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Current Topics in Developmental Biology
|
February 3, 2009
Mouse models for human hereditary deafness
Michel Leibovici, Saaid Safieddine, Christine Petit
Hearing Research
|
April 28, 2005
Initial characterization of kinocilin, a protein of the hair cell kinocilium
Michel 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 membrane
Elisabeth Verpy, Michel Leibovici, Nicolas Michalski, et al.
Development (Cambridge, England)
|
March 25, 2010
Cochlear outer hair cells undergo an apical circumference remodeling constrained by the hair bundle shape
Raphaël Etournay, Léa Lepelletier, Jacques Boutet de Monvel, et al.
Scientific Reports
|
September 27, 2016
A suppressor locus for MODY3-diabetes
Miguel A Garcia-Gonzalez, Claire Carette, Alessia Bagattin, et al.
Scientific Reports
|
October 22, 2016
Erratum: A suppressor locus for MODY3-diabetes
Miguel A Garcia-Gonzalez, Claire Carette, Alessia Bagattin, et al.
Nature
|
October 14, 2008
Stereocilin-deficient mice reveal the origin of cochlear waveform distortions
Elisabeth Verpy, Dominique Weil, Michel Leibovici, et al.
EMBO Molecular Medicine
|
January 6, 2010
Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells
Amel Bahloul, Marie-Christine Simmler, Vincent Michel, et al.
Nature Genetics
|
June 29, 2006
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy
Sedigheh Delmaghani, Francisco J del Castillo, Vincent Michel, 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 DFNB22
Ingrid Zwaenepoel, Mirna Mustapha, Michel Leibovici, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
Current Topics in Developmental Biology
|
February 3, 2009
Mouse models for human hereditary deafness
Michel Leibovici, Saaid Safieddine, Christine Petit
Hearing Research
|
April 28, 2005
Initial characterization of kinocilin, a protein of the hair cell kinocilium
Michel 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 membrane
Elisabeth Verpy, Michel Leibovici, Nicolas Michalski, et al.
Development (Cambridge, England)
|
March 25, 2010
Cochlear outer hair cells undergo an apical circumference remodeling constrained by the hair bundle shape
Raphaël Etournay, Léa Lepelletier, Jacques Boutet de Monvel, et al.
Scientific Reports
|
September 27, 2016
A suppressor locus for MODY3-diabetes
Miguel A Garcia-Gonzalez, Claire Carette, Alessia Bagattin, et al.
Scientific Reports
|
October 22, 2016
Erratum: A suppressor locus for MODY3-diabetes
Miguel A Garcia-Gonzalez, Claire Carette, Alessia Bagattin, et al.
Nature
|
October 14, 2008
Stereocilin-deficient mice reveal the origin of cochlear waveform distortions
Elisabeth Verpy, Dominique Weil, Michel Leibovici, et al.
EMBO Molecular Medicine
|
January 6, 2010
Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells
Amel Bahloul, Marie-Christine Simmler, Vincent Michel, et al.
Nature Genetics
|
June 29, 2006
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy
Sedigheh Delmaghani, Francisco J del Castillo, Vincent Michel, 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 DFNB22
Ingrid Zwaenepoel, Mirna Mustapha, Michel Leibovici, et al.
Page
of 2