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W McIntyre

Showing results (441-450 of 505) with videos related to

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European Journal of Applied Physiology|April 18, 2013
Combined walking exercise and alkali therapy in patients with CKD4-5 regulates intramuscular free amino acid pools and ubiquitin E3 ligase expressionEmma L Watson, George C Kosmadakis, Alice C Smith, et al.
Kidney International|May 5, 2019
Heart failure in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies ConferenceAndrew A House, Christoph Wanner, Mark J Sarnak, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 15, 2006
Selective inhibition of eosinophil influx into the lung by small molecule CC chemokine receptor 3 antagonists in mouse models of allergic inflammationAnuk M Das, Krishna G Vaddi, Kimberly A Solomon, et al.
Journal of Leukocyte Biology|August 5, 2006
A selective small molecule agonist of the melanocortin-1 receptor inhibits lipopolysaccharide-induced cytokine accumulation and leukocyte infiltration in miceLiya Kang, Kim W McIntyre, Kathleen M Gillooly, et al.
Journal of Medicinal Chemistry|May 16, 2003
Rational design and synthesis of an orally active indolopyridone as a novel conformationally constrained cannabinoid ligand possessing antiinflammatory propertiesStephen T Wrobleski, Ping Chen, John Hynes, et al.
Bioorganic & Medicinal Chemistry Letters|February 17, 2006
Discovery and SAR of 2-amino-5-[(thiomethyl)aryl]thiazoles as potent and selective Itk inhibitorsJagabandhu Das, Chunjian Liu, Robert V Moquin, et al.
Bioorganic & Medicinal Chemistry Letters|April 21, 2009
Synthesis, initial SAR and biological evaluation of 1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridin-4-amine derived inhibitors of IkappaB kinaseJames Kempson, Junqing Guo, Jagabandhu Das, et al.
Bioorganic & Medicinal Chemistry Letters|November 18, 2004
Discovery of novel 2-(aminoheteroaryl)-thiazole-5-carboxamides as potent and orally active Src-family kinase p56(Lck) inhibitorsPing Chen, Derek Norris, Jagabandhu Das, et al.
Journal of Medicinal Chemistry|September 30, 2005
5-Cyanopyrimidine derivatives as a novel class of potent, selective, and orally active inhibitors of p38alpha MAP kinaseChunjian Liu, Stephen T Wrobleski, James Lin, et al.
Bioorganic & Medicinal Chemistry Letters|November 2, 2010
5-amino-pyrazoles as potent and selective p38α inhibitorsJagabandhu Das, Robert V Moquin, Alaric J Dyckman, et al.
Pageof 51

Showing results (441-450 of 505) with videos related to

Sort By:
Pageof 51
European Journal of Applied Physiology|April 18, 2013
Combined walking exercise and alkali therapy in patients with CKD4-5 regulates intramuscular free amino acid pools and ubiquitin E3 ligase expressionEmma L Watson, George C Kosmadakis, Alice C Smith, et al.
Kidney International|May 5, 2019
Heart failure in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies ConferenceAndrew A House, Christoph Wanner, Mark J Sarnak, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 15, 2006
Selective inhibition of eosinophil influx into the lung by small molecule CC chemokine receptor 3 antagonists in mouse models of allergic inflammationAnuk M Das, Krishna G Vaddi, Kimberly A Solomon, et al.
Journal of Leukocyte Biology|August 5, 2006
A selective small molecule agonist of the melanocortin-1 receptor inhibits lipopolysaccharide-induced cytokine accumulation and leukocyte infiltration in miceLiya Kang, Kim W McIntyre, Kathleen M Gillooly, et al.
Journal of Medicinal Chemistry|May 16, 2003
Rational design and synthesis of an orally active indolopyridone as a novel conformationally constrained cannabinoid ligand possessing antiinflammatory propertiesStephen T Wrobleski, Ping Chen, John Hynes, et al.
Bioorganic & Medicinal Chemistry Letters|February 17, 2006
Discovery and SAR of 2-amino-5-[(thiomethyl)aryl]thiazoles as potent and selective Itk inhibitorsJagabandhu Das, Chunjian Liu, Robert V Moquin, et al.
Bioorganic & Medicinal Chemistry Letters|April 21, 2009
Synthesis, initial SAR and biological evaluation of 1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridin-4-amine derived inhibitors of IkappaB kinaseJames Kempson, Junqing Guo, Jagabandhu Das, et al.
Bioorganic & Medicinal Chemistry Letters|November 18, 2004
Discovery of novel 2-(aminoheteroaryl)-thiazole-5-carboxamides as potent and orally active Src-family kinase p56(Lck) inhibitorsPing Chen, Derek Norris, Jagabandhu Das, et al.
Journal of Medicinal Chemistry|September 30, 2005
5-Cyanopyrimidine derivatives as a novel class of potent, selective, and orally active inhibitors of p38alpha MAP kinaseChunjian Liu, Stephen T Wrobleski, James Lin, et al.
Bioorganic & Medicinal Chemistry Letters|November 2, 2010
5-amino-pyrazoles as potent and selective p38α inhibitorsJagabandhu Das, Robert V Moquin, Alaric J Dyckman, et al.
Pageof 51