-
1
-
-
36749029515
-
Radiosensitization by the histone deacetylase inhibitor PCI-24781
-
Banuelos CA, Banáth JP, MacPhail SH, et al (2007). Radiosensitization by the histone deacetylase inhibitor PCI-24781. Clin Cancer Res, 13, 6816-26.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 6816-6826
-
-
Banuelos, C.A.1
Banáth, J.P.2
MacPhail, S.H.3
-
2
-
-
0035992780
-
Valproate and valproate-analogues: potent tools to fight against cancer
-
Blaheta RA, Nau H, Michaelis M, et al (2002). Valproate and valproate-analogues: potent tools to fight against cancer. Curr Medic Chem, 9, 1417-33.
-
(2002)
Curr Medic Chem
, vol.9
, pp. 1417-1433
-
-
Blaheta, R.A.1
Nau, H.2
Michaelis, M.3
-
4
-
-
33947578115
-
Retinoic acid and histone deacetylase inhibitor BML-210 inhibit proliferation of human cervical cancer HeLa cells
-
Borutinskaite VV, Navakauskiene R, Magnusson KE (2006). Retinoic acid and histone deacetylase inhibitor BML-210 inhibit proliferation of human cervical cancer HeLa cells. Annal NY Acad Sci, 1091, 346-55.
-
(2006)
Annal NY Acad Sci
, vol.1091
, pp. 346-355
-
-
Borutinskaite, V.V.1
Navakauskiene, R.2
Magnusson, K.E.3
-
5
-
-
33845898832
-
Phase I dose escalation clinical trial of phenylbutyrate sodium administered twice daily to patients with advanced solid tumors
-
Camacho LH, Olson J, Tong WP, et al (2007). Phase I dose escalation clinical trial of phenylbutyrate sodium administered twice daily to patients with advanced solid tumors. Invest New Drugs, 25, 131-8.
-
(2007)
Invest New Drugs
, vol.25
, pp. 131-138
-
-
Camacho, L.H.1
Olson, J.2
Tong, W.P.3
-
6
-
-
0017886958
-
Sodium butyrate inhibits histone deacetylation in cultured cells
-
Candido EPM, Reeves R, Davie JR (1978). Sodium butyrate inhibits histone deacetylation in cultured cells. Cell, 14, 105-13.
-
(1978)
Cell
, vol.14
, pp. 105-113
-
-
Candido, E.P.M.1
Reeves, R.2
Davie, J.R.3
-
7
-
-
0020262762
-
Mechanism of anticonvulsant action of valproate
-
Chapman A, Keane PE, Meldrum BS, et al (1982). Mechanism of anticonvulsant action of valproate. Prog Neurobiol, 19, 315-59.
-
(1982)
Prog Neurobiol
, vol.19
, pp. 315-359
-
-
Chapman, A.1
Keane, P.E.2
Meldrum, B.S.3
-
8
-
-
26844505068
-
Histone acetylation and histone deacetylase activity of magnesium valproate in tumor and peripheral blood of patients with cervical cancer. a phase I study
-
Chávez-Blanco A, Segura-Pacheco B, Pérez-Cárdenas E, et al (2005). Histone acetylation and histone deacetylase activity of magnesium valproate in tumor and peripheral blood of patients with cervical cancer. a phase I study. Mol Cancer, 4, 22.
-
(2005)
Mol Cancer
, vol.4
, pp. 22
-
-
Chávez-Blanco, A.1
Segura-Pacheco, B.2
Pérez-Cárdenas, E.3
-
9
-
-
33645071947
-
Antineoplastic effects of the DNA methylation inhibitor hydralazine and the histone deacetylase inhibitor valproic acid in cancer cell lines
-
Chávez-Blanco A, Perez-Plasencia C, Pérez-Cárdenas E, et al (2006). Antineoplastic effects of the DNA methylation inhibitor hydralazine and the histone deacetylase inhibitor valproic acid in cancer cell lines. Cancer Cell Int, 6.??
-
(2006)
Cancer Cell Int
, vol.6
-
-
Chávez-Blanco, A.1
Perez-Plasencia, C.2
Pérez-Cárdenas, E.3
-
10
-
-
4444278103
-
Antitumor histone deacetylase inhibitors suppress cutaneous radiation syndrome: implications for increasing therapeutic gain in cancer radiotherapy
-
Chung YL, Wang AJ, Yao LF (2004). Antitumor histone deacetylase inhibitors suppress cutaneous radiation syndrome: implications for increasing therapeutic gain in cancer radiotherapy. Mol Cancer Ther, 3, 317-25.
-
(2004)
Mol Cancer Ther
, vol.3
, pp. 317-325
-
-
Chung, Y.L.1
Wang, A.J.2
Yao, L.F.3
-
11
-
-
10544250252
-
Apicidin: a novel antiprotozoal agent that inhibits parasite histone deacetylase
-
Darkin-Rattray SJ, Gurnett AM, Myers RW, et al (1996). Apicidin: a novel antiprotozoal agent that inhibits parasite histone deacetylase. Proc Natl Acad Sci USA, 93, 13143-7.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 13143-13147
-
-
Darkin-Rattray, S.J.1
Gurnett, A.M.2
Myers, R.W.3
-
12
-
-
77955635418
-
Histone deacetylase inhibitor-induced sensitization to TNFalpha/TRAIL-mediated apoptosis in cervical carcinoma cells is dependent on HPV oncogene expression
-
Darvas K, Rosenberger S, Brenner D, et al (2010). Histone deacetylase inhibitor-induced sensitization to TNFalpha/TRAIL-mediated apoptosis in cervical carcinoma cells is dependent on HPV oncogene expression. Int J Cancer, 127, 1384-92.
-
(2010)
Int J Cancer
, vol.127
, pp. 1384-1392
-
-
Darvas, K.1
Rosenberger, S.2
Brenner, D.3
-
13
-
-
78650234864
-
Sodium butyrate with UCN-01 has marked antitumour activity against cervical cancer cells
-
Decrion-Barthod AZ, Bosset M, Plissonnier ML, et al (2010). Sodium butyrate with UCN-01 has marked antitumour activity against cervical cancer cells. Anticancer Res, 30, 4049-61.
-
(2010)
Anticancer Res
, vol.30
, pp. 4049-4061
-
-
Decrion-Barthod, A.Z.1
Bosset, M.2
Plissonnier, M.L.3
-
14
-
-
0033539092
-
Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors
-
Finnin MS, Donigian JR, Cohen A, et al (1999). Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors. Nature, 401, 188-93.
-
(1999)
Nature
, vol.401
, pp. 188-193
-
-
Finnin, M.S.1
Donigian, J.R.2
Cohen, A.3
-
15
-
-
0035833338
-
Inhibitors of histone deacetylase arrest cell cycle and induce apoptosis in cervical carcinoma cells circumventing human papillomavirus oncogene expression
-
Finzer P, Kuntzen C, Soto U, et al (2001). Inhibitors of histone deacetylase arrest cell cycle and induce apoptosis in cervical carcinoma cells circumventing human papillomavirus oncogene expression. Oncogene, 20, 4768-76.
-
(2001)
Oncogene
, vol.20
, pp. 4768-4776
-
-
Finzer, P.1
Kuntzen, C.2
Soto, U.3
-
16
-
-
0344951326
-
Phenylbutyrate inhibits growth of cervical carcinoma cells independent of HPV type and copy number
-
Finzer P, Stöhr M, Seibert N, et al (2003). Phenylbutyrate inhibits growth of cervical carcinoma cells independent of HPV type and copy number. J Cancer Res Clin Oncol, 129, 107-13.
-
(2003)
J Cancer Res Clin Oncol
, vol.129
, pp. 107-113
-
-
Finzer, P.1
Stöhr, M.2
Seibert, N.3
-
17
-
-
0842277812
-
Histone deacetylase (HDAC) inhibitor activation of p21WAF1 involves changes in promoter-associated proteins, including HDAC1
-
Gui CY, Ngo L, Xu WS, et al (2004). Histone deacetylase (HDAC) inhibitor activation of p21WAF1 involves changes in promoter-associated proteins, including HDAC1. Proc Natl Acad Sci USA, 101, 1241-6.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 1241-1246
-
-
Gui, C.Y.1
Ngo, L.2
Xu, W.S.3
-
18
-
-
57749170458
-
The many roles of histone deacetylases in development and physiology: implications for disease and therapy
-
Haberland M, Montgomery RL, Olson EN (2009). The many roles of histone deacetylases in development and physiology: implications for disease and therapy. Nat Rev Genet, 10, 32-42.
-
(2009)
Nat Rev Genet
, vol.10
, pp. 32-42
-
-
Haberland, M.1
Montgomery, R.L.2
Olson, E.N.3
-
19
-
-
0034326799
-
Apicidin, a histone deacetylase inhibitor, inhibits proliferation of tumor cells via induction of p21WAF1/Cip1 and gelsolin
-
Han JW, Ahn SH, Park SH, et al (2000). Apicidin, a histone deacetylase inhibitor, inhibits proliferation of tumor cells via induction of p21WAF1/Cip1 and gelsolin. Cancer Res, 60, 6068-74.
-
(2000)
Cancer Res
, vol.60
, pp. 6068-6074
-
-
Han, J.W.1
Ahn, S.H.2
Park, S.H.3
-
20
-
-
0035839136
-
Translating the histone code
-
Jenuwein T, Allis CD (2001). Translating the histone code. Science, 293, 1074-80.
-
(2001)
Science
, vol.293
, pp. 1074-1080
-
-
Jenuwein, T.1
Allis, C.D.2
-
21
-
-
0033523895
-
Amide analogues of trichostatin A as inhibitors of histone deacetylase and inducers of terminal cell differentiation
-
Jung M, Brosch G, Kölle D, et al (1999). Amide analogues of trichostatin A as inhibitors of histone deacetylase and inducers of terminal cell differentiation. J Medic Chem, 42, 4669-79.
-
(1999)
J Medic Chem
, vol.42
, pp. 4669-4679
-
-
Jung, M.1
Brosch, G.2
Kölle, D.3
-
22
-
-
0035113602
-
MS-275, a histone deacetylase inhibitor, selectively induces transforming growth factor beta type II receptor expression in human breast cancer cells
-
Lee BI, Park SH, Kim JW, et al (2001). MS-275, a histone deacetylase inhibitor, selectively induces transforming growth factor beta type II receptor expression in human breast cancer cells. Cancer Res, 61, 931-4.
-
(2001)
Cancer Res
, vol.61
, pp. 931-934
-
-
Lee, B.I.1
Park, S.H.2
Kim, J.W.3
-
23
-
-
59449084559
-
Combination of proteasome and HDAC inhibitors for uterine cervical cancer treatment
-
Lin Z, Bazzaro M, Wang MC, et al (2009). Combination of proteasome and HDAC inhibitors for uterine cervical cancer treatment. Clin Cancer Res, 15, 570-7.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 570-577
-
-
Lin, Z.1
Bazzaro, M.2
Wang, M.C.3
-
24
-
-
53949094562
-
Apicidin down-regulates human papillomavirus type 16 E6 and E7 transcripts and proteins in SiHa cervical cancer cells
-
Luczak MW, Agodzinski PP (2008). Apicidin down-regulates human papillomavirus type 16 E6 and E7 transcripts and proteins in SiHa cervical cancer cells. Cancer Lett, 272, 53-60.
-
(2008)
Cancer Lett
, vol.272
, pp. 53-60
-
-
Luczak, M.W.1
Agodzinski, P.P.2
-
25
-
-
34247880441
-
Development of histone deacetylase inhibitors for cancer treatment
-
Marchion D, Münster P (2007). Development of histone deacetylase inhibitors for cancer treatment. Expert Rev Anticancer Ther, 7, 583-98.
-
(2007)
Expert Rev Anticancer Ther
, vol.7
, pp. 583-598
-
-
Marchion, D.1
Münster, P.2
-
26
-
-
43049091153
-
A phase II study of vorinostat in the treatment of persistent or recurrent epithelial ovarian or primary peritoneal carcinoma: a Gynecologic Oncology Group study
-
Modesitt SC, Sill M, Hoffman JS, et al (2008). A phase II study of vorinostat in the treatment of persistent or recurrent epithelial ovarian or primary peritoneal carcinoma: a Gynecologic Oncology Group study. Gynecol Oncol, 109, 182-6.
-
(2008)
Gynecol Oncol
, vol.109
, pp. 182-186
-
-
Modesitt, S.C.1
Sill, M.2
Hoffman, J.S.3
-
27
-
-
85008338332
-
Phase I trial of the histone deacetylase inhibitor, valproic acid and the topoisomerase II inhibitor, epirubicin: a clinical and translational study
-
2005 ASCO Annual Meeting Proceedings, 23, abstract no. 3084
-
Munster PN, Marchion DC, Bicaku E, et al (2005). Phase I trial of the histone deacetylase inhibitor, valproic acid and the topoisomerase II inhibitor, epirubicin: a clinical and translational study. J Clin Oncol, 2005 ASCO Annual Meeting Proceedings, 23, abstract no. 3084.
-
(2005)
J Clin Oncol
-
-
Munster, P.N.1
Marchion, D.C.2
Bicaku, E.3
-
28
-
-
64649098653
-
Augmentation of sodium butyrate-induced apoptosis by phosphatidylinositol 3-kinase inhibition in the human cervical cancer cell-line
-
Park JK, Cho CH, Ramachandran S, et al (2006). Augmentation of sodium butyrate-induced apoptosis by phosphatidylinositol 3-kinase inhibition in the human cervical cancer cell-line. Cancer Res Treat, 38, 112-7.
-
(2006)
Cancer Res Treat
, vol.38
, pp. 112-117
-
-
Park, J.K.1
Cho, C.H.2
Ramachandran, S.3
-
29
-
-
0035965343
-
Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen
-
Phiel CJ, Zhang F, Huang EY, et al (2001). Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen. J Biol Chem, 276, 36734-41.
-
(2001)
J Biol Chem
, vol.276
, pp. 36734-36741
-
-
Phiel, C.J.1
Zhang, F.2
Huang, E.Y.3
-
30
-
-
3042785975
-
A review of depsipeptide and other histone deacetylase inhibitors in clinical trials
-
Piekarz R, Bates S (2004). A review of depsipeptide and other histone deacetylase inhibitors in clinical trials. Curr Pharm Design, 10, 2289-98.
-
(2004)
Curr Pharm Design
, vol.10
, pp. 2289-2298
-
-
Piekarz, R.1
Bates, S.2
-
31
-
-
0036132096
-
Estimates of the world-wide prevalence of cancer for 25 sites in the adult population
-
Pisani P, Bray F, Parkin DM (2002). Estimates of the world-wide prevalence of cancer for 25 sites in the adult population. Int J Cancer, 97, 72-81.
-
(2002)
Int J Cancer
, vol.97
, pp. 72-81
-
-
Pisani, P.1
Bray, F.2
Parkin, D.M.3
-
32
-
-
0038079767
-
The histone deacetylase inhibitor MS-275 promotes differentiation or apoptosis in human leukemia cells through a process regulated by generation of reactive oxygen species and induction of p21CIP1/WAF1
-
Rosato RR, Almenara JA, Grant S (2003). The histone deacetylase inhibitor MS-275 promotes differentiation or apoptosis in human leukemia cells through a process regulated by generation of reactive oxygen species and induction of p21CIP1/WAF1. Cancer Res, 63, 3637-45.
-
(2003)
Cancer Res
, vol.63
, pp. 3637-3645
-
-
Rosato, R.R.1
Almenara, J.A.2
Grant, S.3
-
33
-
-
0035845541
-
The histone deacetylase inhibitor and chemotherapeutic agent suberoylanilide hydroxamic acid (SAHA) induces a cell-death pathway characterized by cleavage of Bid and production of reactive oxygen species
-
Ruefli AA, Ausserlechner MJ, Bernhard D, et al (2001). The histone deacetylase inhibitor and chemotherapeutic agent suberoylanilide hydroxamic acid (SAHA) induces a cell-death pathway characterized by cleavage of Bid and production of reactive oxygen species. Proc Natl Acad Sci USA, 98, 10833-8.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 10833-10838
-
-
Ruefli, A.A.1
Ausserlechner, M.J.2
Bernhard, D.3
-
34
-
-
21244458052
-
Phase I and pharmacokinetic study of MS-275, a histone deacetylase inhibitor, in patients with advanced and refractory solid tumors or lymphoma
-
Ryan QC, Headlee D, Acharya M, et al (2005). Phase I and pharmacokinetic study of MS-275, a histone deacetylase inhibitor, in patients with advanced and refractory solid tumors or lymphoma. J Clin Oncol, 23, 3912-22.
-
(2005)
J Clin Oncol
, vol.23
, pp. 3912-3922
-
-
Ryan, Q.C.1
Headlee, D.2
Acharya, M.3
-
35
-
-
0033551152
-
A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors
-
Saito A, Yamashita T, Mariko Y, et al (1999). A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors. Proc Natl Acad Sci USA, 96, 4592-7.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 4592-4597
-
-
Saito, A.1
Yamashita, T.2
Mariko, Y.3
-
36
-
-
55949119320
-
Valproic acid inhibits the growth of cervical cancer both in vitro and in vivo
-
Sami S, Höti N, Xu HM, et al (2008). Valproic acid inhibits the growth of cervical cancer both in vitro and in vivo. J Biochem, 144, 357-62.
-
(2008)
J Biochem
, vol.144
, pp. 357-362
-
-
Sami, S.1
Höti, N.2
Xu, H.M.3
-
37
-
-
0033850625
-
FR901228 causes mitotic arrest but does not alter microtubule polymerization
-
Sandor V, Robbins AR, Robey R, et al (2000). FR901228 causes mitotic arrest but does not alter microtubule polymerization. Anti-Cancer Drugs, 11, 445-54.
-
(2000)
Anti-Cancer Drugs
, vol.11
, pp. 445-454
-
-
Sandor, V.1
Robbins, A.R.2
Robey, R.3
-
38
-
-
0034610814
-
The language of covalent histone modifications
-
Strahl BD, Allis CD (2000). The language of covalent histone modifications. Nature, 403, 41-5.
-
(2000)
Nature
, vol.403
, pp. 41-45
-
-
Strahl, B.D.1
Allis, C.D.2
-
39
-
-
0033614993
-
Synthesis and histone deacetylase inhibitory activity of new benzamide derivatives
-
Suzuki T, Ando T, Tsuchiya K, et al (1999). Synthesis and histone deacetylase inhibitory activity of new benzamide derivatives. J Medic Chem, 42, 3001-3.
-
(1999)
J Medic Chem
, vol.42
, pp. 3001-3003
-
-
Suzuki, T.1
Ando, T.2
Tsuchiya, K.3
-
40
-
-
10044225745
-
Human ovarian carcinoma cells: histone deacetylase inhibitors exhibit antiproliferative activity and potently induce apoptosis
-
Takai N, Kawamata N, Gui D, et al (2004). Human ovarian carcinoma cells: histone deacetylase inhibitors exhibit antiproliferative activity and potently induce apoptosis. Cancer, 101, 2760-70.
-
(2004)
Cancer
, vol.101
, pp. 2760-2770
-
-
Takai, N.1
Kawamata, N.2
Gui, D.3
-
41
-
-
33645817023
-
Anticancer activity of MS-275, a novel histone deacetylase inhibitor, against human endometrial cancer cells
-
Takai N, Ueda T, Nishida M, et al (2006a). Anticancer activity of MS-275, a novel histone deacetylase inhibitor, against human endometrial cancer cells. Anticancer Res, 26, 939-45.
-
(2006)
Anticancer Res
, vol.26
, pp. 939-945
-
-
Takai, N.1
Ueda, T.2
Nishida, M.3
-
42
-
-
33644559077
-
M344 is a novel synthesized histone deacetylase inhibitor that induces growth inhibition, cell cycle arrest, and apoptosis in human endometrial cancer and ovarian cancer cells
-
Takai N, Ueda T, Nishida M, et ak (2006b). M344 is a novel synthesized histone deacetylase inhibitor that induces growth inhibition, cell cycle arrest, and apoptosis in human endometrial cancer and ovarian cancer cells. Gynecol Oncol, 101, 108-13.
-
(2006)
Gynecol Oncol
, vol.101
, pp. 108-113
-
-
Takai, N.1
Ueda, T.2
Nishida, M.3
-
43
-
-
79958796417
-
Histone deacetylase inhibitors induce growth inhibition, cell cycle arrest and apoptosis in human cervical cancer cells
-
Eds Rolland GZ. Nova Science Publishers Inc., Hauppauge, NY, USA
-
Takai N, Koeffler HP, Narahara H (2007a). Histone deacetylase inhibitors induce growth inhibition, cell cycle arrest and apoptosis in human cervical cancer cells. In 'New Research on Cervical Cancer', Eds Rolland GZ. Nova Science Publishers Inc., Hauppauge, NY, USA. pp 175-88.
-
(2007)
New Research on Cervical Cancer
, pp. 175-188
-
-
Takai, N.1
Koeffler, H.P.2
Narahara, H.3
-
44
-
-
35548967147
-
Human endometrial and ovarian cancer cells: histone deacetylase inhibitors exhibit antiproliferative activity, potently induce cell cycle arrest, and stimulate apoptosis
-
Takai N, Narahara H (2007b). Human endometrial and ovarian cancer cells: histone deacetylase inhibitors exhibit antiproliferative activity, potently induce cell cycle arrest, and stimulate apoptosis. Curr Med Chem, 14, 2548-53.
-
(2007)
Curr Med Chem
, vol.14
, pp. 2548-2553
-
-
Takai, N.1
Narahara, H.2
-
45
-
-
79951847599
-
Histone deacetylase inhibitor therapy in epithelial ovarian cancer
-
Takai N, Narahara H (2010a). Histone deacetylase inhibitor therapy in epithelial ovarian cancer. J Oncol, ??.
-
(2010)
J Oncol
-
-
Takai, N.1
Narahara, H.2
-
46
-
-
77957293178
-
Preclinical studies of chemotherapy using histone deacetylase inhibitors in endometrial cancer
-
Takai N, Narahara H (2010b). Preclinical studies of chemotherapy using histone deacetylase inhibitors in endometrial cancer. Obstet Gynecol Int, ??.
-
(2010)
Obstet Gynecol Int
-
-
Takai, N.1
Narahara, H.2
-
47
-
-
0035888083
-
Sodium butyrate induces growth arrest and senescence-like phenotypes in gynecologic cancer cells
-
Terao Y, Nishida J, Horiuchi S, et al (2001). Sodium butyrate induces growth arrest and senescence-like phenotypes in gynecologic cancer cells. Int J Cancer, 94, 257-67.
-
(2001)
Int J Cancer
, vol.94
, pp. 257-267
-
-
Terao, Y.1
Nishida, J.2
Horiuchi, S.3
-
48
-
-
0017284850
-
A new antifungal antibiotic, trichostatin
-
Tsuji N, Kobayashi M, Nagashima K (1976). A new antifungal antibiotic, trichostatin. J Antibiot, 29, 1-6.
-
(1976)
J Antibiot
, vol.29
, pp. 1-6
-
-
Tsuji, N.1
Kobayashi, M.2
Nagashima, K.3
-
49
-
-
0018114158
-
Trichostatin C, a glucopyranosyl hydroxamate
-
Tsuji N, Kobayashi M (1978). Trichostatin C, a glucopyranosyl hydroxamate. J Antibiot, 31, 939-44.
-
(1978)
J Antibiot
, vol.31
, pp. 939-944
-
-
Tsuji, N.1
Kobayashi, M.2
-
50
-
-
33847796188
-
Apicidin, a novel histone deacetylase inhibitor, has profound anti-growth activity in human endometrial and ovarian cancer cells
-
Ueda T, Takai N, Nishida M, et al (2007). Apicidin, a novel histone deacetylase inhibitor, has profound anti-growth activity in human endometrial and ovarian cancer cells. Int J Mol Med, 19, 301-8.
-
(2007)
Int J Mol Med
, vol.19
, pp. 301-308
-
-
Ueda, T.1
Takai, N.2
Nishida, M.3
-
51
-
-
0029693220
-
The expression of a small fraction of cellular genes is changed in response to histone hyperacetylation
-
Van Lint C, Emiliani S, Verdin E (1996). The expression of a small fraction of cellular genes is changed in response to histone hyperacetylation. Gene Expression, 5, 245-53.
-
(1996)
Gene Expression
, vol.5
, pp. 245-253
-
-
Van Lint, C.1
Emiliani, S.2
Verdin, E.3
-
52
-
-
3643104150
-
Therapeutic targeting of transcription in acute promyelocytic leukemia by use of an inhibitor of histone deacetylase
-
Warrell Jr RP, He LZ, Richon V, et al (1998). Therapeutic targeting of transcription in acute promyelocytic leukemia by use of an inhibitor of histone deacetylase. J Natl Cancer Inst, 90, 1621-5.
-
(1998)
J Natl Cancer Inst
, vol.90
, pp. 1621-1625
-
-
Warrell Jr., R.P.1
He, L.Z.2
Richon, V.3
-
53
-
-
33750288048
-
Intrinsic apoptotic and thioredoxin pathways in human prostate cancer cell response to histone deacetylase inhibitor
-
Xu W, Ngo L, Perez G, et al (2006). Intrinsic apoptotic and thioredoxin pathways in human prostate cancer cell response to histone deacetylase inhibitor. Proc Natl Acad Sci USA, 103, 15540-5.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 15540-15545
-
-
Xu, W.1
Ngo, L.2
Perez, G.3
-
54
-
-
3042618526
-
Enhancement of radiation sensitivity of human squamous carcinoma cells by histone deacetylase inhibitors
-
Zhang Y, Jung M, Dritschilo A, et al (2004). Enhancement of radiation sensitivity of human squamous carcinoma cells by histone deacetylase inhibitors. Radiat Res, 161, 667-74.
-
(2004)
Radiat Res
, vol.161
, pp. 667-674
-
-
Zhang, Y.1
Jung, M.2
Dritschilo, A.3
|