MichaelEveretteNanceMDPhD

Physician

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Office
621 S New Ballas Rd
Ste 3019B
Saint Louis, MO 63141
Phone+1 314-509-5305

Fax+1 314-251-4454

Mizzou 18 award University of Missouri Columbia, 2021
Outstanding Medical Student Research Publication (Translational Science). “AAV9 Edits Muscle Stem Cells in Normal and Dystrophic Adult Mice”. University of Missouri Columbia, 2020
Outstanding Poster Presentation Award American Society for Gene and Cell Therapy, 2018
Outstanding Medical Student Research Publication (Basic Science). “Attenuated sarcomere lengthening of the aged murine left ventricle observed using two-photon fluorescence microscopy”. University of Missouri Columbia, 2018
1st place Health Science Research Day poster presentation University of Missouri Columbia, 2017
Hope for Javier Pre-Doctoral Fellowship Hope for Javier Foundation, 2017
Mizzou Advantage/One Health, Travel award University of Missouri Columbia, 2016
Tom and Anne Smith MD-PhD Fellowship University of Missouri Columbia, 2014
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PubMed

38 citations
Perspective on Adeno-Associated Virus Capsid Modification for Duchenne Muscular Dystrophy Gene Therapy
Michael E. Nance, Dongsheng Duan
Human Gene Therapy. 2015-09-16
69 citations
AAV CRISPR editing rescues cardiac and muscle function for 18 months in dystrophic mice.
Chady H. Hakim, Nalinda B. Wasala, Christopher E. Nelson, Lakmini P. Wasala, Yongping Yue
JCI Insight. 2018-12-06
45 citations
AAV9 Edits Muscle Stem Cells in Normal and Dystrophic Adult Mice.
Michael E. Nance, Ruicheng Shi, Chady H. Hakim, Nalinda B. Wasala, Yongping Yue
Molecular Therapy. 2019-09-04

Steps Forward in Treating Duchenne Muscular Dystrophy with Gene Repair TherapyMarch 8th, 2021
Researchers overcome hurdle in CRISPR gene editing for muscular dystrophyMarch 8th, 2021
Gene Editing Enables Researchers to Correct Mutation in Muscle Stem Cells in Muscular Dystrophy Mouse ModelMarch 8th, 2021
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Graduate research assistantMD-PhD student in the lab of Dongsheng Duan. Research focused on genetic engineering, muscle regeneration and muscle stem cell gene therapy.2014 - 2019