Author

P. K. Tari

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Pharmacology & Toxicology· 2

Signature Assays, Organisms & Methods

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Research Focus:drug response / drug discovery· 2 Approach:experimental assay· 2 Organism:mouse· 2 Assay:electrophysiology· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

A. Hussainkhel· 2 shared A. J. Cutts· 2 shared A. Lindgren· 2 shared A. Zenova· 2 shared C. Dehnhardt· 2 shared C. Dube· 2 shared E. Chang· 2 shared G. Bankar· 2 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersPharmacology & Toxicology

A. Hussainkhel

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2 papers

Recent·Most cited

Pharmacology & ToxicologybioRxivPreprintAug 3, 2023

NaV1.6 inhibition drives the efficacy of voltage-gated sodium channel inhibitors to prevent electrically induced seizures in both wild type and Scn8aN1768D/+ gain-of-function mice

J. Johnson, T. Focken, P. K. Tari…·J. R. Empfield

The paper shows that inhibiting NaV1.6 reduces seizures in both wild-type and Scn8aN1768D/+ mice, suggesting NaV1.6 is a key target for anti-seizure drugs.

DOI 10.1101/2023.08.03.551823

mouseelectrophysiology

𝕏 PostBluesky

Pharmacology & ToxicologyeLifePeer-reviewedMar 2, 2022

NBI-921352, a First-in-Class, Na V 1.6 Selective, Sodium Channel Inhibitor That Prevents Seizures in Scn8a Gain-of- Function Mice, and Wild-Type Mice and Rats

J. Johnson, T. Focken, K. Khakh…·W

This paper describes NBI-921352, a selective NaV1.6 inhibitor that prevents seizures in Scn8a gain-of-function mice and wild-type models, with better efficacy and tolerability than existing antiseizure drugs.

DOI 10.7554/elife.72468

mouseexperimental assay

𝕏 PostBluesky