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Dilip Pandey

Showing results (21-30 of 24) with videos related to

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International Journal of Stroke : Official Journal of the International Stroke Society|November 6, 2010
Vertebrobasilar Flow Evaluation and Risk of Transient Ischaemic Attack and Stroke study (VERiTAS): rationale and designSepideh Amin-Hanjani, Linda Rose-Finnell, DeJuran Richardson, et al.
European Journal of Pharmacology|May 31, 2022
Discovery and pre-clinical characterization of a selective PI3Kδ inhibitor, LL-00071210 in rheumatoid arthritisVijay Kanoje, Dilip Pandey, Akshaya Wagh, et al.
Journal of Medicinal Chemistry|November 29, 2021
Discovery of a Novel Potent and Selective Calcium Release-Activated Calcium Channel Inhibitor: 2,6-Difluoro-<i>N</i>-(2'-methyl-3'-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1'-biphenyl]-4-yl)benzamide. Structure-Activity Relationship and Preclinical CharacterizationNilesh Raghunath Khedkar, Nageswara Rao Irlapatti, Disha Dadke, et al.
Journal of Medicinal Chemistry|May 6, 2020
Discovery of Potent, Selective, and State-Dependent Na<sub>V</sub>1.7 Inhibitors with Robust Oral Efficacy in Pain Models: Structure-Activity Relationship and Optimization of Chroman and Indane Aryl SulfonamidesVidya Ramdas, Rashmi Talwar, Vijay Kanoje, et al.
Pageof 3

Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
International Journal of Stroke : Official Journal of the International Stroke Society|November 6, 2010
Vertebrobasilar Flow Evaluation and Risk of Transient Ischaemic Attack and Stroke study (VERiTAS): rationale and designSepideh Amin-Hanjani, Linda Rose-Finnell, DeJuran Richardson, et al.
European Journal of Pharmacology|May 31, 2022
Discovery and pre-clinical characterization of a selective PI3Kδ inhibitor, LL-00071210 in rheumatoid arthritisVijay Kanoje, Dilip Pandey, Akshaya Wagh, et al.
Journal of Medicinal Chemistry|November 29, 2021
Discovery of a Novel Potent and Selective Calcium Release-Activated Calcium Channel Inhibitor: 2,6-Difluoro-<i>N</i>-(2'-methyl-3'-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1'-biphenyl]-4-yl)benzamide. Structure-Activity Relationship and Preclinical CharacterizationNilesh Raghunath Khedkar, Nageswara Rao Irlapatti, Disha Dadke, et al.
Journal of Medicinal Chemistry|May 6, 2020
Discovery of Potent, Selective, and State-Dependent Na<sub>V</sub>1.7 Inhibitors with Robust Oral Efficacy in Pain Models: Structure-Activity Relationship and Optimization of Chroman and Indane Aryl SulfonamidesVidya Ramdas, Rashmi Talwar, Vijay Kanoje, et al.
Pageof 3