(Q33544037)

27 July 2017

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title

Chimeric viral vectors--the best of both worlds? (English)

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27 July 2017

3

Curiel DT

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27 July 2017

Reynolds PN

1

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27 July 2017

Feng M

series ordinal

2

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27 July 2017

publication date

1 January 1999

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Trends in Molecular Medicine

27 July 2017

published in

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27 July 2017

volume

5

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27 July 2017

issue

1

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27 July 2017

page(s)

25-31

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Sounding boards. Gene therapy in human beings: when is it ethical to begin?

27 July 2017

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7 January 2021

Genetic modification of the hematolymphoid compartment for therapeutic purposes

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7 January 2021

Survival of grafts of genetically modified cardiac myocytes transfected with FITC-labeled oligodeoxynucleotides and the beta-galactosidase gene in the noninfarcted area, but not the myocardial infarcted area

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7 January 2021

Ex vivo hepatic gene therapy of a mouse model of Hereditary Tyrosinemia Type I.

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7 January 2021

Adenovirus-mediated in vivo gene transfer

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7 January 2021

Adenovirus mediated expression of therapeutic plasma levels of human factor IX in mice

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7 January 2021

Adenovirus-mediated in vivo gene transfer and expression in normal rat liver

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7 January 2021

HCAR and MCAR: the human and mouse cellular receptors for subgroup C adenoviruses and group B coxsackieviruses

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7 January 2021

Isolation of a common receptor for Coxsackie B viruses and adenoviruses 2 and 5

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7 January 2021

Adenovirus type 5 fiber knob binds to MHC class I alpha2 domain at the surface of human epithelial and B lymphoblastoid cells

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7 January 2021

Integrins alpha v beta 3 and alpha v beta 5 promote adenovirus internalization but not virus attachment

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7 January 2021

Endothelium-Specific In Vivo Gene Transfer

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7 January 2021

In vivo gene transfer into injured carotid arteries. Optimization and evaluation of acute toxicity

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7 January 2021

Targeted gene delivery by tropism-modified adenoviral vectors

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7 January 2021

Increased in vitro and in vivo gene transfer by adenovirus vectors containing chimeric fiber proteins.

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7 January 2021

Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis

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7 January 2021

Acute responses of non-human primates to airway delivery of an adenovirus vector containing the human cystic fibrosis transmembrane conductance regulator cDNA.

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7 January 2021

Innate immune mechanisms dominate elimination of adenoviral vectors following in vivo administration.

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7 January 2021

Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses

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7 January 2021

Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity.

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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

Retroviruses as vectors

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7 January 2021

Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors

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7 January 2021

Direct intramuscular injection with recombinant AAV vectors results in sustained expression in a dog model of hemophilia

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7 January 2021

Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo

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7 January 2021

The pseudotypic paradox

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7 January 2021

Pseudotyping of murine leukemia virus with the envelope glycoproteins of HIV generates a retroviral vector with specificity of infection for CD4-expressing cells

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7 January 2021

Development of amphotropic murine retrovirus vectors resistant to inactivation by human serum

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7 January 2021

VSV-G-pseudotyped retroviral packaging through adenovirus-mediated inducible gene expression

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7 January 2021

Production of infectious recombinant Moloney murine leukemia virus particles in BHK cells using Semliki Forest virus-derived RNA expression vectors

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7 January 2021

A novel adenovirus-adeno-associated virus hybrid vector that displays efficient rescue and delivery of the AAV genome

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7 January 2021

HSV/AAV hybrid amplicon vectors extend transgene expression in human glioma cells.

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7 January 2021

Adenoviral/retroviral vector chimeras: a novel strategy to achieve high-efficiency stable transduction in vivo.

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7 January 2021

Stable in vivo gene transduction via a novel adenoviral/retroviral chimeric vector

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7 January 2021

Human serum lyses RNA tumour viruses

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7 January 2021

Gene therapy for the treatment of brain tumors using intra-tumoral transduction with the thymidine kinase gene and intravenous ganciclovir

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7 January 2021

Plasmoviruses: nonviral/viral vectors for gene therapy.

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7 January 2021

Adenovirus vectors as transcomplementing templates for the production of replication defective retroviral vectors

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7 January 2021

Expanded-capacity adenoviral vectors--the helper-dependent vectors

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7 January 2021

High-efficiency retrovirus-mediated gene transfer into the livers of mice

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7 January 2021

10.1016/S1357-4310(98)01378-1

Identifiers

DOI

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27 July 2017

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