Human genetic variation recognizes functional elements in noncoding sequence.
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RNA editing of nuclear transcripts in Arabidopsis thalianaMining Functional Elements in Messenger RNAs: Overview, Challenges, and PerspectivesThe two stem cell microRNA gene clusters C19MC and miR-371-3 are activated by specific chromosomal rearrangements in a subgroup of thyroid adenomasPredicting functionally important SNP classes based on negative selection.Weak negative and positive selection and the drift load at splice sites.Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus.Late onset sporadic dilated cardiomyopathy caused by a cardiac troponin T mutation.Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypesFrom expression pattern to genetic association in asthma and asthma-related phenotypes.Context-dependent robustness to 5' splice site polymorphisms in human populations.Sequence variants in COL4A1 and COL4A2 genes in Ecuadorian families with keratoconusHPA axis genetic variation, cortisol and psychosis in major depressionSLC6A4 methylation modifies the effect of the number of traumatic events on risk for posttraumatic stress disorder.A Dual Model for Prioritizing Cancer Mutations in the Non-coding Genome Based on Germline and Somatic EventsMutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathyEnhancer-promoter interactions are encoded by complex genomic signatures on looping chromatin.Direct Transcriptional Consequences of Somatic Mutation in Breast CancerAssociation of OPRD1 polymorphisms with heroin dependence in a large case-control series.Global assessment of genetic variation influencing response to retinoid chemoprevention in head and neck cancer patients.Genomic strategies to understand causes of keratoconus.Genetic variations and alternative splicing: the Glioma associated oncogene 1, GLI1.The impact of cis-acting polymorphisms on the human phenotype.Prioritizing single-nucleotide polymorphisms and variants associated with clinical mastitis.Genomic translational research: Paving the way to individualized cardiac functional analyses and personalized cardiology.Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes.Haplotype analysis of XRCC2 gene polymorphisms and association with increased risk of head and neck cancer.Evidence of abundant purifying selection in humans for recently acquired regulatory functions.Analysis of Genes with Alternatively Spliced Transcripts in the Leaf, Root, Panicle and Seed of Rice Using a Long Oligomer Microarray and RNA-Seq.Effects of hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 polymorphisms on fat androstenone level and gene expression in Duroc pigs.Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification.Epigenetic modifications in KDM lysine demethylases associate with survival of early-stage NSCLC.
P2860
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P2860
Human genetic variation recognizes functional elements in noncoding sequence.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
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
2009年论文
@zh
2009年论文
@zh-cn
name
Human genetic variation recognizes functional elements in noncoding sequence.
@en
Human genetic variation recognizes functional elements in noncoding sequence.
@nl
type
label
Human genetic variation recognizes functional elements in noncoding sequence.
@en
Human genetic variation recognizes functional elements in noncoding sequence.
@nl
prefLabel
Human genetic variation recognizes functional elements in noncoding sequence.
@en
Human genetic variation recognizes functional elements in noncoding sequence.
@nl
P2093
P2860
P356
P1433
P1476
Human genetic variation recognizes functional elements in noncoding sequence.
@en
P2093
David Lomelin
Eric Jorgenson
Neil Risch
P2860
P304
P356
10.1101/GR.094151.109
P577
2009-12-23T00:00:00Z