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The Journal of Biological Chemistry
|
June 3, 2006
Association of Catsper1 or -2 with Ca(v)3.3 leads to suppression of T-type calcium channel activity
Di Zhang, Jun Chen, Anita Saraf, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
September 18, 2002
(-)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide (A-278637): a novel ATP-sensitive potassium channel opener efficacious in suppressing urinary bladder contractions. II. in vivo characterization
Michael E Brune, Thomas A Fey, Jorge D Brioni, et al.
Neurourology and Urodynamics
|
February 13, 2003
Effects of ATP-sensitive K+ channel openers and tolterodine on involuntary bladder contractions in a pig model of partial bladder outlet obstruction
Thomas A Fey, Murali Gopalakrishnan, James G Strake, et al.
Assay and Drug Development Technologies
|
April 20, 2004
Automated Parallel Oocyte Electrophysiology Test station (POETs): a screening platform for identification of ligand-gated ion channel modulators
Char-Chang Shieh, Jonathan D Trumbull, Jay F Sarthy, et al.
IS&T International Symposium on Electronic Imaging
|
December 1, 2025
Scale-up Unlearnable Examples Learning with High-Performance Computing
Yanfan Zhu, Issac Lyngaas, Murali Gopalakrishnan Meena, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 29, 2002
Structure-Activity studies for a novel series of tricyclic dihydropyrimidines as K(ATP) channel openers (KCOs)
Irene Drizin, Mark W Holladay, Lin Yi, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
April 25, 2009
In vitro pharmacological characterization of a novel allosteric modulator of alpha 7 neuronal acetylcholine receptor, 4-(5-(4-chlorophenyl)-2-methyl-3-propionyl-1H-pyrrol-1-yl)benzenesulfonamide (A-867744), exhibiting unique pharmacological profile
John Malysz, Jens Halvard Grønlien, David J Anderson, et al.
Journal of Cardiovascular Pharmacology
|
July 10, 2004
(-)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide (A-278637), a novel ATP-sensitive potassium channel opener: hemodynamic comparison to ZD-6169, WAY-133537, and nifedipine in the anesthetized canine
Ryan M Fryer, Lee C Preusser, Samuel V Calzadilla, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 18, 2010
Syntheses and structure-activity relationship (SAR) studies of 2,5-diazabicyclo[2.2.1]heptanes as novel alpha7 neuronal nicotinic receptor (NNR) ligands
Tao Li, William H Bunnelle, Keith B Ryther, et al.
British Journal of Pharmacology
|
January 24, 2003
Pharmacological characterization of a 1,4-dihydropyridine analogue, 9-(3,4-dichlorophenyl)-3,3,6,6-tetramethyl-3,4,6,7,9,10-hexahydro-1,8(2H,5H)-acridinedione (A-184209) as a novelK(ATP) channel inhibitor
Murali Gopalakrishnan, Thomas R Miller, Steven A Buckner, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 83) with videos related to
Sort By:
Page
of 9
The Journal of Biological Chemistry
|
June 3, 2006
Association of Catsper1 or -2 with Ca(v)3.3 leads to suppression of T-type calcium channel activity
Di Zhang, Jun Chen, Anita Saraf, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
September 18, 2002
(-)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide (A-278637): a novel ATP-sensitive potassium channel opener efficacious in suppressing urinary bladder contractions. II. in vivo characterization
Michael E Brune, Thomas A Fey, Jorge D Brioni, et al.
Neurourology and Urodynamics
|
February 13, 2003
Effects of ATP-sensitive K+ channel openers and tolterodine on involuntary bladder contractions in a pig model of partial bladder outlet obstruction
Thomas A Fey, Murali Gopalakrishnan, James G Strake, et al.
Assay and Drug Development Technologies
|
April 20, 2004
Automated Parallel Oocyte Electrophysiology Test station (POETs): a screening platform for identification of ligand-gated ion channel modulators
Char-Chang Shieh, Jonathan D Trumbull, Jay F Sarthy, et al.
IS&T International Symposium on Electronic Imaging
|
December 1, 2025
Scale-up Unlearnable Examples Learning with High-Performance Computing
Yanfan Zhu, Issac Lyngaas, Murali Gopalakrishnan Meena, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 29, 2002
Structure-Activity studies for a novel series of tricyclic dihydropyrimidines as K(ATP) channel openers (KCOs)
Irene Drizin, Mark W Holladay, Lin Yi, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
April 25, 2009
In vitro pharmacological characterization of a novel allosteric modulator of alpha 7 neuronal acetylcholine receptor, 4-(5-(4-chlorophenyl)-2-methyl-3-propionyl-1H-pyrrol-1-yl)benzenesulfonamide (A-867744), exhibiting unique pharmacological profile
John Malysz, Jens Halvard Grønlien, David J Anderson, et al.
Journal of Cardiovascular Pharmacology
|
July 10, 2004
(-)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide (A-278637), a novel ATP-sensitive potassium channel opener: hemodynamic comparison to ZD-6169, WAY-133537, and nifedipine in the anesthetized canine
Ryan M Fryer, Lee C Preusser, Samuel V Calzadilla, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 18, 2010
Syntheses and structure-activity relationship (SAR) studies of 2,5-diazabicyclo[2.2.1]heptanes as novel alpha7 neuronal nicotinic receptor (NNR) ligands
Tao Li, William H Bunnelle, Keith B Ryther, et al.
British Journal of Pharmacology
|
January 24, 2003
Pharmacological characterization of a 1,4-dihydropyridine analogue, 9-(3,4-dichlorophenyl)-3,3,6,6-tetramethyl-3,4,6,7,9,10-hexahydro-1,8(2H,5H)-acridinedione (A-184209) as a novelK(ATP) channel inhibitor
Murali Gopalakrishnan, Thomas R Miller, Steven A Buckner, et al.
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of 9