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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.
Molecular and Biochemical Parasitology|November 30, 2010
The four trypanosomatid eIF4E homologues fall into two separate groups, with distinct features in primary sequence and biological propertiesEden R Freire, Rafael Dhalia, Danielle M N Moura, 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.
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.
EMBO Molecular Medicine|January 6, 2010
Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cellsAmel Bahloul, Marie-Christine Simmler, Vincent Michel, et al.
Annals of Human Genetics|October 1, 2015
Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of HomozygosityNizar Ben Halim, Majdi Nagara, Béatrice Regnault, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1Saber Masmoudi, Abdelaziz Tlili, Marja Majava, et al.
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