Systemic application of AAV vectors targeting GFAP-expressing astrocytes in Z-Q175-KI Huntington's disease mice.
about
Unravelling and Exploiting Astrocyte Dysfunction in Huntington's Disease.Cellular selectivity of AAV serotypes for gene delivery in neurons and astrocytes by neonatal intracerebroventricular injection.In vivo genome editing in animals using AAV-CRISPR system: applications to translational research of human disease.Current Strategies for Brain Drug Delivery.Translation of MicroRNA-Based Huntingtin-Lowering Therapies from Preclinical Studies to the Clinic.The Tiny for the Biggest Answers in Huntington's Disease
P2860
Systemic application of AAV vectors targeting GFAP-expressing astrocytes in Z-Q175-KI Huntington's disease mice.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
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2016年學術文章
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name
Systemic application of AAV ve ...... -KI Huntington's disease mice.
@en
type
label
Systemic application of AAV ve ...... -KI Huntington's disease mice.
@en
prefLabel
Systemic application of AAV ve ...... -KI Huntington's disease mice.
@en
P2093
P921
P1476
Systemic application of AAV ve ...... 5-KI Huntington's disease mice
@en
P2093
Anna Maria Wójtowicz
Rosemarie Grantyn
Tatyana Vagner
P356
10.1016/J.MCN.2016.10.007
P577
2016-10-27T00:00:00Z