Long-term gene transfer to mouse fetuses with recombinant adenovirus and adeno-associated virus (AAV) vectors.
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In utero recombinant adeno-associated virus gene transfer in mice, rats, and primatesIntra-amniotic rAAV-mediated microdystrophin gene transfer improves canine X-linked muscular dystrophy and may induce immune toleranceSystemic delivery of AAV8 in utero results in gene expression in diaphragm and limb muscle: treatment implications for muscle disorders.In utero lung gene transfer using adeno-associated viral and lentiviral vectors in mice.Efficient in vivo targeting of epidermal stem cells by early gestational intraamniotic injection of lentiviral vector driven by the keratin 5 promoter.Kidney-specific expression of GFP by in-utero delivery of pseudotyped adeno-associated virus 9.Modulation of hepatic granulomatous responses by transgene expression of DAP12 or TREM-1-Ig moleculesRecombinant adeno-associated viral (rAAV) vectors as therapeutic tools for Duchenne muscular dystrophy (DMD).Augmentation of transgene-encoded protein after neonatal injection of adeno-associated virus improves hepatic copy number without immune responses.A novel surgical approach for intratracheal administration of bioactive agents in a fetal mouse modelEmbryonic and neonatal phenotyping of genetically engineered mice.Imaging tools for the developmental biologist: ultrasound biomicroscopy of mouse embryonic development.The fetal respiratory system as target for antenatal therapy.Organ targeted prenatal gene therapy--how far are we?Hepatocyte growth factor receptor is a coreceptor for adeno-associated virus type 2 infection.Adeno-associated virus-mediated gene transfer of endostatin inhibits angiogenesis and tumor growth in vivo.Efficient gene transfer into the mouse lung by fetal intratracheal injection of rAAV2/6.2.Comparison of high-capacity and first-generation adenoviral vector gene delivery to murine muscle in utero.Humoral immune response to recombinant adenovirus and adeno-associated virus after in utero administration of viral vectors in mice.Fetal muscle gene transfer is not enhanced by an RGD capsid modification to high-capacity adenoviral vectors.Possible mechanism of gene transfer into early to mid-gestational mouse fetuses by tail vein injection.Evaluation of prenatal intra-amniotic LAMB3 gene delivery in a mouse model of Herlitz disease.Sustained delivery of therapeutic concentrations of human clotting factor IX--a comparison of adenoviral and AAV vectors administered in utero.Adenovirus-mediated prenatal gene transfer to murine central nervous system.The developmental stage determines the distribution and duration of gene expression after early intra-amniotic gene transfer using lentiviral vectors.Brain cytoplasmic RNA 1 suppresses smooth muscle differentiation and vascular development in mice.
P2860
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P2860
Long-term gene transfer to mouse fetuses with recombinant adenovirus and adeno-associated virus (AAV) vectors.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
@zh-hant
name
Long-term gene transfer to mou ...... ssociated virus (AAV) vectors.
@en
Long-term gene transfer to mou ...... rus and adeno-associated virus
@nl
type
label
Long-term gene transfer to mou ...... ssociated virus (AAV) vectors.
@en
Long-term gene transfer to mou ...... rus and adeno-associated virus
@nl
prefLabel
Long-term gene transfer to mou ...... ssociated virus (AAV) vectors.
@en
Long-term gene transfer to mou ...... rus and adeno-associated virus
@nl
P2093
P2860
P356
P1433
P1476
Long-term gene transfer to mou ...... ssociated virus (AAV) vectors.
@en
P2093
P2860
P2888
P304
P356
10.1038/SJ.GT.3301332
P577
2000-12-01T00:00:00Z
P5875
P6179
1026488120