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J H Smith

Showing results (501-510 of 588) with videos related to

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The Annals of Otology, Rhinology, and Laryngology|January 22, 2011
Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian populationMichael S Hildebrand, Kimia Kahrizi, Catherine J Bromhead, et al.
American Journal of Human Genetics|September 8, 2009
Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humansNicolas Grillet, Martin Schwander, Michael S Hildebrand, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2024
A predominately pulmonary activation of complement in a mouse model of severe COVID-19Peter J Szachowicz, Christine Wohlford-Lenane, Cobey J Heinen, et al.
Bioinformatics (Oxford, England)|August 16, 2014
Cordova: web-based management of genetic variation dataSean S Ephraim, Nikhil Anand, Adam P DeLuca, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2017
DNA methylation of intragenic CpG islands depends on their transcriptional activity during differentiation and diseaseDanuta M Jeziorska, Robert J S Murray, Marco De Gobbi, et al.
Ophthalmic Genetics|April 14, 2020
Is it Usher syndrome? Collaborative diagnosis and molecular genetics of patients with visual impairment and hearing lossHeather A Stiff, Christina M Sloan-Heggen, Ashley Ko, et al.
Plos One|August 30, 2018
Grxcr2 is required for stereocilia morphogenesis in the cochleaMatthew R Avenarius, Jae-Yun Jung, Charles Askew, et al.
Human Genetics|August 23, 2021
The natural history of OTOF-related auditory neuropathy spectrum disorders: a multicenter studyRyan K Thorpe, Hela Azaiez, Peina Wu, et al.
Journal of the American Society of Nephrology : JASN|August 19, 2015
High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 GlomerulopathiesFengxiao Bu, Nicolo Ghiringhelli Borsa, Michael B Jones, et al.
Plos Genetics|March 28, 2015
HOMER2, a stereociliary scaffolding protein, is essential for normal hearing in humans and miceHela Azaiez, Amanda R Decker, Kevin T Booth, et al.
Pageof 59

Showing results (501-510 of 588) with videos related to

Sort By:
Pageof 59
The Annals of Otology, Rhinology, and Laryngology|January 22, 2011
Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian populationMichael S Hildebrand, Kimia Kahrizi, Catherine J Bromhead, et al.
American Journal of Human Genetics|September 8, 2009
Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humansNicolas Grillet, Martin Schwander, Michael S Hildebrand, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2024
A predominately pulmonary activation of complement in a mouse model of severe COVID-19Peter J Szachowicz, Christine Wohlford-Lenane, Cobey J Heinen, et al.
Bioinformatics (Oxford, England)|August 16, 2014
Cordova: web-based management of genetic variation dataSean S Ephraim, Nikhil Anand, Adam P DeLuca, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2017
DNA methylation of intragenic CpG islands depends on their transcriptional activity during differentiation and diseaseDanuta M Jeziorska, Robert J S Murray, Marco De Gobbi, et al.
Ophthalmic Genetics|April 14, 2020
Is it Usher syndrome? Collaborative diagnosis and molecular genetics of patients with visual impairment and hearing lossHeather A Stiff, Christina M Sloan-Heggen, Ashley Ko, et al.
Plos One|August 30, 2018
Grxcr2 is required for stereocilia morphogenesis in the cochleaMatthew R Avenarius, Jae-Yun Jung, Charles Askew, et al.
Human Genetics|August 23, 2021
The natural history of OTOF-related auditory neuropathy spectrum disorders: a multicenter studyRyan K Thorpe, Hela Azaiez, Peina Wu, et al.
Journal of the American Society of Nephrology : JASN|August 19, 2015
High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 GlomerulopathiesFengxiao Bu, Nicolo Ghiringhelli Borsa, Michael B Jones, et al.
Plos Genetics|March 28, 2015
HOMER2, a stereociliary scaffolding protein, is essential for normal hearing in humans and miceHela Azaiez, Amanda R Decker, Kevin T Booth, et al.
Pageof 59