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The Clinical Manifestation of p.Asp50Asn Heterozygous Mutation of GJB2 Gene in 3 Members of a Family Is Similar to That of Clouston Syndrome

Annals of dermatology, 2022-10, Vol.34 (5), p.382-386

2022

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Methylselenocysteine Promotes Etoposide Cytotoxicity by Enhancing Homotypic Gap Junctions Composed of Connexin 26

Sichuan da xue xue bao. Journal of Sichuan University. Yi xue ban, 2023-05, Vol.54 (3), p.532-538

2023

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INNOVATIONS IN RESEARCH OF HEREDITARY DEAFNESS

הרפואה, 2020-02, Vol.159 (1), p.117

2020

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Analysis of the results for genetic disease screening among 1 000 newborns from Huzhou

Zhonghua yi xue yi chuan xue za zhi, 2024-05, Vol.41 (5), p.551

2024

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A prospective study of genetic screening of 2 060 neonates by high-throughput sequencing

Zhonghua yi xue yi chuan xue za zhi, 2023-06, Vol.40 (6), p.641

2023

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Screening of mutations of deafness-related genes in women of child-bearing age from Shijiazhuang area

Zhonghua yi xue yi chuan xue za zhi, 2016-08, Vol.33 (4), p.462

2016

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Congenital sensorineural deafness with microtia and Michel aplasia

Laryngo- rhino- otologie, 2015-03, Vol.94 (3), p.182

2015

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A follow-up study of abnormal mutation in neonatal deafness gene screening

Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery, 2019-12, Vol.54 (12), p.881

2019

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Analysis of GJB2, SLC26A4, GJB3 and 12S rRNA gene mutations among patients with nonsyndromic hearing loss from eastern Shandong

Zhonghua yi xue yi chuan xue za zhi, 2019-05, Vol.36 (5), p.433

2019

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La mutation 35delG du gène de la connexine 26, une cause fréquente des surdités non syndromiques autosomiques récessives au Maroc

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2007-05, Vol.14 (5), p.450-453

2007

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Pseudodominanz zweier rezessiver Connexin-Mutationen bei nicht-syndromaler Hörstörung?

Laryngo- rhino- otologie, 2006-03, Vol.85 (3), p.191-196

2006

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New recurrent extended deletion, including GJB2 and GJB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive type of inheritance

Genetika, 2014-04, Vol.50 (4), p.474

2014

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Expression of gap junction protein connexin 26 in human hepatocellular carcinoma and its significance

Zhejiang da xue xue bao. Journal of Zhejiang University. Medical sciences. Yi xue ban, 2015-09, Vol.44 (5), p.517

2015

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The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances

Vestnik otorinolaringologii, 2014 (2), p.37

2014

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A novel technique for simultaneous multi-gene mutation screening in 225 patients with nonsyndromic hearing loss

Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery, 2016-03, Vol.51 (3), p.203

2016

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Lentivirus-mediated shRNA interference of Cx26 suppresses epithelial mesenchymal transition and invasion of highly invasive hepatocellular carcinoma cells in vitro

Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2014-12, Vol.34 (12), p.1743

2014

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Screening of common deafness gene mutations in 17 000 Chinese newborns from Chengdu based on microarray analysis

Zhonghua yi xue yi chuan xue za zhi, 2014-10, Vol.31 (5), p.547

2014

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Distribution characteristics and correlation analysis of GJB2 variation in patients with auditory neuropathy

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery, 2024-01, Vol.38 (1), p.23

2024

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Pesquisa audiológica y molecular para pérdida auditiva por mutación 35delG en el gen de la conexina 26 e infección congénita por citomegalovirus

Archivos argentinos de pediatría, 2011-12, Vol.109 (6), p.479-484

2011

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Screening of common deaf genes in pregnant women and prevention of deafness at birth

Zhonghua yi xue yi chuan xue za zhi, 2015-06, Vol.32 (3), p.339

2015

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Analysis of common mutations of deafness-related genes in 2725 newborns

Zhonghua yi xue yi chuan xue za zhi, 2015-06, Vol.32 (3), p.335

2015

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Progressive hearing impairment with deletion in GJB2 gene despite normal newborn hearing screening

Laryngo- rhino- otologie, 2014-04, Vol.93 (4), p.244

2014

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Study of newborn hearing and genetic screening in Jinan

Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery, 2015-05, Vol.50 (5), p.401

2015

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Combined hearing and deafness gene mutation screening of 11,046 Chinese newborns

Zhonghua yi xue yi chuan xue za zhi, 2015-12, Vol.32 (6), p.766

2015

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Influence of Cx26/Cx32 gap junction channel on antineoplastic effect of etoposide in Hela cells

Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2012-03, Vol.32 (3), p.329

2012

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The Clinical Manifestation of p.Asp50Asn Heterozygous Mutation of GJB2 Gene in 3 Members of a Family Is Similar to That of Clouston Syndrome

Methylselenocysteine Promotes Etoposide Cytotoxicity by Enhancing Homotypic Gap Junctions Composed of Connexin 26

INNOVATIONS IN RESEARCH OF HEREDITARY DEAFNESS

Analysis of the results for genetic disease screening among 1 000 newborns from Huzhou

A prospective study of genetic screening of 2 060 neonates by high-throughput sequencing

Screening of mutations of deafness-related genes in women of child-bearing age from Shijiazhuang area

Congenital sensorineural deafness with microtia and Michel aplasia

A follow-up study of abnormal mutation in neonatal deafness gene screening

Analysis of GJB2, SLC26A4, GJB3 and 12S rRNA gene mutations among patients with nonsyndromic hearing loss from eastern Shandong

La mutation 35delG du gène de la connexine 26, une cause fréquente des surdités non syndromiques autosomiques récessives au Maroc

Pseudodominanz zweier rezessiver Connexin-Mutationen bei nicht-syndromaler Hörstörung?

New recurrent extended deletion, including GJB2 and GJB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive type of inheritance

Expression of gap junction protein connexin 26 in human hepatocellular carcinoma and its significance

The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances

A novel technique for simultaneous multi-gene mutation screening in 225 patients with nonsyndromic hearing loss

Lentivirus-mediated shRNA interference of Cx26 suppresses epithelial mesenchymal transition and invasion of highly invasive hepatocellular carcinoma cells in vitro

Screening of common deafness gene mutations in 17 000 Chinese newborns from Chengdu based on microarray analysis

Distribution characteristics and correlation analysis of GJB2 variation in patients with auditory neuropathy

Pesquisa audiológica y molecular para pérdida auditiva por mutación 35delG en el gen de la conexina 26 e infección congénita por citomegalovirus

Screening of common deaf genes in pregnant women and prevention of deafness at birth

Analysis of common mutations of deafness-related genes in 2725 newborns

Progressive hearing impairment with deletion in GJB2 gene despite normal newborn hearing screening

Study of newborn hearing and genetic screening in Jinan

Combined hearing and deafness gene mutation screening of 11,046 Chinese newborns

Influence of Cx26/Cx32 gap junction channel on antineoplastic effect of etoposide in Hela cells

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