Author

L. Maves

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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Bioengineering· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:drug response / drug discovery· 2 Approach:experimental assay· 2 Research Focus:differential expression· 1 Organism:zebrafish· 1

Frequent Co-Authors

A. Gomez· 1 shared A. S. T. Smith· 1 shared B. J. Berry· 1 shared C. Henry· 1 shared D. L. Mack· 1 shared D. Lih· 1 shared E. C. Fisher· 1 shared E. Kilroy· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperPharmacology & Toxicology

A. Gomez

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2 papers

Recent·Most cited

High-throughput, real-time monitoring of engineered skeletal muscle function using magnetic sensing

A. S. T. Smith, S. M. Luttrell, J.-B. Dupont, K. Gray, D. Lih, J. W. Fleming, N. J. Cunningham, S. Jepson, J. Hesson, J. Mathieu, L. Maves, B. J. Berry, E. C. Fisher, N. Sniadecki, N. A. Geisse, D. L. Mack

This paper introduces a magnetic sensing system for real-time monitoring of engineered skeletal muscle function, showing improved contractility over time and enabling drug screening and disease modeling.

bioRxiv · May 20, 2022Bioengineering

A novel drug-combination screen in zebrafish identifies epigenetic small molecule candidates for Duchenne muscular dystrophy

G. H. Farr, M. Morris, A. Gomez, T. Pham, E. U. Parker, E. Kilroy, S. Said, C. Henry, L. Maves

The paper identifies two epigenetic small molecules, oxamflatin and salermide, that improve skeletal muscle structure in zebrafish models of Duchenne muscular dystrophy through a drug-combination screen.

bioRxiv · Feb 19, 2020Pharmacology & Toxicology