Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29

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Claudin-1 and -2: Novel Integral Membrane Proteins Localizing at Tight Junctions with No Sequence Similarity to Occludin

1998 • 2,005 citations

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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Junctional Adhesion Molecule, a Novel Member of the Immunoglobulin Superfamily That Distributes at Intercellular Junctions and Modulates Monocyte Transmigration

1998 • 1,356 citations

Paracellin-1, a Renal Tight Junction Protein Required for Paracellular Mg ²⁺ Resorption

1999 • 1,107 citations

Claudin multigene family encoding four-transmembrane domain protein components of tight junction strands

1999 • 1,100 citations

Direct Binding of Three Tight Junction-Associated Maguks, Zo-1, Zo-2, and Zo-3, with the Cooh Termini of Claudins

1999 • 1,094 citations

Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in Recombination

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FRACTURE FACES OF ZONULAE OCCLUDENTES FROM "TIGHT" AND "LEAKY" EPITHELIA

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A Single Gene Product, Claudin-1 or -2, Reconstitutes Tight Junction Strands and Recruits Occludin in Fibroblasts

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Interpreting cDNA sequences: Some insights from studies on translation

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Manner of Interaction of Heterogeneous Claudin Species within and between Tight Junction Strands

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Avoiding Recomputation in Linkage Analysis

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CNS Myelin and Sertoli Cell Tight Junction Strands Are Absent in Osp/Claudin-11 Null Mice

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Clostridium perfringens Enterotoxin Fragment Removes Specific Claudins from Tight Junction Strands

1999 • 609 citations

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Mutations in the Connexin 26 Gene (GJB2) among Ashkenazi Jews with Nonsyndromic Recessive Deafness

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Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

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Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment

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Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

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Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

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Dominant modifier DFNM1 suppresses recessive deafness DFNB26

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Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.

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Early Onset of Presbyacusis in Down Syndrome

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Refined Localization of Autosomal Recessive Nonsyndromic Deafness DFNB10 Locus Using 34 Novel Microsatellite Markers, Genomic Structure, and Exclusion of Six Known Genes in the Region

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The junctions of the spindle-shaped cells of the stria vascularis: A link that completes the barrier between perilymph and endolymph

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