A robust approach to identifying tissue-specific gene expression regulatory variants using personalized human induced pluripotent stem cells.
about
P1343
RNA-guided human genome engineering via Cas9New technologies for integrating genomic, environmental and trait dataA public resource facilitating clinical use of genomesThe genetic and mechanistic basis for variation in gene regulationMeta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fractureSomatic coding mutations in human induced pluripotent stem cellsAn integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.Fluorescent in situ sequencing (FISSEQ) of RNA for gene expression profiling in intact cells and tissues.Genetic validation of whole-transcriptome sequencing for mapping expression affected by cis-regulatory variation.Global analysis of the impact of environmental perturbation on cis-regulation of gene expressionAllele-specific methylation is prevalent and is contributed by CpG-SNPs in the human genomeNext-generation DNA sequencing-based assay for measuring allelic expression imbalance (AEI) of candidate neuropsychiatric disorder genes in human brainHighly multiplexed subcellular RNA sequencing in situ.Rapid neurogenesis through transcriptional activation in human stem cells.Genetic analysis identifies DDR2 as a novel gene affecting bone mineral density and osteoporotic fractures in Chinese population.Multi-kilobase homozygous targeted gene replacement in human induced pluripotent stem cells.Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndrome.Personal genomes in progress: from the human genome project to the personal genome projectTranscriptome Signature and Regulation in Human Somatic Cell Reprogramming.Quantitative approaches for investigating the spatial context of gene expression.Functional Maturation of Human Stem Cell-Derived Neurons in Long-Term CulturesLarge-scale identification of sequence variants influencing human transcription factor occupancy in vivoCrispr-mediated Gene Targeting of Human Induced Pluripotent Stem CellsErasure and reestablishment of random allelic expression imbalance after epigenetic reprogrammingTranscriptome study of differential expression in schizophrenia.Mediators and dynamics of DNA methylation.Investigating monogenic and complex diseases with pluripotent stem cells.Integrative genomics and transcriptomics analysis of human embryonic and induced pluripotent stem cells.Identification of three new cis-regulatory IRF5 polymorphisms: in vitro studies.Therapeutic genome engineering via CRISPR-Cas systems.IDP-ASE: haplotyping and quantifying allele-specific expression at the gene and gene isoform level by hybrid sequencing.Stochastic choice of allelic expression in human neural stem cells.Genome editing in human stem cells.
P2860
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P2860
A robust approach to identifying tissue-specific gene expression regulatory variants using personalized human induced pluripotent stem cells.
description
2009 nî lūn-bûn
@nan
2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
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
name
A robust approach to identifyi ...... nduced pluripotent stem cells.
@ast
A robust approach to identifyi ...... nduced pluripotent stem cells.
@en
type
label
A robust approach to identifyi ...... nduced pluripotent stem cells.
@ast
A robust approach to identifyi ...... nduced pluripotent stem cells.
@en
altLabel
A robust approach to identifyi ...... induced pluripotent stem cells
@en
prefLabel
A robust approach to identifyi ...... nduced pluripotent stem cells.
@ast
A robust approach to identifyi ...... nduced pluripotent stem cells.
@en
P2093
P2860
P1433
P1476
A robust approach to identifyi ...... nduced pluripotent stem cells.
@en
P2093
P2860
P304
P356
10.1371/JOURNAL.PGEN.1000718
P407
P4510
P577
2009-11-13T00:00:00Z