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Kenneth R Johnson

Showing results (41-50 of 61) with videos related to

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Human Molecular Genetics|October 2, 2003
Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c geneKenneth R Johnson, Leona H Gagnon, Lisa S Webb, et al.
Genetics|January 6, 2018
Deletion of a Long-Range <i>Dlx5</i> Enhancer Disrupts Inner Ear Development in MiceKenneth R Johnson, Leona H Gagnon, Cong Tian, et al.
Human Molecular Genetics|November 13, 2004
Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humansQing Yin Zheng, Denise Yan, Xiao Mei Ouyang, et al.
Academic Journal of Xian Jiaotong University : AJXJTU = Xi'An Jiao Tong Da Xue Xue Bao (Yi Wen Ban)|December 24, 2010
Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10Qing Yin Zheng, Belinda S Harris, Patricia F Ward-Bailey, et al.
Hearing Research|August 13, 2021
CACHD1-deficient mice exhibit hearing and balance deficits associated with a disruption of calcium homeostasis in the inner earCong Tian, Kenneth R Johnson, Jaclynn M Lett, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 12, 2009
The podosomal-adaptor protein SH3PXD2B is essential for normal postnatal developmentMao Mao, Daniel R Thedens, Bo Chang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 6, 2006
The chloride intracellular channel protein CLIC5 is expressed at high levels in hair cell stereocilia and is essential for normal inner ear functionLeona H Gagnon, Chantal M Longo-Guess, Mark Berryman, et al.
Aging|March 16, 2016
N-acetyl-cysteine prevents age-related hearing loss and the progressive loss of inner hair cells in γ-glutamyl transferase 1 deficient miceDalian Ding, Haiyan Jiang, Guang-Di Chen, et al.
Cytoskeleton (Hoboken, N.J.)|November 29, 2013
CLIC5 stabilizes membrane-actin filament linkages at the base of hair cell stereocilia in a molecular complex with radixin, taperin, and myosin VIFelipe T Salles, Leonardo R Andrade, Soichi Tanda, et al.
Human Molecular Genetics|July 26, 2002
Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6Kristina L Mitchem, Ellen Hibbard, Lisa A Beyer, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|October 2, 2003
Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c geneKenneth R Johnson, Leona H Gagnon, Lisa S Webb, et al.
Genetics|January 6, 2018
Deletion of a Long-Range <i>Dlx5</i> Enhancer Disrupts Inner Ear Development in MiceKenneth R Johnson, Leona H Gagnon, Cong Tian, et al.
Human Molecular Genetics|November 13, 2004
Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humansQing Yin Zheng, Denise Yan, Xiao Mei Ouyang, et al.
Academic Journal of Xian Jiaotong University : AJXJTU = Xi'An Jiao Tong Da Xue Xue Bao (Yi Wen Ban)|December 24, 2010
Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10Qing Yin Zheng, Belinda S Harris, Patricia F Ward-Bailey, et al.
Hearing Research|August 13, 2021
CACHD1-deficient mice exhibit hearing and balance deficits associated with a disruption of calcium homeostasis in the inner earCong Tian, Kenneth R Johnson, Jaclynn M Lett, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 12, 2009
The podosomal-adaptor protein SH3PXD2B is essential for normal postnatal developmentMao Mao, Daniel R Thedens, Bo Chang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 6, 2006
The chloride intracellular channel protein CLIC5 is expressed at high levels in hair cell stereocilia and is essential for normal inner ear functionLeona H Gagnon, Chantal M Longo-Guess, Mark Berryman, et al.
Aging|March 16, 2016
N-acetyl-cysteine prevents age-related hearing loss and the progressive loss of inner hair cells in γ-glutamyl transferase 1 deficient miceDalian Ding, Haiyan Jiang, Guang-Di Chen, et al.
Cytoskeleton (Hoboken, N.J.)|November 29, 2013
CLIC5 stabilizes membrane-actin filament linkages at the base of hair cell stereocilia in a molecular complex with radixin, taperin, and myosin VIFelipe T Salles, Leonardo R Andrade, Soichi Tanda, et al.
Human Molecular Genetics|July 26, 2002
Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6Kristina L Mitchem, Ellen Hibbard, Lisa A Beyer, et al.
Pageof 7