Showing results (11-20 of 36) with videos related to
Sort By:
Pageof 4
Pflugers Archiv : European Journal of Physiology|October 15, 2013
Dual depolarization responses generated within the same lateral septal neurons by TRPC4-containing channelsJinbin Tian, Dhananjay P Thakur, Yungang Lu, et al.Scientific Reports|March 21, 2015
Biochemical and pharmacological characterizations of ESI-09 based EPAC inhibitors: defining the ESI-09 "therapeutic window"Yingmin Zhu, Haijun Chen, Stephen Boulton, et al.Langmuir : the ACS Journal of Surfaces and Colloids|September 13, 2024
An Atomistic Level Investigation of the PFDTES-Graphene Interfacial Shear Strength and the Stick-Slip MechanismJi Zhang, Haiyan Zhang, Tarek Ragab, et al.The Journal of Biological Chemistry|January 11, 2011
Cyclic adenosine diphosphate ribose activates ryanodine receptors, whereas NAADP activates two-pore domain channelsOluseye A Ogunbayo, Yingmin Zhu, Daniela Rossi, et al.ACS Medicinal Chemistry Letters|January 30, 2018
Structure-Activity Relationship Studies with Tetrahydroquinoline Analogs as EPAC InhibitorsYogesh A Sonawane, Yingmin Zhu, Jered C Garrison, et al.Bioorganic & Medicinal Chemistry Letters|November 5, 2017
Structure-activity relationships of 2-substituted phenyl-N-phenyl-2-oxoacetohydrazonoyl cyanides as novel antagonists of exchange proteins directly activated by cAMP (EPACs)Zhiqing Liu, Yingmin Zhu, Haiying Chen, et al.European Journal of Medicinal Chemistry|April 12, 2017
Identification of novel 2-(benzo[d]isoxazol-3-yl)-2-oxo-N-phenylacetohydrazonoyl cyanide analoguesas potent EPAC antagonistsNa Ye, Yingmin Zhu, Zhiqing Liu, et al.ACS Medicinal Chemistry Letters|May 19, 2016
Functionalized N,N-Diphenylamines as Potent and Selective EPAC2 InhibitorsChristopher T Wild, Yingmin Zhu, Ye Na, et al.The Journal of Biological Chemistry|December 3, 2014
Organelle-specific subunit interactions of the vertebrate two-pore channel familyOluseye A Ogunbayo, Yingmin Zhu, Bing Shen, et al.Journal of Medicinal Chemistry|July 8, 2015
Structure-Activity Relationship Studies of Substituted 2-(Isoxazol-3-yl)-2-oxo-N'-phenyl-acetohydrazonoyl Cyanide Analogues: Identification of Potent Exchange Proteins Directly Activated by cAMP (EPAC) AntagonistsNa Ye, Yingmin Zhu, Haijun Chen, et al.Pageof 4