Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector.
about
Francis Crick's legacy for neuroscience: between the alpha and the OmegaConstruction and molecular analysis of gene transfer systems derived from bovine immunodeficiency virusLentiviral vectors in gene therapy: their current status and future potentialHIV-1 nuclear import: matrix protein is back on center stage, this time together with VprEfficient delivery of Cre-recombinase to neurons in vivo and stable transduction of neurons using adeno-associated and lentiviral vectorsIdentification of unique reciprocal and non reciprocal cross packaging relationships between HIV-1, HIV-2 and SIV reveals an efficient SIV/HIV-2 lentiviral vector system with highly favourable features for in vivo testing and clinical usageAssessment of the AAV-mediated expression of channelrhodopsin-2 and halorhodopsin in brainstem neurons mediating auditory signalingDynamic analysis of vascular morphogenesis using transgenic quail embryosTelencephalic neurons monosynaptically link brainstem and forebrain premotor networks necessary for song.A third-generation lentivirus vector with a conditional packaging systemLentiviral delivery of a vesicular glutamate transporter 1 (VGLUT1)-targeting short hairpin RNA vector into the mouse hippocampus impairs cognitionHemato-endothelial differentiation from lentiviral-transduced human embryonic stem cells retains durable reporter gene expression under the control of ubiquitin promoter.Restricted transgene expression in the brain with cell-type specific neuronal promoters.An adeno-associated viral vector transduces the rat hypothalamus and amygdala more efficient than a lentiviral vectorRequirements for efficient production and transduction of human immunodeficiency virus type 1-based vectors.Gene delivery of human apolipoprotein E alters brain Abeta burden in a mouse model of Alzheimer's disease.Midbrain injection of recombinant adeno-associated virus encoding rat glial cell line-derived neurotrophic factor protects nigral neurons in a progressive 6-hydroxydopamine-induced degeneration model of Parkinson's disease in rats.Development of a self-inactivating lentivirus vector.Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery.Development of multigene and regulated lentivirus vectors.Lentivirus vector gene expression during ES cell-derived hematopoietic development in vitroA murine leukemia virus (MuLV) long terminal repeat derived from rhesus macaques in the context of a lentivirus vector and MuLV gag sequence results in high-level gene expression in human T lymphocytesA Rev-independent human immunodeficiency virus type 1 (HIV-1)-based vector that exploits a codon-optimized HIV-1 gag-pol gene.Minimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors.Gene delivery to the spinal cord: comparison between lentiviral, adenoviral, and retroviral vector delivery systemsComparison of AAV serotypes for gene delivery to dorsal root ganglion neurons.Characterization of promoter function and cell-type-specific expression from viral vectors in the nervous system.A central nervous system-restricted isoform of the interleukin-1 receptor accessory protein modulates neuronal responses to interleukin-1Delivery of the Cre recombinase by a self-deleting lentiviral vector: efficient gene targeting in vivo.Nonneurotropic adenovirus: a vector for gene transfer to the brain and gene therapy of neurological disordersGene therapy: design and prospects for craniofacial regeneration.Adeno-associated virus effectively mediates conditional gene modification in the brainFunctional correction of established central nervous system deficits in an animal model of lysosomal storage disease with feline immunodeficiency virus-based vectors.Transduction of human NOD/SCID-repopulating cells with both lymphoid and myeloid potential by foamy virus vectors.alpha -Synucleinopathy and selective dopaminergic neuron loss in a rat lentiviral-based model of Parkinson's disease.Induction of cell cycle arrest by human T-cell lymphotropic virus type 1 Tax in hematopoietic progenitor (CD34+) cells: modulation of p21cip1/waf1 and p27kip1 expression.Inhibition of soluble TNF signaling in a mouse model of Alzheimer's disease prevents pre-plaque amyloid-associated neuropathology.Versatile somatic gene transfer for modeling neurodegenerative diseases.Efficient and stable gene expression into human osteoclasts using an HIV-1-based lentiviral vectorIn vivo assessment of gene delivery to keratinocytes by lentiviral vectors
P2860
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P2860
Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector.
@ast
Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector.
@en
type
label
Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector.
@ast
Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector.
@en
prefLabel
Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector.
@ast
Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector.
@en
P2093
P2860
P1433
P1476
Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector
@en
P2093
P2860
P304
P407
P577
1997-09-01T00:00:00Z