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Kenneth R Johnson

Showing results (51-60 of 61) with videos related to

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Human Molecular Genetics|September 22, 2017
Hearing loss without overt metabolic acidosis in ATP6V1B1 deficient MRL mice, a new genetic model for non-syndromic deafness with enlarged vestibular aqueductsCong Tian, Leona H Gagnon, Chantal Longo-Guess, et al.
BMC Developmental Biology|April 22, 2009
Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body massRobert J Munroe, Vinay Prabhu, Greg M Acland, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 28, 2007
Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid miceI Jill Karolyi, Gary A Dootz, Karin Halsey, et al.
Genomics|February 8, 2003
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5Kenneth R Johnson, Priscilla W Lane, Susan A Cook, et al.
Plos One|January 10, 2013
Retrotransposon insertion in the T-cell acute lymphocytic leukemia 1 (Tal1) gene is associated with severe renal disease and patchy alopecia in Hairpatches (Hpt) miceVishnu Hosur, Melissa L Cox, Lisa M Burzenski, et al.
The Journal of Endocrinology|December 25, 2009
A novel spontaneous mutation of Irs1 in mice results in hyperinsulinemia, reduced growth, low bone mass and impaired adipogenesisVictoria E DeMambro, Masanobu Kawai, Thomas L Clemens, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 20, 2004
New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in miceBettina Lorenz-Depiereux, Victoria E Guido, Kenneth R Johnson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 28, 2010
The R109H variant of fascin-2, a developmentally regulated actin crosslinker in hair-cell stereocilia, underlies early-onset hearing loss of DBA/2J miceJung-Bum Shin, Chantal M Longo-Guess, Leona H Gagnon, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 13, 2003
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisisLeah Rae Donahue, Bo Chang, Subburaman Mohan, et al.
Blood|October 23, 2009
The mouse mutation "thrombocytopenia and cardiomyopathy" (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemiaThomas H Chase, Bonnie L Lyons, Roderick T Bronson, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|September 22, 2017
Hearing loss without overt metabolic acidosis in ATP6V1B1 deficient MRL mice, a new genetic model for non-syndromic deafness with enlarged vestibular aqueductsCong Tian, Leona H Gagnon, Chantal Longo-Guess, et al.
BMC Developmental Biology|April 22, 2009
Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body massRobert J Munroe, Vinay Prabhu, Greg M Acland, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 28, 2007
Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid miceI Jill Karolyi, Gary A Dootz, Karin Halsey, et al.
Genomics|February 8, 2003
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5Kenneth R Johnson, Priscilla W Lane, Susan A Cook, et al.
Plos One|January 10, 2013
Retrotransposon insertion in the T-cell acute lymphocytic leukemia 1 (Tal1) gene is associated with severe renal disease and patchy alopecia in Hairpatches (Hpt) miceVishnu Hosur, Melissa L Cox, Lisa M Burzenski, et al.
The Journal of Endocrinology|December 25, 2009
A novel spontaneous mutation of Irs1 in mice results in hyperinsulinemia, reduced growth, low bone mass and impaired adipogenesisVictoria E DeMambro, Masanobu Kawai, Thomas L Clemens, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 20, 2004
New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in miceBettina Lorenz-Depiereux, Victoria E Guido, Kenneth R Johnson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 28, 2010
The R109H variant of fascin-2, a developmentally regulated actin crosslinker in hair-cell stereocilia, underlies early-onset hearing loss of DBA/2J miceJung-Bum Shin, Chantal M Longo-Guess, Leona H Gagnon, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 13, 2003
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisisLeah Rae Donahue, Bo Chang, Subburaman Mohan, et al.
Blood|October 23, 2009
The mouse mutation "thrombocytopenia and cardiomyopathy" (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemiaThomas H Chase, Bonnie L Lyons, Roderick T Bronson, et al.
Pageof 7