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Showing results (151-160 of 167) with videos related to

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Molecular Endocrinology (Baltimore, Md.)|June 1, 2002
Regulation of cholesterol homeostasis by the liver X receptors in the central nervous systemKarl D Whitney, Michael A Watson, Jon L Collins, et al.
Nature Communications|June 3, 2026
Turbulence drives seabed modification by offshore windfarmsChristopher A Unsworth, Connor J McCarron, Richard J S Whitehouse, et al.
Bioorganic & Medicinal Chemistry Letters|March 16, 2010
Identification of SD-0006, a potent diaryl pyrazole inhibitor of p38 MAP kinaseJohn K Walker, Shaun R Selness, Rajesh V Devraj, et al.
Pathology Oncology Research : POR|September 28, 2004
Short term arterial remodelling in the aortae of cholesterol fed New Zealand white rabbits shown in vivo by high-resolution magnetic resonance imaging - implications for human pathologyLaszlo Hegyi, Paul D Hockings, Martin G Benson, et al.
Biochemistry|June 6, 2009
Structural bioinformatics-based prediction of exceptional selectivity of p38 MAP kinase inhibitor PH-797804Li Xing, Huey S Shieh, Shaun R Selness, et al.
Endocrine Reviews|February 16, 2017
ERRγ Regulates Cardiac, Gastric, and Renal Potassium HomeostasisWilliam A Alaynick, James M Way, Stephanie A Wilson, et al.
Molecular Endocrinology (Baltimore, Md.)|December 8, 2009
ERRgamma regulates cardiac, gastric, and renal potassium homeostasisWilliam A Alaynick, James M Way, Stephanie A Wilson, et al.
The Journal of Biological Chemistry|December 24, 2002
The orphan G protein-coupled receptor GPR40 is activated by medium and long chain fatty acidsCelia P Briscoe, Mohammad Tadayyon, John L Andrews, et al.
Bioorganic & Medicinal Chemistry Letters|September 16, 2009
Discovery of N-substituted pyridinones as potent and selective inhibitors of p38 kinaseShaun R Selness, Rajesh V Devraj, Joseph B Monahan, et al.
Bioorganic & Medicinal Chemistry Letters|July 28, 2009
Optimization of the aminopyridopyrazinones class of PDE5 inhibitors: discovery of 3-[(trans-4-hydroxycyclohexyl)amino]-7-(6-methoxypyridin-3-yl)-1-(2-propoxyethyl)pyrido[3,4-b]pyrazin-2(1H)-oneRobert O Hughes, John K Walker, D Joseph Rogier, et al.
Pageof 17

Showing results (151-160 of 167) with videos related to

Sort By:
Pageof 17
Molecular Endocrinology (Baltimore, Md.)|June 1, 2002
Regulation of cholesterol homeostasis by the liver X receptors in the central nervous systemKarl D Whitney, Michael A Watson, Jon L Collins, et al.
Nature Communications|June 3, 2026
Turbulence drives seabed modification by offshore windfarmsChristopher A Unsworth, Connor J McCarron, Richard J S Whitehouse, et al.
Bioorganic & Medicinal Chemistry Letters|March 16, 2010
Identification of SD-0006, a potent diaryl pyrazole inhibitor of p38 MAP kinaseJohn K Walker, Shaun R Selness, Rajesh V Devraj, et al.
Pathology Oncology Research : POR|September 28, 2004
Short term arterial remodelling in the aortae of cholesterol fed New Zealand white rabbits shown in vivo by high-resolution magnetic resonance imaging - implications for human pathologyLaszlo Hegyi, Paul D Hockings, Martin G Benson, et al.
Biochemistry|June 6, 2009
Structural bioinformatics-based prediction of exceptional selectivity of p38 MAP kinase inhibitor PH-797804Li Xing, Huey S Shieh, Shaun R Selness, et al.
Endocrine Reviews|February 16, 2017
ERRγ Regulates Cardiac, Gastric, and Renal Potassium HomeostasisWilliam A Alaynick, James M Way, Stephanie A Wilson, et al.
Molecular Endocrinology (Baltimore, Md.)|December 8, 2009
ERRgamma regulates cardiac, gastric, and renal potassium homeostasisWilliam A Alaynick, James M Way, Stephanie A Wilson, et al.
The Journal of Biological Chemistry|December 24, 2002
The orphan G protein-coupled receptor GPR40 is activated by medium and long chain fatty acidsCelia P Briscoe, Mohammad Tadayyon, John L Andrews, et al.
Bioorganic & Medicinal Chemistry Letters|September 16, 2009
Discovery of N-substituted pyridinones as potent and selective inhibitors of p38 kinaseShaun R Selness, Rajesh V Devraj, Joseph B Monahan, et al.
Bioorganic & Medicinal Chemistry Letters|July 28, 2009
Optimization of the aminopyridopyrazinones class of PDE5 inhibitors: discovery of 3-[(trans-4-hydroxycyclohexyl)amino]-7-(6-methoxypyridin-3-yl)-1-(2-propoxyethyl)pyrido[3,4-b]pyrazin-2(1H)-oneRobert O Hughes, John K Walker, D Joseph Rogier, et al.
Pageof 17