-
1
-
-
57049120498
-
Drug insight: Histone deacetylase inhibitor-based therapies for cutaneous T-cell lymphomas
-
Khan O, La Thangue NB. Drug insight: histone deacetylase inhibitor-based therapies for cutaneous T-cell lymphomas. Nat Clin Pract Oncol. 2008;5:714-726.
-
(2008)
Nat Clin Pract Oncol
, vol.5
, pp. 714-726
-
-
Khan, O.1
La Thangue, N.B.2
-
2
-
-
0037444803
-
Histone deacetylases (HDACs): Characterization of the classical HDAC family
-
De Ruijter AJM, Van Gennip AH, Caron HN, Demp S, Van Kuilenbur ABP. Histone deacetylases (HDACs): characterization of the classical HDAC family. Biochem J. 2003;370:737-749.
-
(2003)
Biochem J
, vol.370
, pp. 737-749
-
-
De Ruijter, A.J.M.1
Van Gennip, A.H.2
Caron, H.N.3
Demp, S.4
Van Kuilenbur, A.B.P.5
-
3
-
-
0030834976
-
Isolation and characterization of cDNA corresponding to an additional member of the human histone deacetylase gene family
-
Yang W-M, Yao Y-L, Sun J-M, et al. Isolation and characterization of cDNA corresponding to an additional member of the human histone deacetylase gene family. J Biol Chem. 1997;272:28001-28007.
-
(1997)
J Biol Chem
, vol.272
, pp. 28001-28007
-
-
Yang, W.-M.1
Yao, Y.-L.2
Sun, J.-M.3
-
4
-
-
0034730127
-
Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone deacetylase
-
Richon VM, Sandhoff TW, Rifkind RA, Marks PA. Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone deacetylase. Proc Natl Acad Sci U S A. 2000;97:10014-10019.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 10014-10019
-
-
Richon, V.M.1
Sandhoff, T.W.2
Rifkind, R.A.3
Marks, P.A.4
-
5
-
-
0035965343
-
Histone Deacetylase is a Direct Target of Valproic Acid, a Potent Anticonvulsant, Mood Stabilizer, and Teratogen
-
DOI 10.1074/jbc.M101287200
-
Pheil DJ, Zhang F, Huang EY, et al. Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen. J Biol Chem. 2001;276:36734-36741. (Pubitemid 37384288)
-
(2001)
Journal of Biological Chemistry
, vol.276
, Issue.39
, pp. 36734-36741
-
-
Phiel, C.J.1
Zhang, F.2
Huang, E.Y.3
Guenther, M.G.4
Lazar, M.A.5
Klein, P.S.6
-
6
-
-
34247860871
-
Vorinostat for treatment of cutaneous manifestations of advanced primary cutaneous T-cell lymphoma
-
DOI 10.1158/1078-0432.CCR-06-2672
-
Mann BS, Johnson JR, He K, et al. Vorinostat for treatment of cutaneous manifestations of advanced primary cutaneous T-cell lymphoma. Clin Cancer Res. 2007;13:2318-2322. (Pubitemid 46698579)
-
(2007)
Clinical Cancer Research
, vol.13
, Issue.8
, pp. 2318-2322
-
-
Mann, B.S.1
Johnson, J.R.2
He, K.3
Sridhara, R.4
Abraham, S.5
Booth, B.P.6
Verbois, L.7
Morse, D.E.8
Jee, J.M.9
Pope, S.10
Harapanhalli, R.S.11
Dagher, R.12
Farrell, A.13
Justice, R.14
Pazdur, R.15
-
7
-
-
33846142183
-
HDAC inhibitors overcome first hurdle
-
DOI 10.1038/nbt0107-17, PII NBT010717
-
Garber K. HDAC inhibitors overcome first hurdle. Nat Biotechnol. 2007;25:17-19. (Pubitemid 46087886)
-
(2007)
Nature Biotechnology
, vol.25
, Issue.1
, pp. 17-19
-
-
Garber, K.1
-
8
-
-
33846122993
-
Dimethyl sulfoxide to vorinostat: Development of this histone deacetylase inhibitor as an anticancer drug
-
DOI 10.1038/nbt1272, PII NBT1272
-
Marks PA, Breslow R. Dimethyl sulfoxide to vorinostat: development of this histone deacetylase inhibitor as an anticancer drug. Nat Biotechnol. 2007;25:84-90. (Pubitemid 46087907)
-
(2007)
Nature Biotechnology
, vol.25
, Issue.1
, pp. 84-90
-
-
Marks, P.A.1
Breslow, R.2
-
9
-
-
67349095775
-
Development of vorinostat: Current applications and future perspectives for cancer therapy
-
Richon VM, Garcia-Vargas J, Hardwick JS. Development of vorinostat: current applications and future perspectives for cancer therapy. Cancer Lett. 2009;280:201-210.
-
(2009)
Cancer Lett
, vol.280
, pp. 201-210
-
-
Richon, V.M.1
Garcia-Vargas, J.2
Hardwick, J.S.3
-
10
-
-
33847239896
-
Assessment of developmental toxicity of vorinostat, a histone deacetylase inhibitor, in Sprague-Dawley rats and Dutch Belted rabbits
-
Wise LD, Turner KJ, Kerr JS. Assessment of developmental toxicity of vorinostat, a histone deacetylase inhibitor, in Sprague-Dawley rats and Dutch Belted rabbits. Birth Defects Res (Part B). 2007;80:57-68.
-
(2007)
Birth Defects Res (Part B)
, vol.80
, pp. 57-68
-
-
Wise, L.D.1
Turner, K.J.2
Kerr, J.S.3
-
11
-
-
39849097353
-
Assessment of female and male fertility in Sprague-Dawley rats administered vorinostat, a histone deacetylase inhibitor
-
Wise LD, Spence S, Saldutti LP, Kerr JS. Assessment of female and male fertility in Sprague-Dawley rats administered vorinostat, a histone deacetylase inhibitor. Birth Defects Res (Part B). 2008;83:19-26.
-
(2008)
Birth Defects Res (Part B)
, vol.83
, pp. 19-26
-
-
Wise, L.D.1
Spence, S.2
Saldutti, L.P.3
Kerr, J.S.4
-
12
-
-
84888416010
-
Bacterial reverse mutation test
-
OECD, Section 4, Guideline 471 updated and adopted July 21, Accessed October 25, 2009
-
OECD, Bacterial reverse mutation test. OECD Guidelines for Testing of Chemicals, Section 4, Guideline 471 updated and adopted July 21, 1997. http://oberon.sourceoecd.org/vl=686174/cl=21/nw=1/rpsv/cw/vhosts/oecdjournals/ 1607310x/v1n4/contp1-1.htm. Accessed October 25, 2009.
-
(1997)
OECD Guidelines for Testing of Chemicals
-
-
-
13
-
-
0006898158
-
In vitro mammalian chromosome aberration test
-
OECD, Section 4, Guideline 473 updated and adopted July 21, Accessed October 25, 2009
-
OECD, In vitro mammalian chromosome aberration test. OECD Guidelines for Testing of Chemicals, Section 4, Guideline 473 updated and adopted July 21, 1997. http://oberon.sourceoecd.org/vl=686174/cl=21/nw=1/rpsv/cw/vhosts/ oecdjournals/1607310x/v1n4/contp1-1.htm. Accessed October 25, 2009.
-
(1997)
OECD Guidelines for Testing of Chemicals
-
-
-
14
-
-
84874562357
-
Mammalian erythrocyte micronucleus test
-
OECD, Section 4, Guideline 474 adopted 21 Jul Accessed October 25, 2009
-
OECD, Mammalian erythrocyte micronucleus test. OECD Guidelines for Testing of Chemicals, Section 4, Guideline 474 adopted 21 Jul 1997. http://oberon.sourceoecd.org/vl=686174/cl=21/nw=1/rpsv/cw/vhosts/oecdjournals/ 1607310x/v1n4/contp1-1.htm. Accessed October 25, 2009.
-
(1997)
OECD Guidelines for Testing of Chemicals
-
-
-
15
-
-
0028341175
-
Report from working group on in vitro tests for chromosomal aberrations
-
Galloway SM, Aardema MJ, Ishidate M Jr, et al. Report from working group on in vitro tests for chromosomal aberrations. Mutat Res. 1994;312:1-261.
-
(1994)
Mutat Res
, vol.312
, pp. 1-261
-
-
Galloway, S.M.1
Aardema, M.J.2
Ishidate Jr., M.3
-
16
-
-
33846654082
-
Chromosome aberrations in Chinese hamster and human cells: A comparison using compounds with various genotoxicity profiles
-
Hilliard C, Hill R, Armstrong M, et al. Chromosome aberrations in Chinese hamster and human cells: a comparison using compounds with various genotoxicity profiles. Mutat Res. 2007;616:103-118.
-
(2007)
Mutat Res
, vol.616
, pp. 103-118
-
-
Hilliard, C.1
Hill, R.2
Armstrong, M.3
-
17
-
-
0032565516
-
DNA synthesis inhibition as an indirect mechanism of chromosome aberrations: Comparison of DNA-reactive and non-DNA-reactive clastogens
-
Galloway SM, Miller JE, Armstrong MJ, et al. DNA synthesis inhibition as an indirect mechanism of chromosome aberrations: comparison of DNA-reactive and non-DNA-reactive clastogens. Mutat Res. 1998;400:169-186.
-
(1998)
Mutat Res
, vol.400
, pp. 169-186
-
-
Galloway, S.M.1
Miller, J.E.2
Armstrong, M.J.3
-
18
-
-
0016685233
-
Methods for detecting mutagens with Salmonella/mammalian-microsome mutagenicity test
-
Ames BN, McCann J, Yamasaki E. Methods for detecting mutagens with Salmonella/mammalian-microsome mutagenicity test. Mutat Res. 1975;31:347-364.
-
(1975)
Mutat Res
, vol.31
, pp. 347-364
-
-
Ames, B.N.1
McCann, J.2
Yamasaki, E.3
-
19
-
-
0020533372
-
Revised methods for the Salmonella mutagenicity test
-
Maron DM, Ames BN. Revised methods for the Salmonella mutagenicity test. Mutat Res. 1983;113:173-215. (Pubitemid 13120319)
-
(1983)
Mutation Research
, vol.113
, Issue.3-4
, pp. 173-215
-
-
Maron, D.M.1
Ames, B.N.2
-
20
-
-
25844530777
-
A low volume, high-throughput forward mutation assay in Salmonella typhimurium based on fluorouracil resistance
-
Miller JE, Vlasakova K, Glaab WE, Skopek TR. A low volume, high-throughput forward mutation assay in Salmonella typhimurium based on fluorouracil resistance. Mutat Res. 2005;578:210-224.
-
(2005)
Mutat Res
, vol.578
, pp. 210-224
-
-
Miller, J.E.1
Vlasakova, K.2
Glaab, W.E.3
Skopek, T.R.4
-
21
-
-
25844433671
-
5-Fluorouracil forward mutation assay in Salmonella: Determination of mutational target and spontaneous mutational spectra
-
Glaab WE, Mitchell LS, Miller JE, et al. 5-Fluorouracil forward mutation assay in Salmonella: determination of mutational target and spontaneous mutational spectra. Mutat Res. 2005;578:238-246.
-
(2005)
Mutat Res
, vol.578
, pp. 238-246
-
-
Glaab, W.E.1
Mitchell, L.S.2
Miller, J.E.3
-
22
-
-
0033514454
-
Rapid method for improving slide quality in the bone marrow micronucleus assay; an adapted cellulose column procedure
-
Sun JT, Armstrong MJ, Galloway SM. Rapid method for improving slide quality in the bone marrow micronucleus assay; an adapted cellulose column procedure. Mutat Res. 1999;439:121-126.
-
(1999)
Mutat Res
, vol.439
, pp. 121-126
-
-
Sun, J.T.1
Armstrong, M.J.2
Galloway, S.M.3
-
23
-
-
33646766140
-
+ channels and ultrarapidly activating delayed rectifier potassium current
-
DOI 10.1124/jpet.106.101162
-
Lagrutta A, Wang JX, Fermini B, Salata J. Novel, potent inhibitors of human Kv1.5K+ channels and ultrarapidly activating delayed rectifier potassium current. J Pharmacol Exp Ther. 2006;317:1054-1063. (Pubitemid 43764108)
-
(2006)
Journal of Pharmacology and Experimental Therapeutics
, vol.317
, Issue.3
, pp. 1054-1063
-
-
Lagrutta, A.1
Wang, J.2
Fermini, B.3
Salata, J.J.4
-
24
-
-
33746430610
-
Flunarizine is a highly potent inhibitor of cardiac hERG potassium current
-
Trepakova ES, Dech SJ, Salata JJ. Flunarizine is a highly potent inhibitor of cardiac hERG potassium current. J Cardiovasc Pharm. 2006;47:211-220.
-
(2006)
J Cardiovasc Pharm
, vol.47
, pp. 211-220
-
-
Trepakova, E.S.1
Dech, S.J.2
Salata, J.J.3
-
25
-
-
33644551239
-
Electrocardiogram, hemodynamics, and core body temperatures of the normal freely moving laboratory beagle dog by remote radiotelemetry
-
DOI 10.1016/j.vascn.2005.11.004, PII S1056871905001437
-
Gauvin DV, Tilley LP, Smith FWK Jr, Baird TJ. Electrocardiogram, hemodynamics and core body temperatures of the normal freely moving laboratory beagle dog by remote radiotelemetry. J Pharm Tox Methods. 2006;53:128-139. (Pubitemid 43295660)
-
(2006)
Journal of Pharmacological and Toxicological Methods
, vol.53
, Issue.2
, pp. 128-139
-
-
Gauvin, D.V.1
Tilley, L.P.2
Smith Jr., F.W.K.3
Baird, T.J.4
-
26
-
-
34548480697
-
A highly sensitive canine telemetry model for detection of QT interval prolongation: Studies with moxifloxacin, haloperidol and MK-499
-
Chaves AA, Zingaro GJ, Yordy MA, et al. A highly sensitive canine telemetry model for detection of QT interval prolongation: studies with moxifloxacin, haloperidol and MK-499. J Pharm Tox Methods. 2007;56:103-114.
-
(2007)
J Pharm Tox Methods
, vol.56
, pp. 103-114
-
-
Chaves, A.A.1
Zingaro, G.J.2
Yordy, M.A.3
-
27
-
-
84980098899
-
Die systolendauer in elektrokardiogramm bei normalen menschen und beiherzkranken
-
Fridericia L. Die systolendauer in elektrokardiogramm bei normalen menschen und beiherzkranken. Acta Med Scand. 1920;53:469-486.
-
(1920)
Acta Med Scand
, vol.53
, pp. 469-486
-
-
Fridericia, L.1
-
28
-
-
22444445123
-
Spectrum of effects detected in the rat functional observational battery following oral administration of non-CNS targeted compounds
-
DOI 10.1016/j.vascn.2005.04.005, PII S1056871905000535, Second Annual Focus on Safety Pharmacology
-
Redfern WS, Strang I, Storey S, et al. Spectrum of effects detected in the rat functional observational battery following oral administration of non-CNS targeted compounds. J Pharm Tox Methods. 2005;52:77-82. (Pubitemid 41008631)
-
(2005)
Journal of Pharmacological and Toxicological Methods
, vol.52
, Issue.1
, pp. 77-82
-
-
Redfern, W.S.1
Strang, I.2
Storey, S.3
Heys, C.4
Barnard, C.5
Lawton, K.6
Hammond, T.G.7
Valentin, J.-P.8
-
29
-
-
34548495324
-
An optimised methodology for the neurobehavioural assessment in rodents
-
DOI 10.1016/j.vascn.2007.03.007, PII S1056871907001967, Special Issue: Fourth Annual Focus on Safety Pharmacology
-
Moscardo E, Maurin A, Dorigatti R, et al. An optimised methodology for the neurobehavioural assessment in rodents. J Pharm Tox Methods. 2007;56:239-255. (Pubitemid 47376971)
-
(2007)
Journal of Pharmacological and Toxicological Methods
, vol.56
, Issue.2
, pp. 239-255
-
-
Moscardo, E.1
Maurin, A.2
Dorigatti, R.3
Champeroux, P.4
Richard, S.5
-
30
-
-
0024325823
-
An improved method to correct the QT interval of the electrocardiogram for changes in heart rate
-
DOI 10.1016/0160-5402(89)90015-6
-
Van de Water A, Verheyen J, Xhonneux R, Reneman RS. An improved method to correct the QT interval of the electrocardiogram for change in heart rate. J Pharm Methods. 1989;22:207-217. (Pubitemid 19275446)
-
(1989)
Journal of Pharmacological Methods
, vol.22
, Issue.3
, pp. 207-217
-
-
Van De Water, A.1
Verheyen, J.2
Xhonneux, R.3
Reneman, R.S.4
-
31
-
-
33845615494
-
Cancer biology: Mechanism of antitumour action of vorinostat (suberoylanilide hydroxamic acid), a novel histone deacetylase inhibitor
-
DOI 10.1038/sj.bjc.6603463, PII 6603463
-
Richon VM. Cancer biology: mechanism of antitumour action of vorinostat (suberoylanilide hydroxamic acid), a novel histone deacetylase inhibitor. Br. J Cancer. 2006;95:S2-S6. (Pubitemid 44950782)
-
(2006)
British Journal of Cancer
, vol.95
, Issue.SUPPL. 1
-
-
Richon, V.M.1
-
32
-
-
0019161442
-
Mutagenicity of hydroxamic acids and the probable involvement of carbamoylation
-
Skipper PL, Tannenbaum SR, Thilly WG, et al. Mutagenicity of hydroxamic acids and the probable involvement of carbamoylation. Cancer Res. 1980;40:4704-4708.
-
(1980)
Cancer Res
, vol.40
, pp. 4704-4708
-
-
Skipper, P.L.1
Tannenbaum, S.R.2
Thilly, W.G.3
-
33
-
-
0018905445
-
Mutagenicity of platinum coordination complexes in Salmonella typhimurium
-
Beck DJ, Fisch JE. Mutagenicity of platinum coordination complexes in Salmonella typhimurium. Mutat Res. 1980;77:45-54. (Pubitemid 10163610)
-
(1980)
Mutation Research
, vol.77
, Issue.1
, pp. 45-54
-
-
Beck, D.J.1
Fisch, J.E.2
-
34
-
-
33748754280
-
The histone deacetylase inhibitor trichostatin a has genotoxic effects in human lymphoblasts in vitro
-
DOI 10.1093/toxsci/kfl068
-
Olaharski AJ, Ji Z, Woo J-Y, et al. The histone deacetylase inhibitor Trichostatin A has genotoxic effects in human lymphoblasts in vitro. Toxicol Sci. 2006;93:341-347. (Pubitemid 44400452)
-
(2006)
Toxicological Sciences
, vol.93
, Issue.2
, pp. 341-347
-
-
Olaharski, A.J.1
Ji, Z.2
Woo, J.-Y.3
Lim, S.4
Hubbard, A.E.5
Zhang, L.6
Smith, M.T.7
-
35
-
-
28744449121
-
Comparative mutagenicity of apicidin and apicidin derivatives (SD-0203 and SD-2007), histone deacetylase inhibitors
-
Yoo EJ, Lee BM. Comparative mutagenicity of apicidin and apicidin derivatives (SD-0203 and SD-2007), histone deacetylase inhibitors. J Toxicol Environ Health Part A. 2005;68:2097-2109.
-
(2005)
J Toxicol Environ Health Part A
, vol.68
, pp. 2097-2109
-
-
Yoo, E.J.1
Lee, B.M.2
-
36
-
-
0032965702
-
Characterization of p53 in Chinese hamster cell lines CHO-K1, CHO-WBL and CHL; implications for genotoxicity testing
-
Hu T, Miller CM, Ridder GM, Aardema M. Characterization of p53 in Chinese hamster cell lines CHO-K1, CHO-WBL and CHL; implications for genotoxicity testing. Mutat Res. 1999;426:51-62.
-
(1999)
Mutat Res
, vol.426
, pp. 51-62
-
-
Hu, T.1
Miller, C.M.2
Ridder, G.M.3
Aardema, M.4
-
39
-
-
0034086168
-
Histone deacetylase inhibitors trigger a G2 checkpoint in normal cells that is defective in tumor cells
-
Qiu L, Burgess A, Fairlie DP, et al. Histone deacetylase inhibitors trigger a G2 checkpoint in normal cells that is defective in tumor cells. Mol Biol Cell. 2000;11:2069-2083. (Pubitemid 30408065)
-
(2000)
Molecular Biology of the Cell
, vol.11
, Issue.6
, pp. 2069-2083
-
-
Qiu, L.1
Burgess, A.2
Fairlie, D.P.3
Leonard, H.4
Parsons, P.G.5
Gabrielli, B.G.6
-
40
-
-
0038677606
-
Inhibition of histone deacetylase activity increases chromosomal instability by the aberrant regulation of mitotic checkpoint activation
-
Shin H-J, Baek K-W, Jeaon A-E, et al. Inhibition of histone deacetylase activity increases chromosomal instability by the aberrant regulation of mitotic checkpoint activation. Oncogene. 2003;22:3853-3858.
-
(2003)
Oncogene
, vol.22
, pp. 3853-3858
-
-
Shin, H.-J.1
Baek, K.-W.2
Jeaon, A.-E.3
-
41
-
-
39849093997
-
Histone deacetylase inhibitors induce mitotic slippage
-
DOI 10.1038/sj.onc.1210779, PII 1210779
-
Stevens FE, Beamish H, Warrener R, Gabrelli B. Histone deacetylase inhibitors induce mitotic slippage. Oncogene. 2008;27:1345-1354. (Pubitemid 351317466)
-
(2008)
Oncogene
, vol.27
, Issue.10
, pp. 1345-1354
-
-
Stevens, F.E.1
Beamish, H.2
Warrener, R.3
Gabrielli, B.4
-
42
-
-
24744434639
-
Induction of polyploidy by histone deacetylase inhibitors: A pathway for antitumor effects
-
Xu W-S, Perez G, Ngo L, et al. Induction of polyploidy by histone deacetylase inhibitors: a pathway for antitumor effects. Cancer Res. 2008;54:7832-7839.
-
(2008)
Cancer Res
, vol.54
, pp. 7832-7839
-
-
Xu, W.-S.1
Perez, G.2
Ngo, L.3
-
43
-
-
0141744707
-
Histone hyperacetylation in mitosis prevents sister chromatid separation and produces chromosome segregation defects
-
DOI 10.1091/mbc.E03-01-0860
-
Cimini D, Mattiuzzo M, Torosantucci L, Degrassi L. Histone deactylation in mitosis prevents sister chromatid separation and produces chromosome segregation defects. Mol Biol Cell. 2003;14:3821-3833. (Pubitemid 37151628)
-
(2003)
Molecular Biology of the Cell
, vol.14
, Issue.9
, pp. 3821-3833
-
-
Cimini, D.1
Mattiuzzo, M.2
Torosantucci, L.3
Degrassi, F.4
-
44
-
-
33846186786
-
Report of the IWGT working group on strategies and interpretation of regulatory in vivo tests. I. Increases in micronucleated bone marrow cells in rodents that do not indicate genotoxic hazards
-
Tweats DJ, Blakey D, Heflich RH, et al. Report of the IWGT working group on strategies and interpretation of regulatory in vivo tests. I. Increases in micronucleated bone marrow cells in rodents that do not indicate genotoxic hazards. Mutat Res. 2007;627:78-91.
-
(2007)
Mutat Res
, vol.627
, pp. 78-91
-
-
Tweats, D.J.1
Blakey, D.2
Heflich, R.H.3
-
45
-
-
33745687975
-
Cardiac monitoring in phase I trials of a novel histone deacetylase (HDAC) inhibitor LAQ824 in patients with advanced solid tumors and hematologic malignancies
-
abstract 3131
-
Rowinsky EK, de Bono J, Deangelo DJ, et al. Cardiac monitoring in phase I trials of a novel histone deacetylase (HDAC) inhibitor LAQ824 in patients with advanced solid tumors and hematologic malignancies [abstract 3131]. J Clin Oncol. 2005;23:22.
-
(2005)
J Clin Oncol
, vol.23
, pp. 22
-
-
Rowinsky, E.K.1
De Bono, J.2
Deangelo, D.J.3
-
46
-
-
33748063974
-
A phase I study of intravenous LBH589, a novel cinnamic hydroxamic acid analogue histone deacetylase inhibitor, in patients with refractory hematologic malignancies
-
DOI 10.1158/1078-0432.CCR-06-0511
-
Giles F, Fischer T, Cortes J, et al. A phase I study of intravenous LBH589, a novel cinnamic hydroxamic acid analogue histone deacetylase inhibitor, in patients with refractory hematologic malignancies. Clin Cancer Res. 2006;12:4628-4635. (Pubitemid 44297814)
-
(2006)
Clinical Cancer Research
, vol.12
, Issue.15
, pp. 4628-4635
-
-
Giles, F.1
Fischer, T.2
Cortes, J.3
Garcia-Manero, G.4
Beck, J.5
Ravandi, F.6
Masson, E.7
Rae, P.8
Laird, G.9
Sharma, S.10
Kantarjian, H.11
Dugan, M.12
Albitar, M.13
Bhalla, K.14
-
47
-
-
21244464349
-
Phase I study of an oral histone deacetylase inhibitor, suberoylanilide hydroxamic acid, in patients with advanced cancer
-
Kelly WK, O'Conner OA, Krug LM, et al. Phase I study of an oral histone deacetylase inhibitor, suberoylanilide hydroxamic acid, in patients with advanced cancer. J Clin Oncol. 2005;23:3923-3931.
-
(2005)
J Clin Oncol
, vol.23
, pp. 3923-3931
-
-
Kelly, W.K.1
O'Conner, O.A.2
Krug, L.M.3
-
48
-
-
72549108593
-
A single supratherapeutic dose of vorinostat does not prolong the QTc interval in patients with advanced cancer
-
in press. Doi:10.1158/1078-0432.CCR-09-1214
-
Munster PN, Rubin EH, Van Belle S et al. A single supratherapeutic dose of vorinostat does not prolong the QTc interval in patients with advanced cancer. Clin Cancer Res. 2009; in press. Doi:10.1158/1078-0432.CCR-09-1214.
-
(2009)
Clin Cancer Res
-
-
Munster, P.N.1
Rubin, E.H.2
Van Belle, S.3
-
49
-
-
33746035691
-
Cardiotoxicity of histone deacetylase inhibitor depsipeptide in patients with metastatic neuroendocrine tumors
-
DOI 10.1158/1078-0432.CCR-05-2689
-
Shah MH, Binkley P, Chan K, et al. Cardiotoxicity of histone deacetylase inhibitor depsipeptide in patients with metastatic neuroendocrine tumors. Clin Cancer Res. 2006;12:3997-4003. (Pubitemid 44078086)
-
(2006)
Clinical Cancer Research
, vol.12
, Issue.13
, pp. 3997-4003
-
-
Shah, M.H.1
Binkley, P.2
Chan, K.3
Xiao, J.4
Arbogast, D.5
Collamore, M.6
Farra, Y.7
Young, D.8
Grever, M.9
-
50
-
-
65249099500
-
Disposition of vorinostat, a novel histone deacetylase inhibitor and anti-cancer agent, in preclinical species
-
Sandhu P, Andrews PA, Baker MP, et al. Disposition of vorinostat, a novel histone deacetylase inhibitor and anti-cancer agent, in preclinical species. Drug Metab Lett. 2007;1:153-161.
-
(2007)
Drug Metab Lett
, vol.1
, pp. 153-161
-
-
Sandhu, P.1
Andrews, P.A.2
Baker, M.P.3
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