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Kenneth R Johnson

Showing results (31-40 of 61) with videos related to

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Brain Research|February 28, 2006
A comparison of vestibular and auditory phenotypes in inbred mouse strainsSherri M Jones, Timothy A Jones, Kenneth R Johnson, et al.
Molecular Endocrinology (Baltimore, Md.)|April 19, 2007
Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2Kenneth R Johnson, Coleen C Marden, Patricia Ward-Bailey, et al.
Hearing Research|December 6, 2011
Genetic background effects on age-related hearing loss associated with Cdh23 variants in miceKelly L Kane, Chantal M Longo-Guess, Leona H Gagnon, et al.
Plos One|May 9, 2014
A lack of immune system genes causes loss in high frequency hearing but does not disrupt cochlear synapse maturation in miceMelissa A Calton, Dasom Lee, Srividya Sundaresan, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 21, 2005
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) miceChantal M Longo-Guess, Leona H Gagnon, Susan A Cook, et al.
Journal of the Association for Research in Otolaryngology : JARO|October 20, 2005
A quantitative survey of gravity receptor function in mutant mouse strainsSherri M Jones, Kenneth R Johnson, Heping Yu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 10, 2017
ELMOD1 Stimulates ARF6-GTP Hydrolysis to Stabilize Apical Structures in Developing Vestibular Hair CellsJocelyn F Krey, Rachel A Dumont, Philip A Wilmarth, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 20, 2019
Genetic variation in thyroid folliculogenesis influences susceptibility to hypothyroidism-induced hearing impairmentAmanda H Mortensen, Qing Fang, Michelle T Fleming, et al.
Cell|December 11, 2012
TMHS is an integral component of the mechanotransduction machinery of cochlear hair cellsWei Xiong, Nicolas Grillet, Heather M Elledge, et al.
Genetics|August 16, 2011
A modifier gene alleviates hypothyroidism-induced hearing impairment in Pou1f1dw dwarf miceQing Fang, Chantal Longo-Guess, Leona H Gagnon, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Brain Research|February 28, 2006
A comparison of vestibular and auditory phenotypes in inbred mouse strainsSherri M Jones, Timothy A Jones, Kenneth R Johnson, et al.
Molecular Endocrinology (Baltimore, Md.)|April 19, 2007
Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2Kenneth R Johnson, Coleen C Marden, Patricia Ward-Bailey, et al.
Hearing Research|December 6, 2011
Genetic background effects on age-related hearing loss associated with Cdh23 variants in miceKelly L Kane, Chantal M Longo-Guess, Leona H Gagnon, et al.
Plos One|May 9, 2014
A lack of immune system genes causes loss in high frequency hearing but does not disrupt cochlear synapse maturation in miceMelissa A Calton, Dasom Lee, Srividya Sundaresan, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 21, 2005
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) miceChantal M Longo-Guess, Leona H Gagnon, Susan A Cook, et al.
Journal of the Association for Research in Otolaryngology : JARO|October 20, 2005
A quantitative survey of gravity receptor function in mutant mouse strainsSherri M Jones, Kenneth R Johnson, Heping Yu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 10, 2017
ELMOD1 Stimulates ARF6-GTP Hydrolysis to Stabilize Apical Structures in Developing Vestibular Hair CellsJocelyn F Krey, Rachel A Dumont, Philip A Wilmarth, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 20, 2019
Genetic variation in thyroid folliculogenesis influences susceptibility to hypothyroidism-induced hearing impairmentAmanda H Mortensen, Qing Fang, Michelle T Fleming, et al.
Cell|December 11, 2012
TMHS is an integral component of the mechanotransduction machinery of cochlear hair cellsWei Xiong, Nicolas Grillet, Heather M Elledge, et al.
Genetics|August 16, 2011
A modifier gene alleviates hypothyroidism-induced hearing impairment in Pou1f1dw dwarf miceQing Fang, Chantal Longo-Guess, Leona H Gagnon, et al.
Pageof 7