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Elisabeth Verpy

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

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Science Advances|February 26, 2019
Cochlear outer hair cell horizontal top connectors mediate mature stereocilia bundle mechanicsAlexander X Cartagena-Rivera, Sébastien Le Gal, Kerianne Richards, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 29, 2019
Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membranePaul Avan, Sébastien Le Gal, Vincent Michel, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 15, 2001
Twister mutant mice are defective for otogelin, a component specific to inner ear acellular membranesMarie Christine Simmler, Ingrid Zwaenepoel, Elisabeth Verpy, et al.
Brain Sciences|November 25, 2023
Detecting Central Auditory Processing Disorders in Awake MiceCamille Dejean, Typhaine Dupont, Elisabeth Verpy, et al.
Hearing Research|April 28, 2005
Initial characterization of kinocilin, a protein of the hair cell kinociliumMichel Leibovici, Elisabeth Verpy, Richard J Goodyear, et al.
The Journal of Comparative Neurology|December 18, 2010
Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membraneElisabeth Verpy, Michel Leibovici, Nicolas Michalski, et al.
Current Biology : CB|January 25, 2006
Inactivation of NADPH oxidase organizer 1 results in severe imbalancePéter J Kiss, Judit Knisz, Yuzhou Zhang, et al.
Human Genetics|July 24, 2002
Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafnessXiao Mei Ouyang, Xia Juan Xia, Elisabeth Verpy, et al.
Nature|October 14, 2008
Stereocilin-deficient mice reveal the origin of cochlear waveform distortionsElisabeth Verpy, Dominique Weil, Michel Leibovici, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 2002
Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22Ingrid Zwaenepoel, Mirna Mustapha, Michel Leibovici, et al.
Pageof 2

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

Sort By:
Pageof 2
Science Advances|February 26, 2019
Cochlear outer hair cell horizontal top connectors mediate mature stereocilia bundle mechanicsAlexander X Cartagena-Rivera, Sébastien Le Gal, Kerianne Richards, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 29, 2019
Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membranePaul Avan, Sébastien Le Gal, Vincent Michel, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 15, 2001
Twister mutant mice are defective for otogelin, a component specific to inner ear acellular membranesMarie Christine Simmler, Ingrid Zwaenepoel, Elisabeth Verpy, et al.
Brain Sciences|November 25, 2023
Detecting Central Auditory Processing Disorders in Awake MiceCamille Dejean, Typhaine Dupont, Elisabeth Verpy, et al.
Hearing Research|April 28, 2005
Initial characterization of kinocilin, a protein of the hair cell kinociliumMichel Leibovici, Elisabeth Verpy, Richard J Goodyear, et al.
The Journal of Comparative Neurology|December 18, 2010
Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membraneElisabeth Verpy, Michel Leibovici, Nicolas Michalski, et al.
Current Biology : CB|January 25, 2006
Inactivation of NADPH oxidase organizer 1 results in severe imbalancePéter J Kiss, Judit Knisz, Yuzhou Zhang, et al.
Human Genetics|July 24, 2002
Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafnessXiao Mei Ouyang, Xia Juan Xia, Elisabeth Verpy, et al.
Nature|October 14, 2008
Stereocilin-deficient mice reveal the origin of cochlear waveform distortionsElisabeth Verpy, Dominique Weil, Michel Leibovici, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 2002
Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22Ingrid Zwaenepoel, Mirna Mustapha, Michel Leibovici, et al.
Pageof 2