Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Daniel M. Hathaway"'
Autor:
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, Marcos Sotomayor, Artur A. Indzhykulian, David P. Corey
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-21 (2023)
Abstract Usher syndrome type 1 F (USH1F), caused by mutations in the protocadherin-15 gene (PCDH15), is characterized by congenital deafness, lack of balance, and progressive blindness. In hair cells, the receptor cells of the inner ear, PCDH15 is a
Externí odkaz:
https://doaj.org/article/7c07a295a0974ee8b332825242a40ad2
Autor:
Maryna V. Ivanchenko, Killian S. Hanlon, Daniel M. Hathaway, Alex J. Klein, Cole W. Peters, Yaqiao Li, Panos I. Tamvakologos, Josette Nammour, Casey A. Maguire, David P. Corey
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 21, Iss , Pp 382-398 (2021)
Gene therapy strategies using adeno-associated virus (AAV) vectors to treat hereditary deafnesses have shown remarkable efficacy in some mouse models of hearing loss. Even so, there are few AAV capsids that transduce both inner and outer hair cells
Externí odkaz:
https://doaj.org/article/475fe1182acd4ea6b521c663f3fd4d5c
Autor:
Killian S. Hanlon, Casey A. Maguire, Daniel M. Hathaway, David P. Corey, Alex J. Klein, Josette Nammour, Panos I. Tamvakologos, Yaqiao Li, Maryna V. Ivanchenko, Cole Peters
Publikováno v:
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 21, Iss, Pp 382-398 (2021)
Molecular Therapy: Methods & Clinical Development, Vol 21, Iss, Pp 382-398 (2021)
Gene therapy strategies using adeno-associated virus (AAV) vectors to treat hereditary deafnesses have shown remarkable efficacy in some mouse models of hearing loss. Even so, there are few AAV capsids that transduce both inner and outer hair cells