Kulp SK - Search Results

1

Identification and characterization of a novel integrin-linked kinase inhibitor.

Lee SL, Hsu EC, Chou CC, Chuang HC, Bai LY, Kulp SK, Chen CS. Lee SL, et al. Among authors: kulp sk. J Med Chem. 2011 Sep 22;54(18):6364-74. doi: 10.1021/jm2007744. Epub 2011 Aug 24. J Med Chem. 2011. PMID: 21823616 Free PMC article.

2

Cyclooxygenase-2, player or spectator in cyclooxygenase-2 inhibitor-induced apoptosis in prostate cancer cells.

Song X, Lin HP, Johnson AJ, Tseng PH, Yang YT, Kulp SK, Chen CS. Song X, et al. Among authors: kulp sk. J Natl Cancer Inst. 2002 Apr 17;94(8):585-91. doi: 10.1093/jnci/94.8.585. J Natl Cancer Inst. 2002. PMID: 11959891

3

3-phosphoinositide-dependent protein kinase-1/Akt signaling represents a major cyclooxygenase-2-independent target for celecoxib in prostate cancer cells.

Kulp SK, Yang YT, Hung CC, Chen KF, Lai JP, Tseng PH, Fowble JW, Ward PJ, Chen CS. Kulp SK, et al. Cancer Res. 2004 Feb 15;64(4):1444-51. doi: 10.1158/0008-5472.can-03-2396. Cancer Res. 2004. PMID: 14973075

4

From the cyclooxygenase-2 inhibitor celecoxib to a novel class of 3-phosphoinositide-dependent protein kinase-1 inhibitors.

Zhu J, Huang JW, Tseng PH, Yang YT, Fowble J, Shiau CW, Shaw YJ, Kulp SK, Chen CS. Zhu J, et al. Among authors: kulp sk. Cancer Res. 2004 Jun 15;64(12):4309-18. doi: 10.1158/0008-5472.CAN-03-4063. Cancer Res. 2004. PMID: 15205346

5

Growth inhibitory effects of celecoxib in human umbilical vein endothelial cells are mediated through G1 arrest via multiple signaling mechanisms.

Lin HP, Kulp SK, Tseng PH, Yang YT, Yang CC, Chen CS, Chen CS. Lin HP, et al. Among authors: kulp sk. Mol Cancer Ther. 2004 Dec;3(12):1671-80. Mol Cancer Ther. 2004. PMID: 15634661

6

Peroxisome proliferator-activated receptor gamma-independent ablation of cyclin D1 by thiazolidinediones and their derivatives in breast cancer cells.

Huang JW, Shiau CW, Yang YT, Kulp SK, Chen KF, Brueggemeier RW, Shapiro CL, Chen CS. Huang JW, et al. Among authors: kulp sk. Mol Pharmacol. 2005 Apr;67(4):1342-8. doi: 10.1124/mol.104.007732. Epub 2005 Jan 13. Mol Pharmacol. 2005. PMID: 15653552

7

Thiazolidenediones mediate apoptosis in prostate cancer cells in part through inhibition of Bcl-xL/Bcl-2 functions independently of PPARgamma.

Shiau CW, Yang CC, Kulp SK, Chen KF, Chen CS, Huang JW, Chen CS. Shiau CW, et al. Among authors: kulp sk. Cancer Res. 2005 Feb 15;65(4):1561-9. doi: 10.1158/0008-5472.CAN-04-1677. Cancer Res. 2005. PMID: 15735046

8

Antitumor effects of a novel phenylbutyrate-based histone deacetylase inhibitor, (S)-HDAC-42, in prostate cancer.

Kulp SK, Chen CS, Wang DS, Chen CY, Chen CS. Kulp SK, et al. Clin Cancer Res. 2006 Sep 1;12(17):5199-206. doi: 10.1158/1078-0432.CCR-06-0429. Clin Cancer Res. 2006. Retraction in: Clin Cancer Res. 2019 May 1;25(9):2940. doi: 10.1158/1078-0432.CCR-19-0731 PMID: 16951239 Retracted.

9

Histone deacetylase inhibitors sensitize prostate cancer cells to agents that produce DNA double-strand breaks by targeting Ku70 acetylation.

Chen CS, Wang YC, Yang HC, Huang PH, Kulp SK, Yang CC, Lu YS, Matsuyama S, Chen CY, Chen CS. Chen CS, et al. Among authors: kulp sk. Cancer Res. 2007 Jun 1;67(11):5318-27. doi: 10.1158/0008-5472.CAN-06-3996. Cancer Res. 2007. Retraction in: Cancer Res. 2018 Jul 15;78(14):4097. doi: 10.1158/0008-5472.CAN-18-1291 PMID: 17545612 Retracted.

10

Chemopreventive and bioenergetic signaling effects of PDK1/Akt pathway inhibition in a transgenic mouse model of prostate cancer.

Sargeant AM, Klein RD, Rengel RC, Clinton SK, Kulp SK, Kashida Y, Yamaguchi M, Wang X, Chen CS. Sargeant AM, et al. Among authors: kulp sk. Toxicol Pathol. 2007 Jun;35(4):549-61. doi: 10.1080/01926230701338966. Toxicol Pathol. 2007. PMID: 17562488

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