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个人简介
For the past decade he has worked specifically on the stereocilia bundle of vertebrate hair cells—its structure, development, mechanics and role in mechanotransduction. This has included work to elucidate the molecular and cell biological basis of hereditary deafness. Mutations in most of these proteins cause deafness, while many also cause blindness in Usher syndrome.
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论文共 45 篇作者统计合作学者相似作者
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Christopher J. Buswinka, David B. Rosenberg,Rubina G. Simikyan, Richard T. Osgood,Katharine Fernandez, Hidetomi Nitta,Yushi Hayashi, Leslie W. Liberman, Emily Nguyen,Erdem Yildiz, Jinkyung Kim,Amandine Jarysta,
Shelby E. Redfield,Pedro De-la-Torre,Mina Zamani, Hanjun Wang, Hina Khan, Tyler Morris,Gholamreza Shariati, Majid Karimi,Margaret A. Kenna,Go Hun Seo,Hongen Xu,Wei Lu,
Pedro De-la-Torre, Claudia Martinez-Garcia, Paul Gratias, Matthew Mun,Paula Santana,Nurunisa Akyuz,Wendy Gonzalez,Artur A Indzhykulian,David Ramirez
biorxiv(2024)
bioRxiv : the preprint server for biology (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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Molecular Therapyno. 8 (2023): 2439-2453
Maryna V. Ivanchenko,Daniel M. Hathaway,Alex J. Klein,Bifeng Pan,Olga Strelkova,Pedro De-la-Torre,Xudong Wu,Cole W. Peters,Eric M. Mulhall,Kevin T. Booth, Corey Goldstein, Joseph Brower,
Shelby E. Redfield,Pedro De-la-Torre,Mina Zamani, Hina Khan, Tyler Morris,Gholamreza Shariati, Majid Karimi,Margaret A. Kenna,Go Hun Seo,Sadaf Naz,Hamid Galehdari,Artur A. Indzhykulian,
medRxiv : the preprint server for health sciences (2023)
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