Highly efficient transient gene expression and gene targeting in primate embryonic stem cells with helper-dependent adenoviral vectors. - Wikidata - awgldk - TriplyDB

Highly efficient transient gene expression and gene targeting in primate embryonic stem cells with helper-dependent adenoviral vectors.

Highly efficient transient gene expression and gene targeting in primate embryonic stem cells with helper-dependent adenoviral vectors.

http://www.wikidata.org/entity/Q36893512

about

Progressive degeneration of human neural stem cells caused by pathogenic LRRK2 Human induced pluripotent stem cells for monogenic disease modelling and therapy Hematopoietic stem cell engineering at a crossroads Quantitative comparison of constitutive promoters in human ES cells Toward pluripotency by reprogramming: mechanisms and application Efficient targeting of expressed and silent genes in human ESCs and iPSCs using zinc-finger nucleases The use of induced pluripotent stem cells to reveal pathogenic gene mutations and explore treatments for retinitis pigmentosa.Efficient integration of transgenes into a defined locus in human embryonic stem cells.An evolved adeno-associated viral variant enhances gene delivery and gene targeting in neural stem cells Engineering of human pluripotent stem cells by AAV-mediated gene targeting.Gene correction in human embryonic and induced pluripotent stem cells: promises and challenges ahead.Targeting of the human coagulation factor IX gene at rDNA locus of human embryonic stem cells.Human pluripotent stem cells: an emerging model in developmental biology.Simple monitoring of gene targeting efficiency in human somatic cell lines using the PIGA gene.Present state and future perspectives of using pluripotent stem cells in toxicology research VCre/VloxP and SCre/SloxP: new site-specific recombination systems for genome engineering.Modelling Fanconi anemia pathogenesis and therapeutics using integration-free patient-derived iPSCs Induced pluripotent stem cells: applications in regenerative medicine, disease modeling, and drug discovery.Modeling human neurological disorders with induced pluripotent stem cells.Site-specific gene correction of a point mutation in human iPS cells derived from an adult patient with sickle cell disease.Efficient and accurate homologous recombination in hESCs and hiPSCs using helper-dependent adenoviral vectors.Targeted gene correction of laminopathy-associated LMNA mutations in patient-specific iPSCs Chromatin structure of two genomic sites for targeted transgene integration in induced pluripotent stem cells and hematopoietic stem cells.Progress and prospects in stem cell therapy.Find and replace: editing human genome in pluripotent stem cells Gene targeting of a disease-related gene in human induced pluripotent stem and embryonic stem cells.A targeted neuroglial reporter line generated by homologous recombination in human embryonic stem cells.Homology Requirements for Efficient, Footprintless Gene Editing at the CFTR Locus in Human iPSCs with Helper-dependent Adenoviral Vectors.Helper-Dependent Adenoviral Vectors.A cut above the rest: targeted genome editing technologies in human pluripotent stem cells.Disease correction the iPSC way: advances in iPSC-based therapy.Genetic strategies for the treatment of sickle cell anaemia.Concise review: Human cell engineering: cellular reprogramming and genome editing.Genome editing of human pluripotent stem cells to generate human cellular disease models.Genetic correction using engineered nucleases for gene therapy applications.Helper-dependent adenoviral vectors for liver-directed gene therapy of primary hyperoxaluria type 1.Viral Vector-Based Innovative Approaches to Directly Abolishing Tumorigenic Pluripotent Stem Cells for Safer Regenerative Medicine.Genome engineering tools for building cellular models of disease.BTK gene targeting by homologous recombination using a helper-dependent adenovirus/adeno-associated virus hybrid vector.Generation of mouse induced pluripotent stem cells by protein transduction.

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P2860

Highly efficient transient gene expression and gene targeting in primate embryonic stem cells with helper-dependent adenoviral vectors.

http://www.wikidata.org/entity/Q36893512

description

2008 nî lūn-bûn

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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2008年论文

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2008年论文

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name

Highly efficient transient gen ...... -dependent adenoviral vectors.

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Highly efficient transient gen ...... -dependent adenoviral vectors.

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Highly efficient transient gen ...... -dependent adenoviral vectors.

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PNAS.0806976105

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Highly efficient transient gen ...... -dependent adenoviral vectors.

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P2093

Eihachiro Kawase

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Emi Aizawa

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Hirofumi Suemori

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Kaoru Mitsui

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Keiichiro Suzuki

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Kohnosuke Mitani

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Kouichi Hasegawa

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Norio Nakatsuji

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Toshiyuki Yamagishi

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Yoshihiko Shimizu

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P2860

Gene targeting of mutant COL1A2 alleles in mesenchymal stem cells from individuals with osteogenesis imperfecta

Gene targeting in stem cells from individuals with osteogenesis imperfecta

Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells

Induced pluripotent stem cell lines derived from human somatic cells

Establishment in culture of pluripotential cells from mouse embryos

One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products

Induction of pluripotent stem cells from adult human fibroblasts by defined factors

Embryonic stem cell lines derived from human blastocysts

A variant of yellow fluorescent protein with fast and efficient maturation for cell-biological applications

Reprogramming of human somatic cells to pluripotency with defined factors

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13781-13786

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10.1073/PNAS.0806976105

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37

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105

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23235558

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18768795

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2544531

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