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David Weaver

Showing results (131-140 of 173) with videos related to

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ACS Medicinal Chemistry Letters|January 12, 2013
Discovery of N-Aryl Piperazines as Selective mGlu(5) Potentiators with Efficacy in a Rodent Model Predictive of Anti-Psychotic ActivityYa Zhou, Jason T Manka, Alice L Rodriguez, et al.
Cell Metabolism|June 11, 2013
MICU1 controls both the threshold and cooperative activation of the mitochondrial Ca²⁺ uniporterGyörgy Csordás, Tünde Golenár, Erin L Seifert, et al.
ACS Chemical Biology|April 20, 2021
Ten-Year Retrospective of the Vanderbilt Institute of Chemical Biology Chemical Synthesis CoreKwangho Kim, Plamen P Christov, Ian Romaine, et al.
Letters in Drug Design & Discovery|March 24, 2020
Challenges in the Discovery and Optimization of mGlu<sub>2/4</sub> Heterodimer Positive Allosteric ModulatorsMark Gallant Fulton, Matthew Thomas Loch, Caroline Anne Cuoco, et al.
Plos One|November 7, 2014
Discovery and characterization of a potent and selective inhibitor of Aedes aegypti inward rectifier potassium channelsRene Raphemot, Matthew F Rouhier, Daniel R Swale, et al.
Scientific Reports|May 19, 2026
Tissue transcriptional programs stratify Crohn's disease by therapeutic response and clinical outcomesAyesh Awad, Benjamin Huan, Michael T Shanahan, et al.
Bioorganic & Medicinal Chemistry Letters|January 4, 2011
Discovery and optimization of a novel, selective and brain penetrant M1 positive allosteric modulator (PAM): the development of ML169, an MLPCN probePaul R Reid, Thomas M Bridges, Douglas J Sheffler, et al.
Journal of Medicinal Chemistry|January 21, 2011
Discovery, synthesis, and structure-activity relationship development of a series of N-(4-acetamido)phenylpicolinamides as positive allosteric modulators of metabotropic glutamate receptor 4 (mGlu(4)) with CNS exposure in ratsDarren W Engers, Julie R Field, Uyen Le, et al.
Nature Chemical Biology|May 29, 2012
A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimerStefanie Blättermann, Lucas Peters, Philipp Aaron Ottersbach, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 2014
Loss of Miro1-directed mitochondrial movement results in a novel murine model for neuron diseaseTammy T Nguyen, Sang S Oh, David Weaver, et al.
Pageof 18

Showing results (131-140 of 173) with videos related to

Sort By:
Pageof 18
ACS Medicinal Chemistry Letters|January 12, 2013
Discovery of N-Aryl Piperazines as Selective mGlu(5) Potentiators with Efficacy in a Rodent Model Predictive of Anti-Psychotic ActivityYa Zhou, Jason T Manka, Alice L Rodriguez, et al.
Cell Metabolism|June 11, 2013
MICU1 controls both the threshold and cooperative activation of the mitochondrial Ca²⁺ uniporterGyörgy Csordás, Tünde Golenár, Erin L Seifert, et al.
ACS Chemical Biology|April 20, 2021
Ten-Year Retrospective of the Vanderbilt Institute of Chemical Biology Chemical Synthesis CoreKwangho Kim, Plamen P Christov, Ian Romaine, et al.
Letters in Drug Design & Discovery|March 24, 2020
Challenges in the Discovery and Optimization of mGlu<sub>2/4</sub> Heterodimer Positive Allosteric ModulatorsMark Gallant Fulton, Matthew Thomas Loch, Caroline Anne Cuoco, et al.
Plos One|November 7, 2014
Discovery and characterization of a potent and selective inhibitor of Aedes aegypti inward rectifier potassium channelsRene Raphemot, Matthew F Rouhier, Daniel R Swale, et al.
Scientific Reports|May 19, 2026
Tissue transcriptional programs stratify Crohn's disease by therapeutic response and clinical outcomesAyesh Awad, Benjamin Huan, Michael T Shanahan, et al.
Bioorganic & Medicinal Chemistry Letters|January 4, 2011
Discovery and optimization of a novel, selective and brain penetrant M1 positive allosteric modulator (PAM): the development of ML169, an MLPCN probePaul R Reid, Thomas M Bridges, Douglas J Sheffler, et al.
Journal of Medicinal Chemistry|January 21, 2011
Discovery, synthesis, and structure-activity relationship development of a series of N-(4-acetamido)phenylpicolinamides as positive allosteric modulators of metabotropic glutamate receptor 4 (mGlu(4)) with CNS exposure in ratsDarren W Engers, Julie R Field, Uyen Le, et al.
Nature Chemical Biology|May 29, 2012
A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimerStefanie Blättermann, Lucas Peters, Philipp Aaron Ottersbach, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 2014
Loss of Miro1-directed mitochondrial movement results in a novel murine model for neuron diseaseTammy T Nguyen, Sang S Oh, David Weaver, et al.
Pageof 18