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Human Molecular Genetics|March 12, 2021
Mutant Nmnat1 leads to a retina-specific decrease of NAD+ accompanied by increased poly(ADP-ribose) in a mouse model of NMNAT1-associated retinal degenerationScott H Greenwald, Emily E Brown, Michael J Scandura, et al.
Mededportal : the Journal of Teaching and Learning Resources|February 26, 2019
Measuring Assessment Quality With an Assessment Utility Rubric for Medical EducationJorie M Colbert-Getz, Michael Ryan, Erin Hennessey, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 30, 2025
Systematic empirical evaluation of individual base editing targets: Validating therapeutic targets in USH2A and comparison of methodsYuki Tachida, Kannan V Manian, Rossano Butcher, et al.
Molecular Therapy. Methods & Clinical Development|August 11, 2020
Gene Therapy Preserves Retinal Structure and Function in a Mouse Model of NMNAT1-Associated Retinal DegenerationScott H Greenwald, Emily E Brown, Michael J Scandura, et al.
Nature Biomedical Engineering|January 16, 2020
Cytosine and adenine base editing of the brain, liver, retina, heart and skeletal muscle of mice via adeno-associated virusesJonathan M Levy, Wei-Hsi Yeh, Nachiket Pendse, et al.
American Journal of Respiratory Cell and Molecular Biology|May 6, 2026
Lentiviral-mediated gene complementation to rescue pathogenic ABCA3 variantsAshley L Cooney, Shakayla Lamer, Ping Yang, et al.
Biorxiv : the Preprint Server for Biology|September 5, 2025
Lentiviral-mediated gene complementation rescues pathogenic ABCA3 variantsAshley L Cooney, Shakayla Lamer, Ping Yang, et al.
Critical Care Medicine|December 9, 2025
Determination of Adult Critical Care Physician Core Knowledge and Skills: Results of a Multidisciplinary, Modified Delphi ProcessSamuel A Tisherman, Antoinette Spevetz, J Christopher Farmer, et al.
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