The challenges of developing a gene therapy for amyotrophic lateral sclerosis.

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The challenges of developing a gene therapy for amyotrophic lateral sclerosis.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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2017年论文

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2017年论文

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The challenges of developing a gene therapy for amyotrophic lateral sclerosis.

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The challenges of developing a gene therapy for amyotrophic lateral sclerosis.

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The challenges of developing a gene therapy for amyotrophic lateral sclerosis.

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P1476

The challenges of developing a gene therapy for amyotrophic lateral sclerosis

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P2093

Jason John Lamanna

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Nicholas M Boulis

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Orion Paul Keifer

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P2860

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

From animal models to human disease: a genetic approach for personalized medicine in ALS

CRISPR/Cas9: a powerful genetic engineering tool for establishing large animal models of neurodegenerative diseases

Modeling ALS with motor neurons derived from human induced pluripotent stem cells

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

Adeno-associated virus-delivered artificial microRNA extends survival and delays paralysis in an amyotrophic lateral sclerosis mouse model.

Highly efficient retrograde gene transfer into motor neurons by a lentiviral vector pseudotyped with fusion glycoprotein.

Human neural stem cell transplantation in ALS: initial results from a phase I trial.

Therapeutic AAV9-mediated suppression of mutant SOD1 slows disease progression and extends survival in models of inherited ALS

Species-dependent neuropathology in transgenic SOD1 pigs.

P304

323-325

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scholarly article

editorial

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10.1080/14737175.2017.1287565

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P433

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P478

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Muhibullah Tora

P577

2017-02-22T00:00:00Z

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P698

28132569

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P921

amyotrophic lateral sclerosis

gene therapy