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Results of search for 'au:"POIROT, M"', page 2 of 2
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Authors
Baron, B M
Bayard, F
Chailleux, C
Delarue, F
Fargin, A
Faye, J C
Kedjouar, B
Kehne, J H
Klaebe, A
McCloskey, T C
Mesange, F
Mésange, F
POIROT, M
Perie, J J
Poirot, M
Poirot, M K
Reichmann, M E
Schnitzlein, W M
Siegel, B W
Traore, M
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Animals
Binding Sites
Binding, Competitive
Breast Neoplasms
Cell Division
Cell Line
Estrogen Antagonists
Female
Humans
Kinetics
Male
Mice
Rats
Receptors, Drug
Tamoxifen
chemistry
drug effects
metabolism
pharmacology
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Your search returned 24 results.
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21.
In vitro and in vivo characterization of MDL 105,212A, a nonpeptide NK-1/NK-2 tachykinin receptor antagonist.
[electronic resource]
by
Kudlacz, E M
Shatzer, S A
Knippenberg, R W
Logan, D E
Poirot, M
van Giersbergen, P L
Burkholder, T P
Producer:
19960627
In:
The Journal of pharmacology and experimental therapeutics
vol. 277
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22.
Microsomal epoxide hydrolase of rat liver is a subunit of theanti-oestrogen-binding site.
[electronic resource]
by
Mésange, F
Sebbar, M
Kedjouar, B
Capdevielle, J
Guillemot, J C
Ferrara, P
Bayard, F
Delarue, F
Faye, J C
Poirot, M
Producer:
19981008
In:
The Biochemical journal
vol. 334 ( Pt 1)
Online resources:
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23.
MDL 100,458 and MDL 102,288: two potent and selective glycine receptor antagonists with different functional profiles.
[electronic resource]
by
Kehne, J H
Baron, B M
Harrison, B L
McCloskey, T C
Palfreyman, M G
Poirot, M
Salituro, F G
Siegel, B W
Slone, A L
Van Giersbergen, P L
Producer:
19960220
In:
European journal of pharmacology
vol. 284
Online resources:
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24.
Preclinical characterization of the potential of the putative atypical antipsychotic MDL 100,907 as a potent 5-HT2A antagonist with a favorable CNS safety profile.
[electronic resource]
by
Kehne, J H
Baron, B M
Carr, A A
Chaney, S F
Elands, J
Feldman, D J
Frank, R A
van Giersbergen, P L
McCloskey, T C
Johnson, M P
McCarty, D R
Poirot, M
Senyah, Y
Siegel, B W
Widmaier, C
Producer:
19960627
In:
The Journal of pharmacology and experimental therapeutics
vol. 277
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