Frank L. Conlon

Affiliations: 
2001- University of North Carolina, Chapel Hill, Chapel Hill, NC 
Area:
Molecular Biology, Cell Biology, Physiology, Biology, Genetics
Website:
https://www.conlon-lab.com/
Google:
"Frank Conlon"
Cross-listing: Physiology Academic Tree

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Publications

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Shi W, Wasson LK, Dorr KM, et al. (2024) CHD4 and SMYD1 repress common transcriptional programs in the developing heart. Development (Cambridge, England)
Conlon FL, Arnold AP. (2023) Sex chromosome mechanisms in cardiac development and disease. Nature Cardiovascular Research. 2: 340-350
Edwards W, Bussey OK, Conlon FL. (2023) The Tbx20-TLE interaction is essential for the maintenance of the second heart field. Development (Cambridge, England)
Shi W, Scialdone AP, Emerson JI, et al. (2023) Missense Mutation in Human CHD4 Causes Ventricular Noncompaction by Repressing ADAMTS1. Circulation Research
Edwards W, Greco TM, Miner GE, et al. (2023) Quantitative proteomic profiling identifies global protein network dynamics in murine embryonic heart development. Developmental Cell
Robbe ZL, Shi W, Wasson LK, et al. (2022) CHD4 is recruited by GATA4 and NKX2-5 to repress noncardiac gene programs in the developing heart. Genes & Development. 36: 468-482
Hoppler S, Conlon FL. (2019) : Experimental Access to Cardiovascular Development, Regeneration Discovery, and Cardiovascular Heart-Defect Modeling. Cold Spring Harbor Perspectives in Biology
Akerberg BN, Gu F, VanDusen NJ, et al. (2019) A reference map of murine cardiac transcription factor chromatin occupancy identifies dynamic and conserved enhancers. Nature Communications. 10: 4907
Federspiel JD, Tandon P, Wilczewski CM, et al. (2019) Conservation and divergence of protein pathways in the vertebrate heart. Plos Biology. 17: e3000437
Dorr KM, Conlon FL. (2019) Proteomic-based approaches to cardiac development and disease. Current Opinion in Chemical Biology. 48: 150-157
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