Targeted Gene Addition of Microdystrophin in Mice Skeletal Muscle via Human Myoblast Transplantation. - Wikidata - awgldk - TriplyDB

Targeted Gene Addition of Microdystrophin in Mice Skeletal Muscle via Human Myoblast Transplantation.

Targeted Gene Addition of Microdystrophin in Mice Skeletal Muscle via Human Myoblast Transplantation.

http://www.wikidata.org/entity/Q41844091

about

Genome-editing Technologies for Gene and Cell Therapy Engineered Viruses as Genome Editing Devices Advances in gene therapy for muscular dystrophies Multiplex CRISPR/Cas9-based genome editing for correction of dystrophin mutations that cause Duchenne muscular dystrophy.Correction of dystrophin expression in cells from Duchenne muscular dystrophy patients through genomic excision of exon 51 by zinc finger nucleases.CRISPR-Cas9: a promising tool for gene editing on induced pluripotent stem cells.Emerging gene editing strategies for Duchenne muscular dystrophy targeting stem cells.Neuromuscular electrical stimulation promotes development in mice of mature human muscle from immortalized human myoblasts.Adenoviral vector DNA for accurate genome editing with engineered nucleases.Therapeutic gene editing: delivery and regulatory perspectives Genome engineering: a new approach to gene therapy for neuromuscular disorders.

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Targeted Gene Addition of Microdystrophin in Mice Skeletal Muscle via Human Myoblast Transplantation.

http://www.wikidata.org/entity/Q41844091

description

2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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Targeted Gene Addition of Micr ...... uman Myoblast Transplantation.

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Targeted Gene Addition of Micr ...... uman Myoblast Transplantation.

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Targeted Gene Addition of Micr ...... uman Myoblast Transplantation.

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Molecular therapy. Nucleic acids

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Targeted Gene Addition of Micr ...... uman Myoblast Transplantation.

@en

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Arnaud Duval

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Basma F Benabdallah

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Christian M Beauséjour

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Eli Haddad

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

Jacques P Tremblay

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Joel Rousseau

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Michael C Holmes

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Pierre Chapdelaine

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P2860

Retroviral integrations in gene therapy trials

Highly efficient endogenous human gene correction using designed zinc-finger nucleases

Revealing off-target cleavage specificities of zinc-finger nucleases by in vitro selection

Gene editing in human stem cells using zinc finger nucleases and integrase-defective lentiviral vector delivery

Resistance to HIV-1 infection in caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene

Establishment of HIV-1 resistance in CD4+ T cells by genome editing using zinc-finger nucleases

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

Expression of dog microdystrophin in mouse and dog muscles by gene therapy

Human hematopoietic stem/progenitor cells modified by zinc-finger nucleases targeted to CCR5 control HIV-1 in vivo.

Defective myoblasts identified in Duchenne muscular dystrophy.

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10.1038/MTNA.2012.55

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2

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2013-01-29T00:00:00Z

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