-
1
-
-
0035862199
-
The human histone deacetylase family
-
Gray SG, Ekstrom TJ. The human histone deacetylase family. Exp Cell Res 2001;262:75-83.
-
(2001)
Exp Cell Res
, vol.262
, pp. 75-83
-
-
Gray, S.G.1
Ekstrom, T.J.2
-
2
-
-
0344407016
-
Histone deacetylases: Unique players in shaping the epigenetic histone code
-
Thiagalingam S, Cheng KH, Lee HJ, Mineva N, Thiagalingam A, Ponte JF. Histone deacetylases: unique players in shaping the epigenetic histone code. Ann N Y Acad Sci 2003;983:84-100.
-
(2003)
Ann N Y Acad Sci
, vol.983
, pp. 84-100
-
-
Thiagalingam, S.1
Cheng, K.H.2
Lee, H.J.3
Mineva, N.4
Thiagalingam, A.5
Ponte, J.F.6
-
3
-
-
25144496904
-
The Sir 2 family of protein deacetylases
-
Denu JM. The Sir 2 family of protein deacetylases. Curr Opin Chem Biol 2005;9:431-40.
-
(2005)
Curr Opin Chem Biol
, vol.9
, pp. 431-440
-
-
Denu, J.M.1
-
4
-
-
2642573581
-
-
Buck SW, Gallo CM, Smith JS. Diversity in the Sir2 family of protein deacetylases. J Leukoc Biol 2004;75:939-50.
-
Buck SW, Gallo CM, Smith JS. Diversity in the Sir2 family of protein deacetylases. J Leukoc Biol 2004;75:939-50.
-
-
-
-
5
-
-
0029932598
-
A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p. Science New York N Y
-
Taunton J, Hassig CA, Schreiber SL. A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p. Science New York N Y 1996;272:408-11.
-
(1996)
, vol.272
, pp. 408-411
-
-
Taunton, J.1
Hassig, C.A.2
Schreiber, S.L.3
-
6
-
-
0029850458
-
Transcriptional repression by YY1 is mediated by interaction with a mammalian homolog of the yeast global regulator RPD3
-
Yang WM, Inouye C, Zeng Y, Bearss D, Seto E. Transcriptional repression by YY1 is mediated by interaction with a mammalian homolog of the yeast global regulator RPD3. Proc Natl Acad Sci U S A 1996;93:12845-50.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 12845-12850
-
-
Yang, W.M.1
Inouye, C.2
Zeng, Y.3
Bearss, D.4
Seto, E.5
-
7
-
-
0030834976
-
Isolation and characterization of cDNAs corresponding to an additional member of the human histone deacetylase gene family
-
Yang WM, Yao YL, Sun JM, Davie JR, Seto E. Isolation and characterization of cDNAs corresponding to an additional member of the human histone deacetylase gene family. J Biol Chem 1997;272:28001-7.
-
(1997)
J Biol Chem
, vol.272
, pp. 28001-28007
-
-
Yang, W.M.1
Yao, Y.L.2
Sun, J.M.3
Davie, J.R.4
Seto, E.5
-
8
-
-
0034725990
-
Cloning and characterization of human histone deacetylase 8
-
Van den Wyngaert I, de Vries W, Kremer A, et al. Cloning and characterization of human histone deacetylase 8. FEBS Lett 2000;478:77-83.
-
(2000)
FEBS Lett
, vol.478
, pp. 77-83
-
-
Van den Wyngaert, I.1
de Vries, W.2
Kremer, A.3
-
9
-
-
0034685766
-
Cloning and characterization of a novel human class I histone deacetylase that functions as a transcription repressor
-
Hu E, Chen Z, Fredrickson T, et al. Cloning and characterization of a novel human class I histone deacetylase that functions as a transcription repressor. J Biol Chem 2000;275:15254-64.
-
(2000)
J Biol Chem
, vol.275
, pp. 15254-15264
-
-
Hu, E.1
Chen, Z.2
Fredrickson, T.3
-
10
-
-
0033597115
-
A new family of human histone deacetylases related to Saccharomyces cerevisiae HDA1p
-
Fischle W, Emiliani S, Hendzel MJ, et al. A new family of human histone deacetylases related to Saccharomyces cerevisiae HDA1p. J Biol Chem 1999;274:11713-20.
-
(1999)
J Biol Chem
, vol.274
, pp. 11713-11720
-
-
Fischle, W.1
Emiliani, S.2
Hendzel, M.J.3
-
11
-
-
0033609055
-
Three proteins define a class of human histone deacetylases related to yeast Hda1p
-
Grozinger CM, Hassig CA, Schreiber SL. Three proteins define a class of human histone deacetylases related to yeast Hda1p. Proc Natl Acad Sci U S A 1999;96:4868-73.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 4868-4873
-
-
Grozinger, C.M.1
Hassig, C.A.2
Schreiber, S.L.3
-
12
-
-
0032696590
-
HDAC4, a human histone deacetylase related to yeast HDA1, is a transcriptional corepressor
-
Wang AH, Bertos NR, Vezmar M, et al. HDAC4, a human histone deacetylase related to yeast HDA1, is a transcriptional corepressor. Mol Cell Biol 1999;19:7816-27.
-
(1999)
Mol Cell Biol
, vol.19
, pp. 7816-7827
-
-
Wang, A.H.1
Bertos, N.R.2
Vezmar, M.3
-
13
-
-
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. Isolation of a novel histone deacetylase reveals that class I and class II deacetylases promote SMRT-mediated repression. Genes Dev 2000;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
-
14
-
-
0035845539
-
Cloning and characterization of a histone deacetylase, HDAC9
-
Zhou X, Marks PA, Rifkind RA, Richon VM. Cloning and characterization of a histone deacetylase, HDAC9. Proc Natl Acad Sci U S A 2001;98:10572-7.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 10572-10577
-
-
Zhou, X.1
Marks, P.A.2
Rifkind, R.A.3
Richon, V.M.4
-
15
-
-
0037016696
-
Isolation and characterization of mammalian HDAC10, a novel histone deacetylase
-
Kao HY, Lee CH, Komarov A, Han CC, Evans RM. Isolation and characterization of mammalian HDAC10, a novel histone deacetylase. J Biol Chem 2002;277:187-93.
-
(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
-
16
-
-
0037067696
-
Cloning and functional characterization of HDAC11, a novel member of the human histone deacetylase family
-
Gao L, Cueto MA, Asselbergs F, Atadja P. Cloning and functional characterization of HDAC11, a novel member of the human histone deacetylase family. J Biol Chem 2002;277:25748-55.
-
(2002)
J Biol Chem
, vol.277
, pp. 25748-25755
-
-
Gao, L.1
Cueto, M.A.2
Asselbergs, F.3
Atadja, P.4
-
17
-
-
20144388146
-
Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer
-
Fraga MF, Ballestar E, Villar-Garea A, et al. Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer. Nat Genet 2005;37:391-400.
-
(2005)
Nat Genet
, vol.37
, pp. 391-400
-
-
Fraga, M.F.1
Ballestar, E.2
Villar-Garea, A.3
-
18
-
-
0035676731
-
Expression profile of histone deacetylase 1 in gastric cancer tissues
-
Choi JH, Kwon HJ, Yoon BI, et al. Expression profile of histone deacetylase 1 in gastric cancer tissues. Jpn J Cancer Res 2001;92:1300-4.
-
(2001)
Jpn J Cancer Res
, vol.92
, pp. 1300-1304
-
-
Choi, J.H.1
Kwon, H.J.2
Yoon, B.I.3
-
19
-
-
1842631408
-
Upregulation and nuclear recruitment of HDAC1 in hormone refractory prostate cancer
-
Halkidou K, Gaughan L, Cook S, Leung HY, Neal DE, Robson CN. Upregulation and nuclear recruitment of HDAC1 in hormone refractory prostate cancer. Prostate 2004;59:177-89.
-
(2004)
Prostate
, vol.59
, pp. 177-189
-
-
Halkidou, K.1
Gaughan, L.2
Cook, S.3
Leung, H.Y.4
Neal, D.E.5
Robson, C.N.6
-
20
-
-
0142122363
-
Overexpression of histone deacetylase HDAC1 modulates breast cancer progression by negative regulation of estrogen receptor a
-
Kawai H, Li H, Avraham S, Jiang S, Avraham HK. Overexpression of histone deacetylase HDAC1 modulates breast cancer progression by negative regulation of estrogen receptor a. Int J Cancer 2003;107:353-8.
-
(2003)
Int J Cancer
, vol.107
, pp. 353-358
-
-
Kawai, H.1
Li, H.2
Avraham, S.3
Jiang, S.4
Avraham, H.K.5
-
21
-
-
33744956666
-
Histone deacetylase 3 (HDAC3) and other class I HDACs regulate colon cell maturation and p21 expression and are deregulated in human colon cancer
-
Wilson AJ, Byun DS, Popova N, et al. Histone deacetylase 3 (HDAC3) and other class I HDACs regulate colon cell maturation and p21 expression and are deregulated in human colon cancer. J Biol Chem 2006;281:13548-58.
-
(2006)
J Biol Chem
, vol.281
, pp. 13548-13558
-
-
Wilson, A.J.1
Byun, D.S.2
Popova, N.3
-
22
-
-
2342603414
-
Induction of HDAC2 expression upon loss of APC in colorectal tumorigenesis
-
Zhu P, Martin E, Mengwasser J, Schlag P, Janssen KP, Gottlicher M. Induction of HDAC2 expression upon loss of APC in colorectal tumorigenesis. Cancer Cell 2004;5:455-63.
-
(2004)
Cancer Cell
, vol.5
, pp. 455-463
-
-
Zhu, P.1
Martin, E.2
Mengwasser, J.3
Schlag, P.4
Janssen, K.P.5
Gottlicher, M.6
-
23
-
-
0036014986
-
Histone deacetylases as therapeutic targets in hematologic malignancies
-
Melnick A, Licht JD. Histone deacetylases as therapeutic targets in hematologic malignancies. Curr Opin Hematol 2002;9:322-32.
-
(2002)
Curr Opin Hematol
, vol.9
, pp. 322-332
-
-
Melnick, A.1
Licht, J.D.2
-
24
-
-
21844448876
-
Acute myeloid leukemia: Therapeutic impact of epigenetic drugs
-
Altucci L, Clarke N, Nebbioso A, Scognamiglio A, Gronemeyer H. Acute myeloid leukemia: therapeutic impact of epigenetic drugs. Int J Biochem Cell Biol 2005;37:1752-62.
-
(2005)
Int J Biochem Cell Biol
, vol.37
, pp. 1752-1762
-
-
Altucci, L.1
Clarke, N.2
Nebbioso, A.3
Scognamiglio, A.4
Gronemeyer, H.5
-
25
-
-
0036527775
-
Histone-deacetylase inhibitors: Novel drugs for the treatment of cancer
-
Johnstone RW. Histone-deacetylase inhibitors: novel drugs for the treatment of cancer. Nat Rev 2002;1:287-99.
-
(2002)
Nat Rev
, vol.1
, pp. 287-299
-
-
Johnstone, R.W.1
-
26
-
-
0035755974
-
Histone deacetylases and cancer: Causes and therapies
-
Marks P, Rifkind RA, Richon VM, Breslow R, Miller T, Kelly WK. Histone deacetylases and cancer: causes and therapies. Nat Rev Cancer 2001;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
-
27
-
-
34247109089
-
Histone deacetylase inhibitors for epigenetic therapy of cancer
-
Monneret C. Histone deacetylase inhibitors for epigenetic therapy of cancer. Anticancer Drugs 2007;18:363-70.
-
(2007)
Anticancer Drugs
, vol.18
, pp. 363-370
-
-
Monneret, C.1
-
28
-
-
33748451151
-
Anticancer activities of histone-deacetylase inhibitors
-
Bolden JE, Peart MJ, Johnstone RW. Anticancer activities of histone-deacetylase inhibitors. Nat Rev 2006;5:769-84.
-
(2006)
Nat Rev
, vol.5
, pp. 769-784
-
-
Bolden, J.E.1
Peart, M.J.2
Johnstone, R.W.3
-
29
-
-
20444479514
-
Drug insight: Histone deacetylase inhibitors-development of the new targeted anticancer agent suberoylanilide hydroxamic acid
-
Kelly WK, Marks PA. Drug insight: histone deacetylase inhibitors-development of the new targeted anticancer agent suberoylanilide hydroxamic acid. Nat Clin Pract 2005;2:150-7.
-
(2005)
Nat Clin Pract
, vol.2
, pp. 150-157
-
-
Kelly, W.K.1
Marks, P.A.2
-
30
-
-
30344477367
-
Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer
-
Minucci S, Pelicci PG. Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer. Nat Rev Cancer 2006;6:38-51.
-
(2006)
Nat Rev Cancer
, vol.6
, pp. 38-51
-
-
Minucci, S.1
Pelicci, P.G.2
-
31
-
-
34547864236
-
Histone deacetylase inhibitors: Molecular mechanisms of action
-
Xu WS, Parmigiani RB, Marks PA. Histone deacetylase inhibitors: molecular mechanisms of action. Oncogene 2007;26:5541-52.
-
(2007)
Oncogene
, vol.26
, pp. 5541-5552
-
-
Xu, W.S.1
Parmigiani, R.B.2
Marks, P.A.3
-
32
-
-
0032539890
-
A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases
-
Richon VM, Emiliani S, Verdin E, et al. A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases. Proc Natl Acad Sci U S A 1998;95:3003-7.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 3003-3007
-
-
Richon, V.M.1
Emiliani, S.2
Verdin, E.3
-
33
-
-
20844444898
-
Combination of the histone deacetylase inhibitor LBH589 and the hsp90 inhibitor 17-AAG is highly active against human CML-BC cells and AML cells with activating mutation of FLT-3
-
George P, Bali P, Annavarapu S, et al. Combination of the histone deacetylase inhibitor LBH589 and the hsp90 inhibitor 17-AAG is highly active against human CML-BC cells and AML cells with activating mutation of FLT-3. Blood 2005;105:1768-76.
-
(2005)
Blood
, vol.105
, pp. 1768-1776
-
-
George, P.1
Bali, P.2
Annavarapu, S.3
-
34
-
-
1642453460
-
Pharmacodynamic response and inhibition of growth of human tumor xenografts by the novel histone deacetylase inhibitor PXD101
-
Plumb JA, Finn PW, Williams RJ, et al. Pharmacodynamic response and inhibition of growth of human tumor xenografts by the novel histone deacetylase inhibitor PXD101. Mol Cancer Ther 2003;2:721-8.
-
(2003)
Mol Cancer Ther
, vol.2
, pp. 721-728
-
-
Plumb, J.A.1
Finn, P.W.2
Williams, R.J.3
-
35
-
-
0036735385
-
FK228 (depsipeptide) as a natural prodrug that inhibits class I histone deacetylases
-
Furumai R, Matsuyama A, Kobashi N, et al. FK228 (depsipeptide) as a natural prodrug that inhibits class I histone deacetylases. Cancer Res 2002;62:4916-21.
-
(2002)
Cancer Res
, vol.62
, pp. 4916-4921
-
-
Furumai, R.1
Matsuyama, A.2
Kobashi, N.3
-
36
-
-
33847258674
-
Discovery and development of SAHA as an anticancer agent
-
Marks PA. Discovery and development of SAHA as an anticancer agent. Oncogene 2007;26:1351-6.
-
(2007)
Oncogene
, vol.26
, pp. 1351-1356
-
-
Marks, P.A.1
-
37
-
-
0033551152
-
A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors
-
Saito A, Yamashita T, Mariko Y, et al. A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors. Proc Natl Acad Sci U S A 1999;96:4592-7.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 4592-4597
-
-
Saito, A.1
Yamashita, T.2
Mariko, Y.3
-
38
-
-
0142179154
-
Identification of novel isoform-selective inhibitors within class I histone deacetylases
-
Hu E, Dul E, Sung CM, et al. Identification of novel isoform-selective inhibitors within class I histone deacetylases. J Pharmacol Exp Ther 2003;307:720-8.
-
(2003)
J Pharmacol Exp Ther
, vol.307
, pp. 720-728
-
-
Hu, E.1
Dul, E.2
Sung, C.M.3
-
39
-
-
33845514708
-
Will broad-spectrum histone deacetylase inhibitors be superseded by more specific compounds?
-
Karagiannis TC, El-Osta A. Will broad-spectrum histone deacetylase inhibitors be superseded by more specific compounds? Leukemia 2007;21:61-5.
-
(2007)
Leukemia
, vol.21
, pp. 61-65
-
-
Karagiannis, T.C.1
El-Osta, A.2
-
40
-
-
0017795309
-
Resolution of histones by polyacrylamide gel electrophoresis in presence of nonionic detergents
-
Zweidler A. Resolution of histones by polyacrylamide gel electrophoresis in presence of nonionic detergents. Methods Cell Biol 1978;17:223-33.
-
(1978)
Methods Cell Biol
, vol.17
, pp. 223-233
-
-
Zweidler, A.1
-
41
-
-
0141570564
-
Role of class I and class II histone deacetylases in carcinoma cells using siRNA
-
Glaser KB, Li J, Staver MJ, Wei RQ, Albert DH, Davidsen SK. Role of class I and class II histone deacetylases in carcinoma cells using siRNA. Biochem Biophys Res Commun 2003;310:529-36.
-
(2003)
Biochem Biophys Res Commun
, vol.310
, pp. 529-536
-
-
Glaser, K.B.1
Li, J.2
Staver, M.J.3
Wei, R.Q.4
Albert, D.H.5
Davidsen, S.K.6
-
42
-
-
18444414332
-
Essential function of histone deacetylase 1 in proliferation control and CDK inhibitor repression
-
Lagger G, O'Carroll D, Rembold M, et al. Essential function of histone deacetylase 1 in proliferation control and CDK inhibitor repression. EMBO J 2002;21:2672-81.
-
(2002)
EMBO J
, vol.21
, pp. 2672-2681
-
-
Lagger, G.1
O'Carroll, D.2
Rembold, M.3
-
43
-
-
34347339526
-
Role for histone deacetylase 1 in human tumor cell proliferation
-
Senese S, Zaragoza K, Minardi S, et al. Role for histone deacetylase 1 in human tumor cell proliferation. Mol Cell Biol 2007;27:4784-95.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 4784-4795
-
-
Senese, S.1
Zaragoza, K.2
Minardi, S.3
-
45
-
-
0034665124
-
Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo
-
Butler LM, Agus DB, Scher HI, et al. Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo. Cancer Res 2000;60:5165-70.
-
(2000)
Cancer Res
, vol.60
, pp. 5165-5170
-
-
Butler, L.M.1
Agus, D.B.2
Scher, H.I.3
-
46
-
-
34547094822
-
Distinct pharmacological properties of second generation HDAC inhibitors with the benzamide or hydroxamate head group
-
Beckers T, Burkhardt C, Wieland H, et al. Distinct pharmacological properties of second generation HDAC inhibitors with the benzamide or hydroxamate head group. Int J Cancer 2007;121:1138-48.
-
(2007)
Int J Cancer
, vol.121
, pp. 1138-1148
-
-
Beckers, T.1
Burkhardt, C.2
Wieland, H.3
-
47
-
-
0033539092
-
Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors
-
Finnin MS, Donigian JR, Cohen A, et al. Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors. Nature 1999;401:188-93.
-
(1999)
Nature
, vol.401
, pp. 188-193
-
-
Finnin, M.S.1
Donigian, J.R.2
Cohen, A.3
-
48
-
-
36148950575
-
Novel aminophenyl benzamide-type histone deacetylase inhibitors with enhanced potency and selectivity
-
Moradei OM, Mallais TC, Frechette S, et al. Novel aminophenyl benzamide-type histone deacetylase inhibitors with enhanced potency and selectivity. J Med Chem 2007;50:5543-6.
-
(2007)
J Med Chem
, vol.50
, pp. 5543-5546
-
-
Moradei, O.M.1
Mallais, T.C.2
Frechette, S.3
-
49
-
-
33845357791
-
Clinical activity and safety of the histone deacetylase inhibitor MGCD0103: Results of a phase I study in patients with leukemia or myelodysplastic syndromes (MDS)
-
Garcia-Manero G, Minden M, Estrov Z, et al. Clinical activity and safety of the histone deacetylase inhibitor MGCD0103: results of a phase I study in patients with leukemia or myelodysplastic syndromes (MDS). 2006 ASCO Annual Meeting. J Clin Oncol 2006;24:6500.
-
(2006)
ASCO Annual Meeting. J Clin Oncol
, vol.24
, pp. 6500
-
-
Garcia-Manero, G.1
Minden, M.2
Estrov, Z.3
-
50
-
-
42249099883
-
-
Younes A, Fanale M, Pro B, et al. A phase II study of a novel oral isotype-selective histone deacetylase (HDAC) inhibitor in patients with relapsed or refractory Hodgkin lymphoma. 2007 ASCO Annual Meeting. J Clin Oncol 2007;25:8000.
-
Younes A, Fanale M, Pro B, et al. A phase II study of a novel oral isotype-selective histone deacetylase (HDAC) inhibitor in patients with relapsed or refractory Hodgkin lymphoma. 2007 ASCO Annual Meeting. J Clin Oncol 2007;25:8000.
-
-
-
|