Published in Genome Biol on May 29, 2012
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Gfi1 and Gfi1b act equivalently in haematopoiesis, but have distinct, non-overlapping functions in inner ear development. EMBO Rep (2006) 1.21
Myosin VI is required for structural integrity of the apical surface of sensory hair cells in zebrafish. Dev Biol (2004) 1.21
Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss. Am J Hum Genet (2005) 1.20
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Calcium oxalate stone formation in the inner ear as a result of an Slc26a4 mutation. J Biol Chem (2010) 1.08
Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84. J Med Genet (2010) 1.07
A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells. PLoS Genet (2008) 1.07
A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment. Mamm Genome (2004) 1.07
Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population. Hum Genomics (2006) 1.06
Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia. Hum Mol Genet (2003) 1.02
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The DFNA15 deafness mutation affects POU4F3 protein stability, localization, and transcriptional activity. Mol Cell Biol (2003) 0.99
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A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA. Mamm Genome (2010) 0.96
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A novel SLC26A4 (PDS) deafness mutation retained in the endoplasmic reticulum. Arch Otolaryngol Head Neck Surg (2008) 0.89
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Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and mice. Hum Mutat (2013) 0.86
A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective trafficking of the connexin 31 protein. Hum Mol Genet (2002) 0.85
Connexins in hearing loss: a comprehensive overview. J Basic Clin Physiol Pharmacol (2005) 0.85
microRNAs: the art of silencing in the ear. EMBO Mol Med (2012) 0.84
The structural context of disease-causing mutations in gap junctions. J Biol Chem (2006) 0.82
Egr2::cre mediated conditional ablation of dicer disrupts histogenesis of mammalian central auditory nuclei. PLoS One (2012) 0.82
Time-dependent gene expression analysis of the developing superior olivary complex. J Biol Chem (2013) 0.81
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Progressive vestibular mutation leads to elevated anxiety. Brain Res (2010) 0.78
The clinical presentation of DFNA15/POU4F3. Adv Otorhinolaryngol (2002) 0.78
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A "Tric" to tighten cell-cell junctions in the cochlea for hearing. J Clin Invest (2013) 0.77
The many faces of sensorineural hearing loss: one founder and two novel mutations affecting one family of mixed Jewish ancestry. Genet Test Mol Biomarkers (2013) 0.77
Functional characterization of pendrin mutations found in the Israeli and Palestinian populations. Cell Physiol Biochem (2011) 0.77
Rescue from hearing loss in Usher's syndrome. N Engl J Med (2013) 0.77
Integration of human and mouse genetics reveals pendrin function in hearing and deafness. Cell Physiol Biochem (2011) 0.77
Atrophic thyroid follicles and inner ear defects reminiscent of cochlear hypothyroidism in Slc26a4-related deafness. Mamm Genome (2014) 0.76
Apparent phenotypic anticipation in autosomal dominant connexin 26 deafness. J Basic Clin Physiol Pharmacol (2014) 0.75
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Israel Society for Auditory Research (ISAR): 2013 Annual Scientific Conference. J Basic Clin Physiol Pharmacol (2013) 0.75
Single cell analysis of the inner ear sensory organs. Int J Dev Biol (2017) 0.75
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