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Human Reproduction (Oxford, England)
|
January 1, 1989
Glucose phosphate isomerase activity in mouse and human eggs and pre-embryos
J D West, J H Flockhart, R R Angell, et al.
British Journal of Pharmacology
|
March 22, 2005
GW274150 and GW273629 are potent and highly selective inhibitors of inducible nitric oxide synthase in vitro and in vivo
Wendy K Alderton, Anthony D R Angell, Caroline Craig, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
January 6, 2011
GSK256066, an exceptionally high-affinity and selective inhibitor of phosphodiesterase 4 suitable for administration by inhalation: in vitro, kinetic, and in vivo characterization
Cathy J Tralau-Stewart, Richard A Williamson, Anthony T Nials, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 13, 2011
Heteroalicyclic carboxamidines as inhibitors of inducible nitric oxide synthase; the identification of (2R)-2-pyrrolidinecarboxamidine as a potent and selective haem-co-ordinating inhibitor
Robert J Young, Wendy Alderton, Anthony D R Angell, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 10, 2008
Pyrazolopyridines as a novel structural class of potent and selective PDE4 inhibitors
J Nicole Hamblin, Tony D R Angell, Stuart P Ballantine, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 45) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 45 results.
Human Reproduction (Oxford, England)
|
January 1, 1989
Glucose phosphate isomerase activity in mouse and human eggs and pre-embryos
J D West, J H Flockhart, R R Angell, et al.
British Journal of Pharmacology
|
March 22, 2005
GW274150 and GW273629 are potent and highly selective inhibitors of inducible nitric oxide synthase in vitro and in vivo
Wendy K Alderton, Anthony D R Angell, Caroline Craig, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
January 6, 2011
GSK256066, an exceptionally high-affinity and selective inhibitor of phosphodiesterase 4 suitable for administration by inhalation: in vitro, kinetic, and in vivo characterization
Cathy J Tralau-Stewart, Richard A Williamson, Anthony T Nials, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 13, 2011
Heteroalicyclic carboxamidines as inhibitors of inducible nitric oxide synthase; the identification of (2R)-2-pyrrolidinecarboxamidine as a potent and selective haem-co-ordinating inhibitor
Robert J Young, Wendy Alderton, Anthony D R Angell, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 10, 2008
Pyrazolopyridines as a novel structural class of potent and selective PDE4 inhibitors
J Nicole Hamblin, Tony D R Angell, Stuart P Ballantine, et al.
Page
of 5