Author

R. K. Finol-Urdaneta

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

Biology Disciplines

Click to filter author papers

Pharmacology & Toxicology· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

D. J. Adams· 3 shared J. R. McArthur· 3 shared A. Aboelela· 1 shared A. Hung· 1 shared A. Rangel· 1 shared A. S. Kristensen· 1 shared B. J. Buckley· 1 shared B. Olivera· 1 shared

Activity by Year

2022-2022 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 26 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersPharmacology & Toxicology

D. J. Adams

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Pharmacology & ToxicologyeLifePeer-reviewedJul 20, 2022

{micro}-Theraphotoxin-Pn3a inhibition of Cav3.3 channels reveals a novel isoform-selective drug binding site

J. R. McArthur, J. Wen, A. Hung…·D. J. Adams

This study identifies Pn3a as a subtype-selective inhibitor of CaV3.3 T-type calcium channels, revealing a novel isoform-specific binding site with therapeutic potential.

DOI 10.7554/elife.74040

electrophysiologycomparative / phylogenetic analysis

𝕏 PostBluesky

BiochemistrybioRxivJul 4, 2022

Identification of a sensory neuron Cav2.3 inhibitor within a new superfamily of macro-conotoxins

C. M. Hackney, P. Florez Salcedo, E. Mueller…·L. Ellgaard

The paper identifies a new macro-conotoxin, Mu8.1, which selectively inhibits Cav2.3 calcium channels in sensory neurons, highlighting its potential as a molecular tool for studying neuronal subclasses.

DOI 10.1371/journal.pbio.3002217

mouseproteomics

𝕏 PostBluesky

Pharmacology & ToxicologybioRxivMar 12, 2022

Automated patch clamp screening of amiloride and 5-N,N-hexamethyleneamiloride (HMA) analogs identifies 6-iodoamiloride as a potent acid-sensing ion channel inhibitor.

R. K. Finol-Urdaneta, J. R. McArthur, A. Aboelela…·B. J. Buckley

The paper screens amiloride analogs using automated patch-clamp to identify 6-iodoamiloride as a more potent ASIC1 inhibitor than amiloride.

DOI 10.1021/acs.molpharmaceut.2c01083

ratelectrophysiology

𝕏 PostBluesky