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Andrew J Griffith

Showing results (51-60 of 109) with videos related to

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Archives of Otolaryngology--Head & Neck Surgery|May 18, 2005
Investigation of the role of congenital cytomegalovirus infection in the etiology of enlarged vestibular aqueductsShannon P Pryor, Gail J Demmler, Anne C Madeo, et al.
Plos Genetics|October 8, 2011
Cell type-specific transcriptome analysis reveals a major role for Zeb1 and miR-200b in mouse inner ear morphogenesisRonna Hertzano, Ran Elkon, Kiyoto Kurima, et al.
Human Genetics|September 25, 2003
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east AsiansDenise Yan, Hong-Joon Park, Xiao Mei Ouyang, et al.
The Laryngoscope|November 19, 2016
Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele of SLC26A4Jane Rose, Julie A Muskett, Kelly A King, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 9, 2017
Acute genetic ablation of pendrin lowers blood pressure in miceFrancesco Trepiccione, Christelle Soukaseum, Veronique Baudrie, et al.
Research Square|October 27, 2023
Transgenic Tg(Kcnj10-ZsGreen) Fluorescent Reporter Mice Allow Visualization of Intermediate Cells in the Stria VascularisDillon Strepay, Rafal T Olszewski, Sydney Nixon, et al.
Scientific Reports|February 6, 2024
Transgenic Tg(Kcnj10-ZsGreen) fluorescent reporter mice allow visualization of intermediate cells in the stria vascularisDillon Strepay, Rafal T Olszewski, Sydney Nixon, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domainTomoko Makishima, Anne C Madeo, Carmen C Brewer, et al.
BMC Medical Genetics|February 11, 2011
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndromeSaima Riazuddin, Zubair M Ahmed, Rashmi S Hegde, et al.
European Journal of Human Genetics : EJHG|July 16, 2009
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3Shahid Yar Khan, Saima Riazuddin, Mohsin Shahzad, et al.
Pageof 11

Showing results (51-60 of 109) with videos related to

Sort By:
Pageof 11
Archives of Otolaryngology--Head & Neck Surgery|May 18, 2005
Investigation of the role of congenital cytomegalovirus infection in the etiology of enlarged vestibular aqueductsShannon P Pryor, Gail J Demmler, Anne C Madeo, et al.
Plos Genetics|October 8, 2011
Cell type-specific transcriptome analysis reveals a major role for Zeb1 and miR-200b in mouse inner ear morphogenesisRonna Hertzano, Ran Elkon, Kiyoto Kurima, et al.
Human Genetics|September 25, 2003
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east AsiansDenise Yan, Hong-Joon Park, Xiao Mei Ouyang, et al.
The Laryngoscope|November 19, 2016
Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele of SLC26A4Jane Rose, Julie A Muskett, Kelly A King, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 9, 2017
Acute genetic ablation of pendrin lowers blood pressure in miceFrancesco Trepiccione, Christelle Soukaseum, Veronique Baudrie, et al.
Research Square|October 27, 2023
Transgenic Tg(Kcnj10-ZsGreen) Fluorescent Reporter Mice Allow Visualization of Intermediate Cells in the Stria VascularisDillon Strepay, Rafal T Olszewski, Sydney Nixon, et al.
Scientific Reports|February 6, 2024
Transgenic Tg(Kcnj10-ZsGreen) fluorescent reporter mice allow visualization of intermediate cells in the stria vascularisDillon Strepay, Rafal T Olszewski, Sydney Nixon, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domainTomoko Makishima, Anne C Madeo, Carmen C Brewer, et al.
BMC Medical Genetics|February 11, 2011
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndromeSaima Riazuddin, Zubair M Ahmed, Rashmi S Hegde, et al.
European Journal of Human Genetics : EJHG|July 16, 2009
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3Shahid Yar Khan, Saima Riazuddin, Mohsin Shahzad, et al.
Pageof 11