Genetic background drives transcriptional variation in human induced pluripotent stem cells.
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Genome-edited human stem cell-derived beta cells: a powerful tool for drilling down on type 2 diabetes GWAS biologyConcise review: making and using clinically compliant pluripotent stem cell linesModeling chemotherapeutic neurotoxicity with human induced pluripotent stem cell-derived neuronal cellsUtilizing induced pluripotent stem cells (iPSCs) to understand the actions of estrogens in human neuronsPresent and future challenges of induced pluripotent stem cellsModeling Human Bone Marrow Failure Syndromes Using Pluripotent Stem Cells and Genome EngineeringIntegrated Genomic Analysis of Diverse Induced Pluripotent Stem Cells from the Progenitor Cell Biology ConsortiumA Novel Protocol for Directed Differentiation of C9orf72-Associated Human Induced Pluripotent Stem Cells Into Contractile Skeletal Myotubes.Transcriptome Profiling of Patient-Specific Human iPSC-Cardiomyocytes Predicts Individual Drug Safety and Efficacy Responses In Vitro.iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types.Understanding RNA modifications: the promises and technological bottlenecks of the 'epitranscriptome'.Taming Human Genetic Variability: Transcriptomic Meta-Analysis Guides the Experimental Design and Interpretation of iPSC-Based Disease Modeling.A comparison of genetically matched cell lines reveals the equivalence of human iPSCs and ESCs.An integrative analysis of reprogramming in human isogenic system identified a clone selection criterion.Induced Pluripotent Stem Cells Meet Genome EditingTranscriptomic analysis across nasal, temporal, and macular regions of human neural retina and RPE/choroid by RNA-SeqHuman induced hepatic lineage-oriented stem cells: autonomous specification of human iPS cells toward hepatocyte-like cells without any exogenous differentiation factors.Reprogramming LCLs to iPSCs Results in Recovery of Donor-Specific Gene Expression SignatureAdvances in reprogramming-based study of neurologic disordersExpression quantitative trait locus analysis for translational medicine.SOX2 and SOX2-MYC Reprogramming Process of Fibroblasts to the Neural Stem Cells Compromised by Senescence.Genetic Variability Overrides the Impact of Parental Cell Type and Determines iPSC Differentiation Potential.Transcriptional profiling of macrophages derived from monocytes and iPS cells identifies a conserved response to LPS and novel alternative transcriptionGenetic Variation, Not Cell Type of Origin, Underlies the Majority of Identifiable Regulatory Differences in iPSCsStrong Components of Epigenetic Memory in Cultured Human Fibroblasts Related to Site of Origin and Donor AgeMutational History of a Human Cell Lineage from Somatic to Induced Pluripotent Stem CellsvariancePartition: interpreting drivers of variation in complex gene expression studies.Analysis of Transcriptional Variability in a Large Human iPSC Library Reveals Genetic and Non-genetic Determinants of Heterogeneity.A high-content platform to characterise human induced pluripotent stem cell linesEffects of cellular origin on differentiation of human induced pluripotent stem cell-derived endothelial cells.Insights into islet development and biology through characterization of a human iPSC-derived endocrine pancreas model.Modeling psychiatric disorders: from genomic findings to cellular phenotypesReprogramming Methods Do Not Affect Gene Expression Profile of Human Induced Pluripotent Stem Cells.Proteasome impairment in neural cells derived from HMSN-P patient iPSCs.Making it stick: chasing the optimal stem cells for cardiac regeneration.Evaluation of inter-batch differences in stem-cell derived neurons.A developmental framework for induced pluripotency.Modeling Alzheimer's disease with human induced pluripotent stem (iPS) cells.Editing the genome of hiPSC with CRISPR/Cas9: disease models.The mitochondrial protein CHCHD2 primes the differentiation potential of human induced pluripotent stem cells to neuroectodermal lineages.
P2860
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P2860
Genetic background drives transcriptional variation in human induced pluripotent stem cells.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Genetic background drives tran ...... nduced pluripotent stem cells.
@ast
Genetic background drives tran ...... nduced pluripotent stem cells.
@en
type
label
Genetic background drives tran ...... nduced pluripotent stem cells.
@ast
Genetic background drives tran ...... nduced pluripotent stem cells.
@en
prefLabel
Genetic background drives tran ...... nduced pluripotent stem cells.
@ast
Genetic background drives tran ...... nduced pluripotent stem cells.
@en
P2093
P2860
P50
P1433
P1476
Genetic background drives tran ...... nduced pluripotent stem cells.
@en
P2093
Foad Rouhani
Miguel Cardoso de Brito
Natsuhiko Kumasaka
P2860
P304
P356
10.1371/JOURNAL.PGEN.1004432
P577
2014-06-05T00:00:00Z