Abundant contribution of short tandem repeats to gene expression variation in humans. - Wikidata - thesis-toulmin - TriplyDB

Abundant contribution of short tandem repeats to gene expression variation in humans.

Abundant contribution of short tandem repeats to gene expression variation in humans.

http://www.wikidata.org/entity/Q34504259

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Lineage-specific genomics: Frequent birth and death in the human genome: The human genome contains many lineage-specific elements created by both sequence and functional turnover PISMA: A Visual Representation of Motif Distribution in DNA Sequences.Characterization of porcine simple sequence repeat variation on a population scale with genome resequencing data.An accurate and efficient method for large-scale SSR genotyping and applications.Genome-wide profiling of heritable and de novo STR variations.Population-Scale Sequencing Data Enable Precise Estimates of Y-STR Mutation Rates Direct Identification of Hundreds of Expression-Modulating Variants using a Multiplexed Reporter Assay.Genetic polymorphism of heme oxygenase 1 promoter in the occurrence and severity of chronic obstructive pulmonary disease: a meta-analysis An improved genome assembly uncovers prolific tandem repeats in Atlantic cod Microsatellite polymorphisms associated with human behavioural and psychological phenotypes including a gene-environment interaction Population and clinical genetics of human transposable elements in the (post) genomic era.Differences of Variable Number Tandem Repeats in XRCC5 Promoter Are Associated with Increased or Decreased Risk of Breast Cancer in BRCA Gene Mutation Carriers Indels, structural variation, and recombination drive genomic diversity in Plasmodium falciparum.Deep resequencing of CFTR in 762 F508del homozygotes reveals clusters of non-coding variants associated with cystic fibrosis disease traits.The mechanism of transactivation regulation due to polymorphic short tandem repeats (STRs) using IGF1 promoter as a model.Systematic Profiling of Short Tandem Repeats in the Cattle Genome.Transcriptome-Derived Tetranucleotide Microsatellites and Their Associated Genes from the Giant Panda (Ailuropoda melanoleuca).The human RIT2 core promoter short tandem repeat predominant allele is species-specific in length: a selective advantage for human evolution?Structural variants in SNCA gene and the implication to synucleinopathies.Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.popSTR: population-scale detection of STR variants.Enabling Privacy-Preserving GWASs in Heterogeneous Human Populations.α-synuclein genetic variability: A biomarker for dementia in Parkinson disease.Genome-wide DNA methylation analysis of senescence in repetitively infected memory CTLs DNA methylation analysis of repetitively infected memory CTLs.Interpreting Gene Expression Effects of Disease-Associated Variants: A Lesson from SNCA rs356168.Functional Mechanisms of Microsatellite DNA in Eukaryotic Genomes.STRScan: targeted profiling of short tandem repeats in whole-genome sequencing data.The impact of structural variation on human gene expression.The SSV Evaluation System: A Tool to Prioritize Short Structural Variants for Studies of Possible Regulatory and Causal Variants Tandem repeat variation near the HIC1 (hypermethylated in cancer 1) promoter predicts outcome of oxaliplatin-based chemotherapy in patients with metastatic colorectal cancer.Interpreting short tandem repeat variations in humans using mutational constraint.Allelic Expression Imbalance in the Human Retinal Transcriptome and Potential Impact on Inherited Retinal Diseases.A microsatellite repeat in PCA3 long non-coding RNA is associated with prostate cancer risk and aggressiveness.The effects of transcription and recombination on mutational dynamics of short tandem repeats.Obligatory and facilitative allelic variation in the DNA methylome within common disease-associated loci.Evolutionary Origin of OwlRep, a Megasatellite DNA Associated with Adaptation of Owl Monkeys to Nocturnal Lifestyle.Profiling of Short-Tandem-Repeat Disease Alleles in 12,632 Human Whole Genomes.Synthetic transcription elongation factors license transcription across repressive chromatin.Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31.The central role of DNA damage and repair in CAG repeat diseases.

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Abundant contribution of short tandem repeats to gene expression variation in humans.

http://www.wikidata.org/entity/Q34504259

description

2015 nî lūn-bûn

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2015 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2015 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Abundant contribution of short tandem repeats to gene expression variation in humans.

@ast

Abundant contribution of short tandem repeats to gene expression variation in humans.

@en

Abundant contribution of short tandem repeats to gene expression variation in humans.

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type

label

Abundant contribution of short tandem repeats to gene expression variation in humans.

@ast

Abundant contribution of short tandem repeats to gene expression variation in humans.

@en

Abundant contribution of short tandem repeats to gene expression variation in humans.

@nl

prefLabel

Abundant contribution of short tandem repeats to gene expression variation in humans.

@ast

Abundant contribution of short tandem repeats to gene expression variation in humans.

@en

Abundant contribution of short tandem repeats to gene expression variation in humans.

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Nature Genetics

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Abundant contribution of short tandem repeats to gene expression variation in humans.

@en

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Alkes L Price

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Andrew J Sharp

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Audrey Guilmatre

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Barak Markus

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Haoyang Zeng

http://www.w3.org/2001/XMLSchema#string

Jonathan K Pritchard

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Melissa Gymrek

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Stoyan Georgiev

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Thomas Willems

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Yaniv Erlich

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Chimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatellite

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22-29

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scholarly article

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10.1038/NG.3461

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1

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48

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Mark Joseph Daly

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2015-12-07T00:00:00Z

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26642241

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4909355

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