(Q34513628)

English

Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease

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scholarly article

1 reference

Europe PubMed Central

2 August 2017

Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease (English)

1 reference

Europe PubMed Central

2 August 2017

1 reference

based on heuristic

inferred from title

Meniere's disease

1 reference

based on heuristic

inferred from title

sensorineural hearing loss

1 reference

based on heuristic

inferred from title

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25397881%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

3

1 reference

Europe PubMed Central

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8 June 2020

Manuel Martinez Bueno

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25397881%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Gabriel Trinidad-Ruiz

7

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25397881%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Eduardo Martín-Sanz

10

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8 June 2020

Marta E Alarcón-Riquelme

13

1 reference

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8 June 2020

Angel Batuecas-Caletrio

14

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8 June 2020

Juan M Espinosa-Sanchez

15

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8 June 2020

Jose A Lopez-Escamez

17

1 reference

Europe PubMed Central

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8 June 2020

Paz Pérez-Vázquez

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author name string

Sonia Cabrera

1

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8 June 2020

Jesus Benitez

5

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Europe PubMed Central

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8 June 2020

Nicolas Perez

6

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8 June 2020

Andrés Soto-Varela

8

1 reference

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8 June 2020

Sofía Santos-Perez

9

1 reference

Europe PubMed Central

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8 June 2020

Jesus Fraile

11

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8 June 2020

Paz Perez

12

1 reference

Europe PubMed Central

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8 June 2020

Ismael Aran

16

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8 June 2020

language of work or name

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publication date

14 November 2014

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Europe PubMed Central

2 August 2017

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Europe PubMed Central

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8 June 2020

9

1 reference

Europe PubMed Central

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8 June 2020

11

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25397881%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

e112171

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25397881%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

copyright license

Creative Commons Attribution 4.0 International

14 November 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Mining immune epitopes in the inner ear.

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7 July 2018

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

1 reference

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7 July 2018

Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis

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7 July 2018

Annotation of functional variation in personal genomes using RegulomeDB

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7 July 2018

A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies

1 reference

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7 July 2018

Seven newly identified loci for autoimmune thyroid disease

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7 July 2018

Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases

1 reference

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7 July 2018

Meniere's disease might be an autoimmune condition?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4232390

7 July 2018

seeQTL: a searchable database for human eQTLs

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7 July 2018

HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants

1 reference

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7 July 2018

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

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7 July 2018

High prevalence of systemic autoimmune diseases in patients with Menière's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4232390

7 July 2018

Confirmation of TNIP1 and IL23A as susceptibility loci for psoriatic arthritis

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7 July 2018

Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production

1 reference

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7 July 2018

IL-1β is overexpressed and aberrantly regulated in corticosteroid nonresponders with autoimmune inner ear disease.

1 reference

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7 July 2018

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7 July 2018

Biological, clinical and population relevance of 95 loci for blood lipids

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Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci

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7 July 2018

Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4232390

7 July 2018

Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus

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7 July 2018

Selective activation of nuclear factor kappa B in the cochlea by sensory and inflammatory stress

1 reference

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7 July 2018

Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways

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The role of innate immune responses in autoimmune disease development

1 reference

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7 July 2018

PLINK: a tool set for whole-genome association and population-based linkage analyses

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A haplotype map of the human genome

1 reference

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7 July 2018

Toll-like receptor signalling

1 reference

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7 July 2018

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7 July 2018

A nuclear export signal in the N-terminal regulatory domain of IkappaBalpha controls cytoplasmic localization of inactive NF-kappaB/IkappaBalpha complexes

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7 July 2018

Diagnostic and prognostic utility of measuring tumor necrosis factor in the peripheral circulation of patients with immune-mediated sensorineural hearing loss.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0112171

21 January 2018

MICA-STR A.4 is associated with slower hearing loss progression in patients with Ménière's disease.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0112171

21 January 2018

Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere's disease.

1 reference

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21 January 2018

Prevalence, associated factors, and comorbid conditions for Ménière's disease

1 reference

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21 January 2018

Identification of multiple independent susceptibility loci in the HLA region in Behçet's disease

1 reference

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21 January 2018

Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.

1 reference

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27 October 2018

Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4232390

27 October 2018

HLA-DRB1*1101 allele may be associated with bilateral Méniére's disease in southern European population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4232390

27 October 2018

Characteristics of patients with unilateral and bilateral Ménière's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/25397881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Committee on Hearing and Equilibrium guidelines for the diagnosis and evaluation of therapy in Menière's disease. American Academy of Otolaryngology-Head and Neck Foundation, Inc

1 reference

https://pubmed.ncbi.nlm.nih.gov/25397881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0112171

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25397881%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

2014PLoSO...9k2171C

0 references

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25397881%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25397881%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

ResearchGate publication ID

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