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Dominique Weil

Showing results (51-60 of 84) with videos related to

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Development (Cambridge, England)|March 25, 2010
Cochlear outer hair cells undergo an apical circumference remodeling constrained by the hair bundle shapeRaphaël Etournay, Léa Lepelletier, Jacques Boutet de Monvel, et al.
European Journal of Human Genetics : EJHG|June 25, 2002
Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutationsMyrna Medlej-Hashim, Mirna Mustapha, Eliane Chouery, et al.
Human Genetics|April 10, 2002
A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25Mirna Mustapha, Eliane Chouery, Delphine Torchard-Pagnez, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 15, 2007
Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioningNicolas Michalski, Vincent Michel, Amel Bahloul, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factorElise Chapiro, Delphine Feldmann, Françoise Denoyelle, et al.
Nature|October 14, 2008
Stereocilin-deficient mice reveal the origin of cochlear waveform distortionsElisabeth Verpy, Dominique Weil, Michel Leibovici, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|July 4, 2018
Tau/DDX6 interaction increases microRNA activityAlban Chauderlier, Melissa Gilles, Andrea Spolcova, et al.
RNA (New York, N.Y.)|July 28, 2012
Multiple binding of repressed mRNAs by the P-body protein Rck/p54Michèle Ernoult-Lange, Sonia Baconnais, Maryannick Harper, et al.
Gut|November 5, 2011
CPEB1, a novel gene silenced in gastric cancer: a Drosophila approachJoana Caldeira, Joana Simões-Correia, Joana Paredes, et al.
Human Molecular Genetics|February 18, 2003
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmoninDominique Weil, Aziz El-Amraoui, Saber Masmoudi, et al.
Pageof 9

Showing results (51-60 of 84) with videos related to

Sort By:
Pageof 9
Development (Cambridge, England)|March 25, 2010
Cochlear outer hair cells undergo an apical circumference remodeling constrained by the hair bundle shapeRaphaël Etournay, Léa Lepelletier, Jacques Boutet de Monvel, et al.
European Journal of Human Genetics : EJHG|June 25, 2002
Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutationsMyrna Medlej-Hashim, Mirna Mustapha, Eliane Chouery, et al.
Human Genetics|April 10, 2002
A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25Mirna Mustapha, Eliane Chouery, Delphine Torchard-Pagnez, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 15, 2007
Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioningNicolas Michalski, Vincent Michel, Amel Bahloul, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factorElise Chapiro, Delphine Feldmann, Françoise Denoyelle, et al.
Nature|October 14, 2008
Stereocilin-deficient mice reveal the origin of cochlear waveform distortionsElisabeth Verpy, Dominique Weil, Michel Leibovici, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|July 4, 2018
Tau/DDX6 interaction increases microRNA activityAlban Chauderlier, Melissa Gilles, Andrea Spolcova, et al.
RNA (New York, N.Y.)|July 28, 2012
Multiple binding of repressed mRNAs by the P-body protein Rck/p54Michèle Ernoult-Lange, Sonia Baconnais, Maryannick Harper, et al.
Gut|November 5, 2011
CPEB1, a novel gene silenced in gastric cancer: a Drosophila approachJoana Caldeira, Joana Simões-Correia, Joana Paredes, et al.
Human Molecular Genetics|February 18, 2003
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmoninDominique Weil, Aziz El-Amraoui, Saber Masmoudi, et al.
Pageof 9