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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>1.7
Robert 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-42253432
Brian 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-47965567
Anindya 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 antagonist
Brian 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 Exploration
François P Bischoff, Sven Van Brandt, Marcel Viellevoye, et al.
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Showing results (11-20 of 16) with videos related to
Sort By:
Page
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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>1.7
Robert 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-42253432
Brian 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-47965567
Anindya 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 antagonist
Brian 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 Exploration
François P Bischoff, Sven Van Brandt, Marcel Viellevoye, et al.
Page
of 2