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Robert A Neff

Showing results (11-20 of 16) with videos related to

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The Journal of Biological Chemistry|December 25, 2019
Comprehensive engineering of the tarantula venom peptide huwentoxin-IV to inhibit the human voltage-gated sodium channel hNa<sub>v</sub>1.7Robert A Neff, Mack Flinspach, Alan Gibbs, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 2, 2014
Pharmacology of a novel central nervous system-penetrant P2X7 antagonist JNJ-42253432Brian Lord, Leah Aluisio, James R Shoblock, et al.
British Journal of Pharmacology|July 30, 2013
Pharmacological characterization of a novel centrally permeable P2X7 receptor antagonist: JNJ-47965567Anindya Bhattacharya, Qi Wang, Hong Ao, et al.
British Journal of Pharmacology|May 14, 2025
Pharmacological characterisation of JNJ-78911118, a novel, centrally-penetrant, selective GluN2A antagonistBrian Lord, Sirak Simavorian, Ian Fraser, et al.
The Journal of Biological Chemistry|June 14, 2013
Analysis of the structural and molecular basis of voltage-sensitive sodium channel inhibition by the spider toxin huwentoxin-IV (μ-TRTX-Hh2a)Natali A Minassian, Alan Gibbs, Amy Y Shih, et al.
Journal of Medicinal Chemistry|February 17, 2025
Design, Synthesis, and Characterization of GluN2A Negative Allosteric Modulators Suitable for In Vivo ExplorationFrançois P Bischoff, Sven Van Brandt, Marcel Viellevoye, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
The Journal of Biological Chemistry|December 25, 2019
Comprehensive engineering of the tarantula venom peptide huwentoxin-IV to inhibit the human voltage-gated sodium channel hNa<sub>v</sub>1.7Robert A Neff, Mack Flinspach, Alan Gibbs, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 2, 2014
Pharmacology of a novel central nervous system-penetrant P2X7 antagonist JNJ-42253432Brian Lord, Leah Aluisio, James R Shoblock, et al.
British Journal of Pharmacology|July 30, 2013
Pharmacological characterization of a novel centrally permeable P2X7 receptor antagonist: JNJ-47965567Anindya Bhattacharya, Qi Wang, Hong Ao, et al.
British Journal of Pharmacology|May 14, 2025
Pharmacological characterisation of JNJ-78911118, a novel, centrally-penetrant, selective GluN2A antagonistBrian Lord, Sirak Simavorian, Ian Fraser, et al.
The Journal of Biological Chemistry|June 14, 2013
Analysis of the structural and molecular basis of voltage-sensitive sodium channel inhibition by the spider toxin huwentoxin-IV (μ-TRTX-Hh2a)Natali A Minassian, Alan Gibbs, Amy Y Shih, et al.
Journal of Medicinal Chemistry|February 17, 2025
Design, Synthesis, and Characterization of GluN2A Negative Allosteric Modulators Suitable for In Vivo ExplorationFrançois P Bischoff, Sven Van Brandt, Marcel Viellevoye, et al.
Pageof 2