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Molecular screening of patients with profound hearing loss from Chengdu, China

Acta oto-laryngologica, 2022, Vol.142 (1), p.57-60

2022

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Molecular composition and distribution of gap junctions in the sensory epithelium of the human cochlea-a super-resolution structured illumination microscopy (SR-SIM) study

Upsala journal of medical sciences, 2017-08, Vol.122 (3), p.160-170

2017

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Permeation Pathway of Homomeric Connexin 26 and Connexin 30 Channels Investigated by Molecular Dynamics

Journal of biomolecular structure & dynamics, 2012, Vol.29 (5), p.985-998

2012

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The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in Austria

Acta oto-laryngologica, 2017-04, Vol.137 (4), p.356-360

2017

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Is deafness etiology important for prediction of functional outcomes in pediatric cochlear implantation?

Acta oto-laryngologica, 2014-06, Vol.134 (6), p.571-578

2014

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Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China

Acta oto-laryngologica, 2015-06, Vol.135 (6), p.586-591

2015

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Eventual proapoptotic or anti-apoptotic impact of aberrantly expressed Cx43 and Cx26 can depend on ER-alpha overexpression in human endometrioid adenocarcinoma

Gynecological endocrinology, 2015-08, Vol.31 (8), p.604-608

2015

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The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness

International journal of audiology, 2015-02, Vol.54 (2), p.124-130

2015

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Patients with CDH23 mutations and the 1555A>G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS)

Acta oto-laryngologica, 2012-04, Vol.132 (4), p.377-384

2012

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Spectrum and frequency of GJB2 mutations in a cohort of 264 Portuguese nonsyndromic sensorineural hearing loss patients

International journal of audiology, 2013-07, Vol.52 (7), p.466-471

2013

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Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants

Acta oto-laryngologica, 2014-04, Vol.134 (4), p.373-381

2014

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GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population

International journal of audiology, 2012-03, Vol.51 (3), p.181-185

2012

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Prognostic indicators in paediatric cochlear implant surgery: a systematic literature review

Cochlear implants international, 2011-05, Vol.12 (2), p.67-93

2011

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Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord

Acta oto-laryngologica, 2011-09, Vol.131 (9), p.976-982

2011

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Expression of gap junction proteins connexins 26, 30, and 43 in Dupuytren's disease

Acta orthopaedica, 2014-02, Vol.85 (1), p.97-101

2014

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Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China

Acta oto-laryngologica, 2014-09, Vol.134 (9), p.924-929

2014

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Additional difficulties associated with aetiologies of deafness: outcomes from a parent questionnaire of 540 children using cochlear implants

Cochlear implants international, 2016, Vol.17 (1), p.21-30

2016

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The deafness-causing mutation c.508_511dup in the GJB2 gene and a literature review

Acta oto-laryngologica, 2015-09, Vol.135 (9), p.914-918

2015

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Identification of Cells Expressing Cx43, Cx30, Cx26, Cx32 and Cx36 in Gap Junctions of Rat Brain and Spinal Cord

Cell communication & adhesion, 2001, Vol.8 (4-6), p.315-320

2001

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The search of a genetic basis for noise-induced hearing loss (NIHL)

Annals of human biology, 2011-03, Vol.38 (2), p.210-218

2011

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Paediatric cochlear implantation: Adverse prognostic factors and trends from a review of 174 cases

Cochlear implants international, 2014-03, Vol.15 (2), p.62-77

2014

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Statistical study of 35delG mutation of GJB2 gene: A meta-analysis of carrier frequency

International journal of audiology, 2009, Vol.48 (6), p.363-370

2009

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Outcome of cochlear implantation in children with congenital cytomegalovirus infection or GJB2 mutation

Acta oto-laryngologica, 2012-06, Vol.132 (6), p.597-602

2012

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Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China

Acta oto-laryngologica, 2013-09, Vol.133 (9), p.930-934

2013

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Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss

Acta oto-laryngologica, 2013-08, Vol.133 (8), p.833-841

2013

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Molecular screening of patients with profound hearing loss from Chengdu, China

Molecular composition and distribution of gap junctions in the sensory epithelium of the human cochlea-a super-resolution structured illumination microscopy (SR-SIM) study

Permeation Pathway of Homomeric Connexin 26 and Connexin 30 Channels Investigated by Molecular Dynamics

The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in Austria

Is deafness etiology important for prediction of functional outcomes in pediatric cochlear implantation?

Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China

Eventual proapoptotic or anti-apoptotic impact of aberrantly expressed Cx43 and Cx26 can depend on ER-alpha overexpression in human endometrioid adenocarcinoma

The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness

Patients with CDH23 mutations and the 1555A>G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS)

Spectrum and frequency of GJB2 mutations in a cohort of 264 Portuguese nonsyndromic sensorineural hearing loss patients

Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants

GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population

Prognostic indicators in paediatric cochlear implant surgery: a systematic literature review

Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord

Expression of gap junction proteins connexins 26, 30, and 43 in Dupuytren's disease

Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China

Additional difficulties associated with aetiologies of deafness: outcomes from a parent questionnaire of 540 children using cochlear implants

The deafness-causing mutation c.508_511dup in the GJB2 gene and a literature review

Identification of Cells Expressing Cx43, Cx30, Cx26, Cx32 and Cx36 in Gap Junctions of Rat Brain and Spinal Cord

The search of a genetic basis for noise-induced hearing loss (NIHL)

Paediatric cochlear implantation: Adverse prognostic factors and trends from a review of 174 cases

Statistical study of 35delG mutation of GJB2 gene: A meta-analysis of carrier frequency

Outcome of cochlear implantation in children with congenital cytomegalovirus infection or GJB2 mutation

Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China

Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss

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