Expression of GJB2 and GJB6 is reduced in a novel DFNB1 allele.
暂无分享,去创建一个
Mei Zhu | Kirk B. Burkhart | R. Fisher | E. Wilch | K. Friderici | J. Elfenbein | K. Burkhart | M. Regier
[1] Mustafa Tekin,et al. GJB2 mutations and degree of hearing loss: a multicenter study. , 2005, American journal of human genetics.
[2] J. Common,et al. Specific loss of connexin 26 expression in ductal sweat gland epithelium associated with the deletion mutation del(GJB6‐D13S1830) , 2005, Clinical and experimental dermatology.
[3] A. Pandya,et al. A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment , 2005, Journal of Medical Genetics.
[4] J. Lamartine,et al. Gene structure and promoter analysis of the human GJB6 gene encoding connexin30 , 2005 .
[5] A. Forge,et al. Gap junctions in the inner ear: Comparison of distribution patterns in different vertebrates and assessement of connexin composition in mammals , 2003, The Journal of comparative neurology.
[6] X. Estivill,et al. Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study. , 2003, American journal of human genetics.
[7] Xi Lin,et al. Connexins 26 and 30 are co-assembled to form gap junctions in the cochlea of mice. , 2003, Biochemical and biophysical research communications.
[8] D. Jagger,et al. The Inner Ear Contains Heteromeric Channels Composed of Cx26 and Cx30 and Deafness-Related Mutations in Cx26 Have a Dominant Negative Effect on Cx30 , 2003, Cell communication & adhesion.
[9] Philine Wangemann,et al. K+ cycling and the endocochlear potential , 2002, Hearing Research.
[10] F. Moreno,et al. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment. , 2002, The New England journal of medicine.
[11] I. Lerer,et al. A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non‐syndromic deafness: A novel founder mutation in Ashkenazi Jews , 2001, Human mutation.
[12] Joe C. Adams,et al. Gap junction systems in the mammalian cochlea , 2000, Brain Research Reviews.
[13] X. Estivill,et al. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus , 1999, Nature Genetics.
[14] D. Kiang,et al. Mapping and characterization of the basal promoter of the human connexin26 gene. , 1998, Biochimica et biophysica acta.
[15] D. Kiang,et al. Upstream genomic sequence of the human connexin26 gene. , 1997, Gene.
[16] A. Dean. On a chromosome far, far away: LCRs and gene expression. , 2006, Trends in genetics : TIG.
[17] M. Claustres,et al. A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect? , 2002, European Journal of Human Genetics.
[18] H. Dahl,et al. A simple PCR test to detect the common 35delG mutation in the connexin 26 gene. , 2000, Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology.