Lentiviral vector design and imaging approaches to visualize the early stages of cellular reprogramming.
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Nanopatterned Human iPSC-Based Model of a Dystrophin-Null Cardiomyopathic PhenotypeGlycomic Characterization of Induced Pluripotent Stem Cells Derived from a Patient Suffering from Phosphomannomutase 2 Congenital Disorder of Glycosylation (PMM2-CDG)Nrf2, a regulator of the proteasome, controls self-renewal and pluripotency in human embryonic stem cellsPoly(A)-specific ribonuclease (PARN) mediates 3'-end maturation of the telomerase RNA componentDystrophin-deficient cardiomyocytes derived from human urine: new biologic reagents for drug discovery.Dynamic migration and cell-cell interactions of early reprogramming revealed by high-resolution time-lapse imaging.Modified lentiviral LTRs allow Flp recombinase-mediated cassette exchange and in vivo tracing of "factor-free" induced pluripotent stem cells.GAA Deficiency in Pompe Disease Is Alleviated by Exon Inclusion in iPSC-Derived Skeletal Muscle Cells.Enhancement of β-Globin Gene Expression in Thalassemic IVS2-654 Induced Pluripotent Stem Cell-Derived Erythroid Cells by Modified U7 snRNA.Differential role of nonhomologous end joining factors in the generation, DNA damage response, and myeloid differentiation of human induced pluripotent stem cells.miRNA screening reveals a new miRNA family stimulating iPS cell generation via regulation of Meox2.High-risk human papillomavirus E6 protein promotes reprogramming of Fanconi anemia patient cells through repression of p53 but does not allow for sustained growth of induced pluripotent stem cells.Epigenetic characterization of the FMR1 promoter in induced pluripotent stem cells from human fibroblasts carrying an unmethylated full mutationA Comparative View on Human Somatic Cell Sources for iPSC GenerationInduction of pluripotent stem cells from a cynomolgus monkey using a polycistronic simian immunodeficiency virus-based vector, differentiation toward functional cardiomyocytes, and generation of stably expressing reporter lines.Erythroid differentiation of human induced pluripotent stem cells is independent of donor cell type of origin.Novel codon-optimized mini-intronic plasmid for efficient, inexpensive, and xeno-free induction of pluripotency.Stable X chromosome reactivation in female human induced pluripotent stem cellsFAS-based cell depletion facilitates the selective isolation of mouse induced pluripotent stem cellsRetroviral vectors: post entry events and genomic alterations.An in vivo model of human small intestine using pluripotent stem cellsProperties of neurons derived from induced pluripotent stem cells of Gaucher disease type 2 patient fibroblasts: potential role in neuropathology.Rescue of DNA-PK Signaling and T-Cell Differentiation by Targeted Genome Editing in a prkdc Deficient iPSC Disease Model.Mesenchymal Stem/Stromal Cells Derived from Induced Pluripotent Stem Cells Support CD34(pos) Hematopoietic Stem Cell Propagation and Suppress Inflammatory Reaction.Inhibition of CD26/DPP-IV enhances donor muscle cell engraftment and stimulates sustained donor cell proliferationReticular dysgenesis-associated AK2 protects hematopoietic stem and progenitor cell development from oxidative stress.Overcoming reprogramming resistance of Fanconi anemia cells.Pathogenesis of ELANE-mutant severe neutropenia revealed by induced pluripotent stem cellsTRIM32 modulates pluripotency entry and exit by directly regulating Oct4 stabilityOct4-induced oligodendrocyte progenitor cells enhance functional recovery in spinal cord injury modelOvercoming Pluripotent Stem Cell Dependence on the Repair of Endogenous DNA DamageA robust model of natural hepatitis C infection using hepatocyte-like cells derived from human induced pluripotent stem cells as a long-term hostSustained knockdown of a disease-causing gene in patient-specific induced pluripotent stem cells using lentiviral vector-based gene therapy.Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells.Molecular advances in reporter genes: the need to witness the function of stem cells in failing heart in vivo.Imaging of Induced Pluripotent Stem Cells: From Cellular Reprogramming to Transplantation.Concise review: managing genotoxicity in the therapeutic modification of stem cells.miRNAs involved in the generation, maintenance, and differentiation of pluripotent cells.The role of induced pluripotent stem cells in research and therapy of primary immunodeficiencies.
P2860
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P2860
Lentiviral vector design and imaging approaches to visualize the early stages of cellular reprogramming.
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Lentiviral vector design and i ...... ges of cellular reprogramming.
@ast
Lentiviral vector design and i ...... ges of cellular reprogramming.
@en
type
label
Lentiviral vector design and i ...... ges of cellular reprogramming.
@ast
Lentiviral vector design and i ...... ges of cellular reprogramming.
@en
prefLabel
Lentiviral vector design and i ...... ges of cellular reprogramming.
@ast
Lentiviral vector design and i ...... ges of cellular reprogramming.
@en
P2093
P2860
P50
P356
P1433
P1476
Lentiviral vector design and i ...... ages of cellular reprogramming
@en
P2093
Adam A Filipczyk
Axel Schambach
Christopher Baum
Eva Warlich
Johannes Kuehle
Melanie Galla
Tobias Maetzig
P2860
P304
P356
10.1038/MT.2010.314
P577
2011-02-01T00:00:00Z