Stable integration of recombinant adeno-associated virus vector genomes after transduction of murine hematopoietic stem cells.
about
Adeno-associated virus vector integrationComparative analysis of DNA nanoparticles and AAVs for ocular gene deliverySynthesis and characterization of glycol chitosan DNA nanoparticles for retinal gene delivery.Efficient intrathymic gene transfer following in situ administration of a rAAV serotype 8 vector in mice and nonhuman primates.Adeno-associated virus-mediated gene transferHigh-efficiency transduction of primary human hematopoietic stem cells and erythroid lineage-restricted expression by optimized AAV6 serotype vectors in vitro and in a murine xenograft model in vivoCellular fusion for gene delivery to SCA1 affected Purkinje neurons.Protein replacement therapy and gene transfer in canine models of hemophilia A, hemophilia B, von willebrand disease, and factor VII deficiency.AAV and compacted DNA nanoparticles for the treatment of retinal disorders: challenges and future prospects.Recombinant AAV-directed gene therapy for type I glycogen storage diseases.Self-complementary adeno-associated viral vectors for gene therapy of hemophilia B: progress and challengesGene transfer properties and structural modeling of human stem cell-derived AAV.Three-dimensional multipotent progenitor cell aggregates for expansion, osteogenic differentiation and 'in vivo' tracing with AAV vector serotype 6.G-protein-coupled receptors in adult neurogenesis.The SLC37 family of phosphate-linked sugar phosphate antiporters.Analysis of adeno-associated virus progenitor cell transduction in mouse lung.Towards a rAAV-based gene therapy for ADA-SCID: from ADA deficiency to current and future treatment strategies.Safety profile of recombinant adeno-associated viral vectors: focus on alipogene tiparvovec (Glybera®).Identification of adeno-associated viral vectors suitable for intestinal gene delivery and modulation of experimental colitis.Enhanced long-term transduction and multilineage engraftment of human hematopoietic stem cells transduced with tyrosine-modified recombinant adeno-associated virus serotype 2.DsAAV8-mediated expression of glucagon-like peptide-1 in pancreatic beta-cells ameliorates streptozotocin-induced diabetes.
P2860
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P2860
Stable integration of recombinant adeno-associated virus vector genomes after transduction of murine hematopoietic stem cells.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Stable integration of recombin ...... rine hematopoietic stem cells.
@en
Stable integration of recombin ...... rine hematopoietic stem cells.
@nl
type
label
Stable integration of recombin ...... rine hematopoietic stem cells.
@en
Stable integration of recombin ...... rine hematopoietic stem cells.
@nl
prefLabel
Stable integration of recombin ...... rine hematopoietic stem cells.
@en
Stable integration of recombin ...... rine hematopoietic stem cells.
@nl
P2093
P50
P356
P1433
P1476
Stable integration of recombin ...... urine hematopoietic stem cells
@en
P2093
Arun Srivastava
Kirsten A Weigel-Van Aken
Mervin C Yoder
Nitin S Chouthai
Njeri Maina
William B Slayton
Xiaomiao Li
Zhongbo Hu
P304
P356
10.1089/HUM.2007.161
P577
2008-03-01T00:00:00Z