-
1
-
-
0034023070
-
Progress in the diagnosis and treatment of rhabdomyosarcoma and related soft tissue sarcomas
-
Ruymann, F. B., and Grovas, A. C. Progress in the diagnosis and treatment of rhabdomyosarcoma and related soft tissue sarcomas. Cancer Investig., 18: 223-241, 2000.
-
(2000)
Cancer Investig.
, vol.18
, pp. 223-241
-
-
Ruymann, F.B.1
Grovas, A.C.2
-
2
-
-
0028964049
-
The Third Intergroup Rhabdomyosarcoma Study
-
Crist, W., Gehan, E. A., Ragab, A. H., Dickman, P. S., Donaldson, S. S., Fryer, C., Hammond, D., Hays, D. M., Herrmann, J., and Heyn, R. The Third Intergroup Rhabdomyosarcoma Study. J. Clin. Oncol., 13: 610-630, 1995.
-
(1995)
J. Clin. Oncol.
, vol.13
, pp. 610-630
-
-
Crist, W.1
Gehan, E.A.2
Ragab, A.H.3
Dickman, P.S.4
Donaldson, S.S.5
Fryer, C.6
Hammond, D.7
Hays, D.M.8
Herrmann, J.9
Heyn, R.10
-
3
-
-
0033950402
-
Preoperative staging, prognostic factors, and outcome for extremity rhabdomyosarcoma: A preliminary report from the Intergroup Rhabdomyosarcoma Study IV (1991-1997)
-
Neville, H. L., Andrassy, R. J., Lobe, T. E., Bagwell, C. E., Anderson, J. R., Womer, R. B., Crist, W. M., and Wiener, E. S. Preoperative staging, prognostic factors, and outcome for extremity rhabdomyosarcoma: a preliminary report from the Intergroup Rhabdomyosarcoma Study IV (1991-1997). J. Pediatr. Surg., 35: 317-321, 2000.
-
(2000)
J. Pediatr. Surg.
, vol.35
, pp. 317-321
-
-
Neville, H.L.1
Andrassy, R.J.2
Lobe, T.E.3
Bagwell, C.E.4
Anderson, J.R.5
Womer, R.B.6
Crist, W.M.7
Wiener, E.S.8
-
4
-
-
0035008973
-
Rhabdomyosarcoma and undifferentiated sarcoma in the first two decades of life: A selective review of Intergroup Rhabdomyosarcoma Study Group experience and rationale for Intergroup Rhabdomyosarcoma Study V
-
Raney, R. B., Anderson, J. R., Barr, F. G., Donaldson, S. S., Pappo, A. S., Qualman, S. J., Wiener, E. S., Maurer, H. M., and Crist, W. M. Rhabdomyosarcoma and undifferentiated sarcoma in the first two decades of life: a selective review of Intergroup Rhabdomyosarcoma Study Group experience and rationale for Intergroup Rhabdomyosarcoma Study V. Am. J. Pediatr. Hematol. Oncol., 23: 215-220, 2001.
-
(2001)
Am J. Pediatr. Hematol. Oncol.
, vol.23
, pp. 215-220
-
-
Raney, R.B.1
Anderson, J.R.2
Barr, F.G.3
Donaldson, S.S.4
Pappo, A.S.5
Qualman, S.J.6
Wiener, E.S.7
Maurer, H.M.8
Crist, W.M.9
-
5
-
-
0030798245
-
Histone acetylation in chromatin structure and transcription
-
Grunstein, M., Histone acetylation in chromatin structure and transcription. Nature (Lond.), 389: 349-352, 1997.
-
(1997)
Nature (Lond.)
, vol.389
, pp. 349-352
-
-
Grunstein, M.1
-
6
-
-
0032539890
-
A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases
-
Richon, V. M., Emiliani, S., Verdin, E., Webb, Y., Breslow, R., Rifkind, R. A., and Marks, P. A. A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases. Proc. Natl. Acad. Sci. USA, 95: 3003-3007, 1998.
-
(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
-
7
-
-
0033520944
-
Histone deacetylase inhibition selectively alters the activity and expression of cell cycle proteins leading to specific chromatin acetylation and antiproliferative effects
-
Sambucetti, L. C., Fischer, D. D., Zabludoff, S., Kwon, P. O., Chamberlin, H., Trogani, N., Xu, H., and Cohen, D. 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.
-
(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
-
9
-
-
0032030770
-
Histone acetylation and transcriptional regulatory mechanisms
-
Struhl, K. Histone acetylation and transcriptional regulatory mechanisms. Genes Dev., 12: 599-606, 1998.
-
(1998)
Genes Dev.
, vol.12
, pp. 599-606
-
-
Struhl, K.1
-
10
-
-
0024996768
-
Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A
-
Yoshida, M., Kijima, M., Akita, M., and Beppu, T. Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A. J. Biol. Chem., 265: 17174-17179, 1990.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 17174-17179
-
-
Yoshida, M.1
Kijima, M.2
Akita, M.3
Beppu, T.4
-
11
-
-
0017886958
-
Sodium butyrate inhibits histone deacetylation in cultured cells
-
Candido, E. P. M., Reeves, R., and Davie, J. R. Sodium butyrate inhibits histone deacetylation in cultured cells. Cell, 14: 105-113, 1978.
-
(1978)
Cell
, vol.14
, pp. 105-113
-
-
Candido, E.P.M.1
Reeves, R.2
Davie, J.R.3
-
12
-
-
0344431240
-
FR901228, a potent antitumor antibiotic, is a novel histone deacetylase inhibitor
-
Nakajima, H., Kim, Y. B., Terano, H., Yoshida, M., and Horinouchi, S. FR901228, a potent antitumor antibiotic, is a novel histone deacetylase inhibitor. Exp. Cell Res., 241: 126-133, 1998.
-
(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
-
13
-
-
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., and Nakanishi, O. 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.
-
(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
-
14
-
-
1542588471
-
Second generation hybrid polar compounds are potent inducers of transformed cell differentiation
-
Richon, V. M., Webb, Y., Merger, R., Sheppard, T., Jursic, B., Ngo, L., Civoli, F., Breslow, R., Rifkind, R. A., and Marks, P. A. Second generation hybrid polar compounds are potent inducers of transformed cell differentiation. Proc. Natl. Acad. Sci. USA, 93: 5705-5708, 1996.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 5705-5708
-
-
Richon, V.M.1
Webb, Y.2
Merger, R.3
Sheppard, T.4
Jursic, B.5
Ngo, L.6
Civoli, F.7
Breslow, R.8
Rifkind, R.A.9
Marks, P.A.10
-
15
-
-
0033199896
-
Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma
-
Glick, R. D., Swendeman, S. L., Coffey, D. C., Rifkind, R. A., Marks, P. A., Richon, V. M., and LaQuaglia, M. P. Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma. Cancer Res., 59: 4392-4399, 1999.
-
(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
LaQuaglia, M.P.7
-
16
-
-
0034665124
-
Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo
-
Butler, L. M., Agus, D. B., Scher, H. I., Higgins, B., Rose, A., Cordon-Cardo, C., Thaler, H. T., Rifkind, R. A., Marks, P. A., and Richon, V. M. Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo. Cancer Res., 60: 5165-5170, 2000.
-
(2000)
Cancer Res.
, vol.60
, pp. 5165-5170
-
-
Butler, L.M.1
Agus, D.B.2
Scher, H.I.3
Higgins, B.4
Rose, A.5
Cordon-Cardo, C.6
Thaler, H.T.7
Rifkind, R.A.8
Marks, P.A.9
Richon, V.M.10
-
17
-
-
0034905872
-
Inhibition of transformed cell growth and induction of cellular differentiation by pyroxamide, an inhibitor of histone deacetylase
-
Butler, L. M., Webb, Y., Agus, D. B., Higgins, B., Tolentino, T. R., Kutko, M. C., LaQuaglia, M. P., Drobnjak, M., Cordon-Cardo, C., Scher, H. I., Breslow, R., Richon, V. M., Rifkind, R. A., and Marks, P. A. Inhibition of transformed cell growth and induction of cellular differentiation by pyroxamide, an inhibitor of histone deacetylase. Clin. Cancer Res., 7: 962-970, 2001.
-
(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
Breslow, R.11
Richon, V.M.12
Rifkind, R.A.13
Marks, P.A.14
-
18
-
-
0036906832
-
Histone deacetylase inhibitors: From target to clinical trials
-
Kelly, W. K., O'Connor, O. A., and Marks, P. A. Histone deacetylase inhibitors: from target to clinical trials. Expert Opin. Investig. Drugs, 11: 1695-1713, 2002.
-
(2002)
Expert Opin. Investig. Drugs
, vol.11
, pp. 1695-1713
-
-
Kelly, W.K.1
O'Connor, O.A.2
Marks, P.A.3
-
19
-
-
12444321545
-
Phase 1 clinical trial of histone deacetylase inhibitor: Suberoylanilide hydroxamic acid (SAHA) administered intravenously
-
Kelly, W. K., Richon, V. M., O'Connor, O., Curley, T., MacGregor-Curtelli, B., Tong, W., Klang, M., Schwartz, L., Richardson, S., Rosa, E., Drobnjak, M., Cordon-Cordo, C., Chiao, J. H., Rifkind, R., Marks, P. A., and Scher, H. Phase 1 clinical trial of histone deacetylase inhibitor: suberoylanilide hydroxamic acid (SAHA) administered intravenously. Clin. Cancer Res., 9: 3578-3588, 2003.
-
(2003)
Clin. Cancer Res.
, vol.9
, pp. 3578-3588
-
-
Kelly, W.K.1
Richon, V.M.2
O'Connor, O.3
Curley, T.4
MacGregor-Curtelli, B.5
Tong, W.6
Klang, M.7
Schwartz, L.8
Richardson, S.9
Rosa, E.10
Drobnjak, M.11
Cordon-Cordo, C.12
Chiao, J.H.13
Rifkind, R.14
Marks, P.A.15
Scher, H.16
-
20
-
-
0032842703
-
1 arrest and apoptosis in myeloid leukemia cells: Structure-function analysis
-
1 arrest and apoptosis in myeloid leukemia cells: structure-function analysis. Leukemia (Baltimore), 13: 1243-1253, 1999.
-
(1999)
Leukemia (Baltimore)
, vol.13
, pp. 1243-1253
-
-
DiGiuseppe, J.A.1
Weng, L.J.2
Yu, K.H.3
Fu, S.4
Kastan, M.B.5
Samid, D.6
Gore, S.D.7
-
21
-
-
0033561497
-
Oxamflatin is a novel antitumor compound that inhibits mammalian histone deacetylase
-
Kim, Y. B., Lee, K. H., Sugita, K., Yoshida, M., and Horinouchi, S. Oxamflatin is a novel antitumor compound that inhibits mammalian histone deacetylase. Oncogene, 18: 2461-2470, 1999.
-
(1999)
Oncogene
, vol.18
, pp. 2461-2470
-
-
Kim, Y.B.1
Lee, K.H.2
Sugita, K.3
Yoshida, M.4
Horinouchi, S.5
-
22
-
-
0033646839
-
Histone deacetylase inhibitors and retinoic acids inhibit growth of human neuroblastoma in vitro
-
Coffey, D. C., Kutko, M. C., Glick, R. D., Swendeman, S. L., Butler, L. M., Rifkind, R. A., Marks, P. A., Richon, V. M., and LaQuaglia, M. P. Histone deacetylase inhibitors and retinoic acids inhibit growth of human neuroblastoma in vitro. Med. Pediatr. Oncol., 35: 577-581, 2000.
-
(2000)
Med. Pediatr. Oncol.
, vol.35
, pp. 577-581
-
-
Coffey, D.C.1
Kutko, M.C.2
Glick, R.D.3
Swendeman, S.L.4
Butler, L.M.5
Rifkind, R.A.6
Marks, P.A.7
Richon, V.M.8
LaQuaglia, M.P.9
-
23
-
-
0035328528
-
The histone deacetylase inhibitor, CBHA, inhibits growth of human neuroblastoma xenografts in vivo, alone and synergistically with all-trans retinoic acid
-
Coffey, D. C., Kutko, M. C., Glick, R. D., Butler, L. M., Heller, G., Rifkind, R. A., Marks, P. A., Richon, V. M., and Laquaglia, M. P. The histone deacetylase inhibitor, CBHA, inhibits growth of human neuroblastoma xenografts in vivo, alone and synergistically with all-trans retinoic acid. Cancer Res., 61: 3591-3594, 2001.
-
(2001)
Cancer Res.
, vol.61
, pp. 3591-3594
-
-
Coffey, D.C.1
Kutko, M.C.2
Glick, R.D.3
Butler, L.M.4
Heller, G.5
Rifkind, R.A.6
Marks, P.A.7
Richon, V.M.8
Laquaglia, M.P.9
-
24
-
-
0033367018
-
Chemoprevention of carcinogen-induced mammary tumorigenesis by the hybrid polar cytodifferentiation agent, suberanilohydroxamic acid (SAHA)
-
Cohen, L. A., Amin, S., Marks, P. A., Rifkind, R. A., Desai, D., and Richon, V. M. Chemoprevention of carcinogen-induced mammary tumorigenesis by the hybrid polar cytodifferentiation agent, suberanilohydroxamic acid (SAHA). Anticancer Res., 19: 4999-5005, 1999.
-
(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
-
25
-
-
0037236445
-
Chemopreventive efficacy of suberoylanilide hydroxamic acid (SAHA) against 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-induced lung tumorigenesis in female A/J mice
-
Desai, D., Das, A., Cohen, L., El-Bayoumy, K., and Amin, S. Chemopreventive efficacy of suberoylanilide hydroxamic acid (SAHA) against 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-induced lung tumorigenesis in female A/J mice. Anticancer Res. 23(1A): 499-503, 2003.
-
(2003)
Anticancer Res.
, vol.23
, Issue.1 A
, pp. 499-503
-
-
Desai, D.1
Das, A.2
Cohen, L.3
El-Bayoumy, K.4
Amin, S.5
-
26
-
-
0033118754
-
Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: An introduction
-
Feinberg, A. P. Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: an introduction. Cancer Res., 59 (Suppl.): 1743s-1746s, 1999.
-
(1999)
Cancer Res.
, vol.59
, Issue.SUPPL.
-
-
Feinberg, A.P.1
-
27
-
-
0027366917
-
Fusion of PAX3 to a member of the forkhead family of transcription factors in human alveolar rhabdomyosarcoma
-
Shapiro, D. N., Sublett, J. E., Li, B., Downing, J. R., and Naeve, C. W. Fusion of PAX3 to a member of the forkhead family of transcription factors in human alveolar rhabdomyosarcoma. Cancer Res., 53: 5108-5112, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 5108-5112
-
-
Shapiro, D.N.1
Sublett, J.E.2
Li, B.3
Downing, J.R.4
Naeve, C.W.5
-
28
-
-
0028364374
-
Fusion of PAX7 to FHRK by the variant t(1;13)(p36;q14) translocation in alveolar rhabdomyosarcoma
-
Davis, R. J., D'Cruz, C. M., Lovell, M. A., Biegel, J. A., and Barr, F. G. Fusion of PAX7 to FHRK by the variant t(1;13)(p36;q14) translocation in alveolar rhabdomyosarcoma. Cancer Res., 54: 2869-2872, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 2869-2872
-
-
Davis, R.J.1
D'Cruz, C.M.2
Lovell, M.A.3
Biegel, J.A.4
Barr, F.G.5
-
29
-
-
0033562343
-
Both Sp1 and Sp3 are responsible for p21/WAF1 promoter activity induced by histone deacetylase inhibitor in NIH3T3 cells
-
Xiao, H., Hasegawa, T., and Isobe, K. Both Sp1 and Sp3 are responsible for p21/WAF1 promoter activity induced by histone deacetylase inhibitor in NIH3T3 cells. J. Cell. Biochem., 73: 291-302, 1999.
-
(1999)
J. Cell. Biochem.
, vol.73
, pp. 291-302
-
-
Xiao, H.1
Hasegawa, T.2
Isobe, K.3
-
30
-
-
0034730127
-
Histone deacetylase inhibitor selectively induces p21/WAF1 expression and gene-associated histone acetylation
-
Richon, V. M., Sandhoff, T. W., Rifkind, R. A., and Marks, P. A. Histone deacetylase inhibitor selectively induces p21/WAF1 expression and gene-associated histone acetylation. Proc. Natl. Acad. Sci. USA, 97: 10014-10019, 2000.
-
(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
-
31
-
-
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., and Sakai, T. Histone deacetylase inhibitor activates the p21/WAF1/Cip1 gene promoter through the Sp1 sites. Ann. N. Y. Acad. Sci., 886: 195-199, 1999.
-
(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
-
32
-
-
0030772026
-
Butyrate activates the WAF1/Cip1 gene promoter through Sp1 sites in a p53-negative human colon cancer cell line
-
Nakano, K., Mizuno, T., Sowa, Y., Orita, T., Yoshino, T., Okuyama, Y., Fujita, T., Ohtani-Fujita, N., Matsukawa, Y., Tokino, T., Yamagishi, H., Oka, T., Nomura, H., and Sakai, T. Butyrate activates the WAF1/Cip1 gene promoter through Sp1 sites in a p53-negative human colon cancer cell line. J. Biol. Chem., 272: 22199-22206, 1997.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 22199-22206
-
-
Nakano, K.1
Mizuno, T.2
Sowa, Y.3
Orita, T.4
Yoshino, T.5
Okuyama, Y.6
Fujita, T.7
Ohtani-Fujita, N.8
Matsukawa, Y.9
Tokino, T.10
Yamagishi, H.11
Oka, T.12
Nomura, H.13
Sakai, T.14
|