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Andrew J Griffith

Showing results (1-10 of 109) with videos related to

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Human Genetics|August 4, 2021
Genetic architecture and phenotypic landscape of SLC26A4-related hearing lossKeiji Honda, Andrew J Griffith
Hearing Research|June 15, 2011
Hearing loss associated with enlargement of the vestibular aqueduct: mechanistic insights from clinical phenotypes, genotypes, and mouse modelsAndrew J Griffith, Philine Wangemann
Annual Review of Genomics and Human Genetics|October 7, 2003
Human nonsyndromic sensorineural deafnessThomas B Friedman, Andrew J Griffith
Archives of Otolaryngology--Head & Neck Surgery|January 12, 2002
Auditory function and the M34T allele of connexin 26Andrew J Griffith, Thomas B Friedman
Nature Biotechnology|December 11, 2012
Extracting energy from the inner earKenneth Shepard, Taku Ito, Andrew J Griffith
Behavioural Brain Research|September 8, 2007
Anxiety and otovestibular disorders: linking behavioral phenotypes in men and miceAllan V Kalueff, Kotaro Ishikawa, Andrew J Griffith
Acta Oto-Laryngologica|May 15, 2004
Col11a1 and Col11a2 mRNA expression in the developing mouse cochlea: implications for the correlation of hearing loss phenotype with mutant type XI collagen genotypeKarl B Shpargel, Tomoko Makishima, Andrew J Griffith
Genomics|August 9, 2003
Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformisKiyoto Kurima, Yandan Yang, Katherine Sorber, et al.
Auris, Nasus, Larynx|June 17, 2014
Mutations of TMC1 cause deafness by disrupting mechanoelectrical transductionHiroshi Nakanishi, Kiyoto Kurima, Yoshiyuki Kawashima, et al.
Journal of Visualized Experiments : Jove|April 12, 2021
Dissection of the Endolymphatic Sac from MiceKeiji Honda, Hyun Jae Lee, Andrew J Griffith, et al.
Pageof 11

Showing results (1-10 of 109) with videos related to

Sort By:
Pageof 11
Human Genetics|August 4, 2021
Genetic architecture and phenotypic landscape of SLC26A4-related hearing lossKeiji Honda, Andrew J Griffith
Hearing Research|June 15, 2011
Hearing loss associated with enlargement of the vestibular aqueduct: mechanistic insights from clinical phenotypes, genotypes, and mouse modelsAndrew J Griffith, Philine Wangemann
Annual Review of Genomics and Human Genetics|October 7, 2003
Human nonsyndromic sensorineural deafnessThomas B Friedman, Andrew J Griffith
Archives of Otolaryngology--Head & Neck Surgery|January 12, 2002
Auditory function and the M34T allele of connexin 26Andrew J Griffith, Thomas B Friedman
Nature Biotechnology|December 11, 2012
Extracting energy from the inner earKenneth Shepard, Taku Ito, Andrew J Griffith
Behavioural Brain Research|September 8, 2007
Anxiety and otovestibular disorders: linking behavioral phenotypes in men and miceAllan V Kalueff, Kotaro Ishikawa, Andrew J Griffith
Acta Oto-Laryngologica|May 15, 2004
Col11a1 and Col11a2 mRNA expression in the developing mouse cochlea: implications for the correlation of hearing loss phenotype with mutant type XI collagen genotypeKarl B Shpargel, Tomoko Makishima, Andrew J Griffith
Genomics|August 9, 2003
Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformisKiyoto Kurima, Yandan Yang, Katherine Sorber, et al.
Auris, Nasus, Larynx|June 17, 2014
Mutations of TMC1 cause deafness by disrupting mechanoelectrical transductionHiroshi Nakanishi, Kiyoto Kurima, Yoshiyuki Kawashima, et al.
Journal of Visualized Experiments : Jove|April 12, 2021
Dissection of the Endolymphatic Sac from MiceKeiji Honda, Hyun Jae Lee, Andrew J Griffith, et al.
Pageof 11