Genetic susceptibility to otitis media in childhood. - Wikidata - awgldk - TriplyDB

Genetic susceptibility to otitis media in childhood.

Genetic susceptibility to otitis media in childhood.

http://www.wikidata.org/entity/Q37976616

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Genetics: A New Frontier in Otology.Genome-wide association study to identify the genetic determinants of otitis media susceptibility in childhood Polymorphisms of immunity genes and susceptibility to otitis media in children.Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus.The Role of Obliteration in the Achievement of a Dry Mastoid Bowl.Current concepts in the pathogenesis and treatment of chronic suppurative otitis media.Familial and microbiological contribution to the otitis-prone condition Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene.Genetic susceptibility to chronic otitis media with effusion: candidate gene single nucleotide polymorphisms.Innate Immunity: Orchestrating Inflammation and Resolution of Otitis Media.Understanding the aetiology and resolution of chronic otitis media from animal and human studies.Loss of the homeostatic protein BPIFA1, leads to exacerbation of otitis media severity in the Junbo mouse model.

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Genetic susceptibility to otitis media in childhood.

http://www.wikidata.org/entity/Q37976616

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Genetic susceptibility to otitis media in childhood.

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Genetic susceptibility to otitis media in childhood.

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Genetic susceptibility to otitis media in childhood.

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Genetic susceptibility to otitis media in childhood.

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Genetic susceptibility to otitis media in childhood.

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Genetic susceptibility to otitis media in childhood.

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The Laryngoscope

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Genetic susceptibility to otitis media in childhood

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Jenefer M Blackwell

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Sarra E Jamieson

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Association of the FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family Study

Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

Significant linkage at chromosome 19q for otitis media with effusion and/or recurrent otitis media (COME/ROM).

Evaluation of 15 functional candidate genes for association with chronic otitis media with effusion and/or recurrent otitis media (COME/ROM).

Chronic and recurrent otitis media: a genome scan for susceptibility loci.

Association of surfactant protein A polymorphisms with otitis media in infants at risk for asthma.

Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions.

Association of CD14 promoter polymorphism with otitis media and pneumococcal vaccine responses.

Acute otitis media severity: association with cytokine gene polymorphisms and other risk factors.

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665-675

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scholarly article

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10.1002/LARY.22506

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3

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122

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2012-01-17T00:00:00Z

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