Systematic identification of barriers to human iPSC generation.
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ScreenBEAM: a novel meta-analysis algorithm for functional genomics screens via Bayesian hierarchical modelingThe histone chaperone CAF-1 safeguards somatic cell identity.YAP Induces Human Naive PluripotencyMicroRNA-mediated regulation of extracellular matrix formation modulates somatic cell reprogrammingHiTSelect: a comprehensive tool for high-complexity-pooled screen analysisCollaborative rewiring of the pluripotency network by chromatin and signalling modulating pathwaysMyc and SAGA rewire an alternative splicing network during early somatic cell reprogramming.Advances in reprogramming-based study of neurologic disordersDerivation of Patient Specific Pluripotent Stem Cells Using Clinically Discarded Cumulus CellsAnalysis for Carom complex, signaling and function by database mining.A Serial shRNA Screen for Roadblocks to Reprogramming Identifies the Protein Modifier SUMO2.Optimized Approaches for Generation of Integration-free iPSCs from Human Urine-Derived Cells with Small Molecules and Autologous FeederDirect Cardiac Cellular Reprogramming for Cardiac Regeneration.The SIN3A/HDAC Corepressor Complex Functionally Cooperates with NANOG to Promote Pluripotency.Reprogramming barriers and enhancers: strategies to enhance the efficiency and kinetics of induced pluripotencyBiological Networks Governing the Acquisition, Maintenance, and Dissolution of Pluripotency: Insights from Functional Genomics Approaches.A critical role for p38MAPK signalling pathway during reprogramming of human fibroblasts to iPSCs.Ubiquitin-Dependent Regulation of Stem Cell Biology.The EMT spectrum and therapeutic opportunities.Emerging roles of the histone chaperone CAF-1 in cellular plasticity.A Strong Contractile Actin Fence and Large Adhesions Direct Human Pluripotent Colony Morphology and Adhesion.p73 is required for appropriate BMP-induced mesenchymal-to-epithelial transition during somatic cell reprogramming.Replacing reprogramming factors with antibodies selected from combinatorial antibody libraries.Combining membrane proteomics and computational three-way pathway analysis revealed signalling pathways preferentially regulated in human iPSCs and human ESCs.Dual repression of endocytic players by ESCC microRNAs and the Polycomb complex regulates mouse embryonic stem cell pluripotency.Genomic and Proteomic Resolution of Heterochromatin and Its Restriction of Alternate Fate Genes.Coupling shRNA screens with single-cell RNA-seq identifies a dual role for mTOR in reprogramming-induced senescence.Establishment and Use of Mouse Haploid ES Cells.The Transcriptionally Permissive Chromatin State of Embryonic Stem Cells Is Acutely Tuned to Translational Output.Critical roles of Cyclin D1 in mouse embryonic fibroblast cell reprogramming.Chronophin regulates active vitamin B6 levels and transcriptomic features of glioblastoma cell lines cultured under non-adherent, serum-free conditions.FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells
P2860
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P2860
Systematic identification of barriers to human iPSC generation.
description
2014 nî lūn-bûn
@nan
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
2014年论文
@zh
2014年论文
@zh-cn
name
Systematic identification of barriers to human iPSC generation.
@en
type
label
Systematic identification of barriers to human iPSC generation.
@en
prefLabel
Systematic identification of barriers to human iPSC generation.
@en
P2093
P2860
P50
P1433
P1476
Systematic identification of barriers to human iPSC generation.
@en
P2093
Aaron Diaz
Emily M LeProust
Laure Blouin
Miguel Ramalho-Santos
Priscilia Tanbun
P2860
P304
P356
10.1016/J.CELL.2014.05.040
P407
P577
2014-07-01T00:00:00Z