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Danielle Johnson

Showing results (21-30 of 25) with videos related to

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Plos One|September 5, 2014
Global Nav1.7 knockout mice recapitulate the phenotype of human congenital indifference to painJacinthe Gingras, Sarah Smith, David J Matson, et al.
American Journal of Audiology|August 22, 2025
Impact of Short-Term Hearing Aid Use on Cognitive Performance, Noise Acceptance, and Self-Perceived BenefitErin C Schafer, Sharon Miller, Boji P W Lam, et al.
Cancer Research|December 26, 2003
A fully human monoclonal antibody to the insulin-like growth factor I receptor blocks ligand-dependent signaling and inhibits human tumor growth in vivoDouglas Burtrum, Zhenping Zhu, Dan Lu, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 6, 2017
Pharmacologic Characterization of AMG8379, a Potent and Selective Small Molecule Sulfonamide Antagonist of the Voltage-Gated Sodium Channel Na<sub>V</sub>1.7Thomas J Kornecook, Ruoyuan Yin, Stephen Altmann, et al.
Journal of Medicinal Chemistry|June 4, 2011
Identification of a potent, state-dependent inhibitor of Nav1.7 with oral efficacy in the formalin model of persistent painHoward Bregman, Loren Berry, John L Buchanan, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Plos One|September 5, 2014
Global Nav1.7 knockout mice recapitulate the phenotype of human congenital indifference to painJacinthe Gingras, Sarah Smith, David J Matson, et al.
American Journal of Audiology|August 22, 2025
Impact of Short-Term Hearing Aid Use on Cognitive Performance, Noise Acceptance, and Self-Perceived BenefitErin C Schafer, Sharon Miller, Boji P W Lam, et al.
Cancer Research|December 26, 2003
A fully human monoclonal antibody to the insulin-like growth factor I receptor blocks ligand-dependent signaling and inhibits human tumor growth in vivoDouglas Burtrum, Zhenping Zhu, Dan Lu, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 6, 2017
Pharmacologic Characterization of AMG8379, a Potent and Selective Small Molecule Sulfonamide Antagonist of the Voltage-Gated Sodium Channel Na<sub>V</sub>1.7Thomas J Kornecook, Ruoyuan Yin, Stephen Altmann, et al.
Journal of Medicinal Chemistry|June 4, 2011
Identification of a potent, state-dependent inhibitor of Nav1.7 with oral efficacy in the formalin model of persistent painHoward Bregman, Loren Berry, John L Buchanan, et al.
Pageof 3