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Andrew J Griffith

Showing results (61-70 of 109) with videos related to

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The Journal of Clinical Investigation|November 23, 2011
Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genesYoshiyuki Kawashima, Gwenaëlle S G Géléoc, Kiyoto Kurima, et al.
Elife|October 11, 2017
Molecular architecture underlying fluid absorption by the developing inner earKeiji Honda, Sung Huhn Kim, Michael C Kelly, et al.
Plos Genetics|July 23, 2013
SLC26A4 targeted to the endolymphatic sac rescues hearing and balance in Slc26a4 mutant miceXiangming Li, Joel D Sanneman, Donald G Harbidge, et al.
The Laryngoscope|August 4, 2006
Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndromeAndrew J Griffith, Yandan Yang, Shannon P Pryor, et al.
Human Genetics|July 11, 2002
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHICZubair M Ahmed, Tenesha N Smith, Saima Riazuddin, et al.
Advances in Oto-Rhino-Laryngology|March 2, 2011
Hereditary hearing loss with thyroid abnormalitiesByung Yoon Choi, Julie Muskett, Kelly A King, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 22, 2022
Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher SyndromeKevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Ear and Hearing|August 19, 2003
Recent advances in the understanding of syndromic forms of hearing lossThomas B Friedman, Julie M Schultz, Tamar Ben-Yosef, et al.
Human Molecular Genetics|October 23, 2003
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23Zubair M Ahmed, Saima Riazuddin, Jamil Ahmad, et al.
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 SyndromeKevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Pageof 11

Showing results (61-70 of 109) with videos related to

Sort By:
Pageof 11
The Journal of Clinical Investigation|November 23, 2011
Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genesYoshiyuki Kawashima, Gwenaëlle S G Géléoc, Kiyoto Kurima, et al.
Elife|October 11, 2017
Molecular architecture underlying fluid absorption by the developing inner earKeiji Honda, Sung Huhn Kim, Michael C Kelly, et al.
Plos Genetics|July 23, 2013
SLC26A4 targeted to the endolymphatic sac rescues hearing and balance in Slc26a4 mutant miceXiangming Li, Joel D Sanneman, Donald G Harbidge, et al.
The Laryngoscope|August 4, 2006
Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndromeAndrew J Griffith, Yandan Yang, Shannon P Pryor, et al.
Human Genetics|July 11, 2002
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHICZubair M Ahmed, Tenesha N Smith, Saima Riazuddin, et al.
Advances in Oto-Rhino-Laryngology|March 2, 2011
Hereditary hearing loss with thyroid abnormalitiesByung Yoon Choi, Julie Muskett, Kelly A King, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 22, 2022
Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher SyndromeKevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Ear and Hearing|August 19, 2003
Recent advances in the understanding of syndromic forms of hearing lossThomas B Friedman, Julie M Schultz, Tamar Ben-Yosef, et al.
Human Molecular Genetics|October 23, 2003
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23Zubair M Ahmed, Saima Riazuddin, Jamil Ahmad, et al.
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 SyndromeKevin Isgrig, Jack W Shteamer, Inna A Belyantseva, et al.
Pageof 11