Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Andrew J Griffith

Showing results (21-30 of 109) with videos related to

Pageof 11
Sort By:
European Journal of Human Genetics : EJHG|October 21, 2016
A genotypic ascertainment approach to refute the association of MYO1A variants with non-syndromic deafnessJohn Patton, Carmen Brewer, Wade Chien, 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.
Thyroid Research|June 22, 2011
Influence of dietary iodine deficiency on the thyroid gland in Slc26a4-null mutant miceTomoyuki Iwata, Tadao Yoshida, Masaaki Teranishi, et al.
Human Genetics|August 4, 2005
Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorderTomoko Makishima, Clara I Rodriguez, Nahid G Robertson, et al.
Journal of Human Genetics|January 31, 2009
Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairmentNele Hilgert, Kelly Monahan, Kiyoto Kurima, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|January 18, 2018
Gradual Symmetric Progression of DFNA34 Hearing Loss Caused by an NLRP3 Mutation and Cochlear AutoinflammationHiroshi Nakanishi, Yoshiyuki Kawashima, Kiyoto Kurima, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|June 9, 2007
Disruption of fibroblast growth factor receptor 3 signaling results in defects in cellular differentiation, neuronal patterning, and hearing impairmentChandrakala Puligilla, Feng Feng, Kotaro Ishikawa, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Clinical presentation of DFNB12 and Usher syndrome type 1DJulie M Bork, Robert J Morell, Shaheen Khan, et al.
Journal of the Association for Research in Otolaryngology : JARO|March 11, 2020
Systemic Fluorescent Gentamicin Enters Neonatal Mouse Hair Cells Predominantly Through Sensory Mechanoelectrical Transduction ChannelsAyane Makabe, Yoshiyuki Kawashima, Yuriko Sakamaki, et al.
Pageof 11

Showing results (21-30 of 109) with videos related to

Sort By:
Pageof 11
European Journal of Human Genetics : EJHG|October 21, 2016
A genotypic ascertainment approach to refute the association of MYO1A variants with non-syndromic deafnessJohn Patton, Carmen Brewer, Wade Chien, 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.
Thyroid Research|June 22, 2011
Influence of dietary iodine deficiency on the thyroid gland in Slc26a4-null mutant miceTomoyuki Iwata, Tadao Yoshida, Masaaki Teranishi, et al.
Human Genetics|August 4, 2005
Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorderTomoko Makishima, Clara I Rodriguez, Nahid G Robertson, et al.
Journal of Human Genetics|January 31, 2009
Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairmentNele Hilgert, Kelly Monahan, Kiyoto Kurima, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|January 18, 2018
Gradual Symmetric Progression of DFNA34 Hearing Loss Caused by an NLRP3 Mutation and Cochlear AutoinflammationHiroshi Nakanishi, Yoshiyuki Kawashima, Kiyoto Kurima, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|June 9, 2007
Disruption of fibroblast growth factor receptor 3 signaling results in defects in cellular differentiation, neuronal patterning, and hearing impairmentChandrakala Puligilla, Feng Feng, Kotaro Ishikawa, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Clinical presentation of DFNB12 and Usher syndrome type 1DJulie M Bork, Robert J Morell, Shaheen Khan, et al.
Journal of the Association for Research in Otolaryngology : JARO|March 11, 2020
Systemic Fluorescent Gentamicin Enters Neonatal Mouse Hair Cells Predominantly Through Sensory Mechanoelectrical Transduction ChannelsAyane Makabe, Yoshiyuki Kawashima, Yuriko Sakamaki, et al.
Pageof 11