Author

A. Hung

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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Biophysics· 1 Cell Biology· 1 Microbiology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell signaling & trafficking· 2 Assay:electrophysiology· 2 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Approach:comparative / phylogenetic analysis· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

A. Kuanyshbek· 1 shared A. M. Deutschbauer· 1 shared A. P. Arkin· 1 shared C. A. Reid· 1 shared C. McKenzie· 1 shared D. Ho· 1 shared D. J. Adams· 1 shared E. Bertaggia· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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1 shared paperBiophysics

A. Kuanyshbek

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Different fluorescent labels report distinct components of spHCN channel voltage sensor movement

M. N. Wojciechowski, C. McKenzie, A. Hung, A. Kuanyshbek, M. S. Soh, C. A. Reid, I. C. Forster

This study uses different fluorescent labels to distinguish distinct kinetic components of S4 movement in the spHCN channel voltage sensor.

bioRxiv · Jan 23, 2024 · PreprintBiophysics

Barcoded overexpression screens in gut Bacteroidales identify genes with new roles in carbon utilization and stress resistance

Y. Y. Huang, M. N. Price, A. Hung, O. Gal-Oz, D. Ho, H. Carion, A. M. Deutschbauer, A. P. Arkin

The paper identifies new gene functions in gut Bacteroidales using a barcoded overexpression screen, revealing roles in carbon utilization and stress resistance.

bioRxiv · Oct 10, 2022 · PreprintMicrobiology

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

J. R. McArthur, J. Wen, A. Hung, R. K. Finol-Urdaneta, 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.

bioRxiv · Oct 4, 2021Pharmacology & Toxicology

Bile acid composition regulates the manganese transporter Slc30a10 in intestine

T. R. Ahmad, S. Higuchi, E. Bertaggia, A. Hung, N. Shanmugarajah, N. C. Guilz, J. R. Gamarra, R. A. Haeusler

This study shows that bile acid composition, particularly 12-hydroxylated bile acids, regulates the manganese transporter Slc30a10 in the intestine via lithocholic acid signaling through the vitamin D receptor.

bioRxiv · Feb 11, 2020Cell Biology