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Robert M Jones

Showing results (51-60 of 70) with videos related to

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Molecular Endocrinology (Baltimore, Md.)|November 11, 2009
N-oleoyldopamine enhances glucose homeostasis through the activation of GPR119Zhi-Liang Chu, Chris Carroll, Ruoping Chen, et al.
World Journal of Hepatology|August 8, 2019
Epidemiology and outcomes of acute liver failure in AustraliaPenelope Hey, Timothy P Hanrahan, Marie Sinclair, et al.
HPB : the Official Journal of the International Hepato Pancreato Biliary Association|July 11, 2009
Poorer survival in patients whose explanted hepatocellular carcinoma (HCC) exceeds Milan or UCSF Criteria. An analysis of liver transplantation in HCC in Australia and New ZealandJohn W C Chen, Lilian Kow, Deborah J Verran, et al.
ANZ Journal of Surgery|November 11, 2018
Emergency presentations of acute biliary pain: changing patterns of management in a tertiary instituteDaniel R A Cox, Jonathan Fong, Chon Hann Liew, et al.
Endocrinology|February 10, 2007
A role for beta-cell-expressed G protein-coupled receptor 119 in glycemic control by enhancing glucose-dependent insulin releaseZhi-Liang Chu, Robert M Jones, Hongmei He, et al.
Endocrinology|July 26, 2013
GPR41/FFAR3 and GPR43/FFAR2 as cosensors for short-chain fatty acids in enteroendocrine cells vs FFAR3 in enteric neurons and FFAR2 in enteric leukocytesMark K Nøhr, Maria H Pedersen, Andreas Gille, et al.
Bioorganic & Medicinal Chemistry Letters|December 24, 2014
Design and synthesis of new tricyclic indoles as potent modulators of the S1P1 receptorDaniel J Buzard, Thomas O Schrader, Xiuwen Zhu, et al.
ACS Medicinal Chemistry Letters|December 21, 2017
Discovery of APD371: Identification of a Highly Potent and Selective CB<sub>2</sub> Agonist for the Treatment of Chronic PainSangdon Han, Lars Thoresen, Jae-Kyu Jung, et al.
Bioorganic & Medicinal Chemistry Letters|August 20, 2011
Discovery and characterization of potent and selective 4-oxo-4-(5-(5-phenyl-1,2,4-oxadiazol-3-yl)indolin-1-yl)butanoic acids as S1P₁ agonistsDaniel Buzard, Sangdon Han, Lars Thoresen, et al.
Journal of Medicinal Chemistry|August 14, 2008
Discovery of the first potent and orally efficacious agonist of the orphan G-protein coupled receptor 119Graeme Semple, Beatriz Fioravanti, Guillherme Pereira, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Molecular Endocrinology (Baltimore, Md.)|November 11, 2009
N-oleoyldopamine enhances glucose homeostasis through the activation of GPR119Zhi-Liang Chu, Chris Carroll, Ruoping Chen, et al.
World Journal of Hepatology|August 8, 2019
Epidemiology and outcomes of acute liver failure in AustraliaPenelope Hey, Timothy P Hanrahan, Marie Sinclair, et al.
HPB : the Official Journal of the International Hepato Pancreato Biliary Association|July 11, 2009
Poorer survival in patients whose explanted hepatocellular carcinoma (HCC) exceeds Milan or UCSF Criteria. An analysis of liver transplantation in HCC in Australia and New ZealandJohn W C Chen, Lilian Kow, Deborah J Verran, et al.
ANZ Journal of Surgery|November 11, 2018
Emergency presentations of acute biliary pain: changing patterns of management in a tertiary instituteDaniel R A Cox, Jonathan Fong, Chon Hann Liew, et al.
Endocrinology|February 10, 2007
A role for beta-cell-expressed G protein-coupled receptor 119 in glycemic control by enhancing glucose-dependent insulin releaseZhi-Liang Chu, Robert M Jones, Hongmei He, et al.
Endocrinology|July 26, 2013
GPR41/FFAR3 and GPR43/FFAR2 as cosensors for short-chain fatty acids in enteroendocrine cells vs FFAR3 in enteric neurons and FFAR2 in enteric leukocytesMark K Nøhr, Maria H Pedersen, Andreas Gille, et al.
Bioorganic & Medicinal Chemistry Letters|December 24, 2014
Design and synthesis of new tricyclic indoles as potent modulators of the S1P1 receptorDaniel J Buzard, Thomas O Schrader, Xiuwen Zhu, et al.
ACS Medicinal Chemistry Letters|December 21, 2017
Discovery of APD371: Identification of a Highly Potent and Selective CB<sub>2</sub> Agonist for the Treatment of Chronic PainSangdon Han, Lars Thoresen, Jae-Kyu Jung, et al.
Bioorganic & Medicinal Chemistry Letters|August 20, 2011
Discovery and characterization of potent and selective 4-oxo-4-(5-(5-phenyl-1,2,4-oxadiazol-3-yl)indolin-1-yl)butanoic acids as S1P₁ agonistsDaniel Buzard, Sangdon Han, Lars Thoresen, et al.
Journal of Medicinal Chemistry|August 14, 2008
Discovery of the first potent and orally efficacious agonist of the orphan G-protein coupled receptor 119Graeme Semple, Beatriz Fioravanti, Guillherme Pereira, et al.
Pageof 7