Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain (Q42280576)

19 October 2017

title

Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain (English)

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19 October 2017

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During MJ

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19 October 2017

Kaplitt MG

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19 October 2017

Leone P

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19 October 2017

Samulski RJ

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19 October 2017

Xiao X

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19 October 2017

Pfaff DW

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19 October 2017

O'Malley KL

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19 October 2017

language of work or name

English

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publication date

1 October 1994

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19 October 2017

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19 October 2017

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19 October 2017

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19 October 2017

page(s)

148-154

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Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection

19 October 2017

cites work

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A model system for in vivo gene transfer into the central nervous system using an adenoviral vector

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Adenovirus vectors enter the brain

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In vivo release of dopa and dopamine from genetically engineered cells grafted to the denervated rat striatum

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Long-term correction of rat model of Parkinson's disease by gene therapy

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Adeno-associated virus: a vector system for efficient introduction and integration of DNA into a variety of mammalian cell types

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A new technique for the assay of infectivity of human adenovirus 5 DNA

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A 6-hydroxydopamine-induced selective parkinsonian rat model

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Biochemical and behavioral recovery in a rodent model of Parkinson's disease following stereotactic implantation of dopamine-containing liposomes

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Genetic engineering of novel genomes of large DNA viruses

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Cytotoxicity of a replication-defective mutant of herpes simplex virus type 1

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An adenovirus vector for gene transfer into neurons and glia in the brain

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Transfer of a foreign gene into the brain using adenovirus vectors

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Expression of a functional foreign gene in adult mammalian brain following in Vivo transfer via a herpes simplex virus type 1 defective viral vector

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Preproenkephalin promoter yields region-specific and long-term expression in adult brain after direct in vivo gene transfer via a defective herpes simplex viral vector

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Altering central nervous system physiology with a defective herpes simplex virus vector expressing the glucose transporter gene

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An efficient deletion mutant packaging system for defective herpes simplex virus vectors: potential applications to human gene therapy and neuronal physiology.

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Grafting fibroblasts genetically modified to produce L-dopa in a rat model of Parkinson disease

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Restoration of dopaminergic function by grafting of fetal rat substantia nigra to the caudate nucleus: long-term behavioral, biochemical, and histochemical studies

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Importance of different variables for enhancing in situ detection of PCR-amplified DNA.

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Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vector

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Isolation and characterization of the human tyrosine hydroxylase gene: identification of 5' alternative splice sites responsible for multiple mRNAs

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Primate neostriatal neurons containing tyrosine hydroxylase: immunohistochemical evidence

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7 January 2021

Partial lesions of the dopaminergic nigrostriatal system in rat brain: biochemical characterization

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7 January 2021

Chronic intrastriatal dopamine infusions in rats with unilateral lesions of the substantia nigra

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7 January 2021

Long-term in vivo expression of retrovirus-mediated gene transfer in mouse fibroblast implants

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7 January 2021

Targeted integration of adeno-associated virus (AAV) into human chromosome 19

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7 January 2021

Adeno-associated virus general transduction vectors: analysis of proviral structures

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Characteristics of a human cell line transformed by DNA from human adenovirus type 5

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7 January 2021

Identifiers

DOI

10.1038/NG1094-148

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Dimensions Publication ID

19 October 2017

1039273340

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