-
1
-
-
66149103215
-
Novel inhibitor of Plasmodium histone deacetylase that cures P. berghei-infected mice
-
Agbor-Enoh S, Seudieu C, Davidson E, Dritschilo A, Jung M. 2009. Novel inhibitor of Plasmodium histone deacetylase that cures P. berghei-infected mice. Antimicrob. Agents Chemother. 53:1727-1734.
-
(2009)
Antimicrob. Agents Chemother.
, vol.53
, pp. 1727-1734
-
-
Agbor-Enoh, S.1
Seudieu, C.2
Davidson, E.3
Dritschilo, A.4
Jung, M.5
-
2
-
-
0025183708
-
Basic local alignment search tool
-
Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. 1990. Basic local alignment search tool. J. Mol. Biol. 215:403-410.
-
(1990)
J. Mol. Biol.
, vol.215
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
3
-
-
34548319120
-
A role for natural regulatory T cells in the pathogenesis of experimental cerebral malaria
-
Amante FH, et al. 2007. A role for natural regulatory T cells in the pathogenesis of experimental cerebral malaria. Am. J. Pathol. 171:548-559.
-
(2007)
Am. J. Pathol.
, vol.171
, pp. 548-559
-
-
Amante, F.H.1
-
4
-
-
31944440918
-
Potencies of human immunodeficiency virus protease inhibitors in vitro against Plasmodium falciparum and in vivo against murine malaria
-
Andrews KT, et al. 2006. Potencies of human immunodeficiency virus protease inhibitors in vitro against Plasmodium falciparum and in vivo against murine malaria. Antimicrob. Agents Chemother. 50:639-648.
-
(2006)
Antimicrob. Agents Chemother.
, vol.50
, pp. 639-648
-
-
Andrews, K.T.1
-
6
-
-
42049106596
-
Potent antimalarial activity of histone deacetylase inhibitor analogues
-
Andrews KT, et al. 2008. Potent antimalarial activity of histone deacetylase inhibitor analogues. Antimicrob. Agents Chemother. 52:1454-1461.
-
(2008)
Antimicrob. Agents Chemother.
, vol.52
, pp. 1454-1461
-
-
Andrews, K.T.1
-
8
-
-
0034192770
-
Anti-malarial effect of histone deacetylation inhibitors and mammalian tumour cytodifferentiating agents
-
Andrews KT, et al. 2000. Anti-malarial effect of histone deacetylation inhibitors and mammalian tumour cytodifferentiating agents. Int. J. Parasitol. 30:761-768.
-
(2000)
Int. J. Parasitol.
, vol.30
, pp. 761-768
-
-
Andrews, K.T.1
-
9
-
-
58149178569
-
PlasmoDB: A functional genomic database for malaria parasites
-
Aurrecoechea C, et al. 2009. PlasmoDB: a functional genomic database for malaria parasites. Nucleic Acids Res. 37:D539-D543.
-
(2009)
Nucleic Acids Res.
, vol.37
-
-
Aurrecoechea, C.1
-
10
-
-
22844432021
-
Inhibition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: A novel basis for antileukemia activity of histone deacetylase inhibitors
-
Bali P, et al. 2005. Inhibition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: a novel basis for antileukemia activity of histone deacetylase inhibitors. J. Biol. Chem. 280:26729-26734.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 26729-26734
-
-
Bali, P.1
-
11
-
-
0025289722
-
In vitro effects of primaquine and primaquine metabolites on exoerythrocytic stages of Plasmodium berghei
-
Bates MD, Meshnick SR, Sigler CI, Leland P, Hollingdale MR. 1990. In vitro effects of primaquine and primaquine metabolites on exoerythrocytic stages of Plasmodium berghei. Am. J. Trop. Med. Hyg. 42:532-537.
-
(1990)
Am. J. Trop. Med. Hyg.
, vol.42
, pp. 532-537
-
-
Bates, M.D.1
Meshnick, S.R.2
Sigler, C.I.3
Leland, P.4
Hollingdale, M.R.5
-
12
-
-
0017843255
-
A method for testing for synergy with any number of agents
-
Berenbaum M. 1978. A method for testing for synergy with any number of agents. J. Infect. Dis. 137:122-130.
-
(1978)
J. Infect. Dis.
, vol.137
, pp. 122-130
-
-
Berenbaum, M.1
-
14
-
-
0033954256
-
The Protein Data Bank
-
Berman HM, et al. 2000. The Protein Data Bank. Nucleic Acids Res. 28:235-242.
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 235-242
-
-
Berman, H.M.1
-
15
-
-
78649304686
-
Role of histone deacetylases and their inhibitors in cancer biology and treatment
-
Beumer JH, Tawbi H. 2010. Role of histone deacetylases and their inhibitors in cancer biology and treatment. Curr. Clin. Pharmacol. 5:196-208.
-
(2010)
Curr. Clin. Pharmacol.
, vol.5
, pp. 196-208
-
-
Beumer, J.H.1
Tawbi, H.2
-
16
-
-
77952100365
-
Exploration of the HDAC2 foot pocket: Synthesis and SAR of substituted N-(2-aminophenyl)benzamides
-
Bressi JC, et al. 2010. Exploration of the HDAC2 foot pocket: synthesis and SAR of substituted N-(2-aminophenyl)benzamides. Bioorg. Med. Chem. Lett. 20:3142-3145.
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 3142-3145
-
-
Bressi, J.C.1
-
17
-
-
0035500502
-
Emerging roles for chromatin remodeling in cancer biology
-
Cairns BR. 2001. Emerging roles for chromatin remodeling in cancer biology. Trends Cell Biol. 11:S15-S21.
-
(2001)
Trends Cell Biol.
, vol.11
-
-
Cairns, B.R.1
-
18
-
-
0029078941
-
Interactions of atovaquone with other antimalarial drugs against Plasmodium falciparum in vitro
-
Canfield C, Pudney M, Gutteridge W. 1995. Interactions of atovaquone with other antimalarial drugs against Plasmodium falciparum in vitro. Exp. Parasitol. 80:373-381.
-
(1995)
Exp. Parasitol.
, vol.80
, pp. 373-381
-
-
Canfield, C.1
Pudney, M.2
Gutteridge, W.3
-
19
-
-
77649219343
-
Histone deacetylases play a major role in the transcriptional regulation of the Plasmodium falciparum life cycle
-
doi:10.1371/journal.ppat.1000737
-
Chaal BK, Gupta AP, Wastuwidyaningtyas BD, Luah YH, Bozdech Z. 2010. Histone deacetylases play a major role in the transcriptional regulation of the Plasmodium falciparum life cycle. PLoS Pathog. 6:e1000737. doi:10.1371/journal. ppat.1000737.
-
(2010)
PLoS Pathog.
, vol.6
-
-
Chaal, B.K.1
Gupta, A.P.2
Wastuwidyaningtyas, B.D.3
Luah, Y.H.4
Bozdech, Z.5
-
20
-
-
48149089435
-
Characterisation of the in vitro activity of the depsipeptide histone deacetylase inhibitor spiruchostatin A
-
Crabb SJ, et al. 2008. Characterisation of the in vitro activity of the depsipeptide histone deacetylase inhibitor spiruchostatin A. Biochem. Pharmacol. 76:463-475.
-
(2008)
Biochem. Pharmacol.
, vol.76
, pp. 463-475
-
-
Crabb, S.J.1
-
21
-
-
10544250252
-
Apicidin: A novel antiprotozoal agent that inhibits parasite histone deacetylase
-
Darkin-Rattray SJ, et al. 1996. Apicidin: a novel antiprotozoal agent that inhibits parasite histone deacetylase. Proc. Natl. Acad. Sci. U. S. A. 93: 13143-13147.
-
(1996)
Proc. Natl. Acad. Sci. U. S. A.
, vol.93
, pp. 13143-13147
-
-
Darkin-Rattray, S.J.1
-
22
-
-
36048958965
-
Histone deacetylase inhibitors: Overview and perspectives
-
Dokmanovic M, Clarke C, Marks PA. 2007. Histone deacetylase inhibitors: overview and perspectives. Mol. Cancer Res. 5:981-989.
-
(2007)
Mol. Cancer Res.
, vol.5
, pp. 981-989
-
-
Dokmanovic, M.1
Clarke, C.2
Marks, P.A.3
-
23
-
-
68049123592
-
Artemisinin resistance in Plasmodium falciparum malaria
-
Dondorp AM, et al. 2009. Artemisinin resistance in Plasmodium falciparum malaria. N. Engl. J. Med. 361:455-467.
-
(2009)
N. Engl. J. Med.
, vol.361
, pp. 455-467
-
-
Dondorp, A.M.1
-
24
-
-
54049118868
-
Antimalarial activity of phenylthiazolyl-bearing hydroxamate-based histone deacetylase inhibitors
-
Dow GS, et al. 2008. Antimalarial activity of phenylthiazolyl-bearing hydroxamate-based histone deacetylase inhibitors. Antimicrob. Agents Chemother. 52:3467-3477.
-
(2008)
Antimicrob. Agents Chemother.
, vol.52
, pp. 3467-3477
-
-
Dow, G.S.1
-
25
-
-
20144389848
-
Heterochromatin silencing and locus repositioning linked to regulation of virulence genes in Plasmodium falciparum
-
Duraisingh MT, et al. 2005. Heterochromatin silencing and locus repositioning linked to regulation of virulence genes in Plasmodium falciparum. Cell 121:13-24.
-
(2005)
Cell
, vol.121
, pp. 13-24
-
-
Duraisingh, M.T.1
-
26
-
-
0030767485
-
VERIFY3D: Assessment of protein models with three-dimensional profiles
-
Eisenberg D, Luthy R, Bowie JU. 1997. VERIFY3D: assessment of protein models with three-dimensional profiles. Methods Enzymol. 277 :396-404.
-
(1997)
Methods Enzymol.
, vol.277
, pp. 396-404
-
-
Eisenberg, D.1
Luthy, R.2
Bowie, J.U.3
-
27
-
-
0033539092
-
Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors
-
Finnin MS, et al. 1999. Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors. Nature 401:188-193.
-
(1999)
Nature
, vol.401
, pp. 188-193
-
-
Finnin, M.S.1
-
28
-
-
20144389331
-
Telomeric heterochromatin propagation and histone acetylation control mutually exclusive expression of antigenic variation genes in malaria parasites
-
Freitas-Junior LH, et al. 2005. Telomeric heterochromatin propagation and histone acetylation control mutually exclusive expression of antigenic variation genes in malaria parasites. Cell 121:25-36.
-
(2005)
Cell
, vol.121
, pp. 25-36
-
-
Freitas Jr., L.H.1
-
29
-
-
0037067696
-
Cloning and functional characterization of HDAC11, a novel member of the human histone deacetylase family
-
Gao L, Cueto MA, Asselbergs F, Atadja P. 2002. Cloning and functional characterization of HDAC11, a novel member of the human histone deacetylase family. J. Biol. Chem. 277:25748-25755.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 25748-25755
-
-
Gao, L.1
Cueto, M.A.2
Asselbergs, F.3
Atadja, P.4
-
30
-
-
28044471827
-
Acetylation and deacetylation of non-histone proteins
-
Glozak MA, Sengupta N, Zhang X, Seto E. 2005. Acetylation and deacetylation of non-histone proteins. Gene 363:15-23.
-
(2005)
Gene
, vol.363
, pp. 15-23
-
-
Glozak, M.A.1
Sengupta, N.2
Zhang, X.3
Seto, E.4
-
31
-
-
0036008097
-
Deacetylase enzymes: Biological functions and the use of small-molecule inhibitors
-
Grozinger CM, Schreiber SL. 2002. Deacetylase enzymes: biological functions and the use of small-molecule inhibitors. Chem. Biol. 9:3-16.
-
(2002)
Chem. Biol.
, vol.9
, pp. 3-16
-
-
Grozinger, C.M.1
Schreiber, S.L.2
-
32
-
-
74049111230
-
Transcriptional profiling of growth perturbations of the human malaria parasite Plasmodium falciparum
-
Hu G, et al. 2010. Transcriptional profiling of growth perturbations of the human malaria parasite Plasmodium falciparum. Nat. Biotechnol. 28:91-98.
-
(2010)
Nat. Biotechnol.
, vol.28
, pp. 91-98
-
-
Hu, G.1
-
33
-
-
0027753162
-
A comparison of three methods of estimating EC50 in studies of drug resistance of malaria parasites
-
Huber W, Koella JC. 1993. A comparison of three methods of estimating EC50 in studies of drug resistance of malaria parasites. Acta Trop. 55:257-261.
-
(1993)
Acta Trop.
, vol.55
, pp. 257-261
-
-
Huber, W.1
Koella, J.C.2
-
34
-
-
41349084852
-
Bias, reporting, and sharing: Computational evaluations of docking methods
-
Jain AN. 2008. Bias, reporting, and sharing: computational evaluations of docking methods. J. Comput. Aided Mol. Des. 22:201-212.
-
(2008)
J. Comput. Aided Mol. Des.
, vol.22
, pp. 201-212
-
-
Jain, A.N.1
-
35
-
-
81855206620
-
Preclinical metabolism and disposition of SB939 (pracinostat), an orally active histone deacetylase (HDAC) inhibitor, and prediction of human pharmacokinetics
-
Jayaraman R, et al. 2011. Preclinical metabolism and disposition of SB939 (pracinostat), an orally active histone deacetylase (HDAC) inhibitor, and prediction of human pharmacokinetics. Drug Metab. Dispos. 39:2219-2232.
-
(2011)
Drug Metab. Dispos.
, vol.39
, pp. 2219-2232
-
-
Jayaraman, R.1
-
36
-
-
0033525720
-
Molecular cloning and nuclear localization of a histone deacetylase homologue in Plasmodium falciparum
-
Joshi MB, et al. 1999. Molecular cloning and nuclear localization of a histone deacetylase homologue in Plasmodium falciparum. Mol. Biochem. Parasitol. 99:11-19.
-
(1999)
Mol. Biochem. Parasitol.
, vol.99
, pp. 11-19
-
-
Joshi, M.B.1
-
37
-
-
65549166880
-
HDAC6 modulates Hsp90 chaperone activity and regulates activation of aryl hydrocarbon receptor signaling
-
Kekatpure VD, Dannenberg AJ, Subbaramaiah K. 2009. HDAC6 modulates Hsp90 chaperone activity and regulates activation of aryl hydrocarbon receptor signaling. J. Biol. Chem. 284:7436-7445.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 7436-7445
-
-
Kekatpure, V.D.1
Dannenberg, A.J.2
Subbaramaiah, K.3
-
38
-
-
23744500093
-
Depletion of latent HIV-1 infection in vivo: A proof-of-concept study
-
Lehrman G, et al. 2005. Depletion of latent HIV-1 infection in vivo: a proof-of-concept study. Lancet 366:549-555.
-
(2005)
Lancet
, vol.366
, pp. 549-555
-
-
Lehrman, G.1
-
39
-
-
0035289779
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski CA, Lombardo F, Dominy BW, Feeney PJ. 2001. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 46:3-26.
-
(2001)
Adv. Drug Deliv. Rev.
, vol.46
, pp. 3-26
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
40
-
-
70349100446
-
Histone deacetylase inhibitors: Current status and overview of recent clinical trials
-
Ma X, Ezzeldin HH, Diasio RB. 2009. Histone deacetylase inhibitors: current status and overview of recent clinical trials. Drugs 69:1911-1934.
-
(2009)
Drugs
, vol.69
, pp. 1911-1934
-
-
Ma, X.1
Ezzeldin, H.H.2
Diasio, R.B.3
-
41
-
-
79952341758
-
Ex vivo activity of histone deacetylase inhibitors against multidrug-resistant clinical isolates of Plasmodium falciparum and P. vivax
-
Marfurt J, et al. 2011. Ex vivo activity of histone deacetylase inhibitors against multidrug-resistant clinical isolates of Plasmodium falciparum and P. vivax. Antimicrob. Agents Chemother. 55:961-966.
-
(2011)
Antimicrob. Agents Chemother.
, vol.55
, pp. 961-966
-
-
Marfurt, J.1
-
42
-
-
77955643796
-
The clinical development of histone deacetylase inhibitors as targeted anticancer drugs
-
Marks PA. 2010. The clinical development of histone deacetylase inhibitors as targeted anticancer drugs. Expert Opin. Invest. Drugs 19:1049-1066.
-
(2010)
Expert Opin. Invest. Drugs
, vol.19
, pp. 1049-1066
-
-
Marks, P.A.1
-
43
-
-
79957934393
-
Histone deacetylase inhibitors for purging HIV-1 from the latent reservoir
-
Matalon S, Rasmussen TA, Dinarello CA. 2011. Histone deacetylase inhibitors for purging HIV-1 from the latent reservoir. Mol. Med. 17:466-472.
-
(2011)
Mol. Med.
, vol.17
, pp. 466-472
-
-
Matalon, S.1
Rasmussen, T.A.2
Dinarello, C.A.3
-
44
-
-
30344477367
-
Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer
-
Minucci S, Pelicci PG. 2006. Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer. Nat. Rev. Cancer 6:38-51.
-
(2006)
Nat. Rev. Cancer
, vol.6
, pp. 38-51
-
-
Minucci, S.1
Pelicci, P.G.2
-
45
-
-
79961008996
-
Artemisinin resistance in Plasmodium falciparum is associated with an altered temporal pattern of transcription
-
doi:10.1186/1471-2164-12-391
-
Mok S, et al. 2011. Artemisinin resistance in Plasmodium falciparum is associated with an altered temporal pattern of transcription. BMC Genomics 12:391. doi:10.1186/1471-2164-12-391.
-
(2011)
BMC Genomics
, vol.12
, pp. 391
-
-
Mok, S.1
-
46
-
-
79960359543
-
Apicoplast isoprenoid precursor synthesis and the molecular basis of fosmidomycin resistance in Toxoplasma gondii
-
Nair SC, et al. 2011. Apicoplast isoprenoid precursor synthesis and the molecular basis of fosmidomycin resistance in Toxoplasma gondii. J. Exp. Med. 208:1547-1559.
-
(2011)
J. Exp. Med.
, vol.208
, pp. 1547-1559
-
-
Nair, S.C.1
-
47
-
-
77949714263
-
SB939, a novel potent and orally active histone deacetylase inhibitor with high tumor exposure and efficacy in mouse models of colorectal cancer
-
Novotny-Diermayr V, et al. 2010. SB939, a novel potent and orally active histone deacetylase inhibitor with high tumor exposure and efficacy in mouse models of colorectal cancer. Mol. Cancer Ther. 9:642-652.
-
(2010)
Mol. Cancer Ther.
, vol.9
, pp. 642-652
-
-
Novotny-Diermayr, V.1
-
48
-
-
73349116582
-
Docking of hydroxamic acids into HDAC1 and HDAC8: A rationalization of activity trends and selectivities
-
Ortore G, Di Colo F, Martinelli A. 2009. Docking of hydroxamic acids into HDAC1 and HDAC8: a rationalization of activity trends and selectivities. J. Chem. Infect. Model. 49:2774-2785.
-
(2009)
J. Chem. Infect. Model.
, vol.49
, pp. 2774-2785
-
-
Ortore, G.1
Di Colo, F.2
Martinelli, A.3
-
49
-
-
78649667345
-
Heat shock protein 90 as a drug target against protozoan infections: Biochemical characterization of HSP90 from Plasmodium falciparum and Trypanosoma evansi and evaluation of its inhibitor as a candidate drug
-
Pallavi R, et al. 2010. Heat shock protein 90 as a drug target against protozoan infections: biochemical characterization of HSP90 from Plasmodium falciparum and Trypanosoma evansi and evaluation of its inhibitor as a candidate drug. J. Biol. Chem. 285:37964-37975.
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 37964-37975
-
-
Pallavi, R.1
-
50
-
-
65249174969
-
Identification and characterization of small molecule inhibitors of a class I histone deacetylase from Plasmodium falciparum
-
Patel V, et al. 2009. Identification and characterization of small molecule inhibitors of a class I histone deacetylase from Plasmodium falciparum. J. Med. Chem. 52:2185-2187.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 2185-2187
-
-
Patel, V.1
-
51
-
-
33748694158
-
In vitro activity of tafenoquine against the asexual blood stages of Plasmodium falciparum isolates from Gabon, Senegal, and Djibouti
-
Pradines B, et al. 2006. In vitro activity of tafenoquine against the asexual blood stages of Plasmodium falciparum isolates from Gabon, Senegal, and Djibouti. Antimicrob. Agents Chemother. 50:3225-3226.
-
(2006)
Antimicrob. Agents Chemother.
, vol.50
, pp. 3225-3226
-
-
Pradines, B.1
-
52
-
-
79952280909
-
Phase I clinical, pharmacokinetic and pharmacodynamic study of SB939, an oral histone deacetylase (HDAC) inhibitor, in patients with advanced solid tumours
-
Razak AR, et al. 2011. Phase I clinical, pharmacokinetic and pharmacodynamic study of SB939, an oral histone deacetylase (HDAC) inhibitor, in patients with advanced solid tumours. Br. J. Cancer 104:756-762.
-
(2011)
Br. J. Cancer
, vol.104
, pp. 756-762
-
-
Razak, A.R.1
-
53
-
-
0027136282
-
Comparative protein modelling by satisfaction of spatial restraints
-
Sali A, Blundell TL. 1993. Comparative protein modelling by satisfaction of spatial restraints. J. Mol. Biol. 234:779-815.
-
(1993)
J. Mol. Biol.
, vol.234
, pp. 779-815
-
-
Sali, A.1
Blundell, T.L.2
-
54
-
-
4644314055
-
Plasma pharmacokinetics and metabolism of the histone deacetylase inhibitor trichostatin A after intraperitoneal administration to mice
-
Sanderson L, et al. 2004. Plasma pharmacokinetics and metabolism of the histone deacetylase inhibitor trichostatin A after intraperitoneal administration to mice. Drug Metab. Dispos. 32:1132-1138.
-
(2004)
Drug Metab. Dispos.
, vol.32
, pp. 1132-1138
-
-
Sanderson, L.1
-
55
-
-
79953790348
-
Icacina senegalensis (Icacinaceae), traditionally used for the treatment of malaria, inhibits in vitro Plasmodium falciparum growth without host cell toxicity
-
Sarr SO, et al. 2011. Icacina senegalensis (Icacinaceae), traditionally used for the treatment of malaria, inhibits in vitro Plasmodium falciparum growth without host cell toxicity. Malar. J. 10:85.
-
(2011)
Malar. J.
, vol.10
, pp. 85
-
-
Sarr, S.O.1
-
57
-
-
33749578940
-
Statistical potential for assessment and prediction of protein structures
-
Shen MY, Sali A. 2006. Statistical potential for assessment and prediction of protein structures. Protein Sci. 15:2507-2524.
-
(2006)
Protein Sci.
, vol.15
, pp. 2507-2524
-
-
Shen, M.Y.1
Sali, A.2
-
58
-
-
33846563919
-
Synergistic interactions of the antiretroviral protease inhibitors saquinavir and ritonavir with chloroquine and mefloquine against Plasmodium falciparum in vitro
-
Skinner-Adams TS, Andrews KT, Melville L, McCarthy J, Gardiner DL. 2007. Synergistic interactions of the antiretroviral protease inhibitors saquinavir and ritonavir with chloroquine and mefloquine against Plasmodium falciparum in vitro. Antimicrob. Agents Chemother. 51:759-762.
-
(2007)
Antimicrob. Agents Chemother.
, vol.51
, pp. 759-762
-
-
Skinner-Adams, T.S.1
Andrews, K.T.2
Melville, L.3
McCarthy, J.4
Gardiner, D.L.5
-
59
-
-
3142562372
-
Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases
-
Somoza JR, et al. 2004. Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases. Structure 12:1325-1334.
-
(2004)
Structure
, vol.12
, pp. 1325-1334
-
-
Somoza, J.R.1
-
60
-
-
0027968068
-
CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
-
Thompson JD, Higgins DG, Gibson TJ. 1994. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 22:4673-4680.
-
(1994)
Nucleic Acids Res.
, vol.22
, pp. 4673-4680
-
-
Thompson, J.D.1
Higgins, D.G.2
Gibson, T.J.3
-
61
-
-
65949120199
-
Sir2 paralogues cooperate to regulate virulence genes and antigenic variation in Plasmodium falciparum
-
doi:10.1371/journal.pbio.1000084
-
Tonkin CJ, et al. 2009. Sir2 paralogues cooperate to regulate virulence genes and antigenic variation in Plasmodium falciparum. PLoS Biol. 7:e84. doi:10.1371/journal.pbio.1000084.
-
(2009)
PLoS Biol.
, vol.7
-
-
Tonkin, C.J.1
-
62
-
-
0032982103
-
8-Aminoquinolines active against blood-stage Plasmodium falciparum in vitro inhibit hematin polymerization
-
Vennerstrom JL, et al. 1999. 8-Aminoquinolines active against blood-stage Plasmodium falciparum in vitro inhibit hematin polymerization. Antimicrob. Agents Chemother. 43:598-602.
-
(1999)
Antimicrob. Agents Chemother.
, vol.43
, pp. 598-602
-
-
Vennerstrom, J.L.1
-
63
-
-
79952262759
-
Histone deacetylase (HDAC) inhibitors in recent clinical trials for cancer therapy
-
Wagner JM, Hackanson B, Lubbert M, Jung M. 2010. Histone deacetylase (HDAC) inhibitors in recent clinical trials for cancer therapy. Clin. Epigenet. 1:117-136.
-
(2010)
Clin. Epigenet.
, vol.1
, pp. 117-136
-
-
Wagner, J.M.1
Hackanson, B.2
Lubbert, M.3
Jung, M.4
-
64
-
-
0034678922
-
Protein trafficking to the plastid of Plasmodium falciparum is via the secretory pathway
-
Waller RF, Reed MB, Cowman AF, McFadden GI. 2000. Protein trafficking to the plastid of Plasmodium falciparum is via the secretory pathway. EMBO J. 19:1794-1802.
-
(2000)
EMBO J.
, vol.19
, pp. 1794-1802
-
-
Waller, R.F.1
Reed, M.B.2
Cowman, A.F.3
McFadden, G.I.4
-
65
-
-
79960163508
-
Discovery of (2E)-3-{2-butyl-1-[2-(diethylamino)ethyl]-1H-benzimidazol-5- yl}-N-hydroxyacrylamide (SB939), an orally active histone deacetylase inhibitor with a superior preclinical profile
-
Wang H. 2011. Discovery of (2E)-3-{2-butyl-1-[2-(diethylamino)ethyl]-1H- benzimidazol-5-yl}-N-hydroxyacrylamide (SB939), an orally active histone deacetylase inhibitor with a superior preclinical profile. J. Med. Chem. 54:4694-4720.
-
(2011)
J. Med. Chem.
, vol.54
, pp. 4694-4720
-
-
Wang, H.1
-
66
-
-
0034068284
-
Severe falciparum malaria
-
WHOCommunicable Diseases Cluster
-
WHOCommunicable Diseases Cluster. 2000. Severe falciparum malaria. Trans. R. Soc. Trop. Med. Hyg. 94(Suppl 1):S1-S90.
-
(2000)
Trans. R. Soc. Trop. Med. Hyg.
, vol.94
, Issue.SUPPL. 1
-
-
-
67
-
-
79960113305
-
Phase I and pharmacodynamic study of an orally administered novel inhibitor of histone deacetylases, SB939, in patients with refractory solid malignancies
-
Yong WP, et al. 2011. Phase I and pharmacodynamic study of an orally administered novel inhibitor of histone deacetylases, SB939, in patients with refractory solid malignancies. Ann. Oncol. 22:2516-2522.
-
(2011)
Ann. Oncol.
, vol.22
, pp. 2516-2522
-
-
Yong, W.P.1
|