Progress and prospects in human genetic research into age-related hearing impairment (Q34033991)

30 July 2017

5 references

25 April 2019

20 August 2019

12 October 2019

23 July 2020

10 September 2020

Progress and prospects in human genetic research into age-related hearing impairment (English)

1 reference

25140308

genetic predisposition to disease

30 July 2017

main subject

physiological phenomenon

1 reference

20 August 2019

1 reference

12 October 2019

2 references

23 July 2020

10 September 2020

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25140308%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25140308%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Saiko Sugiura

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25140308%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Hiromi Ueda

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25140308%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Tsutomu Nakashima

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25140308%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

language of work or name

English

0 references

publication date

22 July 2014

5 references

BioMed Research International

30 July 2017

25 April 2019

20 August 2019

12 October 2019

23 July 2020

6 references

25 April 2019

20 August 2019

12 October 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25140308%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

23 July 2020

20 September 2020

2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25140308%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

page(s)

390601

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25140308%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 3.0 Unported

4 June 2020

5 references

25 April 2019

20 August 2019

12 October 2019

23 July 2020

Association of GRM7 variants with different phenotype patterns of age-related hearing impairment in an elderly male Han Chinese population

10 September 2020

copyrighted

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Genetics of hearing loss: focus on DFNA2.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Current concepts in age-related hearing loss: epidemiology and mechanistic pathways.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Mechanistic basis and functional roles of long-term plasticity in auditory neurons induced by a brain-generated estrogen

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

GRM7 variants associated with age-related hearing loss based on auditory perception

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

The genetics and neuropathology of Alzheimer's disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Signaling and Damaging Functions of Free Radicals in Aging-Free Radical Theory, Hormesis, and TOR.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Apoptosis in acquired and genetic hearing impairment: the programmed death of the hair cell

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Molecular genetic epidemiology of age-related hearing impairment

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Hearing impairment risk and interaction of folate metabolism related gene polymorphisms in an aging study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

The transcription factor grainyhead-like 2 regulates the molecular composition of the epithelial apical junctional complex

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Antioxidant enzymes, presbycusis, and ethnic variability

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Energetics, epigenetics, mitochondrial genetics

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Cellular targets of estrogen signaling in regeneration of inner ear sensory epithelia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Quantification of the mitochondrial DNA common deletion in presbycusis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

GRM7 variants confer susceptibility to age-related hearing impairment

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Apolipoprotein E alleles and sensorineural hearing loss

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Distribution and significance of endothelin 1 in guinea pig cochlear lateral wall

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

KCNQ4: a gene for age-related hearing impairment?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

N-acetyltransferase 2 genetic polymorphism: effects of carcinogen and haplotype on urinary bladder cancer risk

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Estrogen and hearing: a summary of recent investigations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

A novel Z-score-based method to analyze candidate genes for age-related hearing impairment

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Mutations of MYO6 are associated with recessive deafness, DFNB37

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

A radical demise. Toxins and trauma share common pathways in hair cell death

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Concise review of the glutathione S-transferases and their significance to toxicology

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

Detection of a specific mitochondrial DNA deletion in tissues of older humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4130297

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

5 July 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

The grainyhead-like 2 gene (GRHL2) single nucleotide polymorphism is not associated with age-related hearing impairment in Han Chinese.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Confirmation of GRHL2 as the gene for the DFNA28 locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

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/10.1155%2F2014%2F390601

Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

The role of the PDZ protein GIPC in regulating NMDA receptor trafficking

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Audioprofiles and antioxidant enzyme genotypes in presbycusis

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

The influence of genetic variation in oxidative stress genes on human noise susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

N-acetyltransferase 2 gene polymorphism and presbycusis

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Characterization of atrazine biotransformation by human and murine glutathione S-transferases

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Mitochondrial DNA haplogroups and age-related hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European population

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Gene dose of apolipoprotein E and age-related hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Sudden hearing loss and MTHFR 677C>T/1298A>C gene polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with sudden sensorineural hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Association of folate with hearing is dependent on the 5,10-methylenetetrahdyrofolate reductase 677C-->T mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Expression and significance of endothelin 1 in spiral ganglion cells of guinea pig.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Endothelin-1 gene polymorphism and hearing impairment in elderly Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

The association between gene polymorphisms in uncoupling proteins and hearing impairment in Japanese elderly

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Correlation of Cochlear Blood Supply with Mitochondrial DNA Common Deletion in Presbyacusis

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F390601

Role of genetic and acquired prothrombotic risk factors in genesis of sudden sensorineural hearing loss

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25140308

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

N-acetyltransferase SNPs: emerging concepts serve as a paradigm for understanding complexities of personalized medicine

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25140308

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25140308

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1155/2014/390601

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25140308%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25140308%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

25140308

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25140308%20AND%20SRC:MED&resulttype=core&format=json