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Showing results (71-80 of 87) with videos related to

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Bioorganic & Medicinal Chemistry Letters|December 11, 2012
Novel cinnoline-based inhibitors of LRRK2 kinase activityAlbert W Garofalo, Marc Adler, Danielle L Aubele, et al.
Bioorganic & Medicinal Chemistry Letters|April 11, 2013
Design and synthesis of thiophene dihydroisoquinolines as novel BACE1 inhibitorsYing-Zi Xu, Shendong Yuan, Simeon Bowers, et al.
Bioorganic & Medicinal Chemistry Letters|May 17, 2011
Highly selective c-Jun N-terminal kinase (JNK) 3 inhibitors with in vitro CNS-like pharmacokinetic properties II. Central core replacementR Jeffrey Neitz, Andrei W Konradi, Hing L Sham, et al.
Stroke|October 4, 2014
RNF213 rare variants in an ethnically diverse population with Moyamoya diseaseAlana C Cecchi, Dongchuan Guo, Zhao Ren, et al.
Bioorganic & Medicinal Chemistry Letters|March 5, 2013
Discovery of 4-alkylamino-7-aryl-3-cyanoquinoline LRRK2 kinase inhibitorsAlbert W Garofalo, Marc Adler, Danielle L Aubele, et al.
Journal of General Internal Medicine|March 20, 2025
Effects of the Nudge Theory-Based Multifaceted Intervention on Reducing Inappropriate Proton Pump Inhibitors Use for Prophylaxis in Hospitalized Patients: A Non-Randomized Controlled StudyChun-Xing Li, Shuo Liang, Yin-Shi Xu, et al.
Bioorganic & Medicinal Chemistry Letters|March 8, 2013
Structure-based design of novel dihydroisoquinoline BACE-1 inhibitors that do not engage the catalytic aspartatesSimeon Bowers, Ying-zi Xu, Shendong Yuan, et al.
Circulation Research|February 4, 2016
LOX Mutations Predispose to Thoracic Aortic Aneurysms and DissectionsDong-chuan Guo, Ellen S Regalado, Limin Gong, et al.
SLAS Discovery : Advancing Life Sciences R & D|July 5, 2021
High-Throughput Screening to Identify Small Molecules That Selectively Inhibit APOL1 Protein Level in PodocytesJonathan Choy, Yanqing Kan, Steve Cifelli, et al.
Bioorganic & Medicinal Chemistry Letters|February 15, 2011
Design and synthesis of a novel, orally active, brain penetrant, tri-substituted thiophene based JNK inhibitorSimeon Bowers, Anh P Truong, R Jeffrey Neitz, et al.
Pageof 9

Showing results (71-80 of 87) with videos related to

Sort By:
Pageof 9
Bioorganic & Medicinal Chemistry Letters|December 11, 2012
Novel cinnoline-based inhibitors of LRRK2 kinase activityAlbert W Garofalo, Marc Adler, Danielle L Aubele, et al.
Bioorganic & Medicinal Chemistry Letters|April 11, 2013
Design and synthesis of thiophene dihydroisoquinolines as novel BACE1 inhibitorsYing-Zi Xu, Shendong Yuan, Simeon Bowers, et al.
Bioorganic & Medicinal Chemistry Letters|May 17, 2011
Highly selective c-Jun N-terminal kinase (JNK) 3 inhibitors with in vitro CNS-like pharmacokinetic properties II. Central core replacementR Jeffrey Neitz, Andrei W Konradi, Hing L Sham, et al.
Stroke|October 4, 2014
RNF213 rare variants in an ethnically diverse population with Moyamoya diseaseAlana C Cecchi, Dongchuan Guo, Zhao Ren, et al.
Bioorganic & Medicinal Chemistry Letters|March 5, 2013
Discovery of 4-alkylamino-7-aryl-3-cyanoquinoline LRRK2 kinase inhibitorsAlbert W Garofalo, Marc Adler, Danielle L Aubele, et al.
Journal of General Internal Medicine|March 20, 2025
Effects of the Nudge Theory-Based Multifaceted Intervention on Reducing Inappropriate Proton Pump Inhibitors Use for Prophylaxis in Hospitalized Patients: A Non-Randomized Controlled StudyChun-Xing Li, Shuo Liang, Yin-Shi Xu, et al.
Bioorganic & Medicinal Chemistry Letters|March 8, 2013
Structure-based design of novel dihydroisoquinoline BACE-1 inhibitors that do not engage the catalytic aspartatesSimeon Bowers, Ying-zi Xu, Shendong Yuan, et al.
Circulation Research|February 4, 2016
LOX Mutations Predispose to Thoracic Aortic Aneurysms and DissectionsDong-chuan Guo, Ellen S Regalado, Limin Gong, et al.
SLAS Discovery : Advancing Life Sciences R & D|July 5, 2021
High-Throughput Screening to Identify Small Molecules That Selectively Inhibit APOL1 Protein Level in PodocytesJonathan Choy, Yanqing Kan, Steve Cifelli, et al.
Bioorganic & Medicinal Chemistry Letters|February 15, 2011
Design and synthesis of a novel, orally active, brain penetrant, tri-substituted thiophene based JNK inhibitorSimeon Bowers, Anh P Truong, R Jeffrey Neitz, et al.
Pageof 9