Connexin26 and -30 in the cochlea and their clinical relevance;Connexin26 und -30 im innenohr und ihre klinische bedeutung

Laryngo- Rhino- Otologie

Volumn 80, Issue 12, 2001, Pages 719-724

  Lautermann, J ^a   Gabriel, H D ^b   Kupsch, P ^b   Winterhager, E ^b   Jahnke, K ^a  

^a Ohrenklinik Essen ^*  (Germany)

^b UNIVERSITY OF DUISBURG ESSEN   (Germany)

Author keywords

Connexins; Gap junctions; Hearing loss

Indexed keywords

CONNEXIN 26; CONNEXIN 30; GAP JUNCTION PROTEIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; CHILD; COCHLEA; CONTROLLED STUDY; GAP JUNCTION; GENE MUTATION; GENETIC SCREENING; GERMANY; HEARING LOSS; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MAJOR CLINICAL STUDY; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; PREVALENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADOLESCENT; ADULT; ANIMALS; CHILD; CHILD, PRESCHOOL; CONNEXINS; DEAFNESS; EAR, INNER; FEMALE; GAP JUNCTIONS; HUMANS; MALE; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PREGNANCY; PREGNANCY TRIMESTER, SECOND; RATS; RATS, WISTAR;

EID: 0035664034     PISSN: 09358943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2001-19576     Document Type: Article

References (28)

1. The gap junction family: Structure, function, chemistry
2. The gap junction communication channel
3. The fine structure of freeze-fractured intercellular junctions in the guinea pig inner ear
4. Die feinstruktur gefriergeätzter zellmembran-haftstellen der stria vascularis
5. Intercellular junctions in the organ of Corti as revealed by freeze fracturing
6. Gap junctions in the rat cochlea: Immunohistochemical and ultrastructural analysis
7. + recycling pathway from inner hair cells
8. Gap junction systems in the mammalian cochlea
9. Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment
10. Expression of the gap-junction connexins 26 and 30 in the rat cochlea
11. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
12. Developmental expression patterns of connexin26 and -30 in the rat cochlea
13. Voltage gating of gap junctions in cochlear supporting cells: Evidence for nonhomotypic channels
14. Ototoxicity in developing mammals
15. Development of the human stria vascularis
16. Development of the human cochlea
17. Clinical phenotype and mutations in connexin26 (DFNB1/GJB2) the most common cause of childhood hearing loss
18. Prelingual deafness: High prevalence of a 30delG mutation in the connexin26 gene
19. Novel mutations in the connexin26 gene (GJB2) that cause autosomal recessive (DFNB 1) hearing loss
20. Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: Implications for genetic counselling
21. Prevalent connexin26 gene (GJB2) mutations in Japanese
22. Connexin-26 mutations in sporadic and inherited sensorineural deafness
23. High carrier frequency of the 35delG deafness mutation in European populations. Genetic analysis consortium of GJB2 35delG
24. Mutations-analyse des Connexin26-Gens bei sporadischen Fällen mittel-bis hochgradiger Schwerhörigkeit
25. Human connexin30 (GJB6), a candidate gene for nonsyndromic hearing loss: Molecular cloning, tissue-specific expression and assignment to chromosome 13q12
26. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
27. Clinical studies of families with hearing loss attributable to mutations in the connexin26 gene
28. Temporal bone histopathology in Connexin26-related hearing loss