Gene transfer into hepatocytes mediated by helper virus-free HSV/AAV hybrid vectors - Wikidata - wikimedia - TriplyDB

Gene transfer into hepatocytes mediated by helper virus-free HSV/AAV hybrid vectors

Gene transfer into hepatocytes mediated by helper virus-free HSV/AAV hybrid vectors

http://www.wikidata.org/entity/Q36438166

about

Methods, potentials, and limitations of gene delivery to regenerate central nervous system cells Gene therapy of hepatic diseases: prospects for the new millennium.HSV-1-based vectors for gene therapy of neurological diseases and brain tumors: part II. Vector systems and applications Herpes simplex virus type 1/adeno-associated virus rep(+) hybrid amplicon vector improves the stability of transgene expression in human cells by site-specific integration.Herpes simplex virus type 1/adeno-associated virus hybrid vectors mediate site-specific integration at the adeno-associated virus preintegration site, AAVS1, on human chromosome 19.Site-specific integration mediated by a hybrid adenovirus/adeno-associated virus vector.BAC-VAC, a novel generation of (DNA) vaccines: A bacterial artificial chromosome (BAC) containing a replication-competent, packaging-defective virus genome induces protective immunity against herpes simplex virus 1.Targeting the central nervous system with herpes simplex virus / Sleeping Beauty hybrid amplicon vectors.An enhanced packaging system for helper-dependent herpes simplex virus vectors.Virion-associated cofactor high-mobility group DNA-binding protein-1 facilitates transposition from the herpes simplex virus/Sleeping Beauty amplicon vector platform Herpes Virus Amplicon Vectors.Efficient site-specific integration of large transgenes by an enhanced herpes simplex virus/adeno-associated virus hybrid amplicon vector.Functional coexpression of HSV-1 thymidine kinase and green fluorescent protein: implications for noninvasive imaging of transgene expression.Herpes simplex virus type 1/adeno-associated virus hybrid vectors.

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P2860

Gene transfer into hepatocytes mediated by helper virus-free HSV/AAV hybrid vectors

http://www.wikidata.org/entity/Q36438166

description

1997 nî lūn-bûn

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1997年の論文

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1997年学术文章

@wuu

1997年学术文章

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1997年学术文章

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1997年学术文章

@zh-my

1997年学术文章

@zh-sg

1997年學術文章

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1997年學術文章

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1997年學術文章

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name

Gene transfer into hepatocytes mediated by helper virus-free HSV/AAV hybrid vectors

@ast

Gene transfer into hepatocytes mediated by helper virus-free HSV/AAV hybrid vectors

@en

type

label

Gene transfer into hepatocytes mediated by helper virus-free HSV/AAV hybrid vectors

@ast

Gene transfer into hepatocytes mediated by helper virus-free HSV/AAV hybrid vectors

@en

prefLabel

Gene transfer into hepatocytes mediated by helper virus-free HSV/AAV hybrid vectors

@ast

Gene transfer into hepatocytes mediated by helper virus-free HSV/AAV hybrid vectors

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Molecular Medicine

P1476

Gene transfer into hepatocytes mediated by helper virus-free HSV/AAV hybrid vectors

@en

P2093

C Fraefel

http://www.w3.org/2001/XMLSchema#string

C Lage

http://www.w3.org/2001/XMLSchema#string

D R Jacoby

http://www.w3.org/2001/XMLSchema#string

F W Alt

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H Hilderbrand

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J A Majzoub

http://www.w3.org/2001/XMLSchema#string

J Y Chou

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X O Breakefield

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P2860

Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a

Adeno-associated virus (AAV) Rep proteins mediate complex formation between AAV DNA and its integration site in human DNA

Persistent expression of human clotting factor IX from mouse liver after intravenous injection of adeno-associated virus vectors

Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesis

Glucose-6-phosphatase dependent substrate transport in the glycogen storage disease type-1a mouse

Isolation of the gene for murine glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1A

Multiple tissues express alpha 1-antitrypsin in transgenic mice and man.

Liver-directed gene therapy: quantitative evaluation of promoter elements by using in vivo retroviral transduction.

Adeno-associated virus vectors preferentially transduce cells in S phase.

Helper virus-free transfer of herpes simplex virus type 1 plasmid vectors into neural cells.

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813-825

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9440115

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vector-borne disease

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2230287

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