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Andrew J Griffith

Showing results (41-50 of 109) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 18, 2008
Hedgehog signaling regulates sensory cell formation and auditory function in mice and humansElizabeth Carroll Driver, Shannon P Pryor, Patrick Hill, et al.
Neuron|July 23, 2013
TMC1 and TMC2 are components of the mechanotransduction channel in hair cells of the mammalian inner earBifeng Pan, Gwenaelle S Géléoc, Yukako Asai, et al.
Nature Cell Biology|January 18, 2005
Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereociliaInna A Belyantseva, Erich T Boger, Sadaf Naz, et al.
Journal of Human Genetics|March 17, 2009
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in PakistanisSaima Anwar, Saima Riazuddin, Zubair M Ahmed, et al.
The Journal of Biological Chemistry|September 12, 2020
Expression of a TMC6-TMC8-CIB1 heterotrimeric complex in lymphocytes is regulated by each of the componentsChuan-Jin Wu, Xing Li, Connie L Sommers, et al.
BMC Medical Genetics|July 4, 2019
SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueductJanet R Chao, Parna Chattaraj, Tina Munjal, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|May 14, 2015
Vestibular Dysfunction in Patients with Enlarged Vestibular AqueductChris K Zalewski, Wade W Chien, Kelly A King, et al.
Journal of the Association for Research in Otolaryngology : JARO|October 17, 2002
Knock-in mouse model for resistance to thyroid hormone (RTH): an RTH mutation in the thyroid hormone receptor beta gene disrupts cochlear morphogenesisAndrew J Griffith, Yvonne M Szymko, Masahiro Kaneshige, et al.
Human Molecular Genetics|October 24, 2002
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28Linda M Peters, David W Anderson, Andrew J Griffith, et al.
American Journal of Medical Genetics. Part A|September 10, 2005
Stickler syndrome: clinical characteristics and diagnostic criteriaPeter S Rose, Howard P Levy, Ruth M Liberfarb, et al.
Pageof 11

Showing results (41-50 of 109) with videos related to

Sort By:
Pageof 11
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 18, 2008
Hedgehog signaling regulates sensory cell formation and auditory function in mice and humansElizabeth Carroll Driver, Shannon P Pryor, Patrick Hill, et al.
Neuron|July 23, 2013
TMC1 and TMC2 are components of the mechanotransduction channel in hair cells of the mammalian inner earBifeng Pan, Gwenaelle S Géléoc, Yukako Asai, et al.
Nature Cell Biology|January 18, 2005
Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereociliaInna A Belyantseva, Erich T Boger, Sadaf Naz, et al.
Journal of Human Genetics|March 17, 2009
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in PakistanisSaima Anwar, Saima Riazuddin, Zubair M Ahmed, et al.
The Journal of Biological Chemistry|September 12, 2020
Expression of a TMC6-TMC8-CIB1 heterotrimeric complex in lymphocytes is regulated by each of the componentsChuan-Jin Wu, Xing Li, Connie L Sommers, et al.
BMC Medical Genetics|July 4, 2019
SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueductJanet R Chao, Parna Chattaraj, Tina Munjal, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|May 14, 2015
Vestibular Dysfunction in Patients with Enlarged Vestibular AqueductChris K Zalewski, Wade W Chien, Kelly A King, et al.
Journal of the Association for Research in Otolaryngology : JARO|October 17, 2002
Knock-in mouse model for resistance to thyroid hormone (RTH): an RTH mutation in the thyroid hormone receptor beta gene disrupts cochlear morphogenesisAndrew J Griffith, Yvonne M Szymko, Masahiro Kaneshige, et al.
Human Molecular Genetics|October 24, 2002
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28Linda M Peters, David W Anderson, Andrew J Griffith, et al.
American Journal of Medical Genetics. Part A|September 10, 2005
Stickler syndrome: clinical characteristics and diagnostic criteriaPeter S Rose, Howard P Levy, Ruth M Liberfarb, et al.
Pageof 11