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Valerie A Street

Showing results (1-10 of 9) with videos related to

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The Journal of Biological Chemistry|March 8, 2011
A DNA variant within the MYO7A promoter regulates YY1 transcription factor binding and gene expression serving as a potential dominant DFNA11 auditory genetic modifierValerie A Street, Jin Li, Carol A Robbins, et al.
Journal of the Peripheral Nervous System : JPNS|December 3, 2003
New gene for CMTValerie A Street, Craig L Bennett, Thomas D Bird, et al.
BMC Medical Genetics|June 4, 2008
A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findingsNaomi F Bramhall, Jeremy C Kallman, Aimee M Verrall, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 1, 2008
In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifierJeremy C Kallman, James O Phillips, Naomi F Bramhall, et al.
Journal of Vestibular Research : Equilibrium & Orientation|September 9, 2008
Vestibular function in families with inherited autosomal dominant hearing lossValerie A Street, Jeremy C Kallman, Paul D Strombom, et al.
American Journal of Human Genetics|November 20, 2001
Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathiesValerie A Street, Jeff D Goldy, Alana S Golden, et al.
American Journal of Medical Genetics. Part A|November 2, 2005
A novel DFNA9 mutation in the vWFA2 domain of COCH alters a conserved cysteine residue and intrachain disulfide bond formation resulting in progressive hearing loss and site-specific vestibular and central oculomotor dysfunctionValerie A Street, Jeremy C Kallman, Nahid G Robertson, et al.
Journal of the Association for Research in Otolaryngology : JARO|June 22, 2014
Resistance to noise-induced hearing loss in 129S6 and MOLF mice: identification of independent, overlapping, and interacting chromosomal regionsValerie A Street, Sharon G Kujawa, Ani Manichaikul, et al.
Annals of Neurology|May 4, 2004
SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerveCraig L Bennett, Andrew J Shirk, Huy M Huynh, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
The Journal of Biological Chemistry|March 8, 2011
A DNA variant within the MYO7A promoter regulates YY1 transcription factor binding and gene expression serving as a potential dominant DFNA11 auditory genetic modifierValerie A Street, Jin Li, Carol A Robbins, et al.
Journal of the Peripheral Nervous System : JPNS|December 3, 2003
New gene for CMTValerie A Street, Craig L Bennett, Thomas D Bird, et al.
BMC Medical Genetics|June 4, 2008
A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findingsNaomi F Bramhall, Jeremy C Kallman, Aimee M Verrall, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 1, 2008
In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifierJeremy C Kallman, James O Phillips, Naomi F Bramhall, et al.
Journal of Vestibular Research : Equilibrium & Orientation|September 9, 2008
Vestibular function in families with inherited autosomal dominant hearing lossValerie A Street, Jeremy C Kallman, Paul D Strombom, et al.
American Journal of Human Genetics|November 20, 2001
Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathiesValerie A Street, Jeff D Goldy, Alana S Golden, et al.
American Journal of Medical Genetics. Part A|November 2, 2005
A novel DFNA9 mutation in the vWFA2 domain of COCH alters a conserved cysteine residue and intrachain disulfide bond formation resulting in progressive hearing loss and site-specific vestibular and central oculomotor dysfunctionValerie A Street, Jeremy C Kallman, Nahid G Robertson, et al.
Journal of the Association for Research in Otolaryngology : JARO|June 22, 2014
Resistance to noise-induced hearing loss in 129S6 and MOLF mice: identification of independent, overlapping, and interacting chromosomal regionsValerie A Street, Sharon G Kujawa, Ani Manichaikul, et al.
Annals of Neurology|May 4, 2004
SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerveCraig L Bennett, Andrew J Shirk, Huy M Huynh, et al.
Pageof 1