Regulatory polymorphisms underlying complex disease traits.
about
The human Major Histocompatibility Complex as a paradigm in genomics researchDNA methylation and histone H3-K9 modifications contribute to MUC17 expressionCommon genetic variants account for differences in gene expression among ethnic groupsPolymiRTS Database: linking polymorphisms in microRNA target sites with complex traitsReverse transcriptional profiling: non-correspondence of transcript level variation and proximal promoter polymorphismA pilot study of host genetic variants associated with influenza-associated deaths among children and young adultsThe maternal ITPK1 gene polymorphism is associated with neural tube defects in a high-risk Chinese populationAcyl coenzyme A synthetase long-chain 1 (ACSL1) gene polymorphism (rs6552828) and elite endurance athletic status: a replication studyNeural mechanisms underlying stress resilience in Ahi1 knockout mice: relevance to neuropsychiatric disordersPopulation genomics of human gene expressionAlterations in the expression of a neurodevelopmental gene exert long-lasting effects on cognitive-emotional phenotypes and functional brain networks: translational evidence from the stress-resilient Ahi1 knockout mouse.Cis-regulatory variations: a study of SNPs around genes showing cis-linkage in segregating mouse populations.High-resolution mapping of expression-QTLs yields insight into human gene regulation.A common variant associated with dyslexia reduces expression of the KIAA0319 geneEvolutionary processes acting on candidate cis-regulatory regions in humans inferred from patterns of polymorphism and divergenceAssociation of a functional microsatellite within intron 1 of the BMP5 gene with susceptibility to osteoarthritis.Modeling expression quantitative trait loci in data combining ethnic populations.The genetics and epigenetics of autoimmune diseases.A functional SNP in the regulatory region of the decay-accelerating factor gene associates with extraocular muscle pareses in myasthenia gravis.Computational identification of gene-social environment interaction at the human IL6 locus.Genome-wide association studies: progress and potential for drug discovery and development.Identifying consensus disease pathways in Parkinson's disease using an integrative systems biology approach.A functional mutation at position -155 in porcine APOE promoter affects gene expression.Germ-line variation at a functional p53 binding site increases susceptibility to breast cancer development.Ranking insertion, deletion and nonsense mutations based on their effect on genetic informationEffects of genetic variations on microRNA: target interactionsPost-GWAS functional characterization of susceptibility variants for chronic lymphocytic leukemia.RNA-Seq alignment to individualized genomes improves transcript abundance estimates in multiparent populations.Single nucleotide polymorphisms in IL1B and the risk of acute coronary syndrome: a Danish case-cohort study.Design and evaluation of a panel of single-nucleotide polymorphisms in microRNA genomic regions for association studies in human disease.Association between single nucleotide polymorphisms in ERCC4 and risk of squamous cell carcinoma of the head and neckPTK2 rs7460 and rs7843014 polymorphisms and exceptional longevity: a functional replication study.Natural variation, functional pleiotropy and transcriptional contexts of odorant binding protein genes in Drosophila melanogaster.The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts.Association of polymorphism in microRNA 604 with susceptibility to persistent hepatitis B virus infection and development of hepatocellular carcinomaFNDC5 (irisin) gene and exceptional longevity: a functional replication study with rs16835198 and rs726344 SNPs.Functional genomics of serotonin receptor 2A (HTR2A): interaction of polymorphism, methylation, expression and disease association.Ultra-rare mutation in long-range enhancer predisposes to thyroid carcinoma with high penetranceFirst evidence for an association of a functional variant in the microRNA-510 target site of the serotonin receptor-type 3E gene with diarrhea predominant irritable bowel syndrome.Polymorphisms in predicted miRNA binding sites and osteoporosis.
P2860
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P2860
Regulatory polymorphisms underlying complex disease traits.
description
2004 nî lūn-bûn
@nan
2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Regulatory polymorphisms underlying complex disease traits.
@ast
Regulatory polymorphisms underlying complex disease traits.
@en
type
label
Regulatory polymorphisms underlying complex disease traits.
@ast
Regulatory polymorphisms underlying complex disease traits.
@en
prefLabel
Regulatory polymorphisms underlying complex disease traits.
@ast
Regulatory polymorphisms underlying complex disease traits.
@en
P2860
P1476
Regulatory polymorphisms underlying complex disease traits.
@en
P2860
P2888
P304
P356
10.1007/S00109-004-0603-7
P577
2004-12-09T00:00:00Z