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J H Smith

Showing results (511-520 of 588) with videos related to

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American Journal of Human Genetics|August 5, 2008
Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null miceJérôme Ruel, Sarah Emery, Régis Nouvian, et al.
Clinical Genetics|July 12, 2008
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11N Hilgert, F Alasti, N Dieltjens, et al.
Human Mutation|January 3, 2013
AudioGene: predicting hearing loss genotypes from phenotypes to guide genetic screeningKyle R Taylor, Adam P Deluca, A Eliot Shearer, et al.
International Journal of Pediatric Otorhinolaryngology|October 13, 2016
International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patientBryan J Liming, John Carter, Alan Cheng, et al.
Hearing Research|September 15, 2012
Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesisRobert W Eppsteiner, A Eliot Shearer, Michael S Hildebrand, et al.
Bone|April 6, 2002
Otosclerosis: a genetically heterogeneous disease involving at least three different genesK Van Den Bogaert, P J Govaerts, E M R De Leenheer, et al.
Scientific Reports|April 12, 2020
Insights into the pathophysiology of DFNA10 hearing loss associated with novel EYA4 variantsMatias Morín, Lucía Borreguero, Kevin T Booth, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 21, 2007
Association of bone morphogenetic proteins with otosclerosisIsabelle Schrauwen, Melissa Thys, Kathleen Vanderstraeten, et al.
Kidney International|June 6, 2024
The role of complement in kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies ConferenceMarina Vivarelli, Jonathan Barratt, Laurence H Beck, et al.
International Journal of Pediatric Otorhinolaryngology|June 15, 2012
The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year studyNiloofar Bazazzadegan, Nooshin Nikzat, Zohreh Fattahi, et al.
Pageof 59

Showing results (511-520 of 588) with videos related to

Sort By:
Pageof 59
American Journal of Human Genetics|August 5, 2008
Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null miceJérôme Ruel, Sarah Emery, Régis Nouvian, et al.
Clinical Genetics|July 12, 2008
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11N Hilgert, F Alasti, N Dieltjens, et al.
Human Mutation|January 3, 2013
AudioGene: predicting hearing loss genotypes from phenotypes to guide genetic screeningKyle R Taylor, Adam P Deluca, A Eliot Shearer, et al.
International Journal of Pediatric Otorhinolaryngology|October 13, 2016
International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patientBryan J Liming, John Carter, Alan Cheng, et al.
Hearing Research|September 15, 2012
Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesisRobert W Eppsteiner, A Eliot Shearer, Michael S Hildebrand, et al.
Bone|April 6, 2002
Otosclerosis: a genetically heterogeneous disease involving at least three different genesK Van Den Bogaert, P J Govaerts, E M R De Leenheer, et al.
Scientific Reports|April 12, 2020
Insights into the pathophysiology of DFNA10 hearing loss associated with novel EYA4 variantsMatias Morín, Lucía Borreguero, Kevin T Booth, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 21, 2007
Association of bone morphogenetic proteins with otosclerosisIsabelle Schrauwen, Melissa Thys, Kathleen Vanderstraeten, et al.
Kidney International|June 6, 2024
The role of complement in kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies ConferenceMarina Vivarelli, Jonathan Barratt, Laurence H Beck, et al.
International Journal of Pediatric Otorhinolaryngology|June 15, 2012
The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year studyNiloofar Bazazzadegan, Nooshin Nikzat, Zohreh Fattahi, et al.
Pageof 59