Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65.
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Correction of Monogenic and Common Retinal Disorders with Gene Therapy.Inclusion of the Woodchuck Hepatitis Virus Posttranscriptional Regulatory Element Enhances AAV2-Driven Transduction of Mouse and Human RetinaLeber's Congenital Amaurosis and Gene Therapy.Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions.Concepts and Strategies in Retinal Gene Therapy.Rare Diseases: Drug Discovery and Informatics Resource.Guiding Lights in Genome Editing for Inherited Retinal Disorders: Implications for Gene and Cell Therapy.A novel adeno-associated virus capsid with enhanced neurotropism corrects a lysosomal transmembrane enzyme deficiency.A Drug-Tunable Gene Therapy for Broad-Spectrum Protection against Retinal Degeneration
P2860
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P2860
Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Development of an optimized AA ...... sis owing to defects in RPE65.
@en
type
label
Development of an optimized AA ...... sis owing to defects in RPE65.
@en
prefLabel
Development of an optimized AA ...... sis owing to defects in RPE65.
@en
P2093
P2860
P50
P356
P1433
P1476
Development of an optimized AA ...... osis owing to defects in RPE65
@en
P2093
B Sünkel-Laing
E Cristante
L Abelleira-Hervas
M Michaelides
S J Robbie
P2860
P2888
P304
P356
10.1038/GT.2016.66
P577
2016-09-22T00:00:00Z
P6179
1020150783