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J Gregg

Showing results (311-320 of 320) with videos related to

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Nature Chemical Biology|January 19, 2021
Characterizing the portability of phage-encoded homologous recombination proteinsGabriel T Filsinger, Timothy M Wannier, Felix B Pedersen, et al.
BMC Public Health|October 5, 2018
The relationship between physical literacy scores and adherence to Canadian physical activity and sedentary behaviour guidelinesKevin Belanger, Joel D Barnes, Patricia E Longmuir, et al.
BMC Public Health|October 5, 2018
Physical literacy levels of Canadian children aged 8-12 years: descriptive and normative results from the RBC Learn to Play-CAPL projectMark S Tremblay, Patricia E Longmuir, Joel D Barnes, et al.
Neuroscience|May 5, 2007
P2X7-related modulation of pathological nociception in ratsS McGaraughty, K L Chu, M T Namovic, et al.
BMC Public Health|October 5, 2018
Cardiorespiratory fitness is associated with physical literacy in a large sample of Canadian children aged 8 to 12 yearsJustin J Lang, Jean-Philippe Chaput, Patricia E Longmuir, et al.
Bioorganic & Medicinal Chemistry|October 23, 2010
Discovery and biological evaluation of potent, selective, orally bioavailable, pyrazine-based blockers of the Na(v)1.8 sodium channel with efficacy in a model of neuropathic painMarc J C Scanio, Lei Shi, Irene Drizin, et al.
Journal of Medicinal Chemistry|May 28, 2004
Synthesis and structure-activity relationships of a novel series of 2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide K(ATP) channel openers: discovery of (-)-(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 potent K(ATP) opener that selectively inhibits spontaneous bladder contractionsWilliam A Carroll, Robert J Altenbach, Hao Bai, et al.
Bioorganic & Medicinal Chemistry Letters|September 22, 2010
Subtype-selective Na(v)1.8 sodium channel blockers: identification of potent, orally active nicotinamide derivativesMichael E Kort, Robert N Atkinson, James B Thomas, et al.
Bioorganic & Medicinal Chemistry|May 27, 2008
Discovery of potent furan piperazine sodium channel blockers for treatment of neuropathic painIrene Drizin, Robert J Gregg, Marc J C Scanio, et al.
Journal of Medicinal Chemistry|January 8, 2008
Discovery and biological evaluation of 5-aryl-2-furfuramides, potent and selective blockers of the Nav1.8 sodium channel with efficacy in models of neuropathic and inflammatory painMichael E Kort, Irene Drizin, Robert J Gregg, et al.
Pageof 32

Showing results (311-320 of 320) with videos related to

Sort By:
Pageof 32
You have reached the last page of results.This site can display upto 320 results.
Nature Chemical Biology|January 19, 2021
Characterizing the portability of phage-encoded homologous recombination proteinsGabriel T Filsinger, Timothy M Wannier, Felix B Pedersen, et al.
BMC Public Health|October 5, 2018
The relationship between physical literacy scores and adherence to Canadian physical activity and sedentary behaviour guidelinesKevin Belanger, Joel D Barnes, Patricia E Longmuir, et al.
BMC Public Health|October 5, 2018
Physical literacy levels of Canadian children aged 8-12 years: descriptive and normative results from the RBC Learn to Play-CAPL projectMark S Tremblay, Patricia E Longmuir, Joel D Barnes, et al.
Neuroscience|May 5, 2007
P2X7-related modulation of pathological nociception in ratsS McGaraughty, K L Chu, M T Namovic, et al.
BMC Public Health|October 5, 2018
Cardiorespiratory fitness is associated with physical literacy in a large sample of Canadian children aged 8 to 12 yearsJustin J Lang, Jean-Philippe Chaput, Patricia E Longmuir, et al.
Bioorganic & Medicinal Chemistry|October 23, 2010
Discovery and biological evaluation of potent, selective, orally bioavailable, pyrazine-based blockers of the Na(v)1.8 sodium channel with efficacy in a model of neuropathic painMarc J C Scanio, Lei Shi, Irene Drizin, et al.
Journal of Medicinal Chemistry|May 28, 2004
Synthesis and structure-activity relationships of a novel series of 2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide K(ATP) channel openers: discovery of (-)-(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 potent K(ATP) opener that selectively inhibits spontaneous bladder contractionsWilliam A Carroll, Robert J Altenbach, Hao Bai, et al.
Bioorganic & Medicinal Chemistry Letters|September 22, 2010
Subtype-selective Na(v)1.8 sodium channel blockers: identification of potent, orally active nicotinamide derivativesMichael E Kort, Robert N Atkinson, James B Thomas, et al.
Bioorganic & Medicinal Chemistry|May 27, 2008
Discovery of potent furan piperazine sodium channel blockers for treatment of neuropathic painIrene Drizin, Robert J Gregg, Marc J C Scanio, et al.
Journal of Medicinal Chemistry|January 8, 2008
Discovery and biological evaluation of 5-aryl-2-furfuramides, potent and selective blockers of the Nav1.8 sodium channel with efficacy in models of neuropathic and inflammatory painMichael E Kort, Irene Drizin, Robert J Gregg, et al.
Pageof 32