Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways.
about
Current concepts in age-related hearing loss: epidemiology and mechanistic pathways.Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair.The Role of the Transcription Factor Foxo3 in Hearing Maintenance: Informed Speculation on a New Player in the CochleaComparison of In Vivo Gene Expression Profiling of RPE/Choroid following Intravitreal Injection of Dexamethasone and Triamcinolone AcetonideGenetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise.Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumptionSevere hearing loss and outer hair cell death in homozygous Foxo3 knockout mice after moderate noise exposure.A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health RecordsAssociation of SNPs in LCP1 and CTIF with hearing in 11 year old children: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort and the G-EAR consortiumEstrogen-related receptor gamma and hearing function: evidence of a role in humans and mice.Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss.Age- and sex-related variations in platelet count in Italy: a proposal of reference ranges based on 40987 subjects' data.Salt-inducible kinase 3, SIK3, is a new gene associated with hearing.Progress and prospects in human genetic research into age-related hearing impairment.Genetic insights into the functional elements of language.Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.Association analysis of bitter receptor genes in five isolated populations identifies a significant correlation between TAS2R43 variants and coffee liking.Evidence that homozygous PTPRD gene microdeletion causes trigonocephaly, hearing loss, and intellectual disability.Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking.Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss.Noise-induced hearing loss: Neuropathic pain via Ntrk1 signalingExpression and replication studies to identify new candidate genes involved in normal hearing function.Age related hearing loss and level of education: An epidemiological study on a large cohort of isolated populationsLifestyle and normal hearing function in Italy and Central Asia: The potential role of coffeeInfluence of age, sex and ethnicity on platelet count in five Italian geographic isolates: mild thrombocytopenia may be physiologicalCx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway
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P2860
Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Hearing function and threshold ...... ntifies new loci and pathways.
@en
Hearing function and threshold ...... ntifies new loci and pathways.
@nl
type
label
Hearing function and threshold ...... ntifies new loci and pathways.
@en
Hearing function and threshold ...... ntifies new loci and pathways.
@nl
prefLabel
Hearing function and threshold ...... ntifies new loci and pathways.
@en
Hearing function and threshold ...... ntifies new loci and pathways.
@nl
P2093
P50
P356
P1476
Hearing function and threshold ...... ntifies new loci and pathways.
@en
P2093
Alan F Wright
Harry Campbell
Laura Portas
Mario Pirastu
Nicholas D Hastie
Paolo Gasparini
Rossella Sorice
P304
P356
10.1136/JMG.2010.088310
P407
P50
P577
2011-04-14T00:00:00Z