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British Journal of Urology
|
February 1, 1986
Objective responses to ketoconazole therapy in patients with relapsed progressive prostatic cancer
G Williams, D J Kerle, H Ware, et al.
British Journal of Urology
|
September 1, 1989
A search for infectious agents in chronic abacterial prostatitis using ultrasound guided biopsy
A Doble, B J Thomas, P M Furr, et al.
Neuropharmacology
|
May 1, 1996
Molecular cloning, functional expression, pharmacological characterization and chromosomal localization of the human metabotropic glutamate receptor type 3
L Emile, L Mercken, F Apiou, et al.
Life Sciences
|
July 28, 1986
PK 11195, an antagonist of peripheral type benzodiazepine receptors, modulates Bay K8644 sensitive but not beta- or H2-receptor sensitive voltage operated calcium channels in the guinea pig heart
M Mestre, T Carriot, G Néliat, et al.
Analytical and Bioanalytical Chemistry
|
December 6, 2023
Spatial distribution of trace metals and associated transport proteins during bacterial infection
Raquel Gonzalez de Vega, David Clases, Bliss A Cunningham, et al.
Metallomics : Integrated Biometal Science
|
February 8, 2017
Age modulates the injury-induced metallomic profile in the brain
Stuart D Portbury, Dominic J Hare, Charlotte J Sgambelloni, et al.
British Journal of Pharmacology
|
January 1, 1992
Pharmacological characterization of RP 62203, a novel 5-hydroxytryptamine 5-HT2 receptor antagonist
A Doble, D Girdlestone, O Piot, et al.
Bioorganic & Medicinal Chemistry
|
August 1, 1994
Synthesis, anticonvulsant and neuroprotective activities of RP 66055, a riluzole derivative
P Jimonet, M Barreau, J C Blanchard, et al.
European Journal of Pharmacology
|
September 9, 1986
Stereoselective inhibition of the binding of [3H]PK 11195 to peripheral-type benzodiazepine binding sites by a quinolinepropanamide derivative
M C Dubroeucq, J Bénavidès, A Doble, et al.
Molecular Pharmacology
|
February 1, 1994
Septide: an agonist for the NK1 receptor acting at a site distinct from substance P
L Pradier, J Ménager, J Le Guern, et al.
Page
of 19
Search research articles
Search
Showing results (131-140 of 181) with videos related to
Sort By:
Page
of 19
British Journal of Urology
|
February 1, 1986
Objective responses to ketoconazole therapy in patients with relapsed progressive prostatic cancer
G Williams, D J Kerle, H Ware, et al.
British Journal of Urology
|
September 1, 1989
A search for infectious agents in chronic abacterial prostatitis using ultrasound guided biopsy
A Doble, B J Thomas, P M Furr, et al.
Neuropharmacology
|
May 1, 1996
Molecular cloning, functional expression, pharmacological characterization and chromosomal localization of the human metabotropic glutamate receptor type 3
L Emile, L Mercken, F Apiou, et al.
Life Sciences
|
July 28, 1986
PK 11195, an antagonist of peripheral type benzodiazepine receptors, modulates Bay K8644 sensitive but not beta- or H2-receptor sensitive voltage operated calcium channels in the guinea pig heart
M Mestre, T Carriot, G Néliat, et al.
Analytical and Bioanalytical Chemistry
|
December 6, 2023
Spatial distribution of trace metals and associated transport proteins during bacterial infection
Raquel Gonzalez de Vega, David Clases, Bliss A Cunningham, et al.
Metallomics : Integrated Biometal Science
|
February 8, 2017
Age modulates the injury-induced metallomic profile in the brain
Stuart D Portbury, Dominic J Hare, Charlotte J Sgambelloni, et al.
British Journal of Pharmacology
|
January 1, 1992
Pharmacological characterization of RP 62203, a novel 5-hydroxytryptamine 5-HT2 receptor antagonist
A Doble, D Girdlestone, O Piot, et al.
Bioorganic & Medicinal Chemistry
|
August 1, 1994
Synthesis, anticonvulsant and neuroprotective activities of RP 66055, a riluzole derivative
P Jimonet, M Barreau, J C Blanchard, et al.
European Journal of Pharmacology
|
September 9, 1986
Stereoselective inhibition of the binding of [3H]PK 11195 to peripheral-type benzodiazepine binding sites by a quinolinepropanamide derivative
M C Dubroeucq, J Bénavidès, A Doble, et al.
Molecular Pharmacology
|
February 1, 1994
Septide: an agonist for the NK1 receptor acting at a site distinct from substance P
L Pradier, J Ménager, J Le Guern, et al.
Page
of 19