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Thomas B Friedman

Showing results (11-20 of 153) with videos related to

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Nature Reviews. Genetics|June 24, 2004
Genetic insights into the morphogenesis of inner ear hair cellsGregory I Frolenkov, Inna A Belyantseva, Thomas B Friedman, et al.
Trends in Molecular Medicine|November 8, 2003
Stereocilia: the long and the short of itInna A Belyantseva, Valentina Labay, Erich T Boger, et al.
The Journal of Physiology|September 16, 2006
Auditory mechanotransduction in the absence of functional myosin-XVaRuben Stepanyan, Inna A Belyantseva, Andrew J Griffith, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 4, 2009
Twinfilin 2 regulates actin filament lengths in cochlear stereociliaAnthony W Peng, Inna A Belyantseva, Patrick D Hsu, et al.
Journal of Medical Genetics|May 6, 2015
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing lossGhulam Mujtaba, Julie M Schultz, Ayesha Imtiaz, et al.
Molecular Vision|September 17, 2009
Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1DAyala Lagziel, Nora Overlack, Steven L Bernstein, et al.
Advances in Oto-Rhino-Laryngology|March 2, 2011
Usher syndrome: hearing loss with vision lossThomas B Friedman, Julie M Schultz, Zubair M Ahmed, et al.
Clinical Genetics|January 21, 2022
Late-onset hearing loss case associated with a heterozygous truncating variant of DIAPH1Bong Jik Kim, Takushi Miyoshi, Taimur Chaudhry, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Clinical manifestations of DFNB29 deafnessZubair M Ahmed, Saima Riazuddin, Thomas B Friedman, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Genetic modifiers of hereditary hearing lossSaima Riazuddin, Zubair M Ahmed, Thomas B Friedman, et al.
Pageof 16

Showing results (11-20 of 153) with videos related to

Sort By:
Pageof 16
Nature Reviews. Genetics|June 24, 2004
Genetic insights into the morphogenesis of inner ear hair cellsGregory I Frolenkov, Inna A Belyantseva, Thomas B Friedman, et al.
Trends in Molecular Medicine|November 8, 2003
Stereocilia: the long and the short of itInna A Belyantseva, Valentina Labay, Erich T Boger, et al.
The Journal of Physiology|September 16, 2006
Auditory mechanotransduction in the absence of functional myosin-XVaRuben Stepanyan, Inna A Belyantseva, Andrew J Griffith, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 4, 2009
Twinfilin 2 regulates actin filament lengths in cochlear stereociliaAnthony W Peng, Inna A Belyantseva, Patrick D Hsu, et al.
Journal of Medical Genetics|May 6, 2015
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing lossGhulam Mujtaba, Julie M Schultz, Ayesha Imtiaz, et al.
Molecular Vision|September 17, 2009
Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1DAyala Lagziel, Nora Overlack, Steven L Bernstein, et al.
Advances in Oto-Rhino-Laryngology|March 2, 2011
Usher syndrome: hearing loss with vision lossThomas B Friedman, Julie M Schultz, Zubair M Ahmed, et al.
Clinical Genetics|January 21, 2022
Late-onset hearing loss case associated with a heterozygous truncating variant of DIAPH1Bong Jik Kim, Takushi Miyoshi, Taimur Chaudhry, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Clinical manifestations of DFNB29 deafnessZubair M Ahmed, Saima Riazuddin, Thomas B Friedman, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Genetic modifiers of hereditary hearing lossSaima Riazuddin, Zubair M Ahmed, Thomas B Friedman, et al.
Pageof 16