about
Low-Dose Gene Therapy for Murine PKU Using Episomal Naked DNA Vectors Expressing PAH from Its Endogenous Liver PromoterGene therapy for monogenic liver diseases: clinical successes, current challenges and future prospects.Gene Therapy 2017: Progress and Future Directions.Gene therapy with an AAV vector expressing human IL-2 alters immune system homeostasis in humanized mice.Adeno-Associated Virus (AAV) as a Vector for Gene Therapy.ssAAVs containing cassettes encoding SaCas9 and guides targeting hepatitis B virus inactivate replication of the virus in cultured cells.AAV serotypes have distinctive interactions with domains of the cellular receptor AAVR.The Promise and Challenge of In Vivo Delivery for Genome Therapeutics.Emerging Issues in AAV-Mediated In Vivo Gene Therapy.Gene Therapy for Hemophilia.Gene Therapy With Regulatory T Cells: A Beneficial Alliance.Direct recognition of hepatocyte-expressed MHC class I alloantigens is required for tolerance induction
P2860
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P2860
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
Adeno-Associated Virus Gene Therapy for Liver Disease.
@en
type
label
Adeno-Associated Virus Gene Therapy for Liver Disease.
@en
prefLabel
Adeno-Associated Virus Gene Therapy for Liver Disease.
@en
P2093
P2860
P921
P356
P1433
P1476
Adeno-Associated Virus Gene Therapy for Liver Disease.
@en
P2093
Christopher H Tipper
Deborah S Geraghty
K Reed Clark
Lisa M Kattenhorn
Lorelei Stoica
Samuel C Wadsworth
Teresa L Wright
P2860
P304
P356
10.1089/HUM.2016.160
P577
2016-11-29T00:00:00Z
2016-12-01T00:00:00Z