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Kim Cryns

Showing results (1-10 of 16) with videos related to

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Audiology & Neuro-Otology|December 17, 2003
Deafness genes and their diagnostic applicationsKim Cryns, Guy Van Camp
Ear and Hearing|August 19, 2003
Nonsyndromic hearing lossLut Van Laer, Kim Cryns, Richard J H Smith, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 1, 2006
Transgenic mice overexpressing glycogen synthase kinase 3beta: a putative model of hyperactivity and maniaJos Prickaerts, Dieder Moechars, Kim Cryns, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 20, 2002
Autosomal dominant low-frequency hearing impairment (DFNA6/14): a clinical and genetic family studySteven J H Bom, Guy Van Camp, Kim Cryns, et al.
Histochemistry and Cell Biology|March 22, 2003
The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cellsKim Cryns, Sofie Thys, Lut Van Laer, et al.
The Journal of Comparative Neurology|December 23, 2003
Circling behavior in the Ecl mouse is caused by lateral semicircular canal defectsKim Cryns, Arjan M van Alphen, Michiel P van Spaendonck, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|July 15, 2006
Lack of lithium-like behavioral and molecular effects in IMPA2 knockout miceKim Cryns, Alon Shamir, Joseph Shapiro, et al.
Archives of Otolaryngology--Head & Neck Surgery|April 23, 2003
Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1)Ronald J E Pennings, Steven J H Bom, Kim Cryns, et al.
Audiology & Neuro-Otology|December 17, 2003
Sex-related hearing impairment in Wolfram syndrome patients identified by inactivating WFS1 mutationsRonald J E Pennings, Patrick L M Huygen, Jody M W van den Ouweland, et al.
Genome Research|April 5, 2002
Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genesKim Cryns, Michiel P Van Spaendonck, Kris Flothmann, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Audiology & Neuro-Otology|December 17, 2003
Deafness genes and their diagnostic applicationsKim Cryns, Guy Van Camp
Ear and Hearing|August 19, 2003
Nonsyndromic hearing lossLut Van Laer, Kim Cryns, Richard J H Smith, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 1, 2006
Transgenic mice overexpressing glycogen synthase kinase 3beta: a putative model of hyperactivity and maniaJos Prickaerts, Dieder Moechars, Kim Cryns, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 20, 2002
Autosomal dominant low-frequency hearing impairment (DFNA6/14): a clinical and genetic family studySteven J H Bom, Guy Van Camp, Kim Cryns, et al.
Histochemistry and Cell Biology|March 22, 2003
The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cellsKim Cryns, Sofie Thys, Lut Van Laer, et al.
The Journal of Comparative Neurology|December 23, 2003
Circling behavior in the Ecl mouse is caused by lateral semicircular canal defectsKim Cryns, Arjan M van Alphen, Michiel P van Spaendonck, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|July 15, 2006
Lack of lithium-like behavioral and molecular effects in IMPA2 knockout miceKim Cryns, Alon Shamir, Joseph Shapiro, et al.
Archives of Otolaryngology--Head & Neck Surgery|April 23, 2003
Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1)Ronald J E Pennings, Steven J H Bom, Kim Cryns, et al.
Audiology & Neuro-Otology|December 17, 2003
Sex-related hearing impairment in Wolfram syndrome patients identified by inactivating WFS1 mutationsRonald J E Pennings, Patrick L M Huygen, Jody M W van den Ouweland, et al.
Genome Research|April 5, 2002
Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genesKim Cryns, Michiel P Van Spaendonck, Kris Flothmann, et al.
Pageof 2