(Q43427708)

English

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

scientific article published on 21 November 2012

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23179933%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

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

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18 February 2020

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based on heuristic

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3

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18 February 2020

Jose A Lopez-Escamez

13

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18 February 2020

author name string

Irene Gázquez

1

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18 February 2020

Antonia Moreno

2

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18 February 2020

Jeff Ohmen

4

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18 February 2020

Sofia Santos-Perez

5

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18 February 2020

Ismael Aran

6

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18 February 2020

Andres Soto-Varela

7

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18 February 2020

Herminio Pérez-Garrigues

8

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18 February 2020

Alicia López-Nevot

9

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18 February 2020

Angel Batuecas

10

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18 February 2020

Rick A Friedman

11

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18 February 2020

Miguel A López-Nevot

12

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18 February 2020

publication date

21 November 2012

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18 February 2020

European Archives of Oto-Rhino-Laryngology

1 reference

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18 February 2020

270

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18 February 2020

4

1 reference

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18 February 2020

1521-1529

1 reference

Europe PubMed Central

PubMed publication ID

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18 February 2020

https://scigraph.springernature.com/pub.10.1007/s00405-012-2268-0

0 references

Human leukocyte antigen-DQB1 and -DRB1 associations in patients with idiopathic sudden sensorineural hearing loss from a defined population of Northwest Spain.

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Molecular changes associated with the endolymphatic hydrops model

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Unstable distortion-product otoacoustic emission phase in Menière's disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Cellular responses to interferon-gamma

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

The macrophage is an important and previously unrecognized source of macrophage migration inhibitory factor

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Mutation screening of the macrophage migration inhibitory factor gene: positive association of a functional polymorphism of macrophage migration inhibitory factor with juvenile idiopathic arthritis

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Multifrequency admittancemetry in Ménière's Disease: a preliminary study for a new diagnostic test

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

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/10.1007%2FS00405-012-2268-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Treatment of corticosteroid-responsive autoimmune inner ear disease with methotrexate: a randomized controlled trial

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Carriage of a tumor necrosis factor polymorphism amplifies the cytotoxic T-lymphocyte antigen 4 attributed risk of primary biliary cirrhosis: evidence for a gene-gene interaction

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Regulation of the expression of inducible nitric oxide synthase

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Impact of bilaterality and headache on health-related quality of life in Meniere's disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Pathophysiology of Meniere's syndrome: are symptoms caused by endolymphatic hydrops?

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Anti-inflammatory properties of pro-inflammatory interferon-gamma

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Elevated antithyroid peroxidase and antinuclear autoantibody titers in Ménière's disease patients: more than a chance association?

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Bilateral Ménière's disease

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Amelioration of dextran sulfate sodium-induced colitis by anti-macrophage migration inhibitory factor antibody in mice

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

In vitro production of IFN-gamma correlates with CA repeat polymorphism in the human IFN-gamma gene.

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

The genetics of clinical outcome in multiple sclerosis.

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Macrophage migration inhibitory factor: gene polymorphisms and susceptibility to inflammatory diseases

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Antibodies to inner ear antigens in Meniere's disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Immunologic and serologic testing in patients with Ménière's disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

A functional variant of IFNgamma gene is associated with coeliac disease

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Evidence of association of macrophage migration inhibitory factor gene polymorphisms with systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Contemporary perspectives on the pathophysiology of Meniere's disease: implications for treatment

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

A promoter polymorphism of tumor necrosis factor alpha associated with systemic lupus erythematosus in African-Americans

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

The vestibular evoked-potential profile of Ménière's disease.

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Blockage of immune-mediated inner ear damage by etanercept

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Effects of a polymorphism in the human tumor necrosis factor alpha promoter on transcriptional activation

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Macrophage Migration Inhibitory Factor Gene Polymorphism is Associated with Psoriasis

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Macrophage migration inhibitory factor gene: Influence on rheumatoid arthritis susceptibility

1 reference

https://api.crossref.org/works/10.1007%2FS00405-012-2268-0

21 January 2018

Association between functional promoter polymorphisms of macrophage migration inhibitory factor (MIF) gene and ulcerative colitis in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/23179933

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms of interferon-gamma gene CA-repeat and interleukin-10 promoter region (-592A/C) in Japanese type I diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23179933

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/23179933

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between dinucleotide repeat in non-coding region of interferon-gamma gene and susceptibility to, and severity of, rheumatoid arthritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23179933

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influence of human leukocyte antigen in the pathogenesis of Ménière's disease in the South Korean population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23179933

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/23179933

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/23179933

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A functional promoter polymorphism in the macrophage migration inhibitory factor (MIF) gene associated with disease severity in rheumatoid arthritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23179933

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00405-012-2268-0

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23179933%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23179933%20AND%20SRC:MED&resulttype=core&format=json

18 February 2020

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