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Nature Biotechnology
|
February 7, 2017
Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c
Bifeng Pan, Charles Askew, Alice Galvin, et al.
Neuron
|
August 24, 2018
TMC1 Forms the Pore of Mechanosensory Transduction Channels in Vertebrate Inner Ear Hair Cells
Bifeng Pan, Nurunisa Akyuz, Xiao-Ping Liu, et al.
Cell Reports
|
September 1, 2015
TMC1 and TMC2 Localize at the Site of Mechanotransduction in Mammalian Inner Ear Hair Cell Stereocilia
Kiyoto Kurima, Seham Ebrahim, Bifeng Pan, et al.
Nature Communications
|
April 26, 2023
Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1F
Maryna V Ivanchenko, Daniel M Hathaway, Alex J Klein, et al.
Nature Medicine
|
July 5, 2019
Allele-specific gene editing prevents deafness in a model of dominant progressive hearing loss
Bence György, Carl Nist-Lund, Bifeng Pan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 21, 2020
Direct Delivery of Antisense Oligonucleotides to the Middle and Inner Ear Improves Hearing and Balance in Usher Mice
Jennifer J Lentz, Bifeng Pan, Abhilash Ponnath, et al.
Nature
|
December 21, 2017
Treatment of autosomal dominant hearing loss by in vivo delivery of genome editing agents
Xue Gao, Yong Tao, Veronica Lamas, et al.
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Search research articles
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Showing results (31-40 of 37) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 37 results.
Nature Biotechnology
|
February 7, 2017
Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c
Bifeng Pan, Charles Askew, Alice Galvin, et al.
Neuron
|
August 24, 2018
TMC1 Forms the Pore of Mechanosensory Transduction Channels in Vertebrate Inner Ear Hair Cells
Bifeng Pan, Nurunisa Akyuz, Xiao-Ping Liu, et al.
Cell Reports
|
September 1, 2015
TMC1 and TMC2 Localize at the Site of Mechanotransduction in Mammalian Inner Ear Hair Cell Stereocilia
Kiyoto Kurima, Seham Ebrahim, Bifeng Pan, et al.
Nature Communications
|
April 26, 2023
Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1F
Maryna V Ivanchenko, Daniel M Hathaway, Alex J Klein, et al.
Nature Medicine
|
July 5, 2019
Allele-specific gene editing prevents deafness in a model of dominant progressive hearing loss
Bence György, Carl Nist-Lund, Bifeng Pan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 21, 2020
Direct Delivery of Antisense Oligonucleotides to the Middle and Inner Ear Improves Hearing and Balance in Usher Mice
Jennifer J Lentz, Bifeng Pan, Abhilash Ponnath, et al.
Nature
|
December 21, 2017
Treatment of autosomal dominant hearing loss by in vivo delivery of genome editing agents
Xue Gao, Yong Tao, Veronica Lamas, et al.
Page
of 4