نتایج جستجو برای: ژن gjb2

تعداد نتایج: 16685  

Journal: :Clinical genetics 2010
E Wilch H Azaiez R A Fisher J Elfenbein A Murgia R Birkenhäger H Bolz S M Da Silva-Costa I Del Castillo T Haaf L Hoefsloot H Kremer C Kubisch C Le Marechal A Pandya E L Sartorato E Schneider G Van Camp W Wuyts R J H Smith K H Friderici

Eleven affected members of a large German-American family segregating recessively inherited, congenital, non-syndromic sensorineural hearing loss (SNHL) were found to be homozygous for the common 35delG mutation of GJB2, the gene encoding the gap junction protein Connexin 26. Surprisingly, four additional family members with bilateral profound SNHL carried only a single 35delG mutation. Previou...

Journal: :JAMA 1999
G E Green D A Scott J M McDonald G G Woodworth V C Sheffield R J Smith

CONTEXT Mutations in the GJB2 gene are the most common known cause of inherited congenital severe-to-profound deafness. The carrier frequency of these mutations is not known. OBJECTIVES To determine the carrier rate of deafness-causing mutations in GJB2 in the midwestern United States and the prevalence of these mutations in persons with congenital sensorineural hearing loss ranging in severi...

2010
Hee-Jung Kim Chang-Hun Park Hee-Jin Kim Ki-O Lee Hong-Hee Won Moon-Hee Ko Hosuk Chu Yang-Sun Cho Won-Ho Chung Jong-Won Kim Sung Hwa Hong

OBJECTIVES Hearing impairment (HI) is the most common sensory deficit in human. The Gap Junction Protein, Beta-2 (GJB2) gene encodes the protein connexin 26, and this gene accounts for up to half of the cases of autosomal recessive nonsyndromic HI. This study was conducted to obtain a set of sequence variations (SVs) of the GJB2 gene among Koreans from the general population for making molecula...

Journal: :Physiological research 2013
D Groh P Seeman M Jilek J Popelář Z Kabelka J Syka

The most frequent hereditary hearing loss is caused by mutations in the GJB2 gene coding for the gap junction beta 2 protein Connexin 26 (Cx26). In contrast to many studies performed in patients with bi-allelic mutations, audiometric studies on heterozygotes are sparse and often contradictory. To evaluate hearing function in heterozygous carriers of the GJB2 c.35delG mutation, audiometry over t...

Journal: :Ear and hearing 2009
Ana Carla Batissoco Ronaldo Serafim Abreu-Silva Maria Cristina Célia Braga Karina Lezirovitz Valter Della-Rosa Tabith Alfredo Paulo Alberto Otto Regina Célia Mingroni-Netto

OBJECTIVE Hereditary nonsyndromic deafness is an autosomal recessive condition in about 80% of cases, and point mutations in the GJB2 gene (connexin 26) and two deletions in the GJB6 gene (connexin 30), del(GJB6-D13S1830) and del(GJB6-D13S1854), are reported to account for 50% of recessive deafness. Aiming at establishing the frequencies of GJB2 mutations and GJB6 deletions in the Brazilian pop...

2015
Jing Zheng Zhengbiao Ying Zhaoyang Cai Dongmei Sun Zheyun He Yinglong Gao Ting Zhang Yi Zhu Ye Chen Min-Xin Guan Klaus Brusgaard

Mutations in Gap Junction Beta 2 (GJB2) have been reported to be a major cause of non-syndromic hearing loss in many populations worldwide. The spectrums and frequencies of GJB2 variants vary substantially among different ethnic groups, and the genotypes among these populations remain poorly understood. In the present study, we carried out a systematic and extended mutational screening of GJB2 ...

Journal: :Hearing research 2014
Yohei Takada Lisa A Beyer Donald L Swiderski Aubrey L O'Neal Diane M Prieskorn Shaked Shivatzki Karen B Avraham Yehoash Raphael

Mutations in the connexin 26 gene (GJB2) are the most common genetic cause of deafness, leading to congenital bilateral non-syndromic sensorineural hearing loss. Here we report the generation of a mouse model for a connexin 26 (Cx26) mutation, in which cre-Sox10 drives excision of the Cx26 gene from non-sensory cells flanking the auditory epithelium. We determined that these conditional knockou...

2012
Jennifer A Easton Steven Donnelly Miriam A F Kamps Peter M Steijlen Patricia E Martin Gianluca Tadini René Janssens Rudolf Happle Michel van Geel Maurice A M van Steensel

Porokeratotic eccrine ostial and dermal duct nevus, or porokeratotic eccrine nevus (PEN), is a hyperkeratotic epidermal nevus. Several cases of widespread involvement have been reported, including one in association with the keratitis-ichthyosis-deafness (KID) syndrome (OMIM #148210), a rare disorder caused by mutations in the GJB2 gene coding for the gap junction protein connexin26 (Cx26). The...

2011
Sandra Iossa Elio Marciano Annamaria Franzé

The GJB2 gene is located on chromosome 13q12 and it encodes the connexin 26, a transmembrane protein involved in cell-cell attachment of almost all tissues. GJB2 mutations cause autosomal recessive (DFNB1) and sometimes dominant (DFNA3) non-syndromic sensorineural hearing loss. Moreover, it has been demonstrated that connexins are involved in regulation of growth and differentiation of epidermi...

Journal: :Human molecular genetics 2003
Takayuki Kudo Shigeo Kure Katsuhisa Ikeda An-Ping Xia Yukio Katori Masaaki Suzuki Kanako Kojima Akiko Ichinohe Yoichi Suzuki Yoko Aoki Toshimitsu Kobayashi Yoichi Matsubara

Hereditary deafness affects about 1 in 2000 children and mutations in the GJB2 gene are the major cause in various ethnic groups. GJB2 encodes connexin26, a putative channel component in cochlear gap junction. However, the pathogenesis of hearing loss caused by the GJB2 mutations remains obscure. The generation of a mouse model to study the function of connexin26 during hearing has been hampere...

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