A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis
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Adult rat bones maintain distinct regionalized expression of markers associated with their developmentMutations and altered expression of SERPINF1 in patients with familial otosclerosisCochlear otosclerosis.Estimates of array and pool-construction variance for planning efficient DNA-pooling genome wide association studiesRapid assessment of genetic ancestry in populations of unknown origin by genome-wide genotyping of pooled samples.Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.Comparative analysis of the transcriptome in tissues secreting purple and white nacre in the pearl mussel Hyriopsis cumingiiVitamin D receptor gene as a candidate gene for Parkinson disease.Complex-disease networks of trait-associated single-nucleotide polymorphisms (SNPs) unveiled by information theory.The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA.Differences in gene expression between the otic capsule and other bones.Detection of otosclerosis-specific measles virus receptor (cd46) protein isoforms.Effects of imatinib and nilotinib on the whole transcriptome of cultured murine osteoblastsThe rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian populationGWAS study using DNA pooling strategy identifies association of variant rs4910623 in OR52B4 gene with anti-VEGF treatment response in age-related macular degeneration.Corticosterone regulates the expression of neuropeptide Y and reelin in MLO-Y4 cells.Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signaling.Nonneuronal roles for the reelin signaling pathway.Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian population.Exclusion of TNFRSF11B as Candidate Gene for Otosclerosis in Campania Population.Involvement of T-cell receptor-beta alterations in the development of otosclerosis linked to OTSC2.Genetic association and altered gene expression of osteoprotegerin in otosclerosis patients.Genetic association and gene expression profiles of TGFB1 and the contribution of TGFB1 to otosclerosis susceptibility.Controversies in RELN/reelin expression in otosclerosis.Pooling-Based Genome-Wide Association Study Identifies Risk Loci in the Pathogenesis of Ovarian Endometrioma in Chinese Han Women.No evidence for disturbed COL1A1 and A2 expression in otosclerosis.Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population.Expression of bone morphogenetic protein 2, 4, 5, and 7 correlates with histological activity of otosclerotic foci
P2860
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P2860
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis
description
2009 nî lūn-bûn
@nan
2009 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մարտին հրատարակված գիտական հոդված
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2009年の論文
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2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
A genome-wide analysis identif ...... e associated with otosclerosis
@ast
A genome-wide analysis identif ...... e associated with otosclerosis
@en
A genome-wide analysis identif ...... e associated with otosclerosis
@nl
type
label
A genome-wide analysis identif ...... e associated with otosclerosis
@ast
A genome-wide analysis identif ...... e associated with otosclerosis
@en
A genome-wide analysis identif ...... e associated with otosclerosis
@nl
prefLabel
A genome-wide analysis identif ...... e associated with otosclerosis
@ast
A genome-wide analysis identif ...... e associated with otosclerosis
@en
A genome-wide analysis identif ...... e associated with otosclerosis
@nl
P2093
P2860
P50
P3181
P1476
A genome-wide analysis identif ...... e associated with otosclerosis
@en
P2093
Cor W R J Cremers
David W Craig
Erik Fransen
Erwin Offeciers
Ingeborg Dhooge
Jason J Corneveaux
Kathleen Vanderstraeten
Matthew J Huentelman
Megan Ealy
Melissa Thys
P2860
P304
P3181
P356
10.1016/J.AJHG.2009.01.023
P407
P577
2009-03-01T00:00:00Z