نتایج جستجو برای: gjb6

تعداد نتایج: 238  

2015
B Vona MAH Hofrichter C Neuner J Schröder A Gehrig JB Hennermann F Kraus W Shehata-Dieler E Klopocki I Nanda T Haaf

Increasing attention has been directed toward assessing mutational fallout of stereocilin (STRC), the gene underlying DFNB16. A major challenge is due to a closely linked pseudogene with 99.6% coding sequence identity. In 94 GJB2/GJB6-mutation negative individuals with non-syndromic sensorineural hearing loss (NSHL), we identified two homozygous and six heterozygous deletions, encompassing the ...

2014
Ralf Birkenhäger Nicola Prera Antje Aschendorff Roland Laszig Susan Arndt

To date, about 165 genetic loci or genes have been identified which are associated with nonsyndromal hearing impairment. In about half the cases, genetic defects in the GJB2 gene (connexin 26) are the most common cause of inner-ear deafness. The genes GJB2 and GJB6 are localized on chromosome 13q11-12 in tandem orientation. Connexins belong to the group of "gap junction" proteins, which form co...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2008
Saida Ortolano Giovanni Di Pasquale Giulia Crispino Fabio Anselmi Fabio Mammano John A Chiorini

Connexin 26 (Cx26) and connexin 30 (Cx30) are encoded by two genes (GJB2 and GJB6, respectively) that are found within 50 kb in the same complex deafness locus, DFNB1. Immunocytochemistry and quantitative PCR analysis of Cx30 KO mouse cultures revealed that Cx26 is downregulated at the protein level and at the mRNA level in nonsensory cells located between outer hair cells and the stria vascula...

Journal: :The Laryngoscope 2011
Michael Lipan Xiaomei Ouyang Denise Yan Simon Angeli Li Lin Du Xue-Zhong Liu

OBJECTIVES The aim of the study is to assess clinical characteristics of individuals with nonsyndromic sensorineural hearing loss (NSSNHL) with genetic mutations in GJB2 and/or GJB6. We describe and compare one group with biallelic mutations against a group of heterozygote mutation carriers. METHODS A total of 350 patients between the ages of 3 months and 80 years referred to a tertiary care ...

Journal: :Human mutation 2006
Juan R González Wenyi Wang Ester Ballana Xavier Estivill

Mutations in the DFNB1 locus, where two connexin genes are located (GJB2 and GJB6), account for half of congenital cases of nonsyndromic autosomal recessive deafness. Because of the high frequency of DFNB1 gene mutations and the availability of genetic diagnostic tests involving these genes, they are the best candidates to develop a risk prediction model of being hearing impaired. People underg...

2010
Juan Rodriguez-Paris Lynn Pique Tahl Colen Joseph Roberson Phyllis Gardner Iris Schrijver

Molecular diagnostic testing of individuals with congenital sensorineural hearing loss typically begins with DNA sequencing of the GJB2 gene. If the cause of the hearing loss is not identified in GJB2, additional testing can be ordered. However, the step-wise analysis of several genes often results in a protracted diagnostic process. The more comprehensive Hereditary Hearing Loss Arrayed Primer...

Journal: :American journal of human genetics 2003
Ignacio Del Castillo Miguel A Moreno-Pelayo Francisco J Del Castillo Zippora Brownstein Sandrine Marlin Quint Adina David J Cockburn Arti Pandya Kirby R Siemering G Parker Chamberlin Ester Ballana Wim Wuyts Andréa Trevas Maciel-Guerra Araceli Alvarez Manuela Villamar Mordechai Shohat Dvorah Abeliovich Hans-Henrik M Dahl Xavier Estivill Paolo Gasparini Tim Hutchin Walter E Nance Edi L Sartorato Richard J H Smith Guy Van Camp Karen B Avraham Christine Petit Felipe Moreno

Mutations in GJB2, the gene encoding connexin-26 at the DFNB1 locus on 13q12, are found in as many as 50% of subjects with autosomal recessive, nonsyndromic prelingual hearing impairment. However, genetic diagnosis is complicated by the fact that 10%-50% of affected subjects with GJB2 mutations carry only one mutant allele. Recently, a deletion truncating the GJB6 gene (encoding connexin-30), n...

2012
E Sukarova Stefanovska M Cakar I Filipce D Plaseska Karanfilska

Hearing impairment is the most common sensory deficit in humans affecting 1 in 1000 newborns. When present in an infant, deafness may have dramatic effects on language acquisition, seriously compromising the quality of their life. Deafness is influenced by both genetic and environmental factors, with inherited causes as the most prominent etiological factor in deafness in developed countries. T...

Journal: :International journal of pediatric otorhinolaryngology 2013
Gabrielle N Manzoli Kiyoko Abe-Sandes Alan H Bittles Danniel S D da Silva Luciene da C Fernandes Roberta M C Paulon Iza Cristina S de Castro Carla M C A Padovani Angelina X Acosta

OBJECTIVE There are many hearing impaired individuals in Monte Santo, a rural municipality in the state of Bahia, Brazil, including multiple familial cases strongly suggestive of a genetic aetiology. METHODS The present study investigated 81 subjects with hearing impairment (HI) recruited from 36 families. Mutations often associated with HI, i.e. the DFNB1 mutations c.35delG in GJB2, deletion...

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