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Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 4, 2017
Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher Syndrome
Kevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Nature Communications
|
October 24, 2022
Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
Young Rae Ji, Yosuke Tona, Talah Wafa, et al.
Genes, Brain, and Behavior
|
June 17, 2023
Spontaneous allelic variant in deafness-blindness gene Ush1g resulting in an expanded phenotype
Vladimir Vartanian, Jocelyn F Krey, Paroma Chatterjee, et al.
Human Molecular Genetics
|
May 6, 2009
Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation
Ruishuang Geng, Scott F Geller, Toshinori Hayashi, et al.
The Journal of Cell Biology
|
September 14, 2017
Heterodimeric capping protein is required for stereocilia length and width regulation
Matthew R Avenarius, Jocelyn F Krey, Rachel A Dumont, et al.
Scientific Reports
|
February 24, 2019
Sodium-activated potassium channels shape peripheral auditory function and activity of the primary auditory neurons in mice
Daniël O J Reijntjes, Jeong Han Lee, Seojin Park, et al.
The Journal of Clinical Investigation
|
August 28, 2013
Tricellulin deficiency affects tight junction architecture and cochlear hair cells
Gowri Nayak, Sue I Lee, Rizwan Yousaf, et al.
Nature Communications
|
January 4, 2020
Retinoic acid degradation shapes zonal development of vestibular organs and sensitivity to transient linear accelerations
Kazuya Ono, James Keller, Omar López Ramírez, et al.
Plos One
|
August 30, 2018
Grxcr2 is required for stereocilia morphogenesis in the cochlea
Matthew R Avenarius, Jae-Yun Jung, Charles Askew, et al.
The Journal of Cell Biology
|
February 17, 2022
ANKRD24 organizes TRIOBP to reinforce stereocilia insertion points
Jocelyn F Krey, Chang Liu, Inna A Belyantseva, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 64) with videos related to
Sort By:
Page
of 7
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 4, 2017
Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher Syndrome
Kevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Nature Communications
|
October 24, 2022
Function of bidirectional sensitivity in the otolith organs established by transcription factor Emx2
Young Rae Ji, Yosuke Tona, Talah Wafa, et al.
Genes, Brain, and Behavior
|
June 17, 2023
Spontaneous allelic variant in deafness-blindness gene Ush1g resulting in an expanded phenotype
Vladimir Vartanian, Jocelyn F Krey, Paroma Chatterjee, et al.
Human Molecular Genetics
|
May 6, 2009
Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation
Ruishuang Geng, Scott F Geller, Toshinori Hayashi, et al.
The Journal of Cell Biology
|
September 14, 2017
Heterodimeric capping protein is required for stereocilia length and width regulation
Matthew R Avenarius, Jocelyn F Krey, Rachel A Dumont, et al.
Scientific Reports
|
February 24, 2019
Sodium-activated potassium channels shape peripheral auditory function and activity of the primary auditory neurons in mice
Daniël O J Reijntjes, Jeong Han Lee, Seojin Park, et al.
The Journal of Clinical Investigation
|
August 28, 2013
Tricellulin deficiency affects tight junction architecture and cochlear hair cells
Gowri Nayak, Sue I Lee, Rizwan Yousaf, et al.
Nature Communications
|
January 4, 2020
Retinoic acid degradation shapes zonal development of vestibular organs and sensitivity to transient linear accelerations
Kazuya Ono, James Keller, Omar López Ramírez, et al.
Plos One
|
August 30, 2018
Grxcr2 is required for stereocilia morphogenesis in the cochlea
Matthew R Avenarius, Jae-Yun Jung, Charles Askew, et al.
The Journal of Cell Biology
|
February 17, 2022
ANKRD24 organizes TRIOBP to reinforce stereocilia insertion points
Jocelyn F Krey, Chang Liu, Inna A Belyantseva, et al.
Page
of 7