Faye JC - Search Results

1

Modifications of benzylphenoxy ethanamine antiestrogen molecules: influence affinity for antiestrogen binding site (AEBS) and cell cytotoxicity.

Delarue F, Kedjouar B, Mésange F, Bayard F, Faye JC, Poirot M. Delarue F, et al. Among authors: faye jc. Biochem Pharmacol. 1999 Mar 15;57(6):657-61. doi: 10.1016/s0006-2952(98)00347-5. Biochem Pharmacol. 1999. PMID: 10037451

2

Insulin and estrogen receptor ligand influence the FGF-2 activities in MCF-7 breast cancer cells.

Garnier M, Giamarchi C, Delrieu I, Rio MC, Chinestra P, Bayard F, Poirot M, Faye JC. Garnier M, et al. Among authors: faye jc. Biochem Pharmacol. 2003 Feb 15;65(4):629-36. doi: 10.1016/s0006-2952(02)01563-0. Biochem Pharmacol. 2003. PMID: 12566092

3

A potent and selective photoaffinity probe for the anti-estrogen binding site of rat liver.

Poirot M, Chailleux C, Fargin A, Bayard F, Faye JC. Poirot M, et al. Among authors: faye jc. J Biol Chem. 1990 Oct 5;265(28):17039-43. J Biol Chem. 1990. PMID: 2211609 Free article.

4

The anti-proliferative properties of 4-benzylphenoxy ethanamine derivatives are mediated by the anti-estrogen binding site (ABS), whereas the anti-estrogenic effects of trifluopromazine are not.

Poirot M, Garnier M, Bayard F, Riviere I, Traore M, Wilson M, Fargin A, Faye JC. Poirot M, et al. Among authors: faye jc. Biochem Pharmacol. 1990 Aug 1;40(3):425-9. doi: 10.1016/0006-2952(90)90539-w. Biochem Pharmacol. 1990. PMID: 2383280

5

Antiestrogens inhibit the replication of the retroviral Moloney murine leukemia virus in vitro.

Chailleux C, Mesange F, Bayard F, Prats AC, Faye JC. Chailleux C, et al. Among authors: faye jc. Mol Pharmacol. 1993 Aug;44(2):324-7. Mol Pharmacol. 1993. PMID: 7689144

6

Ligands of the antiestrogen binding site block endothelial cell proliferation reversibly.

Garnier M, Mésange F, Dupont MA, Gas N, Zanibellato C, Bayard F, Faye JC. Garnier M, et al. Among authors: faye jc. Exp Cell Res. 1993 Mar;205(1):191-4. doi: 10.1006/excr.1993.1075. Exp Cell Res. 1993. PMID: 8453993

7

Ligands of the antiestrogen-binding site are able to inhibit virion production of human immunodeficiency virus 1-infected lymphocytes.

Mesange F, Delarue F, Puel J, Bayard F, Faye JC. Mesange F, et al. Among authors: faye jc. Mol Pharmacol. 1996 Jul;50(1):75-9. Mol Pharmacol. 1996. PMID: 8700122

8

Microsomal epoxide hydrolase of rat liver is a subunit of theanti-oestrogen-binding site.

Mésange F, Sebbar M, Kedjouar B, Capdevielle J, Guillemot JC, Ferrara P, Bayard F, Delarue F, Faye JC, Poirot M. Mésange F, et al. Among authors: faye jc. Biochem J. 1998 Aug 15;334 ( Pt 1)(Pt 1):107-12. doi: 10.1042/bj3340107. Biochem J. 1998. PMID: 9693109 Free PMC article.

9

Structural similitudes between cytotoxic antiestrogen-binding site (AEBS) ligands and cytotoxic sigma receptor ligands. Evidence for a relationship between cytotoxicity and affinity for AEBS or sigma-2 receptor but not for sigma-1 receptor.

Kedjouar B, Daunes S, Vilner BJ, Bowen WD, Klaebe A, Faye JC, Poirot M. Kedjouar B, et al. Among authors: faye jc. Biochem Pharmacol. 1999 Dec 15;58(12):1927-39. doi: 10.1016/s0006-2952(99)00285-3. Biochem Pharmacol. 1999. PMID: 10591147

10

Synthesis, binding and structure-affinity studies of new ligands for the microsomal anti-estrogen binding site (AEBS).

Poirot M, De Medina P, Delarue F, Perie JJ, Klaebe A, Faye JC. Poirot M, et al. Among authors: faye jc. Bioorg Med Chem. 2000 Aug;8(8):2007-16. doi: 10.1016/s0968-0896(00)00119-x. Bioorg Med Chem. 2000. PMID: 11003145

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