-
1
-
-
0030916336
-
What's up and down with histone deacetylation and transcription?
-
Pazin MJ, Kadonaga JT (1997) What's up and down with histone deacetylation and transcription? Cell 89: 325-328
-
(1997)
Cell
, vol.89
, pp. 325-328
-
-
Pazin, M.J.1
Kadonaga, J.T.2
-
2
-
-
0034610814
-
The language of covalent histone modifications
-
Strahl BD, Allis CD (2000) The language of covalent histone modifications. Nature 403: 41-45
-
(2000)
Nature
, vol.403
, pp. 41-45
-
-
Strahl, B.D.1
Allis, C.D.2
-
3
-
-
0032030770
-
Histone acetylation and transcriptional regulatory mechanisms
-
Struhl K (1998) Histone acetylation and transcriptional regulatory mechanisms. Genes Dev 12: 599-606
-
(1998)
Genes Dev
, vol.12
, pp. 599-606
-
-
Struhl, K.1
-
4
-
-
0033000990
-
Histone acetylases and deacetylases in cell proliferation
-
Kouzarides T (1999) Histone acetylases and deacetylases in cell proliferation. Curr Opin Genet Dev 9: 40-48
-
(1999)
Curr Opin Genet Dev
, vol.9
, pp. 40-48
-
-
Kouzarides, T.1
-
5
-
-
0030798245
-
Histone acetylation in chroma tin structure and transcription
-
Grunstein M (1997) Histone acetylation in chroma tin structure and transcription. Nature 389: 349-352
-
(1997)
Nature
, vol.389
, pp. 349-352
-
-
Grunstein, M.1
-
6
-
-
0032055037
-
Covalent modifications of histones: Expression from chromatin templates
-
Davie JR (1998) Covalent modifications of histones: expression from chromatin templates. Curr Opin Genet Dev 8: 173-178
-
(1998)
Curr Opin Genet Dev
, vol.8
, pp. 173-178
-
-
Davie, J.R.1
-
8
-
-
0013857650
-
Structural modifications of histones and their possible role in the regulation of ribonucleic acid synthesis
-
Allfrey VG (1966) Structural modifications of histones and their possible role in the regulation of ribonucleic acid synthesis. Proc Can Cancer Conf 6: 313-335
-
(1966)
Proc Can Cancer Conf
, vol.6
, pp. 313-335
-
-
Allfrey, V.G.1
-
9
-
-
0032142918
-
Roles of histone acetyltransferases and deacetylases in gene regulation
-
Kuo MH, Allis CD (1998) Roles of histone acetyltransferases and deacetylases in gene regulation. Bioessays 20: 615-626
-
(1998)
Bioessays
, vol.20
, pp. 615-626
-
-
Kuo, M.H.1
Allis, C.D.2
-
10
-
-
0033837634
-
Regulation of gene expression by transcription factor acetylation
-
Bannister AJ, Miska EA (2000) Regulation of gene expression by transcription factor acetylation. Cell Mol Life Sci 57: 1184-1192
-
(2000)
Cell Mol Life Sci
, vol.57
, pp. 1184-1192
-
-
Bannister, A.J.1
Miska, E.A.2
-
11
-
-
0029984469
-
Tetrahymena histone acetyltransferase A: A homolog to yeast Gcn5p linking histone acetylation to gene activation
-
Brownell JE, Zhou J, Ranalli T, Kobayashi R, Edmondson DG, Roth SY, Allis CD (1996) Tetrahymena histone acetyltransferase A: a homolog to yeast Gcn5p linking histone acetylation to gene activation. Cell 84: 843-851
-
(1996)
Cell
, vol.84
, pp. 843-851
-
-
Brownell, J.E.1
Zhou, J.2
Ranalli, T.3
Kobayashi, R.4
Edmondson, D.G.5
Roth, S.Y.6
Allis, C.D.7
-
12
-
-
0030606239
-
The transcriptional coactivators p300 and CBP are histone acetyltransferases
-
Ogryzko VV, Schiltz RL, Russanova V, Howard BH, Nakatani Y (1996) The transcriptional coactivators p300 and CBP are histone acetyltransferases. Cell 87: 953-959
-
(1996)
Cell
, vol.87
, pp. 953-959
-
-
Ogryzko, V.V.1
Schiltz, R.L.2
Russanova, V.3
Howard, B.H.4
Nakatani, Y.5
-
13
-
-
0030447943
-
The TAF(II)250 subunit of TFIID has histone acetyltransferase activity
-
Mizzen CA, Yang XJ, Kokubo T, Brownell JE, Bannister AJ, Owen-Hughes T, Workman J, Wang L, Berger SL, Kouzarides T et al (1996) The TAF(II)250 subunit of TFIID has histone acetyltransferase activity. Cell 87: 1261-1270
-
(1996)
Cell
, vol.87
, pp. 1261-1270
-
-
Mizzen, C.A.1
Yang, X.J.2
Kokubo, T.3
Brownell, J.E.4
Bannister, A.J.5
Owen-Hughes, T.6
Workman, J.7
Wang, L.8
Berger, S.L.9
Kouzarides, T.10
-
14
-
-
0030768745
-
Steroid receptor coactivator-1 is a histone acetyltransferase
-
Spencer TE, Jenster G, Burcin MM, Allis CD, Zhou J, Mizzen CA, McKenna NJ, Onate SA, Tsai SY et al (1997) Steroid receptor coactivator-1 is a histone acetyltransferase. Nature 389: 194-198
-
(1997)
Nature
, vol.389
, pp. 194-198
-
-
Spencer, T.E.1
Jenster, G.2
Burcin, M.M.3
Allis, C.D.4
Zhou, J.5
Mizzen, C.A.6
McKenna, N.J.7
Onate, S.A.8
Tsai, S.Y.9
-
16
-
-
0035755974
-
Histone deacetylases and cancer: Causes and therapies
-
Marks P, Rifkind RA, Richon VM, Breslow R, Miller T, Kelly WK (2001) Histone deacetylases and cancer: causes and therapies. Nat Rev Cancer 1: 194-202
-
(2001)
Nat Rev Cancer
, vol.1
, pp. 194-202
-
-
Marks, P.1
Rifkind, R.A.2
Richon, V.M.3
Breslow, R.4
Miller, T.5
Kelly, W.K.6
-
17
-
-
4143140016
-
Histone deacetylase inhibitors open new doors in cancer therapy
-
McLaughlin F, La Thangue NB (2004) Histone deacetylase inhibitors open new doors in cancer therapy. Biochem Pharmacol 68: 1139-1144
-
(2004)
Biochem Pharmacol
, vol.68
, pp. 1139-1144
-
-
McLaughlin, F.1
La Thangue, N.B.2
-
18
-
-
0029932598
-
A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p
-
Taunton J, Hassig CA, Schreiber SL (1996) A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p. Science 272: 408-411
-
(1996)
Science
, vol.272
, pp. 408-411
-
-
Taunton, J.1
Hassig, C.A.2
Schreiber, S.L.3
-
19
-
-
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
-
20
-
-
0029856225
-
HDA1 and RPD3 are members of distinct yeast histone deacetylase complexes that regulate silencing and transcription
-
Rundlett SE, Carmen AA, Kobayashi R, Bavykin S, Turner BM, Grunstein M (1996) HDA1 and RPD3 are members of distinct yeast histone deacetylase complexes that regulate silencing and transcription. Proc Natl Acad Sci USA 93: 14503-14508
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 14503-14508
-
-
Rundlett, S.E.1
Carmen, A.A.2
Kobayashi, R.3
Bavykin, S.4
Turner, B.M.5
Grunstein, M.6
-
21
-
-
0032696590
-
HDAC4, a human histone deacetylase related to yeast HDA1, is a transcriptional corepressor
-
Wang AH, Bertos NR, Vezmar M, Pelletier N, Crosato M, Heng HH, Th'ng J, Han J, Yang XJ (1999) HDAC4, a human histone deacetylase related to yeast HDA1, is a transcriptional corepressor. Mol Cell Biol 19: 7816-7827
-
(1999)
Mol Cell Biol
, vol.19
, pp. 7816-7827
-
-
Wang, A.H.1
Bertos, N.R.2
Vezmar, M.3
Pelletier, N.4
Crosato, M.5
Heng, H.H.6
Th'ng, J.7
Han, J.8
Yang, X.J.9
-
22
-
-
0034608955
-
Regulation of histone deacetylase 4 and 5 and transcriptional activity by 14-3-3-dependent cellular localization
-
Grozinger CM, Schreiber SL (2000) Regulation of histone deacetylase 4 and 5 and transcriptional activity by 14-3-3-dependent cellular localization. Proc Natl Acad Sci USA 97: 7835-7840
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 7835-7840
-
-
Grozinger, C.M.1
Schreiber, S.L.2
-
23
-
-
0034659405
-
Active maintenance of mHDA2/mHDAC6 histone-deacetylase in the cytoplasm
-
Verdel A, Gurtet S, Brocard MP, Rousseaux S, Lemercier C, Yoshida M, Khochbin S (2000) Active maintenance of mHDA2/mHDAC6 histone-deacetylase in the cytoplasm. Curr Biol 10: 747-749
-
(2000)
Curr Biol
, vol.10
, pp. 747-749
-
-
Verdel, A.1
Gurtet, S.2
Brocard, M.P.3
Rousseaux, S.4
Lemercier, C.5
Yoshida, M.6
Khochbin, S.7
-
24
-
-
0033964223
-
Isolation of a novel histone deacetylase reveals that class I and class II deacetylases promote SMRT-mediated repression
-
Kao HY, Downes M, Ordentlich P, Evans RM (2000) Isolation of a novel histone deacetylase reveals that class I and class II deacetylases promote SMRT-mediated repression. Genes Dev 14: 55-66
-
(2000)
Genes Dev
, vol.14
, pp. 55-66
-
-
Kao, H.Y.1
Downes, M.2
Ordentlich, P.3
Evans, R.M.4
-
25
-
-
0035907314
-
A dynamic role for HDAC7 in MEF2-mediated muscle differentiation
-
Dressel U, Bailey PJ, Wang SC, Downes M, Evans RM, Muscat GE (2001) A dynamic role for HDAC7 in MEF2-mediated muscle differentiation. J Biol Chem 276: 17007-17013
-
(2001)
J Biol Chem
, vol.276
, pp. 17007-17013
-
-
Dressel, U.1
Bailey, P.J.2
Wang, S.C.3
Downes, M.4
Evans, R.M.5
Muscat, G.E.6
-
26
-
-
0035862199
-
The human histone deacetylase family
-
Gray SG, Ekstrom TJ (2001) The human histone deacetylase family. Exp Cell Res 262: 75-83
-
(2001)
Exp Cell Res
, vol.262
, pp. 75-83
-
-
Gray, S.G.1
Ekstrom, T.J.2
-
27
-
-
0037016696
-
Isolation and characterization of mammalian HDAC10, a novel histone deacetylase
-
Kao HY, Lee CH, Komarov A, Han CC, Evans RM (2002) Isolation and characterization of mammalian HDAC10, a novel histone deacetylase. J Biol Chem 277: 187-193
-
(2002)
J Biol Chem
, vol.277
, pp. 187-193
-
-
Kao, H.Y.1
Lee, C.H.2
Komarov, A.3
Han, C.C.4
Evans, R.M.5
-
28
-
-
0034677535
-
Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase
-
Imai S, Armstrong CM, Kaeberlein M, Guarente L (2000) Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase. Nature 403: 795-800
-
(2000)
Nature
, vol.403
, pp. 795-800
-
-
Imai, S.1
Armstrong, C.M.2
Kaeberlein, M.3
Guarente, L.4
-
30
-
-
0030959244
-
Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression
-
Alland L, Muhle R, Hou H, Jr., Potes J, Chin L, Schreiber-Agus N, DePinho RA (1997) Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression. Nature 387: 49-55
-
(1997)
Nature
, vol.387
, pp. 49-55
-
-
Alland, L.1
Muhle, R.2
Hou Jr., H.3
Potes, J.4
Chin, L.5
Schreiber-Agus, N.6
DePinho, R.A.7
-
31
-
-
17744413444
-
A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression
-
Heinzel T, Lavinsky RM, Mullen TM, Soderstrom M, Laherty CD, Torchia J, Yang WM, Brard G, Ngo SD, Davie JR et al (1997) A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression. Nature 387: 43-48
-
(1997)
Nature
, vol.387
, pp. 43-48
-
-
Heinzel, T.1
Lavinsky, R.M.2
Mullen, T.M.3
Soderstrom, M.4
Laherty, C.D.5
Torchia, J.6
Yang, W.M.7
Brard, G.8
Ngo, S.D.9
Davie, J.R.10
-
32
-
-
0031837109
-
Methylated DNA and MeCPZ recruit histone deacetylase to repress transcription
-
Jones PL, Veenstra GJ, Wade PA, Vermaak D, Kass SU, Landsberger N, Strouboulis J, Wolffe AP (1998) Methylated DNA and MeCPZ recruit histone deacetylase to repress transcription. Nat Genet 19: 187-191
-
(1998)
Nat Genet
, vol.19
, pp. 187-191
-
-
Jones, P.L.1
Veenstra, G.J.2
Wade, P.A.3
Vermaak, D.4
Kass, S.U.5
Landsberger, N.6
Strouboulis, J.7
Wolffe, A.P.8
-
33
-
-
0032574977
-
Transcriptional repression by the methyl-CpG-binding protein MeCPZ involves a histone deacetylase complex
-
Nan X, Ng HH, Johnson CA, Laherty CD, Turner BM, Eisenman RN, Bird A (1998) Transcriptional repression by the methyl-CpG-binding protein MeCPZ involves a histone deacetylase complex. Nature 393: 386-389
-
(1998)
Nature
, vol.393
, pp. 386-389
-
-
Nan, X.1
Ng, H.H.2
Johnson, C.A.3
Laherty, C.D.4
Turner, B.M.5
Eisenman, R.N.6
Bird, A.7
-
34
-
-
0032450550
-
Histone deacetylase directs the dominant silencing of transcription in chromatin: Association with MeCPZ and the Mi-Z chromodomain SWI/SNF ATPase
-
Wade PA, Jones PL, Vermaak D, Veenstra GJ, Imhof A, Sera T, Tse C, Ge H, Shi YB, Hansen JC et al (1998) Histone deacetylase directs the dominant silencing of transcription in chromatin: association with MeCPZ and the Mi-Z chromodomain SWI/SNF ATPase. Cold Spring Harb Symp Quant Biol 63: 435-445
-
(1998)
Cold Spring Harb Symp Quant Biol
, vol.63
, pp. 435-445
-
-
Wade, P.A.1
Jones, P.L.2
Vermaak, D.3
Veenstra, G.J.4
Imhof, A.5
Sera, T.6
Tse, C.7
Ge, H.8
Shi, Y.B.9
Hansen, J.C.10
-
35
-
-
0033215387
-
Transcriptional repression by wild-type p53 utilizes histone deacetylases, mediated by interaction with mSin3a
-
Murphy M, Ahn J, Walker KK, Hoffman WH, Evans RM, Levine AJ, George DL (1999) Transcriptional repression by wild-type p53 utilizes histone deacetylases, mediated by interaction with mSin3a. Genes Dev 13: 2490-2501
-
(1999)
Genes Dev
, vol.13
, pp. 2490-2501
-
-
Murphy, M.1
Ahn, J.2
Walker, K.K.3
Hoffman, W.H.4
Evans, R.M.5
Levine, A.J.6
George, D.L.7
-
36
-
-
0031007189
-
Histone deacetylase activity is required for full transcriptional repression by mSin3A
-
Hassig CA, Fleischer TC, Billin AN, Schreiber SL, Ayer DE (1997) Histone deacetylase activity is required for full transcriptional repression by mSin3A. Cell 89: 341-347
-
(1997)
Cell
, vol.89
, pp. 341-347
-
-
Hassig, C.A.1
Fleischer, T.C.2
Billin, A.N.3
Schreiber, S.L.4
Ayer, D.E.5
-
37
-
-
0030916729
-
Histone deacetylases and SAP18, a novel polypeptide, are components of a human Sin3 complex
-
Zhang Y, Iratni R, Erdjument-Bromage H, Tempst P, Reinberg D (1997) Histone deacetylases and SAP18, a novel polypeptide, are components of a human Sin3 complex. Cell 89: 357-364
-
(1997)
Cell
, vol.89
, pp. 357-364
-
-
Zhang, Y.1
Iratni, R.2
Erdjument-Bromage, H.3
Tempst, P.4
Reinberg, D.5
-
38
-
-
0034045040
-
Histone deacetylases, transcriptional control, and cancer
-
Cress WD, Seto E (2000) Histone deacetylases, transcriptional control, and cancer. J Cell Physiol 184: 1-16
-
(2000)
J Cell Physiol
, vol.184
, pp. 1-16
-
-
Cress, W.D.1
Seto, E.2
-
39
-
-
0034617261
-
Histone deacetylases specifically down-regulate p53-dependent gene activation
-
Juan LJ, Shia WJ, Chen MH, Yang WM, Seto E, Lin YS, Wu CW (2000) Histone deacetylases specifically down-regulate p53-dependent gene activation. J Biol Chem 275: Z0436-Z0443
-
(2000)
J Biol Chem
, vol.275
-
-
Juan, L.J.1
Shia, W.J.2
Chen, M.H.3
Yang, W.M.4
Seto, E.5
Lin, Y.S.6
Wu, C.W.7
-
40
-
-
0031239891
-
Acetylation of general transcription factors by histone acetyltransferases
-
Imhof A, Yang XJ, Ogryzko W, Nakatani Y, Wolffe AP, Ge H (1997) Acetylation of general transcription factors by histone acetyltransferases. Curr Biol 7: 689-692
-
(1997)
Curr Biol
, vol.7
, pp. 689-692
-
-
Imhof, A.1
Yang, X.J.2
Ogryzko, W.3
Nakatani, Y.4
Wolffe, A.P.5
Ge, H.6
-
41
-
-
0032506542
-
Regulation of activity of the transcription factor GATA-1 by acetylation
-
Boyes J, Byfield P, Nakatani Y, Ogryzko V (1998) Regulation of activity of the transcription factor GATA-1 by acetylation. Nature 396: 594-598
-
(1998)
Nature
, vol.396
, pp. 594-598
-
-
Boyes, J.1
Byfield, P.2
Nakatani, Y.3
Ogryzko, V.4
-
42
-
-
0242637101
-
Direct acetylation of the estrogen receptor alpha hinge region by p300 regulates transactivation and hormone sensitivity
-
Wang C, Fu M, Angeletti RH, Siconolfi-Baez L, Reutens AT, Albanese C, Lisanti MP, Katzenellenbogen BS, Kato S, Hopp T et al (2001) Direct acetylation of the estrogen receptor alpha hinge region by p300 regulates transactivation and hormone sensitivity. J Biol Chem 276: 18375-18383
-
(2001)
J Biol Chem
, vol.276
, pp. 18375-18383
-
-
Wang, C.1
Fu, M.2
Angeletti, R.H.3
Siconolfi-Baez, L.4
Reutens, A.T.5
Albanese, C.6
Lisanti, M.P.7
Katzenellenbogen, B.S.8
Kato, S.9
Hopp, T.10
-
43
-
-
0032484989
-
Retinoblastoma protein recruits histone deacetylase to repress transcription
-
Brehm A, Miska EA, McCance DJ, Reid JL, Bannister AJ, Kouzarides T (1998) Retinoblastoma protein recruits histone deacetylase to repress transcription. Nature 391: 597-601
-
(1998)
Nature
, vol.391
, pp. 597-601
-
-
Brehm, A.1
Miska, E.A.2
McCance, D.J.3
Reid, J.L.4
Bannister, A.J.5
Kouzarides, T.6
-
44
-
-
0032484904
-
Retinoblastoma protein represses transcription by recruiting a histone deacetylase
-
Magnaghi-Jaulin L, Groisman R, Naguibneva I, Robin P, Lorain S, Le Villain JP, Troalen F, Trouche D, Harel-Bellan A (1998) Retinoblastoma protein represses transcription by recruiting a histone deacetylase. Nature 391: 601-605
-
(1998)
Nature
, vol.391
, pp. 601-605
-
-
Magnaghi-Jaulin, L.1
Groisman, R.2
Naguibneva, I.3
Robin, P.4
Lorain, S.5
Le Villain, J.P.6
Troalen, F.7
Trouche, D.8
Harel-Bellan, A.9
-
45
-
-
0037205476
-
Phosphatase inhibition leads to histone deacetylases 1 and 2 phosphorylation and disruption of corepressor interactions
-
Galasinski SC, Resing KA, Goodrich JA, Ahn NG (2002) Phosphatase inhibition leads to histone deacetylases 1 and 2 phosphorylation and disruption of corepressor interactions. J Biol Chem 277: 19618-19626
-
(2002)
J Biol Chem
, vol.277
, pp. 19618-19626
-
-
Galasinski, S.C.1
Resing, K.A.2
Goodrich, J.A.3
Ahn, N.G.4
-
46
-
-
0035724413
-
The smrt and n-cor corepressors are activating cofactors for histone deacetylase 3
-
Guenther MG, Barak O, Lazar MA (2001) The smrt and n-cor corepressors are activating cofactors for histone deacetylase 3. Mol Cell Biol 21: 6091-6101
-
(2001)
Mol Cell Biol
, vol.21
, pp. 6091-6101
-
-
Guenther, M.G.1
Barak, O.2
Lazar, M.A.3
-
47
-
-
0036161439
-
Enzymatic activity associated with class II HDACs is dependent on a multi-protein complex containing HDAC3 and SMRT/N-CoR
-
Fischle W, Dequiedt F, Hendzel MJ, Guenther MG, Lazar MA, Voelter W, Verdin E (2002) Enzymatic activity associated with class II HDACs is dependent on a multi-protein complex containing HDAC3 and SMRT/N-CoR. Mol Cell 9: 45-57
-
(2002)
Mol Cell
, vol.9
, pp. 45-57
-
-
Fischle, W.1
Dequiedt, F.2
Hendzel, M.J.3
Guenther, M.G.4
Lazar, M.A.5
Voelter, W.6
Verdin, E.7
-
49
-
-
0035881078
-
Differential localization of HDAC4 orchestrates muscle differentiation
-
Miska EA, Langley E, Wolf D, Karlsson C, Pines J, Kouzarides T (2001) Differential localization of HDAC4 orchestrates muscle differentiation. Nucleic Acids Res 29: 3439-3447
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 3439-3447
-
-
Miska, E.A.1
Langley, E.2
Wolf, D.3
Karlsson, C.4
Pines, J.5
Kouzarides, T.6
-
50
-
-
0033568028
-
HDAC4 deacetylase associates with and represses the MEF2 transcription factor
-
Miska EA, Karlsson C, Langley E, Nielsen SJ, Pines J, Kouzarides T (1999) HDAC4 deacetylase associates with and represses the MEF2 transcription factor. EMBO J 18: 5099-5107
-
(1999)
EMBO J
, vol.18
, pp. 5099-5107
-
-
Miska, E.A.1
Karlsson, C.2
Langley, E.3
Nielsen, S.J.4
Pines, J.5
Kouzarides, T.6
-
51
-
-
0033568492
-
MEF-2 function is modified by a novel co-repressor, MITR
-
Sparrow DB, Miska EA, Langley E, Reynaud-Deonauth S, Kotecha S, Towers N, Spohr G, Kouzarides T, Mohun TJ (1999) MEF-2 function is modified by a novel co-repressor, MITR. EMBO J 18: 5085-5098
-
(1999)
EMBO J
, vol.18
, pp. 5085-5098
-
-
Sparrow, D.B.1
Miska, E.A.2
Langley, E.3
Reynaud-Deonauth, S.4
Kotecha, S.5
Towers, N.6
Spohr, G.7
Kouzarides, T.8
Mohun, T.J.9
-
52
-
-
0034597816
-
Signal-dependent nuclear export of a histone deacetylase regulates muscle differentiation
-
McKinsey TA, Zhang CL, Lu J, Olson EN (2000) Signal-dependent nuclear export of a histone deacetylase regulates muscle differentiation. Nature 408: 106-111
-
(2000)
Nature
, vol.408
, pp. 106-111
-
-
McKinsey, T.A.1
Zhang, C.L.2
Lu, J.3
Olson, E.N.4
-
53
-
-
18444370302
-
The SUMO E3 ligase RanBP2 promotes modification of the HDAC4 deacetylase
-
Kirsh O, Seeler JS, Pichler A, Gast A, Muller S, Miska E, Mathieu M, Harel-Bellan A, Kouzarides T, Melchior F et al (2002) The SUMO E3 ligase RanBP2 promotes modification of the HDAC4 deacetylase. EMBO J 21: 2682-2691
-
(2002)
EMBO J
, vol.21
, pp. 2682-2691
-
-
Kirsh, O.1
Seeler, J.S.2
Pichler, A.3
Gast, A.4
Muller, S.5
Miska, E.6
Mathieu, M.7
Harel-Bellan, A.8
Kouzarides, T.9
Melchior, F.10
-
54
-
-
0034676439
-
Deacetylation of p53 modulates its effect on cell growth and apoptosis
-
Luo J, Su F, Chen D, Shiloh A, Gu W (2000) Deacetylation of p53 modulates its effect on cell growth and apoptosis. Nature 408: 377-381
-
(2000)
Nature
, vol.408
, pp. 377-381
-
-
Luo, J.1
Su, F.2
Chen, D.3
Shiloh, A.4
Gu, W.5
-
55
-
-
0035913903
-
SIR2(SIRT1) functions as an NAD-dependent p53 deacetylase
-
Vaziri H, Dessain SK, Ng Eaton E, Imai SI, Frye RA, Pandita TK, Guarente L, Weinberg RA (2001) hSIR2(SIRT1) functions as an NAD-dependent p53 deacetylase. Cell 107: 149-159
-
(2001)
Cell
, vol.107
, pp. 149-159
-
-
Vaziri, H.1
Dessain, S.K.2
Ng Eaton, E.3
Imai, S.I.4
Frye, R.A.5
Pandita, T.K.6
Guarente, L.7
Weinberg, R.A.8
-
56
-
-
0035913911
-
Negative control of p53 by Sir2alpha promotes cell survival under stress
-
Luo J, Nikolaev AY, Imai S, Chen D, Su F, Shiloh A, Guarente L, Gu W (2001) Negative control of p53 by Sir2alpha promotes cell survival under stress. Cell 107: 137-148
-
(2001)
Cell
, vol.107
, pp. 137-148
-
-
Luo, J.1
Nikolaev, A.Y.2
Imai, S.3
Chen, D.4
Su, F.5
Shiloh, A.6
Guarente, L.7
Gu, W.8
-
57
-
-
0037093346
-
Human SIR2 deacetylates p53 and antagonizes PML/p53-induced cellular senescence
-
Langley E, Pearson M, Faretta M, Bauer UM, Frye RA, Minucci S, Pelicci PG, Kouzarides T (2002) Human SIR2 deacetylates p53 and antagonizes PML/p53-induced cellular senescence. EMBO J 21: 2383-2396
-
(2002)
EMBO J
, vol.21
, pp. 2383-2396
-
-
Langley, E.1
Pearson, M.2
Faretta, M.3
Bauer, U.M.4
Frye, R.A.5
Minucci, S.6
Pelicci, P.G.7
Kouzarides, T.8
-
58
-
-
0033152703
-
The PML nuclear bodies: Actors or extras?
-
Seeler JS, Dejean A (1999) The PML nuclear bodies: actors or extras? Curr Opin Genet Dev 9: 362-367
-
(1999)
Curr Opin Genet Dev
, vol.9
, pp. 362-367
-
-
Seeler, J.S.1
Dejean, A.2
-
59
-
-
0036898253
-
Acetylation inactivates the transcriptional repressor BCL6
-
Bereshchenko OR, Gu W, Dalla-Favera R (2002) Acetylation inactivates the transcriptional repressor BCL6. Nat Genet 32: 606-613
-
(2002)
Nat Genet
, vol.32
, pp. 606-613
-
-
Bereshchenko, O.R.1
Gu, W.2
Dalla-Favera, R.3
-
60
-
-
0035868764
-
Acetylation of TAF(I)68, a subunit of TIF-IB/SL1, activates RNA polymerase I transcription
-
Muth V, Nadaud S, Grummt I, Voit R (2001) Acetylation of TAF(I)68, a subunit of TIF-IB/SL1, activates RNA polymerase I transcription. EMBO J 20: 1353-1362
-
(2001)
EMBO J
, vol.20
, pp. 1353-1362
-
-
Muth, V.1
Nadaud, S.2
Grummt, I.3
Voit, R.4
-
61
-
-
0037359584
-
The absence of SIR2alpha protein has no effect on global gene silencing in mouse embryonic stem cells
-
McBurney MW, Yang X, Jardine K, Bieman M, Th'ng J, Lemieux M (2003) The absence of SIR2alpha protein has no effect on global gene silencing in mouse embryonic stem cells. Mol Cancer Res 1: 402-409
-
(2003)
Mol Cancer Res
, vol.1
, pp. 402-409
-
-
McBurney, M.W.1
Yang, X.2
Jardine, K.3
Bieman, M.4
Th'ng, J.5
Lemieux, M.6
-
62
-
-
0141814680
-
Developmental defects and p53 hyperacetylation in Sir2 homolog (SIRT1)-deficient mice
-
Cheng HL, Mostoslavsky R, Saito S, Manis JP, Gu Y, Patel P, Bronson R, Appella E, Alt FW, Chua KF (2003) Developmental defects and p53 hyperacetylation in Sir2 homolog (SIRT1)-deficient mice. Proc Natl Acad Sci USA 100: 10794-10799
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 10794-10799
-
-
Cheng, H.L.1
Mostoslavsky, R.2
Saito, S.3
Manis, J.P.4
Gu, Y.5
Patel, P.6
Bronson, R.7
Appella, E.8
Alt, F.W.9
Chua, K.F.10
-
63
-
-
3943054839
-
The Sir2 family of protein deacetylases
-
Blander G, Guarente L (2004) The Sir2 family of protein deacetylases. Annu Rev Biochem 73: 417-435
-
(2004)
Annu Rev Biochem
, vol.73
, pp. 417-435
-
-
Blander, G.1
Guarente, L.2
-
64
-
-
0035962646
-
Chromatin remodeling and transcriptional activation: The cast (in order of appearance)
-
Urnov FD, Wolffe AP (2001) Chromatin remodeling and transcriptional activation: the cast (in order of appearance). Oncogene 20: 2991-3006
-
(2001)
Oncogene
, vol.20
, pp. 2991-3006
-
-
Urnov, F.D.1
Wolffe, A.P.2
-
65
-
-
0034252183
-
Histone acetylation modifiers in the pathogenesis of malignant disease
-
Mahlknecht U, Hoelzer D (2000) Histone acetylation modifiers in the pathogenesis of malignant disease. Mol Med 6: 623-644
-
(2000)
Mol Med
, vol.6
, pp. 623-644
-
-
Mahlknecht, U.1
Hoelzer, D.2
-
67
-
-
0032076229
-
Conjunction dysfunction: CBP/p300 in human disease
-
Giles RH, Peters DJ, Breuning MH (1998) Conjunction dysfunction: CBP/p300 in human disease. Trends Genet 14: 178-183
-
(1998)
Trends Genet
, vol.14
, pp. 178-183
-
-
Giles, R.H.1
Peters, D.J.2
Breuning, M.H.3
-
68
-
-
0034104047
-
Mutations truncating the EP300 acetylase in human cancers
-
Gayther SA, Batley SJ, Linger L, Bannister A, Thorpe K, Chin SF, Daigo Y, Russell P, Wilson A, Sowter HM et al (2000) Mutations truncating the EP300 acetylase in human cancers. Nat Genet 24: 300-303
-
(2000)
Nat Genet
, vol.24
, pp. 300-303
-
-
Gayther, S.A.1
Batley, S.J.2
Linger, L.3
Bannister, A.4
Thorpe, K.5
Chin, S.F.6
Daigo, Y.7
Russell, P.8
Wilson, A.9
Sowter, H.M.10
-
69
-
-
0035339491
-
Defect of histone acetyltransferase activity of the nuclear transcriptional coactivator CBP in Rubinstein-Taybi syndrome
-
Murata T, Kurokawa R, Krones A, Tatsumi K, Ishii M, Taki T, Masuno M, Ohashi H, Yanagisawa M, Rosenfeld MG et al (2001) Defect of histone acetyltransferase activity of the nuclear transcriptional coactivator CBP in Rubinstein-Taybi syndrome. Hum Mol Genet 10: 1071-1076
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1071-1076
-
-
Murata, T.1
Kurokawa, R.2
Krones, A.3
Tatsumi, K.4
Ishii, M.5
Taki, T.6
Masuno, M.7
Ohashi, H.8
Yanagisawa, M.9
Rosenfeld, M.G.10
-
70
-
-
0026632471
-
Loss of heterozygosity on chromosome 16 in hepatocellular carcinoma
-
Sakai K, Nagahara H, Abe K, Obata H (1992) Loss of heterozygosity on chromosome 16 in hepatocellular carcinoma. J Gastroenterol Hepatol 7: 288-292
-
(1992)
J Gastroenterol Hepatol
, vol.7
, pp. 288-292
-
-
Sakai, K.1
Nagahara, H.2
Abe, K.3
Obata, H.4
-
71
-
-
9544220768
-
The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein
-
Borrow J, Stanton VP Jr, Andresen JM, Becher R, Behm FG, Chaganti RS, Civin CI, Disteche C, Dube I, Frischauf AM et al (1996) The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein. Nat Genet 14: 33-41
-
(1996)
Nat Genet
, vol.14
, pp. 33-41
-
-
Borrow, J.1
Stanton Jr., V.P.2
Andresen, J.M.3
Becher, R.4
Behm, F.G.5
Chaganti, R.S.6
Civin, C.I.7
Disteche, C.8
Dube, I.9
Frischauf, A.M.10
-
72
-
-
0032530267
-
Acute mixed lineage leukemia with an inv(8)(p11q13) resulting in fusion of the genes for MOZ and TIF2
-
Liang J, Prouty L, Williams BJ, Dayton MA, Blanchard KL (1998) Acute mixed lineage leukemia with an inv(8)(p11q13) resulting in fusion of the genes for MOZ and TIF2. Blood 92: 2118-2122
-
(1998)
Blood
, vol.92
, pp. 2118-2122
-
-
Liang, J.1
Prouty, L.2
Williams, B.J.3
Dayton, M.A.4
Blanchard, K.L.5
-
73
-
-
0030792867
-
All patients with the T(11;16) (q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders
-
Rowley JD, Reshmi S, Sobulo O, Musvee T, Anastasi J, Raimondi S, Schneider NR, Barredo JC, Cantu ES, Schlegelberger B et al (1997) All patients with the T(11;16) (q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders. Blood 90: 535-541
-
(1997)
Blood
, vol.90
, pp. 535-541
-
-
Rowley, J.D.1
Reshmi, S.2
Sobulo, O.3
Musvee, T.4
Anastasi, J.5
Raimondi, S.6
Schneider, N.R.7
Barredo, J.C.8
Cantu, E.S.9
Schlegelberger, B.10
-
74
-
-
0032433144
-
Role of histone deacetylases in acute leukemia
-
Fenrick R, Hiebert SW (1998) Role of histone deacetylases in acute leukemia. J Cell Biochem Suppl 31: 194-202
-
(1998)
J Cell Biochem Suppl
, vol.31
, pp. 194-202
-
-
Fenrick, R.1
Hiebert, S.W.2
-
75
-
-
0035962636
-
Transcription therapy for cancer
-
Pandolfi PP (2001) Transcription therapy for cancer. Oncogene 20: 3116-3127
-
(2001)
Oncogene
, vol.20
, pp. 3116-3127
-
-
Pandolfi, P.P.1
-
76
-
-
0030747725
-
Identification of positively and negatively acting elements regulating expression of the E2F2 gene in response to cell growth signals
-
Sears R, Ohtani K, Nevins JR (1997) Identification of positively and negatively acting elements regulating expression of the E2F2 gene in response to cell growth signals. Mol Cell Biol 17: 5227-5235
-
(1997)
Mol Cell Biol
, vol.17
, pp. 5227-5235
-
-
Sears, R.1
Ohtani, K.2
Nevins, J.R.3
-
77
-
-
0032451007
-
The Mad protein family links transcriptional repression to cell differentiation
-
McArthur GA, Laherty CD, Queva C, Hurlin PJ, Loo L, James L, Grandori C, Gallant P, Shiio Y, Hokanson WC et al (1998) The Mad protein family links transcriptional repression to cell differentiation. Cold Spring Harb Symp Quant Biol 63: 423-433
-
(1998)
Cold Spring Harb Symp Quant Biol
, vol.63
, pp. 423-433
-
-
McArthur, G.A.1
Laherty, C.D.2
Queva, C.3
Hurlin, P.J.4
Loo, L.5
James, L.6
Grandori, C.7
Gallant, P.8
Shiio, Y.9
Hokanson, W.C.10
-
78
-
-
0032905924
-
Myc target genes involved in cell growth, apoptosis, and metabolism
-
Dang CV (1999) c-Myc target genes involved in cell growth, apoptosis, and metabolism. Mol Cell Biol 19: 1-11
-
(1999)
Mol Cell Biol
, vol.19
, pp. 1-11
-
-
Dang, C.V.1
-
79
-
-
0033557497
-
Ski is a component of the histone deacetylase complex required for transcriptional repression by Mad and thyroid hormone receptor
-
Nomura T, Khan MM, Kaul SC, Dong HD, Wadhwa R, Colmenares C, Kohno I, Ishii S (1999) Ski is a component of the histone deacetylase complex required for transcriptional repression by Mad and thyroid hormone receptor. Genes Dev 13: 412-423
-
(1999)
Genes Dev
, vol.13
, pp. 412-423
-
-
Nomura, T.1
Khan, M.M.2
Kaul, S.C.3
Dong, H.D.4
Wadhwa, R.5
Colmenares, C.6
Kohno, I.7
Ishii, S.8
-
80
-
-
0030678627
-
Role of the retinoblastoma protein in the pathogenesis of human cancer
-
Sellers WR, Kaelin WG Jr (1997) Role of the retinoblastoma protein in the pathogenesis of human cancer. J Clin Oncol 15: 3301-3312
-
(1997)
J Clin Oncol
, vol.15
, pp. 3301-3312
-
-
Sellers, W.R.1
Kaelin Jr., W.G.2
-
81
-
-
0029921317
-
Genetic alterations of cyclins, cyclin-dependent kinases, and Cdk inhibitors in human cancer
-
Hall M, Peters G (1996) Genetic alterations of cyclins, cyclin-dependent kinases, and Cdk inhibitors in human cancer. Adv Cancer Res 68: 67-108
-
(1996)
Adv Cancer Res
, vol.68
, pp. 67-108
-
-
Hall, M.1
Peters, G.2
-
82
-
-
0032546017
-
Role of the histone deacetylase complex in acute promyelocytic leukaemia
-
Lin RJ, Nagy L, Inoue S, Shao W, Miller WH Jr, Evans RM (1998) Role of the histone deacetylase complex in acute promyelocytic leukaemia. Nature 391: 811-814
-
(1998)
Nature
, vol.391
, pp. 811-814
-
-
Lin, R.J.1
Nagy, L.2
Inoue, S.3
Shao, W.4
Miller Jr., W.H.5
Evans, R.M.6
-
83
-
-
17144458786
-
Fusion proteins of the retinoic acid receptor-alpha recruit histone deacetylase in promyelocytic leukaemia
-
Grignani F, De Matteis S, Nervi C, Tomassoni L, Gelmetti V, Cioce M, Fanelli M, Ruthardt M, Ferrara FF, Zamir I et al (1998) Fusion proteins of the retinoic acid receptor-alpha recruit histone deacetylase in promyelocytic leukaemia. Nature 391: 815-818
-
(1998)
Nature
, vol.391
, pp. 815-818
-
-
Grignani, F.1
De Matteis, S.2
Nervi, C.3
Tomassoni, L.4
Gelmetti, V.5
Cioce, M.6
Fanelli, M.7
Ruthardt, M.8
Ferrara, F.F.9
Zamir, I.10
-
84
-
-
0034663431
-
PML/RAR alpha fusion protein expression in normal human hematopoietic progenitors dictates myeloid commitment and the promyelocytic phenotype
-
Grignani F, Valtieri M, Gabbianelli M, Gelmetti V, Botta R, Luchetti L, Masella B, Morsilli O, Pelosi E, Samoggia P et al (2000) PML/RAR alpha fusion protein expression in normal human hematopoietic progenitors dictates myeloid commitment and the promyelocytic phenotype. Blood 96: 1531-1537
-
(2000)
Blood
, vol.96
, pp. 1531-1537
-
-
Grignani, F.1
Valtieri, M.2
Gabbianelli, M.3
Gelmetti, V.4
Botta, R.5
Luchetti, L.6
Masella, B.7
Morsilli, O.8
Pelosi, E.9
Samoggia, P.10
-
85
-
-
0031941912
-
Distinct interactions of PML-RARalpha and PLZF-RARalpha with co-repressors determine differential responses to RA in APL
-
He LZ, Guidez F, Tribioli C, Peruzzi D, Ruthardt M, Zelent A, Pandolfi PP (1998) Distinct interactions of PML-RARalpha and PLZF-RARalpha with co-repressors determine differential responses to RA in APL. Nat Genet 18: 126-135
-
(1998)
Nat Genet
, vol.18
, pp. 126-135
-
-
He, L.Z.1
Guidez, F.2
Tribioli, C.3
Peruzzi, D.4
Ruthardt, M.5
Zelent, A.6
Pandolfi, P.P.7
-
86
-
-
0032531688
-
The LAZ3(BCL-6) oncoprotein recruits a SMRT/mSIN3A/histone deacetylase containing complex to mediate transcriptional repression
-
Dhordain P, Lin RJ, Quief S, Lantoine D, Kerckaert JP, Evans RM, Albagli O (1998) The LAZ3(BCL-6) oncoprotein recruits a SMRT/mSIN3A/histone deacetylase containing complex to mediate transcriptional repression. Nucleic Acids Res 26: 4645-4651
-
(1998)
Nucleic Acids Res
, vol.26
, pp. 4645-4651
-
-
Dhordain, P.1
Lin, R.J.2
Quief, S.3
Lantoine, D.4
Kerckaert, J.P.5
Evans, R.M.6
Albagli, O.7
-
87
-
-
0032101379
-
Interaction and functional cooperation of the leukemia-associated factors AML1 and p300 in myeloid cell differentiation
-
Kitabayashi I, Yokoyama A, Shimizu K, Ohki M (1998) Interaction and functional cooperation of the leukemia-associated factors AML1 and p300 in myeloid cell differentiation. EMBO J 17: 2994-3004
-
(1998)
EMBO J
, vol.17
, pp. 2994-3004
-
-
Kitabayashi, I.1
Yokoyama, A.2
Shimizu, K.3
Ohki, M.4
-
88
-
-
0032169858
-
ETO, fusion partner in t(8;21) acute myeloid leukemia, represses transcription by interaction with the human N-CoR/mSin3/HDAC1 complex
-
Wang J, Hoshino T, Redner RL, Kajigaya S, Liu JM (1998) ETO, fusion partner in t(8;21) acute myeloid leukemia, represses transcription by interaction with the human N-CoR/mSin3/HDAC1 complex. Proc Natl Acad Sci USA 95: 10860-10865
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 10860-10865
-
-
Wang, J.1
Hoshino, T.2
Redner, R.L.3
Kajigaya, S.4
Liu, J.M.5
-
89
-
-
0033564130
-
Inhibitors of histone deacetylase relieve ETO-mediated repression and induce differentiation of AML1-ETO leukemia cells
-
Wang J, Saunthararajah Y, Redner RL, Liu JM (1999) Inhibitors of histone deacetylase relieve ETO-mediated repression and induce differentiation of AML1-ETO leukemia cells. Cancer Res 59: 2766-2769
-
(1999)
Cancer Res
, vol.59
, pp. 2766-2769
-
-
Wang, J.1
Saunthararajah, Y.2
Redner, R.L.3
Liu, J.M.4
-
90
-
-
0017284850
-
A new antifungal antibiotic, trichostatin
-
Tsuji N, Kobayashi M, Nagashima K, Wakisaka Y, Koizumi K (1976) A new antifungal antibiotic, trichostatin. J Antibiot (Tokyo) 29: 1-6
-
(1976)
J Antibiot (Tokyo)
, vol.29
, pp. 1-6
-
-
Tsuji, N.1
Kobayashi, M.2
Nagashima, K.3
Wakisaka, Y.4
Koizumi, K.5
-
91
-
-
0024996768
-
Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A
-
Yoshida M, Kijima M, Akita M, Beppu T (1990) Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A. J Biol Chem 265: 17174-17179
-
(1990)
J Biol Chem
, vol.265
, pp. 17174-17179
-
-
Yoshida, M.1
Kijima, M.2
Akita, M.3
Beppu, T.4
-
92
-
-
0033561497
-
Oxamflatin is a novel antitumor compound that inhibits mammalian histone deacetylase
-
Kim YB, Lee KH, Sugita K, Yoshida M, Horinouchi S (1999) Oxamflatin is a novel antitumor compound that inhibits mammalian histone deacetylase. Oncogene 18: 2461-2470
-
(1999)
Oncogene
, vol.18
, pp. 2461-2470
-
-
Kim, Y.B.1
Lee, K.H.2
Sugita, K.3
Yoshida, M.4
Horinouchi, S.5
-
93
-
-
10744229917
-
N-hydroxy-3-phenyl-2-propenamides as novel inhibitors of human histone deacetylase with in vivo antitumor activity: Discovery of (2E)-N-hydroxy-3-[4- [[(2-hydroxyethyl)[2-(1H-indol-3-yl)-ethyl]amino]methyl]phenyl]-2-propenamide (NVP-LAQ824)
-
Remiszewski SW, Sambucetti LC, Bair KW, Bontempo J, Cesarz D, Chandramouli N, Chen R, Cheung M, Cornell-Kennon S, Dean K et al (2003) N-hydroxy-3-phenyl-2-propenamides as novel inhibitors of human histone deacetylase with in vivo antitumor activity: discovery of (2E)-N-hydroxy-3-[4- [[(2-hydroxyethyl)[2-(1H-indol-3-yl)-ethyl]amino]methyl]phenyl]-2-propenamide (NVP-LAQ824). J Med Chem 46: 4609-4624
-
(2003)
J Med Chem
, vol.46
, pp. 4609-4624
-
-
Remiszewski, S.W.1
Sambucetti, L.C.2
Bair, K.W.3
Bontempo, J.4
Cesarz, D.5
Chandramouli, N.6
Chen, R.7
Cheung, M.8
Cornell-Kennon, S.9
Dean, K.10
-
94
-
-
0032539890
-
A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases
-
Richon VM, Emiliani S, Verdin E, Webb Y, Breslow R, Rifkind RA, Marks PA (1998) A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases. Proc Natl Acad Sci USA 95: 3003-3007
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 3003-3007
-
-
Richon, V.M.1
Emiliani, S.2
Verdin, E.3
Webb, Y.4
Breslow, R.5
Rifkind, R.A.6
Marks, P.A.7
-
95
-
-
0034905872
-
Inhibition of transformed cell growth and induction of cellular differentiation by pyroxamide, an inhibitor of histone deacetylase
-
Butler LM, Webb Y, Agus DB, Higgins B, Tolentino TR, Kutko MC, LaQuaglia MP, Drobnjak M, Cordon-Cardo C, Scher HI et al (2001) Inhibition of transformed cell growth and induction of cellular differentiation by pyroxamide, an inhibitor of histone deacetylase. Clin Cancer Res 7: 962-970
-
(2001)
Clin Cancer Res
, vol.7
, pp. 962-970
-
-
Butler, L.M.1
Webb, Y.2
Agus, D.B.3
Higgins, B.4
Tolentino, T.R.5
Kutko, M.C.6
Laquaglia, M.P.7
Drobnjak, M.8
Cordon-Cardo, C.9
Scher, H.I.10
-
96
-
-
0027378351
-
Trapoxin, an antitumor cyclic tetrapeptide, is an irreversible inhibitor of mammalian histone deacetylase
-
Kijima M, Yoshida M, Sugita K, Horinouchi S, Beppu T (1993) Trapoxin, an antitumor cyclic tetrapeptide, is an irreversible inhibitor of mammalian histone deacetylase. J Biol Chem 268: 22429-22435
-
(1993)
J Biol Chem
, vol.268
, pp. 22429-22435
-
-
Kijima, M.1
Yoshida, M.2
Sugita, K.3
Horinouchi, S.4
Beppu, T.5
-
97
-
-
0016031841
-
Mass spectrometric determination of amino acid sequence in Cyl-2, a novel cyclotetrapeptide from Cylindrocladium scoparium
-
Hirota A, Suzuki A, Aizawa K, Tamura S (1974) Mass spectrometric determination of amino acid sequence in Cyl-2, a novel cyclotetrapeptide from Cylindrocladium scoparium. Biomed Mass Spectrom 1: 15-19
-
(1974)
Biomed Mass Spectrom
, vol.1
, pp. 15-19
-
-
Hirota, A.1
Suzuki, A.2
Aizawa, K.3
Tamura, S.4
-
99
-
-
0020519166
-
Studies on WF-3161, a new antitumor antibiotic
-
Umehara K, Nakahara K, Kiyoto S, Iwami M, Okamoto M, Tanaka H, Kohsaka M, Aoki H, Imanaka H (1983) Studies on WF-3161, a new antitumor antibiotic. J Antibiot (Tokyo) 36: 478-483
-
(1983)
J Antibiot (Tokyo)
, vol.36
, pp. 478-483
-
-
Umehara, K.1
Nakahara, K.2
Kiyoto, S.3
Iwami, M.4
Okamoto, M.5
Tanaka, H.6
Kohsaka, M.7
Aoki, H.8
Imanaka, H.9
-
100
-
-
0016366116
-
Isolation and structural clarification of chlamydocin
-
Glosse A, Huguenin R (1974) Isolation and structural clarification of chlamydocin. Helv Chim Acta 57: 533-545
-
(1974)
Helv Chim Acta
, vol.57
, pp. 533-545
-
-
Glosse, A.1
Huguenin, R.2
-
101
-
-
10544250252
-
Apicidin: A novel antiprotozoal agent that inhibits parasite histone deacetylase
-
Darkin-Rattray SJ, Gurnett AM, Myers RW, Dulski PM, Crumley TM, Allocco JJ, Cannova C, Meinke PT, Colletti SL, Bednarek MA et al (1996) Apicidin: a novel antiprotozoal agent that inhibits parasite histone deacetylase. Proc Natl Acad Sci USA 93: 13143-13147
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 13143-13147
-
-
Darkin-Rattray, S.J.1
Gurnett, A.M.2
Myers, R.W.3
Dulski, P.M.4
Crumley, T.M.5
Allocco, J.J.6
Cannova, C.7
Meinke, P.T.8
Colletti, S.L.9
Bednarek, M.A.10
-
102
-
-
0344431240
-
FR901228, a potent antitumor antibiotic, is a novel histone deacetylase inhibitor
-
Nakajima H, Kim YB, Terano H, Yoshida M, Horinouchi S (1998) FR901228, a potent antitumor antibiotic, is a novel histone deacetylase inhibitor. Exp Cell Res 241: 126-133
-
(1998)
Exp Cell Res
, vol.241
, pp. 126-133
-
-
Nakajima, H.1
Kim, Y.B.2
Terano, H.3
Yoshida, M.4
Horinouchi, S.5
-
103
-
-
0028260120
-
Butyrate as a differentiating agent: Pharmacokinetics, analogues and current status
-
Newmark HL, Lupton JR, Young CW (1994) Butyrate as a differentiating agent: pharmacokinetics, analogues and current status. Cancer Lett 78: 1-5
-
(1994)
Cancer Lett
, vol.78
, pp. 1-5
-
-
Newmark, H.L.1
Lupton, J.R.2
Young, C.W.3
-
104
-
-
3643104150
-
Therapeutic targeting of transcription in acute promyelocytic leukemia by use of an inhibitor of histone deacetylase
-
Warrell RP Jr, He LZ, Richon V, Calleja E, Pandolfi PP (1998) Therapeutic targeting of transcription in acute promyelocytic leukemia by use of an inhibitor of histone deacetylase. J Natl Cancer Inst 90: 1621-1625
-
(1998)
J Natl Cancer Inst
, vol.90
, pp. 1621-1625
-
-
Warrell Jr., R.P.1
He, L.Z.2
Richon, V.3
Calleja, E.4
Pandolfi, P.P.5
-
105
-
-
0001671940
-
Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen
-
Phiel CJ, Zhang F, Huang EY, Guenther MG, Lazar MA, Klein PS (2001) Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen. J Biol Chem 25: 25
-
(2001)
J Biol Chem
, vol.25
, pp. 25
-
-
Phiel, C.J.1
Zhang, F.2
Huang, E.Y.3
Guenther, M.G.4
Lazar, M.A.5
Klein, P.S.6
-
106
-
-
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, Nosaka Y, Tsuchiya K, Ando T, Suzuki T, Tsuruo T, Nakanishi O (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: 4592-4597
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 4592-4597
-
-
Saito, A.1
Yamashita, T.2
Mariko, Y.3
Nosaka, Y.4
Tsuchiya, K.5
Ando, T.6
Suzuki, T.7
Tsuruo, T.8
Nakanishi, O.9
-
107
-
-
0000032126
-
Depudecin induces morphological reversion of transformed fibroblasts via the inhibition of histone deacetylase
-
Kwon HJ, Owa T, Hassig CA, Shimada J, Schreiber SL (1998) Depudecin induces morphological reversion of transformed fibroblasts via the inhibition of histone deacetylase. Proc Natl Acad Sci USA 95: 3356-3361
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 3356-3361
-
-
Kwon, H.J.1
Owa, T.2
Hassig, C.A.3
Shimada, J.4
Schreiber, S.L.5
-
108
-
-
0018114158
-
Trichostatin C, a glucopyranosyl hydroxamate
-
Tsuji N, Kobayashi M (1978) Trichostatin C, a glucopyranosyl hydroxamate. J Antibiot (Tokyo) 31: 939-944
-
(1978)
J Antibiot (Tokyo)
, vol.31
, pp. 939-944
-
-
Tsuji, N.1
Kobayashi, M.2
-
109
-
-
0023195737
-
Effects of trichostatins on differentiation of murine erythroleukemia cells
-
Yoshida M, Nomura S, Beppu T (1987) Effects of trichostatins on differentiation of murine erythroleukemia cells. Cancer Res 47: 3688-3691
-
(1987)
Cancer Res
, vol.47
, pp. 3688-3691
-
-
Yoshida, M.1
Nomura, S.2
Beppu, T.3
-
110
-
-
0029294663
-
Trichostatin A and trapoxin: Novel chemical probes for the role of histone acetylation in chromatin structure and function
-
Yoshida M, Horinouchi S, Beppu T (1995) Trichostatin A and trapoxin: novel chemical probes for the role of histone acetylation in chromatin structure and function. Bioessays 17: 423-430
-
(1995)
Bioessays
, vol.17
, pp. 423-430
-
-
Yoshida, M.1
Horinouchi, S.2
Beppu, T.3
-
111
-
-
0025083327
-
Structural specificity for biological activity of trichostatin A, a specific inhibitor of mammalian cell cycle with potent differentiation-inducing activity in Friend leukemia cells
-
Yoshida M, Hoshikawa Y, Koseki K, Mori K, Beppu T (1990) Structural specificity for biological activity of trichostatin A, a specific inhibitor of mammalian cell cycle with potent differentiation- inducing activity in Friend leukemia cells. J Antibiot (Tokyo) 43: 1101-1106
-
(1990)
J Antibiot (Tokyo)
, vol.43
, pp. 1101-1106
-
-
Yoshida, M.1
Hoshikawa, Y.2
Koseki, K.3
Mori, K.4
Beppu, T.5
-
112
-
-
0023689244
-
Reversible arrest of proliferation of rat 3Y1 fibroblasts in both the G1 and G2 phases by trichostatin A
-
Yoshida M, Beppu T (1988) Reversible arrest of proliferation of rat 3Y1 fibroblasts in both the G1 and G2 phases by trichostatin A. Exp Cell Res 177: 122-131
-
(1988)
Exp Cell Res
, vol.177
, pp. 122-131
-
-
Yoshida, M.1
Beppu, T.2
-
113
-
-
0018371969
-
Different accessibilities in chromatin to histone acetylase
-
Cousens LS, Gallwitz D, Alberts BM (1979) Different accessibilities in chromatin to histone acetylase. J Biol Chem 254: 1716-1723
-
(1979)
J Biol Chem
, vol.254
, pp. 1716-1723
-
-
Cousens, L.S.1
Gallwitz, D.2
Alberts, B.M.3
-
114
-
-
0020025385
-
Effects of sodium butyrate, a new pharmacological agent, on cells in culture
-
Kruh J (1982) Effects of sodium butyrate, a new pharmacological agent, on cells in culture. Mol Cell Biochem 42: 65-82
-
(1982)
Mol Cell Biochem
, vol.42
, pp. 65-82
-
-
Kruh, J.1
-
115
-
-
0025673805
-
Isolation and structural elucidation of new cyclotetrapeptides, trapoxins a and B, having detransformation activities as antitumor agents
-
Itazaki H, Nagashima K, Sugita K, Yoshida H, Kawamura Y, Yasuda Y, Matsumoto K, Ishii K, Uotani N, Nakai H et al (1990) Isolation and structural elucidation of new cyclotetrapeptides, trapoxins A and B, having detransformation activities as antitumor agents. J Antibiot (Tokyo) 43: 1524-1532
-
(1990)
J Antibiot (Tokyo)
, vol.43
, pp. 1524-1532
-
-
Itazaki, H.1
Nagashima, K.2
Sugita, K.3
Yoshida, H.4
Kawamura, Y.5
Yasuda, Y.6
Matsumoto, K.7
Ishii, K.8
Uotani, N.9
Nakai, H.10
-
116
-
-
0034326799
-
Apicidin, a histone deacetylase inhibitor, inhibits proliferation of tumor cells via induction of p21WAF1/Cip1 and gelsolin
-
Han JW, Ahn SH, Park SH, Wang SY, Bae GU, Seo DW, Kwon HK, Hong S, Lee HY, Lee YW et al (2000) Apicidin, a histone deacetylase inhibitor, inhibits proliferation of tumor cells via induction of p21WAF1/Cip1 and gelsolin. Cancer Res 60: 6068-6074
-
(2000)
Cancer Res
, vol.60
, pp. 6068-6074
-
-
Han, J.W.1
Ahn, S.H.2
Park, S.H.3
Wang, S.Y.4
Bae, G.U.5
Seo, D.W.6
Kwon, H.K.7
Hong, S.8
Lee, H.Y.9
Lee, Y.W.10
-
117
-
-
0029094715
-
Depudecin, a microbial metabolite containing two epoxide groups, exhibits anti-angiogenic activity in vivo
-
Oikawa T, Onozawa C, Inose M, Sasaki M (1995) Depudecin, a microbial metabolite containing two epoxide groups, exhibits anti-angiogenic activity in vivo. Biol Pharm Bull 18: 1305-1307
-
(1995)
Biol Pharm Bull
, vol.18
, pp. 1305-1307
-
-
Oikawa, T.1
Onozawa, C.2
Inose, M.3
Sasaki, M.4
-
118
-
-
0029347704
-
Synthesis and cellular characterization of the detransformation agent, (-)-depudecin
-
Shimada J, Kwon HJ, Sawamura M, Schreiber SL (1995) Synthesis and cellular characterization of the detransformation agent, (-)-depudecin. Chem Biol 2: 517-525
-
(1995)
Chem Biol
, vol.2
, pp. 517-525
-
-
Shimada, J.1
Kwon, H.J.2
Sawamura, M.3
Schreiber, S.L.4
-
119
-
-
1642453460
-
Pharmacodynamic response and inhibition of growth of human tumor xenografts by the novel histone deacetylase inhibitor PXD101
-
Plumb JA, Finn PW, Williams RJ, Bandara MJ, Romero MR, Watkins CJ, La Thangue NB, Brown R (2003) Pharmacodynamic response and inhibition of growth of human tumor xenografts by the novel histone deacetylase inhibitor PXD101. Mol Cancer Ther 2: 721-728
-
(2003)
Mol Cancer Ther
, vol.2
, pp. 721-728
-
-
Plumb, J.A.1
Finn, P.W.2
Williams, R.J.3
Bandara, M.J.4
Romero, M.R.5
Watkins, C.J.6
La Thangue, N.B.7
Brown, R.8
-
120
-
-
0033539092
-
Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors
-
Finnin MS, Donigian JR, Cohen A, Richon VM, Rifkind RA, Marks PA, Breslow R, Pavletich NP (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
Donigian, J.R.2
Cohen, A.3
Richon, V.M.4
Rifkind, R.A.5
Marks, P.A.6
Breslow, R.7
Pavletich, N.P.8
-
121
-
-
6344222799
-
Crystal structure of a eukaryotic zinc-dependent histone deacetylase, human HDAC8, complexed with a hydroxamic acid inhibitor
-
Vannini A, Volpari C, Filocamo G, Casavola EC, Brunetti M, Renzoni D, Chakravarty P, Paolini C, De Francesco R, Gallinari P et al (2004) Crystal structure of a eukaryotic zinc-dependent histone deacetylase, human HDAC8, complexed with a hydroxamic acid inhibitor. Proc Natl Acad Sci USA 101: 15064-15069
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 15064-15069
-
-
Vannini, A.1
Volpari, C.2
Filocamo, G.3
Casavola, E.C.4
Brunetti, M.5
Renzoni, D.6
Chakravarty, P.7
Paolini, C.8
De Francesco, R.9
Gallinari, P.10
-
122
-
-
3142562372
-
Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases
-
Somoza JR, Skene RJ, Katz BA, Mol C, Ho JD, Jennings AJ, Luong C, Arvai A, Buggy JJ, Chi E et al (2004) Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases. Structure (Camb) 12: 1325-1334
-
(2004)
Structure (Camb)
, vol.12
, pp. 1325-1334
-
-
Somoza, J.R.1
Skene, R.J.2
Katz, B.A.3
Mol, C.4
Ho, J.D.5
Jennings, A.J.6
Luong, C.7
Arvai, A.8
Buggy, J.J.9
Chi, E.10
-
123
-
-
0035793107
-
Potent histone deacetylase inhibitors built from trichostatin A and cyclic tetrapeptide antibiotics including trapoxin
-
Furumai R, Komatsu Y, Nishino N, Khochbin S, Yoshida M, Horinouchi S (2001) Potent histone deacetylase inhibitors built from trichostatin A and cyclic tetrapeptide antibiotics including trapoxin. Proc Natl Acad Sci USA 98: 87-92
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 87-92
-
-
Furumai, R.1
Komatsu, Y.2
Nishino, N.3
Khochbin, S.4
Yoshida, M.5
Horinouchi, S.6
-
124
-
-
0033614993
-
Synthesis and histone deacetylase inhibitory activity of new benzamide derivatives
-
Suzuki T, Ando T, Tsuchiya K, Fukazawa N, Saito A, Mariko Y, Yamashita T, Nakanishi O (1999) Synthesis and histone deacetylase inhibitory activity of new benzamide derivatives. J Med Chem 42: 3001-3003
-
(1999)
J Med Chem
, vol.42
, pp. 3001-3003
-
-
Suzuki, T.1
Ando, T.2
Tsuchiya, K.3
Fukazawa, N.4
Saito, A.5
Mariko, Y.6
Yamashita, T.7
Nakanishi, O.8
-
125
-
-
0038274087
-
Structural biasing elements for in-cell histone deacetylase paralog selectivity
-
Wong JC, Hong R, Schreiber SL (2003) Structural biasing elements for in-cell histone deacetylase paralog selectivity. J Am Chem Soc 125: 5586-5587
-
(2003)
J Am Chem Soc
, vol.125
, pp. 5586-5587
-
-
Wong, J.C.1
Hong, R.2
Schreiber, S.L.3
-
126
-
-
0038522853
-
Multidimensional chemical genetic analysis of diversity-oriented synthesis-derived deacetylase inhibitors using cell-based assays
-
Haggarty SJ, Koeller KM, Wong JC, Butcher RA, Schreiber SL (2003) Multidimensional chemical genetic analysis of diversity-oriented synthesis-derived deacetylase inhibitors using cell-based assays. Chem Biol 10: 383-396
-
(2003)
Chem Biol
, vol.10
, pp. 383-396
-
-
Haggarty, S.J.1
Koeller, K.M.2
Wong, J.C.3
Butcher, R.A.4
Schreiber, S.L.5
-
127
-
-
18644379759
-
Trifluoromethyl ketones as inhibitors of histone deacetylase
-
Frey RR, Wada CK, Garland RB, Curtin ML, Michaelides MR, Li J, Pease LJ, Glaser KB, Marcotte PA, Bouska JJ et al (2002) Trifluoromethyl ketones as inhibitors of histone deacetylase. Bioorg Med Chem Lett 12: 3443-3447
-
(2002)
Bioorg Med Chem Lett
, vol.12
, pp. 3443-3447
-
-
Frey, R.R.1
Wada, C.K.2
Garland, R.B.3
Curtin, M.L.4
Michaelides, M.R.5
Li, J.6
Pease, L.J.7
Glaser, K.B.8
Marcotte, P.A.9
Bouska, J.J.10
-
128
-
-
10744230376
-
Alpha-keto amides as inhibitors of histone deacetylase
-
Wada CK, Frey RR, Ji Z, Curtin ML, Garland RB, Holms JH, Li J, Pease LJ, Guo J, Glaser KB et al (2003) Alpha-keto amides as inhibitors of histone deacetylase. Bioorg Med Chem Lett 13: 3331-3335
-
(2003)
Bioorg Med Chem Lett
, vol.13
, pp. 3331-3335
-
-
Wada, C.K.1
Frey, R.R.2
Ji, Z.3
Curtin, M.L.4
Garland, R.B.5
Holms, J.H.6
Li, J.7
Pease, L.J.8
Guo, J.9
Glaser, K.B.10
-
129
-
-
10744233418
-
Heterocyclic ketones as inhibitors of histone deacetylase
-
Vasudevan A, Ji Z, Frey RR, Wada CK, Steinman D, Heyman HR, Guo Y, Curtin ML, Guo J, Li J et al (2003) Heterocyclic ketones as inhibitors of histone deacetylase. Bioorg Med Chem Lett 13: 3909-3913
-
(2003)
Bioorg Med Chem Lett
, vol.13
, pp. 3909-3913
-
-
Vasudevan, A.1
Ji, Z.2
Frey, R.R.3
Wada, C.K.4
Steinman, D.5
Heyman, H.R.6
Guo, Y.7
Curtin, M.L.8
Guo, J.9
Li, J.10
-
130
-
-
0345358526
-
Novel histone deacetylase inhibitors: Design, synthesis, enzyme inhibition, and binding mode study of SAHA-based non-hydroxamates
-
Suzuki T, Nagano Y, Matsuura A, Kohara A, Ninomiya S, Kohda K, Miyata N (2003) Novel histone deacetylase inhibitors: design, synthesis, enzyme inhibition, and binding mode study of SAHA-based non-hydroxamates. Bioorg Med Chem Lett 13: 4321-4326
-
(2003)
Bioorg Med Chem Lett
, vol.13
, pp. 4321-4326
-
-
Suzuki, T.1
Nagano, Y.2
Matsuura, A.3
Kohara, A.4
Ninomiya, S.5
Kohda, K.6
Miyata, N.7
-
131
-
-
0346099272
-
Design, synthesis, and activity of HDAC inhibitors with a N-formyl hydroxylamine head group
-
Wu TY, Hassig C, Wu Y, Ding S, Schultz PG (2004) Design, synthesis, and activity of HDAC inhibitors with a N-formyl hydroxylamine head group. Bioorg Med Chem Lett 14: 449-453
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 449-453
-
-
Wu, T.Y.1
Hassig, C.2
Wu, Y.3
Ding, S.4
Schultz, P.G.5
-
132
-
-
2442597872
-
Thiol-based SAHA analogues as potent histone deacetylase inhibitors
-
Suzuki T, Kouketsu A, Matsuura A, Kohara A, Ninomiya S, Kohda K, Miyata N (2004) Thiol-based SAHA analogues as potent histone deacetylase inhibitors. Bioorg Med Chem Lett 14: 3313-3317
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 3313-3317
-
-
Suzuki, T.1
Kouketsu, A.2
Matsuura, A.3
Kohara, A.4
Ninomiya, S.5
Kohda, K.6
Miyata, N.7
-
133
-
-
10644239808
-
Identification of a potent non-hydroxamate histone deacetylase inhibitor by mechanism-based drug design
-
Suzuki T, Matsuura A, Kouketsu A, Nakagawa H, Miyata N (2005) Identification of a potent non-hydroxamate histone deacetylase inhibitor by mechanism-based drug design. Bioorg Med Chem Lett 15: 331-335
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 331-335
-
-
Suzuki, T.1
Matsuura, A.2
Kouketsu, A.3
Nakagawa, H.4
Miyata, N.5
-
135
-
-
0141988610
-
Histone deacetylase inhibitors: The Abbott experience
-
Curtin M, Glaser K (2003) Histone deacetylase inhibitors: the Abbott experience. Curr Med Chem 10: 2373-2392
-
(2003)
Curr Med Chem
, vol.10
, pp. 2373-2392
-
-
Curtin, M.1
Glaser, K.2
-
136
-
-
0346020435
-
The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stress
-
Kawaguchi Y, Kovacs JJ, McLaurin A, Vance JM, Ito A, Yao TP (2003) The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stress. Cell 115: 727-738
-
(2003)
Cell
, vol.115
, pp. 727-738
-
-
Kawaguchi, Y.1
Kovacs, J.J.2
McLaurin, A.3
Vance, J.M.4
Ito, A.5
Yao, T.P.6
-
137
-
-
0033609055
-
Three proteins define a class of human histone deacetylases related to yeast Hdalp
-
Grozinger CM, Hassig CA, Schreiber SL (1999) Three proteins define a class of human histone deacetylases related to yeast Hdalp. Proc Natl Acad Sci USA 96: 4868-4873
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 4868-4873
-
-
Grozinger, C.M.1
Hassig, C.A.2
Schreiber, S.L.3
-
138
-
-
0033593347
-
Identification of a new family of higher eukaryotic histone deacetylases. Coordinate expression of differentiation-dependent chromatin modifiers
-
Verdel A, Khochbin S (1999) Identification of a new family of higher eukaryotic histone deacetylases. Coordinate expression of differentiation- dependent chromatin modifiers. J Biol Chem 274: 2440-2445
-
(1999)
J Biol Chem
, vol.274
, pp. 2440-2445
-
-
Verdel, A.1
Khochbin, S.2
-
139
-
-
0142179154
-
Identification of novel isoform-selective inhibitors within class I histone deacetylases
-
Hu E, Dul E, Sung CM, Chen Z, Kirkpatrick R, Zhang GF, Johanson K, Liu R, Lago A, Hofmann G et al (2003) Identification of novel isoform-selective inhibitors within class I histone deacetylases. J Pharmacol Exp Ther 307: 720-728
-
(2003)
J Pharmacol Exp Ther
, vol.307
, pp. 720-728
-
-
Hu, E.1
Dul, E.2
Sung, C.M.3
Chen, Z.4
Kirkpatrick, R.5
Zhang, G.F.6
Johanson, K.7
Liu, R.8
Lago, A.9
Hofmann, G.10
-
140
-
-
0036735385
-
FK228 (depsipeptide) as a natural pro-drug that inhibits class I histone deacetylases
-
Furumai R, Matsuyama A, Kobashi N, Lee KH, Nishiyama M, Nakajima H, Tanaka A, Komatsu Y, Nishino N, Yoshida M et al (2002) FK228 (depsipeptide) as a natural pro-drug that inhibits class I histone deacetylases. Cancer Res 62: 4916-4921
-
(2002)
Cancer Res
, vol.62
, pp. 4916-4921
-
-
Furumai, R.1
Matsuyama, A.2
Kobashi, N.3
Lee, K.H.4
Nishiyama, M.5
Nakajima, H.6
Tanaka, A.7
Komatsu, Y.8
Nishino, N.9
Yoshida, M.10
-
141
-
-
0035910031
-
Identification of a small molecule inhibitor of Sir2p
-
Bedalov A, Gatbonton T, Irvine WP, Gottschling DE, Simon JA (2001) Identification of a small molecule inhibitor of Sir2p. Proc Natl Acad Sci USA 98: 15113-15118
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 15113-15118
-
-
Bedalov, A.1
Gatbonton, T.2
Irvine, W.P.3
Gottschling, D.E.4
Simon, J.A.5
-
142
-
-
0141719702
-
Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan
-
Howitz KT, Bitterman KJ, Cohen HY, Lamming DW, Lavu S, Wood JG, Zipkin RE, Chung P, Kisielewski A, Zhang LL et al (2003) Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan. Nature 425: 191-196
-
(2003)
Nature
, vol.425
, pp. 191-196
-
-
Howitz, K.T.1
Bitterman, K.J.2
Cohen, H.Y.3
Lamming, D.W.4
Lavu, S.5
Wood, J.G.6
Zipkin, R.E.7
Chung, P.8
Kisielewski, A.9
Zhang, L.L.10
-
143
-
-
0022377598
-
Cellular and molecular changes in 3T3 cells transformed spontaneously or by DNA transfection
-
Wahrman MZ, Gagnier SE, Kobrin DR, Higgins PJ, Augenlicht LH (1985) Cellular and molecular changes in 3T3 cells transformed spontaneously or by DNA transfection. Tumour Biol 6: 41-56
-
(1985)
Tumour Biol
, vol.6
, pp. 41-56
-
-
Wahrman, M.Z.1
Gagnier, S.E.2
Kobrin, D.R.3
Higgins, P.J.4
Augenlicht, L.H.5
-
144
-
-
0017139523
-
Changes in microfilament organization and surface topogrophy upon transformation of chick embryo fibroblasts with Rous sarcoma virus
-
Wang E, Goldberg AR (1976) Changes in microfilament organization and surface topogrophy upon transformation of chick embryo fibroblasts with Rous sarcoma virus. Proc Natl Acad Sci USA 73: 4065-4069
-
(1976)
Proc Natl Acad Sci USA
, vol.73
, pp. 4065-4069
-
-
Wang, E.1
Goldberg, A.R.2
-
145
-
-
0028022785
-
Trichostatin A induces morphological changes and gelsolin expression by inhibiting histone deacetylase in human carcinoma cell lines
-
Hoshikawa Y, Kwon HJ, Yoshida M, Horinouchi S, Beppu T (1994) Trichostatin A induces morphological changes and gelsolin expression by inhibiting histone deacetylase in human carcinoma cell lines. Exp Cell Res 214: 189-197
-
(1994)
Exp Cell Res
, vol.214
, pp. 189-197
-
-
Hoshikawa, Y.1
Kwon, H.J.2
Yoshida, M.3
Horinouchi, S.4
Beppu, T.5
-
146
-
-
0023780588
-
Predominant induction of gelsolin and actin-binding protein during myeloid differentiation
-
Kwiatkowski DJ (1988) Predominant induction of gelsolin and actin-binding protein during myeloid differentiation. J Biol Chem 263: 13857-13862
-
(1988)
J Biol Chem
, vol.263
, pp. 13857-13862
-
-
Kwiatkowski, D.J.1
-
147
-
-
0029144456
-
Gelsolin: A candidate for suppressor of human bladder cancer
-
Tanaka M, Mullauer L, Ogiso Y, Fujita H, Moriya S, Furuuchi K, Harabayashi T, Shinohara N, Koyanagi T, Kuzumaki N (1995) Gelsolin: a candidate for suppressor of human bladder cancer. Cancer Res 55: 3228-3232
-
(1995)
Cancer Res
, vol.55
, pp. 3228-3232
-
-
Tanaka, M.1
Mullauer, L.2
Ogiso, Y.3
Fujita, H.4
Moriya, S.5
Furuuchi, K.6
Harabayashi, T.7
Shinohara, N.8
Koyanagi, T.9
Kuzumaki, N.10
-
148
-
-
0032499756
-
p21(WAF1) is required for butyrate-mediated growth inhibition of human colon cancer cells
-
Archer SY, Meng S, Shei A, Hodin RA (1998) p21(WAF1) is required for butyrate-mediated growth inhibition of human colon cancer cells. Proc Natl Acad Sci USA 95: 6791-6796
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 6791-6796
-
-
Archer, S.Y.1
Meng, S.2
Shei, A.3
Hodin, R.A.4
-
149
-
-
0027970713
-
DNA damage triggers a prolonged p53-dependent G1 arrest and long-term induction of Cip1 in normal human fibroblasts
-
Di Leonardo A, Linke SP, Clarkin K, Wahl GM (1994) DNA damage triggers a prolonged p53-dependent G1 arrest and long-term induction of Cip1 in normal human fibroblasts. Genes Dev 8: 2540-2551
-
(1994)
Genes Dev
, vol.8
, pp. 2540-2551
-
-
Di Leonardo, A.1
Linke, S.P.2
Clarkin, K.3
Wahl, G.M.4
-
150
-
-
0033562343
-
Both Sp1 and Sp3 are responsible for p21waf1 promoter activity induced by histone deacetylase inhibitor in NIH3T3 cells
-
Xiao H, Hasegawa T, Isobe K (1999) Both Sp1 and Sp3 are responsible for p21waf1 promoter activity induced by histone deacetylase inhibitor in NIH3T3 cells. J Cell Biochem 73: 291-302
-
(1999)
J Cell Biochem
, vol.73
, pp. 291-302
-
-
Xiao, H.1
Hasegawa, T.2
Isobe, K.3
-
151
-
-
17744416444
-
Histone deacetylase inhibitor activates the WAF1/Cip1 gene promoter through the Sp1 sites
-
Sowa Y, Orita T, Minamikawa S, Nakano K, Mizuno T, Nomura H, Sakai T (1997) Histone deacetylase inhibitor activates the WAF1/Cip1 gene promoter through the Sp1 sites. Biochem Biophys Res Commun 241: 142-150
-
(1997)
Biochem Biophys Res Commun
, vol.241
, pp. 142-150
-
-
Sowa, Y.1
Orita, T.2
Minamikawa, S.3
Nakano, K.4
Mizuno, T.5
Nomura, H.6
Sakai, T.7
-
152
-
-
0033427145
-
Histone deacetylase inhibitor activates the p21/WAF1/Cip1 gene promoter through the Sp1 sites
-
Sowa Y, Orita T, Hiranabe-Minamikawa S, Nakano K, Mizuno T, Nomura H, Sakai T (1999) Histone deacetylase inhibitor activates the p21/WAF1/Cip1 gene promoter through the Sp1 sites. Ann N Y Acad Sci 886: 195-199
-
(1999)
Ann N Y Acad Sci
, vol.886
, pp. 195-199
-
-
Sowa, Y.1
Orita, T.2
Hiranabe-Minamikawa, S.3
Nakano, K.4
Mizuno, T.5
Nomura, H.6
Sakai, T.7
-
153
-
-
0033822112
-
P21-dependent g(1)arrest with downregulation of cyclin D1 and upregulation of cyclin E by the histone deacetylase inhibitor FR901228
-
Sandor V, Senderowicz A, Mertins S, Sackett D, Sausville E, Blagosklonny MV, Bates SE (2000) P21-dependent g(1)arrest with downregulation of cyclin D1 and upregulation of cyclin E by the histone deacetylase inhibitor FR901228. Br J Cancer 83: 817-825
-
(2000)
Br J Cancer
, vol.83
, pp. 817-825
-
-
Sandor, V.1
Senderowicz, A.2
Mertins, S.3
Sackett, D.4
Sausville, E.5
Blagosklonny, M.V.6
Bates, S.E.7
-
154
-
-
0034802325
-
Up-regulation of p21(WAF1/CIP1) by histone deacetylase inhibitors reduces their cytotoxicity
-
Burgess AJ, Pavey S, Warrener R, Hunter LJ, Piva TJ, Musgrove EA, Saunders N, Parsons PG, Gabrielli BG (2001) Up-regulation of p21(WAF1/CIP1) by histone deacetylase inhibitors reduces their cytotoxicity. Mol Pharmacol 60: 828-837
-
(2001)
Mol Pharmacol
, vol.60
, pp. 828-837
-
-
Burgess, A.J.1
Pavey, S.2
Warrener, R.3
Hunter, L.J.4
Piva, T.J.5
Musgrove, E.A.6
Saunders, N.7
Parsons, P.G.8
Gabrielli, B.G.9
-
155
-
-
0033604457
-
Induction of apoptosis in U937 human leukemia cells by suberoyl-anilide hydroxamic acid (SAHA) proceeds through pathways that are regulated by Bcl-2/Bcl-XL, c-Jun, and p21CIP1, but independent of p53
-
Vrana JA, Decker RH, Johnson CR, Wang Z, Jarvis WD, Richon VM, Ehinger M, Fisher PB, Grant S (1999) Induction of apoptosis in U937 human leukemia cells by suberoyl-anilide hydroxamic acid (SAHA) proceeds through pathways that are regulated by Bcl-2/Bcl-XL, c-Jun, and p21CIP1, but independent of p53. Oncogene 18: 7016-7025
-
(1999)
Oncogene
, vol.18
, pp. 7016-7025
-
-
Vrana, J.A.1
Decker, R.H.2
Johnson, C.R.3
Wang, Z.4
Jarvis, W.D.5
Richon, V.M.6
Ehinger, M.7
Fisher, P.B.8
Grant, S.9
-
156
-
-
0034086168
-
Histone deacetylase inhibitors trigger a G2 checkpoint in normal cells that is defective in tumor cells
-
Qiu L, Burgess A, Fairlie DP, Leonard H, Parsons PG, Gabrielli BG (2000) Histone deacetylase inhibitors trigger a G2 checkpoint in normal cells that is defective in tumor cells. Mol Biol Cell 11: 2069-2083
-
(2000)
Mol Biol Cell
, vol.11
, pp. 2069-2083
-
-
Qiu, L.1
Burgess, A.2
Fairlie, D.P.3
Leonard, H.4
Parsons, P.G.5
Gabrielli, B.G.6
-
157
-
-
0036527775
-
Histone-deacetylase inhibitors: Novel drugs for the treatment of cancer
-
Johnstone RW (2002) Histone-deacetylase inhibitors: novel drugs for the treatment of cancer. Nat Rev Drug Discov 1: 287-299
-
(2002)
Nat Rev Drug Discov
, vol.1
, pp. 287-299
-
-
Johnstone, R.W.1
-
158
-
-
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 Expr 5: 245-253
-
(1996)
Gene Expr
, vol.5
, pp. 245-253
-
-
Van Lint, C.1
Emiliani, S.2
Verdin, E.3
-
159
-
-
0034297220
-
Suberoylanilide hydroxamic acid as a potential therapeutic agent for human breast cancer treatment
-
Huang L, Pardee AB (2000) Suberoylanilide hydroxamic acid as a potential therapeutic agent for human breast cancer treatment. Mol Med 6: 849-866
-
(2000)
Mol Med
, vol.6
, pp. 849-866
-
-
Huang, L.1
Pardee, A.B.2
-
160
-
-
0033520944
-
Histone deacetylase inhibition selectively alters the activity and expression of cell cycle proteins leading to specific chromatin acetylation and antiproliferative effects
-
Sambucetti LC, Fischer DD, Zabludoff S, Kwon PO, Chamberlin H, Trogani N, Xu H, Cohen D (1999) Histone deacetylase inhibition selectively alters the activity and expression of cell cycle proteins leading to specific chromatin acetylation and antiproliferative effects. J Biol Chem 274: 34940-34947
-
(1999)
J Biol Chem
, vol.274
, pp. 34940-34947
-
-
Sambucetti, L.C.1
Fischer, D.D.2
Zabludoff, S.3
Kwon, P.O.4
Chamberlin, H.5
Trogani, N.6
Xu, H.7
Cohen, D.8
-
161
-
-
0034730127
-
Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation
-
Richon VM, Sandhoff TW, Rifkind RA, Marks PA (2000) Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation. Proc Natl Acad Sci USA 97: 10014-10019
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 10014-10019
-
-
Richon, V.M.1
Sandhoff, T.W.2
Rifkind, R.A.3
Marks, P.A.4
-
162
-
-
0033602765
-
Epigenetic regulation of gelsolin expression in human breast cancer cells
-
Mielnicki LM, Ying AM, Head KL, Asch HL, Asch BB (1999) Epigenetic regulation of gelsolin expression in human breast cancer cells. Exp Cell Res 249: 161-176
-
(1999)
Exp Cell Res
, vol.249
, pp. 161-176
-
-
Mielnicki, L.M.1
Ying, A.M.2
Head, K.L.3
Asch, H.L.4
Asch, B.B.5
-
163
-
-
0035878721
-
Telomerase activation by histone deacetylase inhibitor in normal cells
-
Takakura M, Kyo S, Sowa Y, Wang Z, Yatabe N, Maida Y, Tanaka M, Inoue M (2001) Telomerase activation by histone deacetylase inhibitor in normal cells. Nucleic Acids Res 29: 3006-3011
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 3006-3011
-
-
Takakura, M.1
Kyo, S.2
Sowa, Y.3
Wang, Z.4
Yatabe, N.5
Maida, Y.6
Tanaka, M.7
Inoue, M.8
-
164
-
-
0032530486
-
DNA damage activates p53 through a phosphorylation-acetylation cascade
-
Sakaguchi K, Herrera JE, Saito S, Miki T, Bustin M, Vassilev A, Anderson CW, Appella E (1998) DNA damage activates p53 through a phosphorylation- acetylation cascade. Genes Dev 12: 2831-2841
-
(1998)
Genes Dev
, vol.12
, pp. 2831-2841
-
-
Sakaguchi, K.1
Herrera, J.E.2
Saito, S.3
Miki, T.4
Bustin, M.5
Vassilev, A.6
Anderson, C.W.7
Appella, E.8
-
165
-
-
0032906633
-
p53 sites acetylated in vitro by PCAF and p300 are acetylated in vivo in response to DNA damage
-
Liu L, Scolnick DM, Trievel RC, Zhang HB, Marmorstein R, Halazonetis TD, Berger SL (1999) p53 sites acetylated in vitro by PCAF and p300 are acetylated in vivo in response to DNA damage. Mol Cell Biol 19: 1202-209
-
(1999)
Mol Cell Biol
, vol.19
, pp. 1202-1209
-
-
Liu, L.1
Scolnick, D.M.2
Trievel, R.C.3
Zhang, H.B.4
Marmorstein, R.5
Halazonetis, T.D.6
Berger, S.L.7
-
166
-
-
0032544123
-
Acetylation and modulation of erythroid Kruppel-like factor (EKLF) activity by interaction with histone acetyltransferases
-
Zhang W, Bieker JJ (1998) Acetylation and modulation of erythroid Kruppel-like factor (EKLF) activity by interaction with histone acetyltransferases. Proc Natl Acad Sci USA 95: 9855-9860
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 9855-9860
-
-
Zhang, W.1
Bieker, J.J.2
-
167
-
-
0033520325
-
Regulation of hormone-induced histone hyperacetylation and gene activation via acetylation of an acetylase
-
Chen H, Lin RJ, Xie W, Wilpitz D, Evans RM (1999) Regulation of hormone-induced histone hyperacetylation and gene activation via acetylation of an acetylase. Cell 98: 675-686
-
(1999)
Cell
, vol.98
, pp. 675-686
-
-
Chen, H.1
Lin, R.J.2
Xie, W.3
Wilpitz, D.4
Evans, R.M.5
-
168
-
-
0034901985
-
Trichostatin a is a histone deacetylase inhibitor with potent antitumor activity against breast cancer in vivo
-
Vigushin DM, Ali S, Pace PE, Mirsaidi N, Ito K, Adcock I, Coombes RC (2001) Trichostatin A is a histone deacetylase inhibitor with potent antitumor activity against breast cancer in vivo. Clin Cancer Res 7: 971-976
-
(2001)
Clin Cancer Res
, vol.7
, pp. 971-976
-
-
Vigushin, D.M.1
Ali, S.2
Pace, P.E.3
Mirsaidi, N.4
Ito, K.5
Adcock, I.6
Coombes, R.C.7
-
169
-
-
4143114765
-
Acetylation of nuclear receptors in cellular growth and apoptosis
-
Fu M, Wang C, Zhang X, Pestell RG (2004) Acetylation of nuclear receptors in cellular growth and apoptosis. Biochem Pharmacol 68: 1199-1208
-
(2004)
Biochem Pharmacol
, vol.68
, pp. 1199-1208
-
-
Fu, M.1
Wang, C.2
Zhang, X.3
Pestell, R.G.4
-
170
-
-
9744223645
-
Histone deacetylase inhibitor trichostatin A represses estrogen receptor alpha-dependent transcription and promotes proteasomal degradation of cyclin D1 in human breast carcinoma cell lines
-
Alao JP, Lam EW, Ali S, Buluwela L, Bordogna W, Lockey P, Varshochi R, Stavropoulou AV, Coombes RC, Vigushin DM (2004) Histone deacetylase inhibitor trichostatin A represses estrogen receptor alpha-dependent transcription and promotes proteasomal degradation of cyclin D1 in human breast carcinoma cell lines. Clin Cancer Res 10: 8094-8104
-
(2004)
Clin Cancer Res
, vol.10
, pp. 8094-8104
-
-
Alao, J.P.1
Lam, E.W.2
Ali, S.3
Buluwela, L.4
Bordogna, W.5
Lockey, P.6
Varshochi, R.7
Stavropoulou, A.V.8
Coombes, R.C.9
Vigushin, D.M.10
-
171
-
-
0037012344
-
Modulation of p53, ErbB1, ErbB2, and Raf-1 expression in lung cancer cells by depsipeptide FR901228
-
Yu X, Guo ZS, Marcu MG, Neckers L, Nguyen DM, Chen GA, Schrump DS (2002) Modulation of p53, ErbB1, ErbB2, and Raf-1 expression in lung cancer cells by depsipeptide FR901228. J Natl Cancer Inst 94: 504-513
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 504-513
-
-
Yu, X.1
Guo, Z.S.2
Marcu, M.G.3
Neckers, L.4
Nguyen, D.M.5
Chen, G.A.6
Schrump, D.S.7
-
172
-
-
1642490813
-
Histone deacetylase inhibitor LAQ824 down-regulates Her-2 and sensitizes human breast cancer cells to trastuzumab, taxotere, gemcitabine, and epothilone B
-
Fuino L, Bali P, Wittmann S, Donapaty S, Guo F, Yamaguchi H, Wang HG, Atadja P, Bhalla K (2003) Histone deacetylase inhibitor LAQ824 down-regulates Her-2 and sensitizes human breast cancer cells to trastuzumab, taxotere, gemcitabine, and epothilone B. Mol Cancer Ther 2: 971-984
-
(2003)
Mol Cancer Ther
, vol.2
, pp. 971-984
-
-
Fuino, L.1
Bali, P.2
Wittmann, S.3
Donapaty, S.4
Guo, F.5
Yamaguchi, H.6
Wang, H.G.7
Atadja, P.8
Bhalla, K.9
-
173
-
-
0043016178
-
Histone deacetylase inhibitor LAQ824 both lowers expression and promotes proteasomal degradation of Bcr-Abl and induces apoptosis of imatinib mesylate-sensitive or -refractory chronic myelogenous leukemia-blast crisis cells
-
Nimmanapalli R, Fuino L, Bali P, Gasparetto M, Glozak M, Tao J, Moscinski L, Smith C, Wu J, Jove R et al (2003) Histone deacetylase inhibitor LAQ824 both
-
(2003)
Cancer Res
, vol.63
, pp. 5126-5135
-
-
Nimmanapalli, R.1
Fuino, L.2
Bali, P.3
Gasparetto, M.4
Glozak, M.5
Tao, J.6
Moscinski, L.7
Smith, C.8
Wu, J.9
Jove, R.10
-
174
-
-
0017815160
-
DNA associated with hyperacetylated histone is preferentially digested by DNase I
-
Sealy L, Chalkley R (1978) DNA associated with hyperacetylated histone is preferentially digested by DNase I. Nucleic Acids Res 5: 1863-1876
-
(1978)
Nucleic Acids Res
, vol.5
, pp. 1863-1876
-
-
Sealy, L.1
Chalkley, R.2
-
175
-
-
0033564458
-
Carboxy-peptidase A3 (CPA3): A novel gene highly induced by histone deacetylase inhibitors during differentiation of prostate epithelial cancer cells
-
Huang H, Reed CP, Zhang JS, Shridhar V, Wang L, Smith DI (1999) Carboxy-peptidase A3 (CPA3): a novel gene highly induced by histone deacetylase inhibitors during differentiation of prostate epithelial cancer cells. Cancer Res 59: 2981-2988
-
(1999)
Cancer Res
, vol.59
, pp. 2981-2988
-
-
Huang, H.1
Reed, C.P.2
Zhang, J.S.3
Shridhar, V.4
Wang, L.5
Smith, D.I.6
-
176
-
-
0030796349
-
Induction of caspase-3 protease activity and apoptosis by butyrate and trichostatin A (inhibitors of histone deacetylase): Dependence on protein synthesis and synergy with a mitochondrial/cytochrome c-dependent pathway
-
Medina V, Edmonds B, Young GP, James R, Appleton S, Zalewski PD (1997) Induction of caspase-3 protease activity and apoptosis by butyrate and trichostatin A (inhibitors of histone deacetylase): dependence on protein synthesis and synergy with a mitochondrial/cytochrome c-dependent pathway. Cancer Res 57: 3697-3707
-
(1997)
Cancer Res
, vol.57
, pp. 3697-3707
-
-
Medina, V.1
Edmonds, B.2
Young, G.P.3
James, R.4
Appleton, S.5
Zalewski, P.D.6
-
177
-
-
0030597111
-
Involvement of histone hyperacetylation in triggering DNA fragmentation of rat thymocytes undergoing apoptosis
-
Lee E, Furukubo T, Miyabe T, Yamauchi A, Kariya K (1996) Involvement of histone hyperacetylation in triggering DNA fragmentation of rat thymocytes undergoing apoptosis. FEBS Lett 395: 183-187
-
(1996)
FEBS Lett
, vol.395
, pp. 183-187
-
-
Lee, E.1
Furukubo, T.2
Miyabe, T.3
Yamauchi, A.4
Kariya, K.5
-
178
-
-
0032729215
-
Apoptosis induced by the histone deacetylase inhibitor sodium butyrate in human leukemic lymphoblasts
-
Bernhard D, Ausserlechner MJ, Tonko M, Loffler M, Hartmann BL, Csordas A, Kofler R (1999) Apoptosis induced by the histone deacetylase inhibitor sodium butyrate in human leukemic lymphoblasts. FASEB J 13: 1991-2001
-
(1999)
FASEB J
, vol.13
, pp. 1991-2001
-
-
Bernhard, D.1
Ausserlechner, M.J.2
Tonko, M.3
Loffler, M.4
Hartmann, B.L.5
Csordas, A.6
Kofler, R.7
-
179
-
-
0033199896
-
Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma
-
Glick RD, Swendeman SL, Coffey DC, Rifkind RA, Marks PA, Richon VM, La Quaglia MP (1999) Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma. Cancer Res 59: 4392-4399
-
(1999)
Cancer Res
, vol.59
, pp. 4392-4399
-
-
Glick, R.D.1
Swendeman, S.L.2
Coffey, D.C.3
Rifkind, R.A.4
Marks, P.A.5
Richon, V.M.6
La Quaglia, M.P.7
-
180
-
-
0032989027
-
Anti-tumour activity in vitro and in vivo of selective differentiating agents containing hydroxamate
-
Qiu L, Kelso MJ, Hansen C, West ML, Fairlie DP, Parsons PG (1999) Anti-tumour activity in vitro and in vivo of selective differentiating agents containing hydroxamate. Br J Cancer 80: 1252-1258
-
(1999)
Br J Cancer
, vol.80
, pp. 1252-1258
-
-
Qiu, L.1
Kelso, M.J.2
Hansen, C.3
West, M.L.4
Fairlie, D.P.5
Parsons, P.G.6
-
181
-
-
0030786371
-
Tumor selectivity and transcriptional activation by azelaic bishydroxamic acid in human melanocytic cells
-
Parsons PG, Hansen C, Fairlie DP, West ML, Danoy PA, Sturm RA, Dunn IS, Pedley J, Ablett EM (1997) Tumor selectivity and transcriptional activation by azelaic bishydroxamic acid in human melanocytic cells. Biochem Pharmacol 53: 1719-1724
-
(1997)
Biochem Pharmacol
, vol.53
, pp. 1719-1724
-
-
Parsons, P.G.1
Hansen, C.2
Fairlie, D.P.3
West, M.L.4
Danoy, P.A.5
Sturm, R.A.6
Dunn, I.S.7
Pedley, J.8
Ablett, E.M.9
-
182
-
-
0031768386
-
Effects of a novel antitumor depsipeptide, FR901228, on human breast cancer cells
-
Rajgolikar G, Chan KK, Wang HC (1998) Effects of a novel antitumor depsipeptide, FR901228, on human breast cancer cells. Breast Cancer Res Treat 51: 29-38
-
(1998)
Breast Cancer Res Treat
, vol.51
, pp. 29-38
-
-
Rajgolikar, G.1
Chan, K.K.2
Wang, H.C.3
-
183
-
-
0033566643
-
Depsipeptide (FR901228): A novel therapeutic agent with selective, in vitro activity against human B-cell chronic lymphocytic leukemia cells
-
Byrd JC, Shinn C, Ravi R, Willis CR, Waselenko JK, Flinn IW, Dawson NA, Grever MR (1999) Depsipeptide (FR901228): a novel therapeutic agent with selective, in vitro activity against human B-cell chronic lymphocytic leukemia cells. Blood 94: 1401-1408
-
(1999)
Blood
, vol.94
, pp. 1401-1408
-
-
Byrd, J.C.1
Shinn, C.2
Ravi, R.3
Willis, C.R.4
Waselenko, J.K.5
Flinn, I.W.6
Dawson, N.A.7
Grever, M.R.8
-
184
-
-
0033572754
-
IGF-II enhances trichostatin A-induced TGFbeta1 and p21(Waf1,Cip1, sdi1) expression in Hep3B cells
-
Gray SG, Yakovleva T, Hartmann W, Tally M, Bakalkin G, Ekstrom TJ (1999) IGF-II enhances trichostatin A-induced TGFbeta1 and p21(Waf1,Cip1, sdi1) expression in Hep3B cells. Exp Cell Res 253: 618-628
-
(1999)
Exp Cell Res
, vol.253
, pp. 618-628
-
-
Gray, S.G.1
Yakovleva, T.2
Hartmann, W.3
Tally, M.4
Bakalkin, G.5
Ekstrom, T.J.6
-
185
-
-
0034663182
-
Histone deacetylase inhibitors suppress IL-2-mediated gene expression prior to induction of apoptosis
-
Koyama Y, Adachi M, Sekiya M, Takekawa M, Imai K (2000) Histone deacetylase inhibitors suppress IL-2-mediated gene expression prior to induction of apoptosis. Blood 96: 1490-1495
-
(2000)
Blood
, vol.96
, pp. 1490-1495
-
-
Koyama, Y.1
Adachi, M.2
Sekiya, M.3
Takekawa, M.4
Imai, K.5
-
186
-
-
0028986992
-
Trichostatin A inhibits both ras-induced neurite outgrowth of PC12 cells and morphological transformation of NIH3T3 cells
-
Futamura M, Monden Y, Okabe T, Fujita-Yoshigaki J, Yokoyama S, Nishimura S (1995) Trichostatin A inhibits both ras-induced neurite outgrowth of PC12 cells and morphological transformation of NIH3T3 cells. Oncogene 10: 1119-1123
-
(1995)
Oncogene
, vol.10
, pp. 1119-1123
-
-
Futamura, M.1
Monden, Y.2
Okabe, T.3
Fujita-Yoshigaki, J.4
Yokoyama, S.5
Nishimura, S.6
-
187
-
-
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, Sutton VR, Tainton KM, Kofler R, Smyth MJ, Johnstone RW (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: 10833-10838
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 10833-10838
-
-
Ruefli, A.A.1
Ausserlechner, M.J.2
Bernhard, D.3
Sutton, V.R.4
Tainton, K.M.5
Kofler, R.6
Smyth, M.J.7
Johnstone, R.W.8
-
188
-
-
0037052687
-
Suberoylanilide hydroxamic acid (SAHA) overcomes multidrug resistance and induces cell death in P-glycoprotein-expressing cells
-
Ruefli AA, Bernhard D, Tainton KM, Kofler R, Smyth MJ, Johnstone RW (2002) Suberoylanilide hydroxamic acid (SAHA) overcomes multidrug resistance and induces cell death in P-glycoprotein-expressing cells. Int J Cancer 99: 292-298
-
(2002)
Int J Cancer
, vol.99
, pp. 292-298
-
-
Ruefli, A.A.1
Bernhard, D.2
Tainton, K.M.3
Kofler, R.4
Smyth, M.J.5
Johnstone, R.W.6
-
189
-
-
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 1
-
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 1. Cancer Res 63: 3637-3645
-
(2003)
Cancer Res
, vol.63
, pp. 3637-3645
-
-
Rosato, R.R.1
Almenara, J.A.2
Grant, S.3
-
190
-
-
0035866353
-
DNA methyltransferase inhibition enhances apoptosis induced by histone deacetylase inhibitors
-
Zhu WG, Lakshmanan RR, Beal MD, Otterson GA (2001) DNA methyltransferase inhibition enhances apoptosis induced by histone deacetylase inhibitors. Cancer Res 61: 1327-1333
-
(2001)
Cancer Res
, vol.61
, pp. 1327-1333
-
-
Zhu, W.G.1
Lakshmanan, R.R.2
Beal, M.D.3
Otterson, G.A.4
-
191
-
-
0033119780
-
DNA methylation and chromatin modification
-
Ng HH, Bird A (1999) DNA methylation and chromatin modification. Curr Opin Genet Dev 9: 158-163
-
(1999)
Curr Opin Genet Dev
, vol.9
, pp. 158-163
-
-
Ng, H.H.1
Bird, A.2
-
192
-
-
0032845039
-
Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation
-
Wade PA, Gegonne A, Jones PL, Ballestar E, Aubry F, Wolffe AP (1999) Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation. Nat Genet 23: 62-66
-
(1999)
Nat Genet
, vol.23
, pp. 62-66
-
-
Wade, P.A.1
Gegonne, A.2
Jones, P.L.3
Ballestar, E.4
Aubry, F.5
Wolffe, A.P.6
-
193
-
-
0032948005
-
Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer
-
Cameron EE, Bachman KE, Myohanen S, Herman JG, Baylin SB (1999) Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer. Nat Genet 21: 103-107
-
(1999)
Nat Genet
, vol.21
, pp. 103-107
-
-
Cameron, E.E.1
Bachman, K.E.2
Myohanen, S.3
Herman, J.G.4
Baylin, S.B.5
-
194
-
-
0034671304
-
Transcriptional activation of estrogen receptor alpha in human breast cancer cells by histone deacetylase inhibition
-
Yang X, Ferguson AT, Nass SJ, Phillips DL, Butash KA, Wang SM, Herman JG, Davidson NE (2000) Transcriptional activation of estrogen receptor alpha in human breast cancer cells by histone deacetylase inhibition. Cancer Res 60: 6890-6894
-
(2000)
Cancer Res
, vol.60
, pp. 6890-6894
-
-
Yang, X.1
Ferguson, A.T.2
Nass, S.J.3
Phillips, D.L.4
Butash, K.A.5
Wang, S.M.6
Herman, J.G.7
Davidson, N.E.8
-
195
-
-
0035126974
-
Sequential 5-Aza-2 deoxycytidine-depsipeptide FR901228 treatment induces apoptosis preferentially in cancer cells and facilitates their recognition by cytolytic T lymphocytes specific for NY-ESO-1
-
Weiser TS, Guo ZS, Ohnmacht GA, Parkhurst ML, Tong-On P, Marincola FM, Fischette MR, Yu X, Chen GA, Hong JA et al (2001) Sequential 5-Aza-2 deoxycytidine-depsipeptide FR901228 treatment induces apoptosis preferentially in cancer cells and facilitates their recognition by cytolytic T lymphocytes specific for NY-ESO-1. J Immunother 24: 151-161
-
(2001)
J Immunother
, vol.24
, pp. 151-161
-
-
Weiser, T.S.1
Guo, Z.S.2
Ohnmacht, G.A.3
Parkhurst, M.L.4
Tong-On, P.5
Marincola, F.M.6
Fischette, M.R.7
Yu, X.8
Chen, G.A.9
Hong, J.A.10
-
196
-
-
0037137896
-
Histone deacetylase inhibitor FK228 inhibits tumor angiogenesis
-
Kwon HJ, Kim MS, Kim MJ, Nakajima H, Kim KW (2002) Histone deacetylase inhibitor FK228 inhibits tumor angiogenesis. Int J Cancer 97: 290-296
-
(2002)
Int J Cancer
, vol.97
, pp. 290-296
-
-
Kwon, H.J.1
Kim, M.S.2
Kim, M.J.3
Nakajima, H.4
Kim, K.W.5
-
197
-
-
0242610850
-
Inhibition of histone deacetylase increases cytotoxicity to anticancer drugs targeting DNA
-
Kim MS, Blake M, Baek JH, Kohlhagen G, Pommier Y, Carrier F (2003) Inhibition of histone deacetylase increases cytotoxicity to anticancer drugs targeting DNA. Cancer Res 63: 7291-7300
-
(2003)
Cancer Res
, vol.63
, pp. 7291-7300
-
-
Kim, M.S.1
Blake, M.2
Baek, J.H.3
Kohlhagen, G.4
Pommier, Y.5
Carrier, F.6
-
198
-
-
0038066488
-
+ human myeloid leukemia cells
-
+ human myeloid leukemia cells. Cancer Res 63: 2118-2126
-
(2003)
Cancer Res
, vol.63
, pp. 2118-2126
-
-
Yu, C.1
Rahmani, M.2
Almenara, J.3
Subler, M.4
Krystal, G.5
Conrad, D.6
Varticovski, L.7
Dent, P.8
Grant, S.9
-
199
-
-
1642339046
-
The histone deacetylase inhibitor trichostatin A sensitizes estrogen receptor alpha-negative breast cancer cells to tamoxifen
-
Jang ER, Lim SJ, Lee ES, Jeong G, Kim TY, Bang YJ, Lee JS (2004) The histone deacetylase inhibitor trichostatin A sensitizes estrogen receptor alpha-negative breast cancer cells to tamoxifen. Oncogene 23: 1724-1736
-
(2004)
Oncogene
, vol.23
, pp. 1724-1736
-
-
Jang, E.R.1
Lim, S.J.2
Lee, E.S.3
Jeong, G.4
Kim, T.Y.5
Bang, Y.J.6
Lee, J.S.7
-
200
-
-
0028219470
-
Comparison between the effect of butyric acid and its prodrug pivaloyloxymethylbutyrate on histones hyperacetylation in an HL-60 leukemic cell line
-
Aviram A, Zimrah Y, Shaklai M, Nudelman A, Rephaeli A (1994) Comparison between the effect of butyric acid and its prodrug pivaloyloxymethylbutyrate on histones hyperacetylation in an HL-60 leukemic cell line. Int J Cancer 56: 906-909
-
(1994)
Int J Cancer
, vol.56
, pp. 906-909
-
-
Aviram, A.1
Zimrah, Y.2
Shaklai, M.3
Nudelman, A.4
Rephaeli, A.5
-
201
-
-
0028267278
-
FR901228, a novel antitumor bicyclic depsipeptide produced by Chromobacterium violaceum No. 968. III. Antitumor activities on experimental tumors in mice
-
Ueda H, Manda T, Matsumoto S, Mukumoto S, Nishigaki F, Kawamura I, Shimomura K (1994) FR901228, a novel antitumor bicyclic depsipeptide produced by Chromobacterium violaceum No. 968. III. Antitumor activities on experimental tumors in mice. J Antibiot (Tokyo) 47: 315-323
-
(1994)
J Antibiot (Tokyo)
, vol.47
, pp. 315-323
-
-
Ueda, H.1
Manda, T.2
Matsumoto, S.3
Mukumoto, S.4
Nishigaki, F.5
Kawamura, I.6
Shimomura, K.7
-
202
-
-
0034982359
-
In vivo effects of a histone deacetylase inhibitor, FK228, on human acute promyelocytic leukemia in NOD / Shi-scid/scid mice
-
Kosugi H, Ito M, Yamamoto Y, Towatari M, Ueda R, Saito H, Naoe T (2001) In vivo effects of a histone deacetylase inhibitor, FK228, on human acute promyelocytic leukemia in NOD / Shi-scid/scid mice. Jpn J Cancer Res 92: 529-536
-
(2001)
Jpn J Cancer Res
, vol.92
, pp. 529-536
-
-
Kosugi, H.1
Ito, M.2
Yamamoto, Y.3
Towatari, M.4
Ueda, R.5
Saito, H.6
Naoe, T.7
-
203
-
-
0035048449
-
Histone deacetylases induce angiogenesis by negative regulation of tumor suppressor genes
-
Kim MS, Kwon HJ, Lee YM, Baek JH, Jang JE, Lee SW, Moon EJ, Kim HS, Lee SK, Chung HY et al (2001) Histone deacetylases induce angiogenesis by negative regulation of tumor suppressor genes. Nat Med 7: 437-443
-
(2001)
Nat Med
, vol.7
, pp. 437-443
-
-
Kim, M.S.1
Kwon, H.J.2
Lee, Y.M.3
Baek, J.H.4
Jang, J.E.5
Lee, S.W.6
Moon, E.J.7
Kim, H.S.8
Lee, S.K.9
Chung, H.Y.10
-
204
-
-
0034596309
-
Histone deacetylase inhibitors: Inducers of differentiation or apoptosis of transformed cells
-
Marks PA, Richon VM, Rifkind RA (2000) Histone deacetylase inhibitors: inducers of differentiation or apoptosis of transformed cells. J Natl Cancer Inst 92: 1210-1216
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 1210-1216
-
-
Marks, P.A.1
Richon, V.M.2
Rifkind, R.A.3
-
205
-
-
0033367018
-
Chemoprevention of carcinogen-induced mammary tumorigenesis by the hybrid polar cytodifferentiation agent, suberanilohydroxamic acid (SAHA)
-
Cohen LA, Amin S, Marks PA, Rifkind RA, Desai D, Richon VM (1999) Chemoprevention of carcinogen-induced mammary tumorigenesis by the hybrid polar cytodifferentiation agent, suberanilohydroxamic acid (SAHA). Anticancer Res 19: 4999-5005
-
(1999)
Anticancer Res
, vol.19
, pp. 4999-5005
-
-
Cohen, L.A.1
Amin, S.2
Marks, P.A.3
Rifkind, R.A.4
Desai, D.5
Richon, V.M.6
-
206
-
-
0035361402
-
Cyclic hydroxamic-acid-containing peptide 31, a potent synthetic histone deacetylase inhibitor with antitumor activity
-
Komatsu Y, Tomizaki KY, Tsukamoto M, Kato T, Nishino N, Sato S, Yamori T, Tsuruo T, Furumai R, Yoshida M et al (2001) Cyclic hydroxamic-acid-containing peptide 31, a potent synthetic histone deacetylase inhibitor with antitumor activity. Cancer Res 61: 4459-4466
-
(2001)
Cancer Res
, vol.61
, pp. 4459-4466
-
-
Komatsu, Y.1
Tomizaki, K.Y.2
Tsukamoto, M.3
Kato, T.4
Nishino, N.5
Sato, S.6
Yamori, T.7
Tsuruo, T.8
Furumai, R.9
Yoshida, M.10
-
207
-
-
0028269683
-
A phase I and pharmacokinetic study of intravenous phenylacetate in patients with cancer
-
Thibault A, Cooper MR, Figg WD, Venzon DJ, Sartor AO, Tompkins AC, Weinberger MS, Headlee DJ, McCall NA, Samid D et al (1994) A phase I and pharmacokinetic study of intravenous phenylacetate in patients with cancer. Cancer Res 54: 1690-1694
-
(1994)
Cancer Res
, vol.54
, pp. 1690-1694
-
-
Thibault, A.1
Cooper, M.R.2
Figg, W.D.3
Venzon, D.J.4
Sartor, A.O.5
Tompkins, A.C.6
Weinberger, M.S.7
Headlee, D.J.8
McCall, N.A.9
Samid, D.10
-
208
-
-
0031954530
-
Phase I study of the orally administered butyrate prodrug, tributyrin, in patients with solid tumors
-
Conley BA, Egorin MJ, Tait N, Rosen DM, Sausville EA, Dover G, Fram RJ, Van Echo DA (1998) Phase I study of the orally administered butyrate prodrug, tributyrin, in patients with solid tumors. Clin Cancer Res 4: 629-634
-
(1998)
Clin Cancer Res
, vol.4
, pp. 629-634
-
-
Conley, B.A.1
Egorin, M.J.2
Tait, N.3
Rosen, D.M.4
Sausville, E.A.5
Dover, G.6
Fram, R.J.7
Van Echo, D.A.8
-
209
-
-
0033672431
-
Modifying histones to tame cancer: Clinical development of sodium phenylbutyrate and other histone deacetylase inhibitors
-
Gore SD, Carducci MA (2000) Modifying histones to tame cancer: clinical development of sodium phenylbutyrate and other histone deacetylase inhibitors. Expert Opin Investig Drugs 9: 2923-2934
-
(2000)
Expert Opin Investig Drugs
, vol.9
, pp. 2923-2934
-
-
Gore, S.D.1
Carducci, M.A.2
-
210
-
-
0034885248
-
A phase I dose escalation and bioavailability study of oral sodium phenylbutyrate in patients with refractory solid tumor malignancies
-
Gilbert J, Baker SD, Bowling MK, Grochow L, Figg WD, Zabelina Y, Donehower RC, Carducci MA (2001) A phase I dose escalation and bioavailability study of oral sodium phenylbutyrate in patients with refractory solid tumor malignancies. Clin Cancer Res 7: 2292-2300
-
(2001)
Clin Cancer Res
, vol.7
, pp. 2292-2300
-
-
Gilbert, J.1
Baker, S.D.2
Bowling, M.K.3
Grochow, L.4
Figg, W.D.5
Zabelina, Y.6
Donehower, R.C.7
Carducci, M.A.8
-
211
-
-
0020693603
-
Effect of polar organic compounds on leukemic cells. Butyrate-induced partial remission of acute myelogenous leukemia in a child
-
Novogrodsky A, Dvir A, Ravid A, Shkolnik T, Stenzel KH, Rubin AL, Zaizov R (1983) Effect of polar organic compounds on leukemic cells. Butyrate-induced partial remission of acute myelogenous leukemia in a child. Cancer 51: 9-14
-
(1983)
Cancer
, vol.51
, pp. 9-14
-
-
Novogrodsky, A.1
Dvir, A.2
Ravid, A.3
Shkolnik, T.4
Stenzel, K.H.5
Rubin, A.L.6
Zaizov, R.7
-
212
-
-
0035992310
-
A phase I study of pivaloyloxymethyl butyrate, a prodrug of the differentiating agent butyric acid, in patients with advanced solid malignancies
-
Patnaik A, Rowinsky EK, Villalona MA, Hammond LA, Britten CD, Siu LL, Goetz A, Felton SA, Burton S, Valone FH et al (2002) A phase I study of pivaloyloxymethyl butyrate, a prodrug of the differentiating agent butyric acid, in patients with advanced solid malignancies. Clin Cancer Res 8: 2142-2148
-
(2002)
Clin Cancer Res
, vol.8
, pp. 2142-2148
-
-
Patnaik, A.1
Rowinsky, E.K.2
Villalona, M.A.3
Hammond, L.A.4
Britten, C.D.5
Siu, L.L.6
Goetz, A.7
Felton, S.A.8
Burton, S.9
Valone, F.H.10
-
213
-
-
3843151628
-
Phase II trial of the histone deacetylase inhibitor pivaloyl-oxymethyl butyrate (Pivanex, AN-9) in advanced non-small cell lung cancer
-
Reid T, Valone F, Lipera W, Irwin D, Paroly W, Natale R, Sreedharan S, Keer H, Lum B, Scappaticci F et al (2004) Phase II trial of the histone deacetylase inhibitor pivaloyl-oxymethyl butyrate (Pivanex, AN-9) in advanced non-small cell lung cancer. Lung Cancer 45: 381-386
-
(2004)
Lung Cancer
, vol.45
, pp. 381-386
-
-
Reid, T.1
Valone, F.2
Lipera, W.3
Irwin, D.4
Paroly, W.5
Natale, R.6
Sreedharan, S.7
Keer, H.8
Lum, B.9
Scappaticci, F.10
-
214
-
-
18244383806
-
Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells
-
Gottlicher M, Minucci S, Zhu P, Kramer OH, Schimpf A, Giavara S, Sleeman JP, Lo Coco F, Nervi C, Pelicci PG et al (2001) Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells. EMBO J 20: 6969-6978
-
(2001)
EMBO J
, vol.20
, pp. 6969-6978
-
-
Gottlicher, M.1
Minucci, S.2
Zhu, P.3
Kramer, O.H.4
Schimpf, A.5
Giavara, S.6
Sleeman, J.P.7
Lo Coco, F.8
Nervi, C.9
Pelicci, P.G.10
-
215
-
-
0036771408
-
FR-901228 Fujisawa/National Cancer Institute
-
Vigushin DM (2002) FR-901228 Fujisawa/National Cancer Institute. Curr Opin Investig Drugs 3: 1396-1402
-
(2002)
Curr Opin Investig Drugs
, vol.3
, pp. 1396-1402
-
-
Vigushin, D.M.1
-
216
-
-
0030667857
-
Depsipeptide (FR901228, NSC-630176) pharmacokinetics in the rat by LC/MS/MS
-
Chan KK, Bakhtiar R, Jiang C (1997) Depsipeptide (FR901228, NSC-630176) pharmacokinetics in the rat by LC/MS/MS. Invest New Drugs 15: 195-206
-
(1997)
Invest New Drugs
, vol.15
, pp. 195-206
-
-
Chan, K.K.1
Bakhtiar, R.2
Jiang, C.3
-
217
-
-
0036301281
-
Phase I trial of the histone deacetylase inhibitor, depsipeptide (FR901228, NSC 630176), in patients with refractory neoplasms
-
Sandor V, Bakke S, Robey RW, Kang MH, Blagosklonny MV, Bender J, Brooks R, Piekarz RL, Tucker E, Figg WD et al (2002) Phase I trial of the histone deacetylase inhibitor, depsipeptide (FR901228, NSC 630176), in patients with refractory neoplasms. Clin Cancer Res 8: 718-728
-
(2002)
Clin Cancer Res
, vol.8
, pp. 718-728
-
-
Sandor, V.1
Bakke, S.2
Robey, R.W.3
Kang, M.H.4
Blagosklonny, M.V.5
Bender, J.6
Brooks, R.7
Piekarz, R.L.8
Tucker, E.9
Figg, W.D.10
-
218
-
-
0035098155
-
Chronic oral administration of CI-994: A phase 1 study
-
Prakash S, Foster BJ, Meyer M, Wozniak A, Heilbrun LK, Flaherty L, Zalupski M, Radulovic L, Valdivieso M, LoRusso PM (2001) Chronic oral administration of CI-994: a phase 1 study. Invest New Drugs 19: 1-11
-
(2001)
Invest New Drugs
, vol.19
, pp. 1-11
-
-
Prakash, S.1
Foster, B.J.2
Meyer, M.3
Wozniak, A.4
Heilbrun, L.K.5
Flaherty, L.6
Zalupski, M.7
Radulovic, L.8
Valdivieso, M.9
LoRusso, P.M.10
-
219
-
-
10844248177
-
Phase I study of oral CI-994 in combination with carboplatin and paclitaxel in the treatment of patients with advanced solid tumors
-
Pauer LR, Olivares J, Cunningham C, Williams A, Grove W, Kraker A, Olson S, Nemunaitis J (2004) Phase I study of oral CI-994 in combination with carboplatin and paclitaxel in the treatment of patients with advanced solid tumors. Cancer Invest 22: 886-896
-
(2004)
Cancer Invest
, vol.22
, pp. 886-896
-
-
Pauer, L.R.1
Olivares, J.2
Cunningham, C.3
Williams, A.4
Grove, W.5
Kraker, A.6
Olson, S.7
Nemunaitis, J.8
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