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G Mills

Showing results (731-740 of 888) with videos related to

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Bioorganic & Medicinal Chemistry Letters|May 16, 2006
Discovery of 3-arylpropionic acids as potent agonists of sphingosine-1-phosphate receptor-1 (S1P1) with high selectivity against all other known S1P receptor subtypesLin Yan, Pei Huo, George Doherty, et al.
Bioorganic & Medicinal Chemistry Letters|February 25, 2009
Design, synthesis, and structure-activity relationship of novel CCR2 antagonistsShankaran Kothandaraman, Karla L Donnely, Gabor Butora, et al.
The Journal of Clinical Investigation|October 3, 2022
Melanocortin 4 receptor agonism enhances sexual brain processing in women with hypoactive sexual desire disorderLayla Thurston, Tia Hunjan, Edouard G Mills, et al.
Cell Reports|April 15, 2023
Autocrine activation of MAPK signaling mediates intrinsic tolerance to androgen deprivation in LY6D prostate cancer cellsIvana Steiner, Teresita Del N J Flores-Tellez, Renaud Mevel, et al.
Chemical Research in Toxicology|December 21, 2019
CRISPR-Generated Nrf2a Loss- and Gain-of-Function Mutants Facilitate Mechanistic Analysis of Chemical Oxidative Stress-Mediated Toxicity in ZebrafishMargaret G Mills, Richard Ramsden, Eva Y Ma, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Genomic Surveillance for Enhanced Healthcare Outbreak Detection and ControlAlexander J Sundermann, Praveen Kumar, Marissa P Griffith, et al.
Biorxiv : the Preprint Server for Biology|February 23, 2026
Assessing the effects of a 3D pathology tissue-processing workflow on downstream molecular analysesElena Baraznenok, Huai-Ching Hsieh, Lydia Lan, et al.
Bioorganic & Medicinal Chemistry Letters|September 11, 2001
Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 4: synthesis and structure-activity relationships for 1-[N-(methyl)-N-(phenylsulfonyl)amino]-2-(phenyl)-4-(4-(N-(alkyl)-N-(benzyloxycarbonyl)amino)piperidin-1-yl)butanesP E Finke, B Oates, S G Mills, et al.
Bioorganic & Medicinal Chemistry|February 6, 2008
Fused bicyclic pyrrolizinones as new scaffolds for human NK1 antagonistsGregori J Morriello, Robert J Devita, Sander G Mills, et al.
British Journal of Cancer|January 12, 2024
Peroxisomal β-oxidation enzyme, DECR2, regulates lipid metabolism and promotes treatment resistance in advanced prostate cancerChui Yan Mah, An Dieu Trang Nguyen, Takuto Niijima, et al.
Pageof 89

Showing results (731-740 of 888) with videos related to

Sort By:
Pageof 89
Bioorganic & Medicinal Chemistry Letters|May 16, 2006
Discovery of 3-arylpropionic acids as potent agonists of sphingosine-1-phosphate receptor-1 (S1P1) with high selectivity against all other known S1P receptor subtypesLin Yan, Pei Huo, George Doherty, et al.
Bioorganic & Medicinal Chemistry Letters|February 25, 2009
Design, synthesis, and structure-activity relationship of novel CCR2 antagonistsShankaran Kothandaraman, Karla L Donnely, Gabor Butora, et al.
The Journal of Clinical Investigation|October 3, 2022
Melanocortin 4 receptor agonism enhances sexual brain processing in women with hypoactive sexual desire disorderLayla Thurston, Tia Hunjan, Edouard G Mills, et al.
Cell Reports|April 15, 2023
Autocrine activation of MAPK signaling mediates intrinsic tolerance to androgen deprivation in LY6D prostate cancer cellsIvana Steiner, Teresita Del N J Flores-Tellez, Renaud Mevel, et al.
Chemical Research in Toxicology|December 21, 2019
CRISPR-Generated Nrf2a Loss- and Gain-of-Function Mutants Facilitate Mechanistic Analysis of Chemical Oxidative Stress-Mediated Toxicity in ZebrafishMargaret G Mills, Richard Ramsden, Eva Y Ma, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Genomic Surveillance for Enhanced Healthcare Outbreak Detection and ControlAlexander J Sundermann, Praveen Kumar, Marissa P Griffith, et al.
Biorxiv : the Preprint Server for Biology|February 23, 2026
Assessing the effects of a 3D pathology tissue-processing workflow on downstream molecular analysesElena Baraznenok, Huai-Ching Hsieh, Lydia Lan, et al.
Bioorganic & Medicinal Chemistry Letters|September 11, 2001
Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 4: synthesis and structure-activity relationships for 1-[N-(methyl)-N-(phenylsulfonyl)amino]-2-(phenyl)-4-(4-(N-(alkyl)-N-(benzyloxycarbonyl)amino)piperidin-1-yl)butanesP E Finke, B Oates, S G Mills, et al.
Bioorganic & Medicinal Chemistry|February 6, 2008
Fused bicyclic pyrrolizinones as new scaffolds for human NK1 antagonistsGregori J Morriello, Robert J Devita, Sander G Mills, et al.
British Journal of Cancer|January 12, 2024
Peroxisomal β-oxidation enzyme, DECR2, regulates lipid metabolism and promotes treatment resistance in advanced prostate cancerChui Yan Mah, An Dieu Trang Nguyen, Takuto Niijima, et al.
Pageof 89