Literature DB >> 9620796

Connexin 26 gene linked to a dominant deafness.

F Denoyelle, G Lina-Granade, H Plauchu, R Bruzzone, H Chaïb, F Lévi-Acobas, D Weil, C Petit.   

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Year:  1998        PMID： 9620796     DOI： 10.1038/30639

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


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  51 in total

1.  A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.

Authors:  K Fukushima; N Kasai; Y Ueki; K Nishizaki; K Sugata; S Hirakawa; A Masuda; M Gunduz; Y Ninomiya; Y Masuda; M Sato; W T McGuirt; P Coucke; G Van Camp; R J Smith
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

2.  Purinergic control of intercellular communication between Hensen's cells of the guinea-pig cochlea.

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Journal:  J Physiol       Date:  2001-03-15       Impact factor: 5.182

3.  Inherited deafness in childhood--the genetic revolution unmasks the clinical challenge.

Authors:  W Reardon; R F Mueller
Journal:  Arch Dis Child       Date:  2000-04       Impact factor: 3.791

Review 4.  Connexin mutations in skin disease and hearing loss.

Authors:  D P Kelsell; W L Di; M J Houseman
Journal:  Am J Hum Genet       Date:  2001-01-25       Impact factor: 11.025

5.  [Defective gap junctions: variability of the phenotype exemplified by connexin 26 mutations].

Authors:  J Krutmann; J O Funk; B Korge
Journal:  Hautarzt       Date:  2002-09       Impact factor: 0.751

6.  Apparent phenotypic anticipation in autosomal dominant connexin 26 deafness.

Authors:  Meirav Sokolov; Zippora Brownstein; Moshe Frydman; Karen B Avraham
Journal:  J Basic Clin Physiol Pharmacol       Date:  2014-09

7.  Connexin46 mutations in autosomal dominant congenital cataract.

Authors:  D Mackay; A Ionides; Z Kibar; G Rouleau; V Berry; A Moore; A Shiels; S Bhattacharya
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

Review 8.  Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential.

Authors:  Philine Wangemann
Journal:  J Physiol       Date:  2006-07-20       Impact factor: 5.182

9.  Infrequency of two deletion mutations at the DFNB1 locus in patients and controls.

Authors:  Hsiao-Yuan Tang; Monica J Basehore; Gregory L Blakey; Sandra Darilek; John S Oghalai; Benjamin B Roa; Ping Fang; Raye Lynn Alford
Journal:  Am J Med Genet A       Date:  2008-04-01       Impact factor: 2.802

Review 10.  Therapeutic regulation of gene expression in the inner ear using RNA interference.

Authors:  Yukihide Maeda; Abraham M Sheffield; Richard J H Smith
Journal:  Adv Otorhinolaryngol       Date:  2009-06-02
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