Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional - Wikidata - wikimedia - TriplyDB

Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

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Reprogramming towards pluripotency requires AID-dependent DNA demethylation Molecular roadblocks for cellular reprogramming Phenotypic changes in growth-arrested T cell hybrids: a possible avenue to produce functional T cell hybridoma Fusion between Intestinal epithelial cells and macrophages in a cancer context results in nuclear reprogramming Mesenchymal stem cells generate distinct functional hybrids in vitro via cell fusion or entosis.Nuclear reprogramming to a pluripotent state by three approaches.Targeted cell fusion facilitates stable heterokaryon generation in vitro and in vivo.Cell fusion reprogramming leads to a specific hepatic expression pattern during mouse bone marrow derived hepatocyte formation in vivo.Zfp296 is a novel, pluripotent-specific reprogramming factor In-vivo fusion of human cancer and hamster stromal cells permanently transduces and transcribes human DNA.DNA methylation and cellular reprogramming Incomplete reprogramming after fusion of human multipotent stromal cells and bronchial epithelial cells Electrofusion of mesenchymal stem cells and islet cells for diabetes therapy: a rat model Using heterokaryons to understand pluripotency and reprogramming Cell divisions are not essential for the direct conversion of fibroblasts into neuronal cells.Intra-hematopoietic cell fusion as a source of somatic variation in the hematopoietic system.The problem of colliding networks and its relation to cell fusion and cancer Viral-mediated fusion of mesenchymal stem cells with cells of the infarcted heart hinders healing via decreased vascularization and immune modulation Single-cell RNA-seq reveals activation of unique gene groups as a consequence of stem cell-parenchymal cell fusion.AID hits the jackpot when missing the target.Efficiencies and mechanisms of nuclear reprogramming Systematic mapping of occluded genes by cell fusion reveals prevalence and stability of cis-mediated silencing in somatic cells.β-MSCs: successful fusion of MSCs with β-cells results in a β-cell like phenotype.Maintaining differentiated cellular identity.The shock of being united and symphiliosis. Another lesson from plants?

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Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

http://www.wikidata.org/entity/Q24658365

description

2009 nî lūn-bûn

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2009 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2009 թվականի մայիսին հրատարակված գիտական հոդված

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2009年の論文

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年學術文章

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name

Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

@ast

Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

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Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

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type

label

Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

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Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

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Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

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prefLabel

Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

@ast

Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

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Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

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Nuclear reprogramming in heterokaryons is rapid, extensive, and bidirectional

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Adam Palermo

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

Helen M Blau

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

Jason Pomerantz

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

Nidhi Bhutani

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

Ozan Alkan

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Regis Doyonnas

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P2860

Active tissue-specific DNA demethylation conferred by somatic cell nuclei in stable heterokaryons

Cross-species hybridisation of human and bovine orthologous genes on high density cDNA microarrays

In vitro identification and in silico utilization of interspecies sequence similarities using GeneChip technology

Cell-type-specific transcriptomics in chimeric models using transcriptome-based masks

Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors

Generation of germline-competent induced pluripotent stem cells

Nuclear reprogramming of somatic cells after fusion with human embryonic stem cells

Reverse transcriptase template switching: a SMART approach for full-length cDNA library construction.

Activation of muscle-specific genes in pigment, nerve, fat, liver, and fibroblast cell lines by forced expression of MyoD.

Differentiation requires continuous active control.

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1431-40

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scholarly article

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2617898

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10.1096/FJ.08-122903

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5

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23

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19141533

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2669427

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