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

Proceedings of the National Academy of Sciences - PNAS, 2008-09, Vol.105 (37), p.13781-13786

2008

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An inhibitor of fibroblast growth factor receptor-1 (FGFR1) promotes late-stage terminal differentiation from NGN3+ pancreatic endocrine progenitors

Scientific reports, 2016-10, Vol.6 (1), p.35908-35908, Article 35908

2016

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The use of induced pluripotent stem cells to reveal pathogenic gene mutations and explore treatments for retinitis pigmentosa

Molecular brain, 2014-06, Vol.7 (1), p.45-45, Article 45

2014

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Dual usage of a stage-specific fluorescent reporter system based on a helper-dependent adenoviral vector to visualize osteogenic differentiation

Scientific reports, 2019-07, Vol.9 (1), p.9705-10, Article 9705

2019

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Novel human adenovirus strain, Bangladesh

Emerging infectious diseases, 2012-05, Vol.18 (5), p.846-848

2012

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Efficient and Accurate Homologous Recombination in hESCs and hiPSCs Using Helper-dependent Adenoviral Vectors

Molecular therapy, 2012-02, Vol.20 (2), p.424-431

2012

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Simple Derivation of Spinal Motor Neurons from ESCs/iPSCs Using Sendai Virus Vectors

Molecular therapy. Methods & clinical development, 2017-03, Vol.4 (C), p.115-125

2017

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Frequency and Stability of Chromosomal Integration of Adenovirus Vectors

Journal of Virology, 1999-07, Vol.73 (7), p.6141-6146

1999

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A New Hybrid System Capable of Efficient Lentiviral Vector Production and Stable Gene Transfer Mediated by a Single Helper-Dependent Adenoviral Vector

Journal of Virology, 2003-03, Vol.77 (5), p.2964-2971

2003

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Correction of Chromosomal Mutation and Random Integration in Embryonic Stem Cells with Helper-Dependent Adenoviral Vectors

Proceedings of the National Academy of Sciences - PNAS, 2005-09, Vol.102 (38), p.13628-13633

2005

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Helper-Dependent Adenoviral Vectors Efficiently Express Transgenes in Human Dendritic Cells but Still Stimulate Antiviral Immune Responses

The Journal of immunology (1950), 2002-10, Vol.169 (8), p.4651-4656

2002

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Convergence of Notch and β-catenin signaling induces arterial fate in vascular progenitors

The Journal of cell biology, 2010-04, Vol.189 (2), p.325-338

2010

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Gene Therapy of Erectile Dysfunction in the Rat with Penile Neuronal Nitric Oxide Synthase

Biology of reproduction, 2002-07, Vol.67 (1), p.20-28

2002

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A Novel, Helper-Dependent, Adenovirus–Retrovirus Hybrid Vector: Stable Transduction by a Two-Stage Mechanism

Molecular therapy, 2002-05, Vol.5 (5), p.599-608

2002

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Insufficient accumulation of viral late mRNAs restricts the replicative cycle of human adenovirus type 37 in A549 cells

Archives of virology, 2009, Vol.154 (9), p.1401-1407

2009

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Gene targeting in human-induced pluripotent stem cells with adenoviral vectors

Methods in molecular biology (Clifton, N.J.), 2014, Vol.1114, p.163

Mitani, Kohnosuke

2014

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Gene targeting in human pluripotent stem cells with adeno-associated virus vectors

Biochemical and biophysical research communications, 2009-10, Vol.388 (4), p.711-717

2009

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Convergence of Notch and β-catenin signaling induces arterial fate in vascular progenitors

The Journal of cell biology, 2013-07, Vol.202 (1), p.179-179

2013

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gRNA

ファルマシア, 2018, Vol.54(2), pp.150_2-150_2

三谷, 幸之介

2018

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オフターゲット変異

ファルマシア, 2018, Vol.54(2), pp.150_1-150_1

三谷, 幸之介

2018

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ゲノム編集の臨床応用の概要

ファルマシア, 2018, Vol.54(2), pp.118-122

三谷, 幸之介

2018

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A New Adenoviral Vector: Replacement of All Viral Coding Sequences with 28 kb of DNA Independently Expressing Both Full-Length Dystrophin and β -Galactosidase

Proceedings of the National Academy of Sciences - PNAS, 1996-06, Vol.93 (12), p.5731-5736

1996

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Albumin gene targeting in human embryonic stem cells and induced pluripotent stem cells with helper-dependent adenoviral vector to monitor hepatic differentiation

Stem cell research, 2013-03, Vol.10 (2), p.179-194

2013

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Correction of mutant Fanconi anemia gene by homologous recombination in human hematopoietic cells using adeno-associated virus vector

The journal of gene medicine, 2009-11, Vol.11 (11), p.1012-1019

2009

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

An inhibitor of fibroblast growth factor receptor-1 (FGFR1) promotes late-stage terminal differentiation from NGN3+ pancreatic endocrine progenitors

The use of induced pluripotent stem cells to reveal pathogenic gene mutations and explore treatments for retinitis pigmentosa

Dual usage of a stage-specific fluorescent reporter system based on a helper-dependent adenoviral vector to visualize osteogenic differentiation

Novel human adenovirus strain, Bangladesh

Efficient and Accurate Homologous Recombination in hESCs and hiPSCs Using Helper-dependent Adenoviral Vectors

Simple Derivation of Spinal Motor Neurons from ESCs/iPSCs Using Sendai Virus Vectors

Frequency and Stability of Chromosomal Integration of Adenovirus Vectors

A New Hybrid System Capable of Efficient Lentiviral Vector Production and Stable Gene Transfer Mediated by a Single Helper-Dependent Adenoviral Vector

Correction of Chromosomal Mutation and Random Integration in Embryonic Stem Cells with Helper-Dependent Adenoviral Vectors

Helper-Dependent Adenoviral Vectors Efficiently Express Transgenes in Human Dendritic Cells but Still Stimulate Antiviral Immune Responses

Convergence of Notch and β-catenin signaling induces arterial fate in vascular progenitors

Gene Therapy of Erectile Dysfunction in the Rat with Penile Neuronal Nitric Oxide Synthase

A Novel, Helper-Dependent, Adenovirus–Retrovirus Hybrid Vector: Stable Transduction by a Two-Stage Mechanism

Insufficient accumulation of viral late mRNAs restricts the replicative cycle of human adenovirus type 37 in A549 cells

Gene targeting in human-induced pluripotent stem cells with adenoviral vectors

Gene targeting in human pluripotent stem cells with adeno-associated virus vectors

Phototoxicity avoidance is a potential therapeutic approach for retinal dystrophy caused by EYS dysfunction

Convergence of Notch and β-catenin signaling induces arterial fate in vascular progenitors

gRNA

オフターゲット変異

ゲノム編集の臨床応用の概要

A New Adenoviral Vector: Replacement of All Viral Coding Sequences with 28 kb of DNA Independently Expressing Both Full-Length Dystrophin and β -Galactosidase

Albumin gene targeting in human embryonic stem cells and induced pluripotent stem cells with helper-dependent adenoviral vector to monitor hepatic differentiation

Correction of mutant Fanconi anemia gene by homologous recombination in human hematopoietic cells using adeno-associated virus vector

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