Adenoassociated virus serotype 9-mediated gene therapy for x-linked adrenoleukodystrophy.
about
Gene delivery to the spinal cord using MRI-guided focused ultrasoundExtraneuronal pathology in a canine model of CLN2 neuronal ceroid lipofuscinosis after intracerebroventricular gene therapy that delays neurological disease progression.Inhibition of pathological brain angiogenesis through systemic delivery of AAV vector expressing soluble FLT1.Viral vectors for therapy of neurologic diseases.Principles of precision medicine in stroke.Systemic AAV9 gene therapy improves the lifespan of mice with Niemann-Pick disease, type C1.Microglial dysfunction as a key pathological change in adrenomyeloneuropathy.Therapeutic strategies in adrenoleukodystrophy.
P2860
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P2860
Adenoassociated virus serotype 9-mediated gene therapy for x-linked adrenoleukodystrophy.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年學術文章
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2015年學術文章
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2015年學術文章
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name
Adenoassociated virus serotype 9-mediated gene therapy for x-linked adrenoleukodystrophy.
@en
type
label
Adenoassociated virus serotype 9-mediated gene therapy for x-linked adrenoleukodystrophy.
@en
prefLabel
Adenoassociated virus serotype 9-mediated gene therapy for x-linked adrenoleukodystrophy.
@en
P2093
P2860
P356
P1433
P1476
Adenoassociated virus serotype 9-mediated gene therapy for x-linked adrenoleukodystrophy.
@en
P2093
Casey A Maguire
Florian S Eichler
JiaQian Ren
Patricia Musolino
Shilpa Prabhakar
Xandra O Breakefield
P2860
P304
P356
10.1038/MT.2015.6
P577
2015-01-16T00:00:00Z