Published in Am J Hum Genet on October 31, 2006
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Identification of MarvelD3 as a tight junction-associated transmembrane protein of the occludin family. BMC Cell Biol (2009) 1.32
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Enterocytes' tight junctions: From molecules to diseases. World J Gastrointest Pathophysiol (2011) 0.89
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Possible involvement of tight junctions, extracellular matrix and nuclear receptors in epithelial differentiation. J Biomed Biotechnol (2011) 0.87
Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing loss. PLoS One (2014) 0.86
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Deafness in occludin-deficient mice with dislocation of tricellulin and progressive apoptosis of the hair cells. Biol Open (2014) 0.86
Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss. PLoS One (2013) 0.85
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss. PLoS One (2015) 0.84
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A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3. Hum Genet (2008) 0.82
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A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population. BMC Med Genet (2011) 0.80
Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population. J Hum Genet (2012) 0.80
Downsloping high-frequency hearing loss due to inner ear tricellular tight junction disruption by a novel ILDR1 mutation in the Ig-like domain. PLoS One (2015) 0.80
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The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations. Genet Test Mol Biomarkers (2015) 0.78
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DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3. Clin Genet (2011) 0.78
Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss. Hum Genet (2015) 0.78
Tricellular Tight Junctions in the Inner Ear. Biomed Res Int (2016) 0.77
A "Tric" to tighten cell-cell junctions in the cochlea for hearing. J Clin Invest (2013) 0.77
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Mechanisms of otoconia and otolith development. Dev Dyn (2014) 0.77
Viral interactions with the blood-brain barrier: old dog, new tricks. Tissue Barriers (2016) 0.76
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MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin. PLoS One (2015) 0.75
APOC3 induces endothelial dysfunction through TNF-α and JAM-1. Lipids Health Dis (2016) 0.75
Tricellular Tight Junction Protein Tricellulin is targeted by the Enteropathogenic E. coli Effector EspG1 Leading to Epithelial Barrier Disruption. Infect Immun (2016) 0.75
A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect. Hum Genet (2016) 0.75
Tricellular junctions: how to build junctions at the TRICkiest points of epithelial cells. Mol Biol Cell (2017) 0.75
Histone deacetylase inhibition prevents cell death induced by loss of tricellular tight junction proteins in temperature-sensitive mouse cochlear cells. PLoS One (2017) 0.75
Angulin proteins ILDR1 and ILDR2 regulate alternative pre-mRNA splicing through binding to splicing factors TRA2A, TRA2B, or SRSF1. Sci Rep (2017) 0.75
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Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79. Am J Hum Genet (2010) 2.95
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