Ellsworth K - Search Results

1

Expression of the type 1 and 2 steroid 5 alpha-reductases in human fetal tissues.

Ellsworth K, Harris G. Ellsworth K, et al. Biochem Biophys Res Commun. 1995 Oct 13;215(2):774-80. doi: 10.1006/bbrc.1995.2530. Biochem Biophys Res Commun. 1995. PMID: 7488021

2

Effects of finasteride, a type 2 5-alpha reductase inhibitor, on fetal development in the rhesus monkey (Macaca mulatta).

Prahalada S, Tarantal AF, Harris GS, Ellsworth KP, Clarke AP, Skiles GL, MacKenzie KI, Kruk LF, Ablin DS, Cukierski MA, Peter CP, vanZwieten MJ, Hendrickx AG. Prahalada S, et al. Among authors: ellsworth kp. Teratology. 1997 Feb;55(2):119-31. doi: 10.1002/(SICI)1096-9926(199702)55:2<119::AID-TERA1>3.0.CO;2-Z. Teratology. 1997. PMID: 9143092

3

Identification and selective inhibition of an isozyme of steroid 5 alpha-reductase in human scalp.

Harris G, Azzolina B, Baginsky W, Cimis G, Rasmusson GH, Tolman RL, Raetz CR, Ellsworth K. Harris G, et al. Among authors: ellsworth k. Proc Natl Acad Sci U S A. 1992 Nov 15;89(22):10787-91. doi: 10.1073/pnas.89.22.10787. Proc Natl Acad Sci U S A. 1992. PMID: 1438277 Free PMC article.

4

Inhibition of rat alpha-reductases by finasteride: evidence for isozyme differences in the mechanism of inhibition.

Azzolina B, Ellsworth K, Andersson S, Geissler W, Bull HG, Harris GS. Azzolina B, et al. Among authors: ellsworth k. J Steroid Biochem Mol Biol. 1997 Apr;61(1-2):55-64. doi: 10.1016/s0960-0760(97)00002-2. J Steroid Biochem Mol Biol. 1997. PMID: 9328210

5

Cloning, expression and characterization of rhesus macaque types 1 and 2 5alpha-reductase: evidence for mechanism-based inhibition by finasteride.

Ellsworth KP, Azzolina BA, Cimis G, Bull HG, Harris GS. Ellsworth KP, et al. J Steroid Biochem Mol Biol. 1998 Sep;66(5-6):271-9. doi: 10.1016/s0960-0760(98)00059-4. J Steroid Biochem Mol Biol. 1998. PMID: 9749833

6

4-Aza-3-oxo-5 alpha-androst-1-ene-17 beta-N-aryl-carboxamides as dual inhibitors of human type 1 and type 2 steroid 5 alpha-reductases. Dramatic effect of N-aryl substituents on type 1 and type 2 5 alpha-reductase inhibitory potency.

Bakshi RK, Rasmusson GH, Patel GF, Mosley RT, Chang B, Ellsworth K, Harris GS, Tolman RL. Bakshi RK, et al. Among authors: ellsworth k. J Med Chem. 1995 Aug 18;38(17):3189-92. doi: 10.1021/jm00017a001. J Med Chem. 1995. PMID: 7650670 No abstract available.

7

4,7 beta-Dimethyl-4-azacholestan-3-one (MK-386) and related 4-azasteroids as selective inhibitors of human type 1 5 alpha-reductase.

Bakshi RK, Patel GF, Rasmusson GH, Baginsky WF, Cimis G, Ellsworth K, Chang B, Bull H, Tolman RL, Harris GS. Bakshi RK, et al. Among authors: ellsworth k. J Med Chem. 1994 Nov 11;37(23):3871-4. doi: 10.1021/jm00049a003. J Med Chem. 1994. PMID: 7966146 No abstract available.

8

MK386: a potent, selective inhibitor of the human type 1 5alpha-reductase.

Ellsworth K, Azzolina B, Baginsky W, Bull H, Chang B, Cimis G, Mitra S, Toney J, Bakshi RK, Rasmusson GR, Tolman RL, Harris GS. Ellsworth K, et al. J Steroid Biochem Mol Biol. 1996 Jul;58(4):377-84. doi: 10.1016/0960-0760(96)00050-7. J Steroid Biochem Mol Biol. 1996. PMID: 8903421

9

A new class of glycogen phosphorylase inhibitors.

Lu Z, Bohn J, Bergeron R, Deng Q, Ellsworth KP, Geissler WM, Harris G, McCann PE, McKeever B, Myers RW, Saperstein R, Willoughby CA, Yao J, Chapman K. Lu Z, et al. Among authors: ellsworth kp. Bioorg Med Chem Lett. 2003 Nov 17;13(22):4125-8. doi: 10.1016/j.bmcl.2003.08.046. Bioorg Med Chem Lett. 2003. PMID: 14592521

10

Novel 3,4-dihydroquinolin-2(1H)-one inhibitors of human glycogen phosphorylase a.

Rosauer KG, Ogawa AK, Willoughby CA, Ellsworth KP, Geissler WM, Myers RW, Deng Q, Chapman KT, Harris G, Moller DE. Rosauer KG, et al. Among authors: ellsworth kp. Bioorg Med Chem Lett. 2003 Dec 15;13(24):4385-8. doi: 10.1016/j.bmcl.2003.09.022. Bioorg Med Chem Lett. 2003. PMID: 14643331

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