Integrating HDAd5/35++ Vectors as a New Platform for HSC Gene Therapy of Hemoglobinopathies.

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Reactivation of γ-globin in adult β-YAC mice after ex vivo and in vivo hematopoietic stem cell genome editing.Gene Therapy for Hemoglobinopathies

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Integrating HDAd5/35++ Vectors as a New Platform for HSC Gene Therapy of Hemoglobinopathies.

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http://www.wikidata.org/entity/Q55333613

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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2018年學術文章

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Integrating HDAd5/35++ Vectors ...... Therapy of Hemoglobinopathies.

@en

Integrating HDAd5/35++ Vectors ...... Therapy of Hemoglobinopathies.

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type

Item

label

Integrating HDAd5/35++ Vectors ...... Therapy of Hemoglobinopathies.

@en

Integrating HDAd5/35++ Vectors ...... Therapy of Hemoglobinopathies.

@nl

prefLabel

Integrating HDAd5/35++ Vectors ...... Therapy of Hemoglobinopathies.

@en

Integrating HDAd5/35++ Vectors ...... Therapy of Hemoglobinopathies.

@nl

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Integrating HDAd5/35++ Vectors ...... Therapy of Hemoglobinopathies.

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André Lieber

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

Anja Ehrhardt

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

Chang Li

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

Himanshu Bhusan Samal

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

Hongjie Wang

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Manvendra Singh

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Nikoletta Psatha

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

Thalia Papayannopoulou

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

Zsuzsanna Izsvák

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A capsid-modified helper-dependent adenovirus vector containing the beta-globin locus control region displays a nonrandom integration pattern and allows stable, erythroid-specific gene expression.

Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia

Fast gapped-read alignment with Bowtie 2

Molecular evolution of a novel hyperactive Sleeping Beauty transposase enables robust stable gene transfer in vertebrates

Membrane cofactor protein (MCP; CD46) expression in transgenic mice

BEDTools: a flexible suite of utilities for comparing genomic features.

Efficient infection of primitive hematopoietic stem cells by modified adenovirus.

Insertional transformation of hematopoietic cells by self-inactivating lentiviral and gammaretroviral vectors.

Large-scale molecular characterization of adeno-associated virus vector integration in mouse liver.

Efficient gene transfer into human CD34(+) cells by a retargeted adenovirus vector

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142-152

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scholarly article

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10.1016/J.OMTM.2018.02.004

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

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Wenli Zhang

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2018-02-15T00:00:00Z

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29766024

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

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gene therapy

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5948227

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Integrating HDAd5/35++ Vectors as a New Platform for HSC Gene Therapy of Hemoglobinopathies.

about

P2860

P2860

Integrating HDAd5/35++ Vectors as a New Platform for HSC Gene Therapy of Hemoglobinopathies.

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P1433

P1476

P2093

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P50

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