Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Guiscard Seebohm

Showing results (101-110 of 189) with videos related to

Pageof 19
Sort By:
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|September 1, 2007
Alterations in the cytoplasmic domain of CLCN2 result in altered gating kineticsJochen Paul, Sankarganesh Jeyaraj, Stephan M Huber, et al.
European Journal of Medicinal Chemistry|July 14, 2017
Deconstruction - reconstruction approach to analyze the essential structural elements of tetrahydro-3-benzazepine-based antagonists of GluN2B subunit containing NMDA receptorsSougata Dey, Louisa Temme, Julian A Schreiber, et al.
Plos Genetics|January 24, 2014
Bioelectric signaling regulates size in zebrafish finsSimon Perathoner, Jacob M Daane, Ulrike Henrion, et al.
Organic & Biomolecular Chemistry|September 8, 2023
Negative allosteric modulators of NMDA receptors with GluN2B subunit: synthesis of β-aminoalcohols by epoxide opening and subsequent rearrangementMarvin Korff, Judith Lüken, Judith Schmidt, et al.
Journal of Medicinal Chemistry|August 15, 2023
Indazole as a Phenol Bioisostere: Structure-Affinity Relationships of GluN2B-Selective NMDA Receptor AntagonistsJudith Lüken, Gunnar Goerges, Nadine Ritter, et al.
Biochemical and Biophysical Research Communications|April 20, 2011
Inhibition of Kir2.1 (KCNJ2) by the AMP-activated protein kinaseIoana Alesutan, Carlos Munoz, Mentor Sopjani, et al.
Heartrhythm Case Reports|May 12, 2017
Structural interplay of K<sub>V</sub>7.1 and KCNE1 is essential for normal repolarization and is compromised in short QT syndrome 2 (K<sub>V</sub>7.1-A287T)Ina Rothenberg, Ilaria Piccini, Eva Wrobel, et al.
International Journal of Nanomedicine|October 30, 2016
Comparison of cellular effects of starch-coated SPIONs and poly(lactic-co-glycolic acid) matrix nanoparticles on human monocytesDominik Gonnissen, Ying Qu, Klaus Langer, et al.
European Journal of Medicinal Chemistry|January 22, 2022
Synthesis of tropane-based σ<sub>1</sub> receptor antagonists with antiallodynic activityElena Bechthold, Julian A Schreiber, Nadine Ritter, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 11, 2010
Modulation of human ether a gogo related channels by CASQ2 contributes to etiology of catecholaminergic polymorphic ventricular tachycardia (CPVT)Karina Eckey, Nathalie Strutz-Seebohm, Guy Katz, et al.
Pageof 19

Showing results (101-110 of 189) with videos related to

Sort By:
Pageof 19
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|September 1, 2007
Alterations in the cytoplasmic domain of CLCN2 result in altered gating kineticsJochen Paul, Sankarganesh Jeyaraj, Stephan M Huber, et al.
European Journal of Medicinal Chemistry|July 14, 2017
Deconstruction - reconstruction approach to analyze the essential structural elements of tetrahydro-3-benzazepine-based antagonists of GluN2B subunit containing NMDA receptorsSougata Dey, Louisa Temme, Julian A Schreiber, et al.
Plos Genetics|January 24, 2014
Bioelectric signaling regulates size in zebrafish finsSimon Perathoner, Jacob M Daane, Ulrike Henrion, et al.
Organic & Biomolecular Chemistry|September 8, 2023
Negative allosteric modulators of NMDA receptors with GluN2B subunit: synthesis of β-aminoalcohols by epoxide opening and subsequent rearrangementMarvin Korff, Judith Lüken, Judith Schmidt, et al.
Journal of Medicinal Chemistry|August 15, 2023
Indazole as a Phenol Bioisostere: Structure-Affinity Relationships of GluN2B-Selective NMDA Receptor AntagonistsJudith Lüken, Gunnar Goerges, Nadine Ritter, et al.
Biochemical and Biophysical Research Communications|April 20, 2011
Inhibition of Kir2.1 (KCNJ2) by the AMP-activated protein kinaseIoana Alesutan, Carlos Munoz, Mentor Sopjani, et al.
Heartrhythm Case Reports|May 12, 2017
Structural interplay of K<sub>V</sub>7.1 and KCNE1 is essential for normal repolarization and is compromised in short QT syndrome 2 (K<sub>V</sub>7.1-A287T)Ina Rothenberg, Ilaria Piccini, Eva Wrobel, et al.
International Journal of Nanomedicine|October 30, 2016
Comparison of cellular effects of starch-coated SPIONs and poly(lactic-co-glycolic acid) matrix nanoparticles on human monocytesDominik Gonnissen, Ying Qu, Klaus Langer, et al.
European Journal of Medicinal Chemistry|January 22, 2022
Synthesis of tropane-based σ<sub>1</sub> receptor antagonists with antiallodynic activityElena Bechthold, Julian A Schreiber, Nadine Ritter, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 11, 2010
Modulation of human ether a gogo related channels by CASQ2 contributes to etiology of catecholaminergic polymorphic ventricular tachycardia (CPVT)Karina Eckey, Nathalie Strutz-Seebohm, Guy Katz, et al.
Pageof 19