 25-33.
-
(2007)
Biochem. Pharmacol
, vol.73
, pp. 25-33
-
-
Wickström, M.1
Danielsson, K.2
Rickardson, L.3
Gullbo, J.4
Nygren, P.5
Isaksson, A.6
Larsson, R.7
Lövborg, H.8
-
19
-
-
33847668394
-
Image-based screening for the identification of novel proteasome inhibitors
-
Rickardson, L.; Wickström, M.; Larsson, R.; Lövborg, H. Image-based screening for the identification of novel proteasome inhibitors. J. Biomol. Screen. 2007, 12, 203-210.
-
(2007)
J. Biomol. Screen
, vol.12
, pp. 203-210
-
-
Rickardson, L.1
Wickström, M.2
Larsson, R.3
Lövborg, H.4
-
20
-
-
33751285781
-
Disulfiram, a clinically used anti-alcoholism drug and copper-binding agent, induces apoptotic cell death in breast cancer cultures and xenografts via inhibition of the proteasome activity
-
Chen, D.; Cui, Q. C.; Yang, H.; Dou, Q. P. Disulfiram, a clinically used anti-alcoholism drug and copper-binding agent, induces apoptotic cell death in breast cancer cultures and xenografts via inhibition of the proteasome activity. Cancer Res. 2006, 66, 10425-10433.
-
(2006)
Cancer Res
, vol.66
, pp. 10425-10433
-
-
Chen, D.1
Cui, Q.C.2
Yang, H.3
Dou, Q.P.4
-
21
-
-
43649083069
-
Disulfiram promotes the conversion of carcinogenic cadmium to a proteasome inhibitor with pro-apoptotic activity in human cancer cells
-
Li, L.; Yang, H.; Chen, D.; Cui, C.; Dou, Q. P. Disulfiram promotes the conversion of carcinogenic cadmium to a proteasome inhibitor with pro-apoptotic activity in human cancer cells. Toxicol. Appl. Pharmacol. 2008, 229, 206-214.
-
(2008)
Toxicol. Appl. Pharmacol
, vol.229
, pp. 206-214
-
-
Li, L.1
Yang, H.2
Chen, D.3
Cui, C.4
Dou, Q.P.5
-
22
-
-
42149187107
-
Evaluation of copper-dependent proteasome-inhibitory and apoptosis-inducing activities of novel pyrrolidine dithiocarbamate analogues
-
Yu, Z.; Wang, F.; Milacic, V.; Li, X.; Cui, Q. C.; Zhang, B.; Yan, B.; Dou, Q. P. Evaluation of copper-dependent proteasome-inhibitory and apoptosis-inducing activities of novel pyrrolidine dithiocarbamate analogues. Int. J. Mol. Med. 2007, 20, 919-925.
-
(2007)
Int. J. Mol. Med
, vol.20
, pp. 919-925
-
-
Yu, Z.1
Wang, F.2
Milacic, V.3
Li, X.4
Cui, Q.C.5
Zhang, B.6
Yan, B.7
Dou, Q.P.8
-
23
-
-
0030918876
-
The origin of an EPR signal observed in dithiocarbamate-loaded tissues. Copper(II)-dithiocarbamate complexes account for the narrow hyperfine lines
-
Suzuki, Y.; Fujii, S.; Tominaga, T.; Yoshimoto, T.; Yoshimura, T.; Kamada, H. The origin of an EPR signal observed in dithiocarbamate-loaded tissues. Copper(II)-dithiocarbamate complexes account for the narrow hyperfine lines. Biochim. Biophys. Acta 1997, 1335, 242-245.
-
(1997)
Biochim. Biophys. Acta
, vol.1335
, pp. 242-245
-
-
Suzuki, Y.1
Fujii, S.2
Tominaga, T.3
Yoshimoto, T.4
Yoshimura, T.5
Kamada, H.6
-
24
-
-
4644235752
-
Disulfiram inhibits activating transcription factor/cyclic AMP-responsive element binding protein and human melanoma growth in a metal-dependent manner in vitro, in mice and in a patient with metastatic disease
-
Brar, S. S.; Grigg, C.; Wilson, K. S.; Holder Jr, W. D.; Dreau, D.; Austin, C.; Foster, M.; Ghio, A. J.; Whorton, A. R.; Stowell, G.W.; Whittall, L. B.; Whittle, R. R.; White, D. P.; Kennedy, T. P. Disulfiram inhibits activating transcription factor/cyclic AMP-responsive element binding protein and human melanoma growth in a metal-dependent manner in vitro, in mice and in a patient with metastatic disease. Mol. Cancer Ther. 2004, 3, 1049-1060.
-
(2004)
Mol. Cancer Ther
, vol.3
, pp. 1049-1060
-
-
Brar, S.S.1
Grigg, C.2
Wilson, K.S.3
Holder, W.D.4
Dreau, D.5
Austin, C.6
Foster, M.7
Ghio, A.J.8
Whorton, A.R.9
Stowell, G.W.10
Whittall, L.B.11
Whittle, R.R.12
White, D.P.13
Kennedy, T.P.14
-
25
-
-
5344234076
-
The ubiquitin mediated protein degradation pathway in cancer: Therapeutic implications
-
Burger, A. M.; Seth, A. K. The ubiquitin mediated protein degradation pathway in cancer: therapeutic implications. Eur. J. Cancer 2004, 40, 2217-2229.
-
(2004)
Eur. J. Cancer
, vol.40
, pp. 2217-2229
-
-
Burger, A.M.1
Seth, A.K.2
-
26
-
-
79951717343
-
Ubiquitin Ligases and Cancer
-
Sakamoto, K.; Rubin, E. H., Eds.; Springer: New York, NY
-
Burger, A. M.; Seth, A. K. Ubiquitin Ligases and Cancer. In: Modulation of Protein Stability in Cancer Therapy; Sakamoto, K.; Rubin, E. H., Eds.; Springer: New York, NY, 2009, pp. 1-18.
-
(2009)
Modulation of Protein Stability In Cancer Therapy
, pp. 1-18
-
-
Burger, A.M.1
Seth, A.K.2
-
27
-
-
17544404364
-
Evaluation and classification of RING-finger domains encoded by the Arabidopsis genome
-
Kosarev, P.; Mayer, K. F. X.; Hardtke, C. S. Evaluation and classification of RING-finger domains encoded by the Arabidopsis genome. Genome Biol. 2002, 3, 1-12.
-
(2002)
Genome Biol
, vol.3
, pp. 1-12
-
-
Kosarev, P.1
Mayer, K.F.X.2
Hardtke, C.S.3
-
29
-
-
33745674468
-
Drug discovery in the ubiquitin-proteasome system
-
Nalepa, G.; Rolfe, M.; Harper, J. W. Drug discovery in the ubiquitin-proteasome system. Nat. Rev. Drug Discov. 2006, 5, 596-613.
-
(2006)
Nat. Rev. Drug Discov
, vol.5
, pp. 596-613
-
-
Nalepa, G.1
Rolfe, M.2
Harper, J.W.3
-
30
-
-
10744221485
-
In vivo activation of the p53 pathway by smallmolecule antagonists of MDM2
-
Vassilev, L. T.; Vu, B. T.; Graves, B.; Carvajal, D.; Podlaski, F.; Filipovic, Z.; Kong, N.; Kammlott, U.; Lukacs, C.; Klein, C.; Fotouhi, N.; Liu, E. A. In vivo activation of the p53 pathway by smallmolecule antagonists of MDM2. Science 2004, 303, 844-8.
-
(2004)
Science
, vol.303
, pp. 844-848
-
-
Vassilev, L.T.1
Vu, B.T.2
Graves, B.3
Carvajal, D.4
Podlaski, F.5
Filipovic, Z.6
Kong, N.7
Kammlott, U.8
Lukacs, C.9
Klein, C.10
Fotouhi, N.11
Liu, E.A.12
-
31
-
-
72549094296
-
An MDM2 antagonist (MI-319) restores p53 functions and increases the life span of orally treated follicular lymphoma bearing animals
-
Mohammad, R. M.; Wu, J.; Azmi, A. S.; Aboukameel, A.; Sosin, A.; Wu, S.; Yang, D.; Wang, S.; Al-Katib, A-M. An MDM2 antagonist (MI-319) restores p53 functions and increases the life span of orally treated follicular lymphoma bearing animals. Mol. Cancer 2009, 8, 115.
-
(2009)
Mol. Cancer
, vol.8
, pp. 115
-
-
Mohammad, R.M.1
Wu, J.2
Azmi, A.S.3
Aboukameel, A.4
Sosin, A.5
Wu, S.6
Yang, D.7
Wang, S.8
Al-Katib, A.-M.9
-
32
-
-
64749098830
-
An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer
-
Soucy, T. A.; Smith, P. G.; Milhollen, M. A.; Berger, A. J.; Gavin, J. M.; Adhikari, S.; Brownell, J. E.; Burke, K. E.; Cardin, D. P.; Critchley, S.; Cullis, C. A.; Doucette, A.; Garnsey, J. J.; Gaulin, J. L.; Gershman, R. E.; Lublinsky, A. R.; McDonald, A.; Mizutani, H.; Narayanan, U.; Olhava, E. J.; Peluso, S.; Rezaei, M.; Sintchak, M. D.; Talreja, T.; Thomas, M. P.; Traore, T.; Vyskocil, S.; Weatherhead, G. S.; Yu, J.; Zhang, J.; Dick, L. R.; Claiborne, C. F.; Rolfe, M.; Bolen, J. B.; Langston, S. P. An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer. Nature 2009, 458, 732-736.
-
(2009)
Nature
, vol.458
, pp. 732-736
-
-
Soucy, T.A.1
Smith, P.G.2
Milhollen, M.A.3
Berger, A.J.4
Gavin, J.M.5
Adhikari, S.6
Brownell, J.E.7
Burke, K.E.8
Cardin, D.P.9
Critchley, S.10
Cullis, C.A.11
Doucette, A.12
Garnsey, J.J.13
Gaulin, J.L.14
Gershman, R.E.15
Lublinsky, A.R.16
McDonald, A.17
Mizutani, H.18
Narayanan, U.19
Olhava, E.J.20
Peluso, S.21
Rezaei, M.22
Sintchak, M.D.23
Talreja, T.24
Thomas, M.P.25
Traore, T.26
Vyskocil, S.27
Weatherhead, G.S.28
Yu, J.29
Zhang, J.30
Dick, L.R.31
Claiborne, C.F.32
Rolfe, M.33
Bolen, J.B.34
Langston, S.P.35
more..
-
33
-
-
0027523471
-
Inhibition of HIV infectivity by zinc-ejecting aromatic C-nitroso compounds
-
Rice, W. G.; Schaeffer, C. A.; Harten B.; Villinger, F.; South, T. L.; Summers, M. F.; Henderson, L. E.; Bess Jr, J. W.; Arthur, L. O.; McDougal, J. S.; Orloff, S. L.; Mendeleyev, J.; Kun E. Inhibition of HIV infectivity by zinc-ejecting aromatic C-nitroso compounds. Nature 1993, 361, 473-475.
-
(1993)
Nature
, vol.361
, pp. 473-475
-
-
Rice, W.G.1
Schaeffer, C.A.2
Harten, B.3
Villinger, F.4
South, T.L.5
Summers, M.F.6
Henderson, L.E.7
Bess, J.W.8
Arthur, L.O.9
McDougal, J.S.10
Orloff, S.L.11
Mendeleyev, J.12
Kun, E.13
-
34
-
-
16944362355
-
Azodicarbonamide inhibits HIV-1 replication by targeting the nucleocapsid protein
-
Rice, W. G.; Turpin, J. A.; Huang, M.; Clanton, D.; Buckheit Jr, R. W.; Covell, D. G.; Wallqvist, A.; McDonnell, N. B.; DeGuzman, R. N.; Summers, M. F.; Zalkow, L.; Bader, J. P.; Haugwitz, R. D.; Sausville, E. A. Azodicarbonamide inhibits HIV-1 replication by targeting the nucleocapsid protein. Nat. Med. 1997, 3, 341-345.
-
(1997)
Nat. Med
, vol.3
, pp. 341-345
-
-
Rice, W.G.1
Turpin, J.A.2
Huang, M.3
Clanton, D.4
Buckheit, R.W.5
Covell, D.G.6
Wallqvist, A.7
McDonnell, N.B.8
Deguzman, R.N.9
Summers, M.F.10
Zalkow, L.11
Bader, J.P.12
Haugwitz, R.D.13
Sausville, E.A.14
-
35
-
-
0031860825
-
Efficacies of Zinc-Finger-Active Drugs against Giardia lamblia
-
Nash, T.; Rice, W. G. Efficacies of Zinc-Finger-Active Drugs against Giardia lamblia. Antimicrob. Agents Chemother. 1998, 42, 1488-1492.
-
(1998)
Antimicrob. Agents Chemother
, vol.42
, pp. 1488-1492
-
-
Nash, T.1
Rice, W.G.2
-
36
-
-
0033591844
-
Potential drugs against cervical cancer: Zinc-ejecting inhibitors of the human papillomavirus type 16 E6 onco-protein
-
Beerheide, W.; Bernard, H. U.; Tan, Y. J.; Ganesan, A.; Rice, W. G.; Ting, A. E. Potential drugs against cervical cancer: zinc-ejecting inhibitors of the human papillomavirus type 16 E6 onco-protein. J. Natl. Cancer Inst. 1999, 91, 1211-1220.
-
(1999)
J. Natl. Cancer Inst
, vol.91
, pp. 1211-1220
-
-
Beerheide, W.1
Bernard, H.U.2
Tan, Y.J.3
Ganesan, A.4
Rice, W.G.5
Ting, A.E.6
-
37
-
-
33748570421
-
Novel RING E3 ubiquitin ligases in breast cancer
-
Burger, A. M.; Amemiya, Y.; Kitching, R.; Seth, A. K. Novel RING E3 ubiquitin ligases in breast cancer. Neoplasia 2006, 8, 689-695.
-
(2006)
Neoplasia
, vol.8
, pp. 689-695
-
-
Burger, A.M.1
Amemiya, Y.2
Kitching, R.3
Seth, A.K.4
-
38
-
-
28544431575
-
A novel breast cancer associated RING-type ubiquitin ligase correlates with outcome in invasive breast cancer
-
Burger, A. M.; Gao, Y.; Amemiya, Y.; Kahn, H. J.; Kitching, R.; Yang, Y.; Sun, P.; Narod, S. A.; Hanna, W. M.; Seth, A. K. A novel breast cancer associated RING-type ubiquitin ligase correlates with outcome in invasive breast cancer. Cancer Res. 2005, 65, 10401-10412.
-
(2005)
Cancer Res
, vol.65
, pp. 10401-10412
-
-
Burger, A.M.1
Gao, Y.2
Amemiya, Y.3
Kahn, H.J.4
Kitching, R.5
Yang, Y.6
Sun, P.7
Narod, S.A.8
Hanna, W.M.9
Seth, A.K.10
-
39
-
-
0031050622
-
Inhibition of multiple phases of human immunodeficiency virus type 1 replication by a dithiane compound that attacks the conserved zinc fingers of retroviral nucleocapsid proteins
-
Rice, W. G.; Baker, D. C.; Schaeffer, C. A.; Graham, L.; Bu, M.; Terpening, S.; Clanton, D.; Schultz, R.; Bader, J. P.; Buckheit Jr., R. W.; Field, L.; Singh, P. K.; Turpin, J. A. Inhibition of multiple phases of human immunodeficiency virus type 1 replication by a dithiane compound that attacks the conserved zinc fingers of retroviral nucleocapsid proteins. Antimicrob. Agents Chemother. 1997, 419-426.
-
(1997)
Antimicrob. Agents Chemother
, pp. 419-426
-
-
Rice, W.G.1
Baker, D.C.2
Schaeffer, C.A.3
Graham, L.4
Bu, M.5
Terpening, S.6
Clanton, D.7
Schultz, R.8
Bader, J.P.9
Buckheit, R.W.10
Field, L.11
Singh, P.K.12
Turpin, J.A.13
-
40
-
-
77950581975
-
Exploring the structural requirements for inhibition of the ubiquitin E3 ligase breast cancer associated protein 2 (BCA2) as a treatment for breast cancer
-
Brahemi, G.; Kona, F. R.; Fiasella, A.; Buac, D.; Soukupová, J.; Brancale, A.; Burger, A. M.; Westwell, A. D. Exploring the structural requirements for inhibition of the ubiquitin E3 ligase breast cancer associated protein 2 (BCA2) as a treatment for breast cancer. J. Med. Chem. 2010, 53, 2757-2765.
-
(2010)
J. Med. Chem
, vol.53
, pp. 2757-2765
-
-
Brahemi, G.1
Kona, F.R.2
Fiasella, A.3
Buac, D.4
Soukupová, J.5
Brancale, A.6
Burger, A.M.7
Westwell, A.D.8
-
41
-
-
77950551936
-
Targeting leukemic stem cells
-
Bagley, R. G.; Teicher, B. A., Eds., Humana Press: New York, NY
-
Burger, A. M. Targeting leukemic stem cells. In: Stem Cells and Cancer; Bagley, R. G.; Teicher, B. A., Eds., Humana Press: New York, NY, 2009, pp. 263-273.
-
(2009)
Stem Cells and Cancer
, pp. 263-273
-
-
Burger, A.M.1
-
42
-
-
35848955428
-
ALDH1 is a marker of normal and malignant human mammary stem cells and a predictor of poor clinical outcome
-
Ginestier, C.; Hur, M. H.; Charafe-Jauffret, E.; Monville, F.; Dutcher, J.; Brown, M.; Jacquemier, J.; Viens, P.; Kleer, C. G.; Liu, S.; Schott, A.; Hayes, D.; Birnbaum, D.; Wicha, M. S.; Dontu, G. ALDH1 is a marker of normal and malignant human mammary stem cells and a predictor of poor clinical outcome. Cell Stem Cell. 2007, 1, 555-567.
-
(2007)
Cell Stem Cell
, vol.1
, pp. 555-567
-
-
Ginestier, C.1
Hur, M.H.2
Charafe-Jauffret, E.3
Monville, F.4
Dutcher, J.5
Brown, M.6
Jacquemier, J.7
Viens, P.8
Kleer, C.G.9
Liu, S.10
Schott, A.11
Hayes, D.12
Birnbaum, D.13
Wicha, M.S.14
Dontu, G.15
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