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Chantal M Longo-Guess

Showing results (1-10 of 13) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 21, 2015
A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J miceKenneth R Johnson, Chantal M Longo-Guess, Leona H Gagnon
Plos One|May 5, 2012
Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereociliaKenneth R Johnson, Chantal M Longo-Guess, Leona H Gagnon
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 19, 2007
Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutationChantal M Longo-Guess, Leona H Gagnon, Bernd Fritzsch, et al.
Nature Genetics|June 29, 2002
Deletion in Catna2, encoding alpha N-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulationChankyu Park, William Falls, Jacqueline H Finger, et al.
Journal of the Association for Research in Otolaryngology : JARO|December 4, 2013
Hearing impairment in hypothyroid dwarf mice caused by mutations of the thyroid peroxidase geneKenneth R Johnson, Leona H Gagnon, Chantal M Longo-Guess, et al.
The Journal of Clinical Investigation|February 23, 2008
Mutation of the Cyba gene encoding p22phox causes vestibular and immune defects in miceYoko Nakano, Chantal M Longo-Guess, David E Bergstrom, 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.
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.
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.
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.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 21, 2015
A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J miceKenneth R Johnson, Chantal M Longo-Guess, Leona H Gagnon
Plos One|May 5, 2012
Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereociliaKenneth R Johnson, Chantal M Longo-Guess, Leona H Gagnon
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 19, 2007
Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutationChantal M Longo-Guess, Leona H Gagnon, Bernd Fritzsch, et al.
Nature Genetics|June 29, 2002
Deletion in Catna2, encoding alpha N-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulationChankyu Park, William Falls, Jacqueline H Finger, et al.
Journal of the Association for Research in Otolaryngology : JARO|December 4, 2013
Hearing impairment in hypothyroid dwarf mice caused by mutations of the thyroid peroxidase geneKenneth R Johnson, Leona H Gagnon, Chantal M Longo-Guess, et al.
The Journal of Clinical Investigation|February 23, 2008
Mutation of the Cyba gene encoding p22phox causes vestibular and immune defects in miceYoko Nakano, Chantal M Longo-Guess, David E Bergstrom, 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.
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.
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.
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.
Pageof 2