Genome Editing Gene Therapy for Duchenne Muscular Dystrophy. - Wikidata - awgldk - TriplyDB

Genome Editing Gene Therapy for Duchenne Muscular Dystrophy.

Genome Editing Gene Therapy for Duchenne Muscular Dystrophy.

http://www.wikidata.org/entity/Q37589752

about

Cellular Reprogramming, Genome Editing, and Alternative CRISPR Cas9 Technologies for Precise Gene Therapy of Duchenne Muscular Dystrophy.Myopenia and precision (P4) medicine.

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Genome Editing Gene Therapy for Duchenne Muscular Dystrophy.

http://www.wikidata.org/entity/Q37589752

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on September 2015

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vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

@cs

name

Genome Editing Gene Therapy for Duchenne Muscular Dystrophy.

@en

Genome Editing Gene Therapy for Duchenne Muscular Dystrophy.

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type

label

Genome Editing Gene Therapy for Duchenne Muscular Dystrophy.

@en

Genome Editing Gene Therapy for Duchenne Muscular Dystrophy.

@nl

prefLabel

Genome Editing Gene Therapy for Duchenne Muscular Dystrophy.

@en

Genome Editing Gene Therapy for Duchenne Muscular Dystrophy.

@nl

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Journal of neuromuscular diseases

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Genome Editing Gene Therapy for Duchenne Muscular Dystrophy

@en

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Akitsu Hotta

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CRISPR Provides Acquired Resistance Against Viruses in Prokaryotes

CRISPR/Cas9-mediated gene editing in human tripronuclear zygotes

Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study

A highly stable and nonintegrated human artificial chromosome (HAC) containing the 2.4 Mb entire human dystrophin gene

Disease-specific induced pluripotent stem cells

Local restoration of dystrophin expression with the morpholino oligomer AVI-4658 in Duchenne muscular dystrophy: a single-blind, placebo-controlled, dose-escalation, proof-of-concept study

Efficient targeting of a SCID gene by an engineered single-chain homing endonuclease

A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity

Efficient and reproducible myogenic differentiation from human iPS cells: prospects for modeling Miyoshi Myopathy in vitro

Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors

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343-355

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scholarly article

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10.3233/JND-150116

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4

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2015-09-01T00:00:00Z

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27858753

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5240599

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