Expression of connexin 30 in the developing mouse cochlea

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1997 • 1,435 citations

Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease

1993 • 1,055 citations

Connexin-26 mutations in sporadic and inherited sensorineural deafness

1998 • 645 citations

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

1995 • 590 citations

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

1998 • 415 citations

The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequency

1996 • 298 citations

Expression of the gap-junction connexins 26 and 30 in the rat cochlea

1998 • 276 citations

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

2000 • 182 citations

Molecular Cloning and Functional Expression of Mouse Connexin-30,a Gap Junction Gene Highly Expressed in Adult Brain and Skin

1996 • 181 citations

Expression of α and β subunit isoforms of Na,K-ATPase in the mouse inner ear and changes with mutations at the Wv or Sld loci

1994 • 138 citations

Expression of connexin 31 in the developing mouse cochlea

2000 • 84 citations

Development of endocochlear potential and its negative component in mouse cochlea

1995 • 72 citations

Expression of connexin 26 and Na,K-ATPase in the developing mouse cochlear lateral wall: functional implications

1999 • 64 citations

Human Connexin 30 (GJB6), a Candidate Gene for Nonsyndromic Hearing Loss: Molecular Cloning, Tissue-Specific Expression, and Assignment to Chromosome 13q12

1999 • 53 citations

The NA-K-CL Cotransporters in the Rat Cochlea: RT-PCR and Partial Sequence Analysis

1996 • 26 citations