(Q34270661)

1 August 2017

title

DFNA5, a gene involved in hearing loss and cancer: a review (English)

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1 August 2017

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Ken Op de Beeck

1

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1 August 2017

Lut Van Laer

series ordinal

2

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1 August 2017

Guy Van Camp

series ordinal

3

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1 August 2017

publication date

1 March 2012

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Annals of Otology Rhinology and Laryngology

1 August 2017

published in

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1 August 2017

volume

121

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1 August 2017

issue

3

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1 August 2017

page(s)

197-207

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A follow-up study in a family with dominant progressive inner ear deafness.

1 August 2017

cites work

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https://api.crossref.org/works/10.1177%2F000348941212100310

Further delineation of the DFNA5 phenotype: results of speech recognition tests.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15.

21 January 2018

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https://api.crossref.org/works/10.1177%2F000348941212100310

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

A 3-nucleotide deletion in the polypyrimidine tract of intron 7 of the DFNA5 gene causes nonsyndromic hearing impairment in a Chinese family

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

A novel mutation identified in the DFNA5 gene in a Dutch family: a clinical and genetic evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Evidence for a founder mutation causing DFNA5 hearing loss in East Asians

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Is DFNA5 a susceptibility gene for age-related hearing impairment?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

A yeast model for the study of human DFNA5, a gene mutated in nonsyndromic hearing impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families

21 January 2018

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Gasdermin (Gsdm) localizing to mouse Chromosome 11 is predominantly expressed in upper gastrointestinal tract but significantly suppressed in human gastric cancer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Members of a novel gene family, Gsdm, are expressed exclusively in the epithelium of the skin and gastrointestinal tract in a highly tissue-specific manner

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Zebrafish as a genomics research model

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

The deafness gene dfna5 is crucial for ugdh expression and HA production in the developing ear in zebrafish.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

The DFNA5 gene, responsible for hearing loss and involved in cancer, encodes a novel apoptosis-inducing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

DFNA5: hearing impairment exon instead of hearing impairment gene?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

A novel DFNA5 mutation does not cause hearing loss in an Iranian family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Characterization of a gene that is inversely correlated with estrogen receptor expression (ICERE-1) in breast carcinomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

DFNA5 (ICERE-1) contributes to acquired etoposide resistance in melanoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

The potential role of DFNA5, a hearing impairment gene, in p53-mediated cellular response to DNA damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Genomic screening for genes upregulated by demethylation revealed novel targets of epigenetic silencing in breast cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Worms gang up on bacteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Identification of DFNA5 as a target of epigenetic inactivation in gastric cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Aberrant promoter methylation and tumor suppressive activity of the DFNA5 gene in colorectal carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Methylation of the DFNA5 increases risk of lymph node metastasis in human breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Characterization of the murine Dfna5 promoter and regulatory regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Linkage disequilibrium patterns and tagSNP transferability among European populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Frequent DNA methylation but not mutation of the ID4 gene in malignant lymphoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Apoptosis of guinea pig cochlear hair cells following chronic aminoglycoside treatment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Activation of cell death pathways in the inner ear of the aging CBA/J mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Intense noise-induced apoptosis in hair cells of guinea pig cochleae

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

Studies on Progressive Hereditary Perceptive Deafness in A Family of 335 Members: I. Genetical and General Audiological Results

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348941212100310

10.1177/000348941212100310

21 January 2018

Identifiers

DOI

0 references

1 reference