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R F Bruns

Showing results (1-10 of 54) with videos related to

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Biochemical Pharmacology|February 15, 1981
Adenosine antagonism by purines, pteridines and benzopteridines in human fibroblastsR F Bruns
Canadian Journal of Physiology and Pharmacology|June 1, 1980
Adenosine receptor activation in human fibroblasts: nucleoside agonists and antagonistsR F Bruns
Trends in Pharmacological Sciences|May 1, 1996
Conformational induction versus conformational selection: evidence from allosteric enhancersR F Bruns
Annals of the New York Academy of Sciences|January 1, 1990
Adenosine receptors. Roles and pharmacologyR F Bruns
Naunyn-Schmiedeberg'S Archives of Pharmacology|January 1, 1980
Adenosine receptor activation by adenine nucleotides requires conversion of the nucleotides to adenosineR F Bruns
Journal of Medicinal Chemistry|May 1, 1988
[1,2,4]Triazolo[4,3-a]quinoxalin-4-amines: a new class of A1 receptor selective adenosine antagonistsB K Trivedi, R F Bruns
Journal of Medicinal Chemistry|August 1, 1989
C2,N6-disubstituted adenosines: synthesis and structure-activity relationshipsB K Trivedi, R F Bruns
Molecular Pharmacology|December 1, 1990
Allosteric enhancement of adenosine A1 receptor binding and function by 2-amino-3-benzoylthiophenesR F Bruns, J H Fergus
The Journal of Pharmacy and Pharmacology|September 1, 1989
Solubilities of adenosine antagonists determined by radioreceptor assayR F Bruns, J H Fergus
Journal of Neurochemistry|May 1, 1980
Depolarization-evoked accumulation of cyclic AMP in brain slices: the requisite intermediate adenosine is not derived from hydrolysis of released ATPF Pons, R F Bruns, J W Daly
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
Biochemical Pharmacology|February 15, 1981
Adenosine antagonism by purines, pteridines and benzopteridines in human fibroblastsR F Bruns
Canadian Journal of Physiology and Pharmacology|June 1, 1980
Adenosine receptor activation in human fibroblasts: nucleoside agonists and antagonistsR F Bruns
Trends in Pharmacological Sciences|May 1, 1996
Conformational induction versus conformational selection: evidence from allosteric enhancersR F Bruns
Annals of the New York Academy of Sciences|January 1, 1990
Adenosine receptors. Roles and pharmacologyR F Bruns
Naunyn-Schmiedeberg'S Archives of Pharmacology|January 1, 1980
Adenosine receptor activation by adenine nucleotides requires conversion of the nucleotides to adenosineR F Bruns
Journal of Medicinal Chemistry|May 1, 1988
[1,2,4]Triazolo[4,3-a]quinoxalin-4-amines: a new class of A1 receptor selective adenosine antagonistsB K Trivedi, R F Bruns
Journal of Medicinal Chemistry|August 1, 1989
C2,N6-disubstituted adenosines: synthesis and structure-activity relationshipsB K Trivedi, R F Bruns
Molecular Pharmacology|December 1, 1990
Allosteric enhancement of adenosine A1 receptor binding and function by 2-amino-3-benzoylthiophenesR F Bruns, J H Fergus
The Journal of Pharmacy and Pharmacology|September 1, 1989
Solubilities of adenosine antagonists determined by radioreceptor assayR F Bruns, J H Fergus
Journal of Neurochemistry|May 1, 1980
Depolarization-evoked accumulation of cyclic AMP in brain slices: the requisite intermediate adenosine is not derived from hydrolysis of released ATPF Pons, R F Bruns, J W Daly
Pageof 6