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Our laboratory studies the molecular genetic basis of human diseases, particularly Usher syndrome, the leading cause of combined deafness and blindess, and other diseases of the eye and ear.
We use zebrafish and a combination of anatomical, physiological, molecular, and genetic techniques. The goal of our research is to identify disease-causing genes, to elucidate what goes wrong during disease, and to develop preclinical trials for new therapies.
Current research focuses on developing models of human disease. In particular, we are making and studying models of Usher syndrome.
We use zebrafish and a combination of anatomical, physiological, molecular, and genetic techniques. The goal of our research is to identify disease-causing genes, to elucidate what goes wrong during disease, and to develop preclinical trials for new therapies.
Current research focuses on developing models of human disease. In particular, we are making and studying models of Usher syndrome.
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论文共 185 篇作者统计合作学者相似作者
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Jennifer B Phillips, Siena Kulis, Sarah H. Buchner,Eric J Fox,Jeremy Wegner, Judy Pierce,Maryna V Ivanchenko,David P Corey,Jack L Arbiser,Monte Westerfield
biorxiv(2023)
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Maryna Ivanchenko,Alex J. Klein, Daniel M. Hathaway,Jennifer B. Phillips,Kevin T. Booth, Corey Goldstein, Andrew R. Murphy,Jeremy Wegner, Marcelo Cicconet,Artur A. Indzhykulian, Sean G. Megason,Monte Westerfield,
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCEno. 8 (2023)
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INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCEno. 8 (2023)
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Journal of proteomics (2022): 104666-104666
biorxiv(2021)
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