(Q40308939)

English

An adenovirus serotype 5 vector with fibers derived from ovine atadenovirus demonstrates CAR-independent tropism and unique biodistribution in mice

scientific article published on 3 March 2006

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scholarly article

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Europe PubMed Central

PubMed publication ID

19 September 2017

An adenovirus serotype 5 vector with fibers derived from ovine atadenovirus demonstrates CAR-independent tropism and unique biodistribution in mice (English)

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Europe PubMed Central

PubMed publication ID

19 September 2017

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David T. Curiel

9

object named as

David T Curiel

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PubMed publication ID

19 September 2017

author name string

Masaharu Nakayama

1

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19 September 2017

Gerald W Both

2

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19 September 2017

Boglarka Banizs

3

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19 September 2017

Yuko Tsuruta

4

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19 September 2017

Seiji Yamamoto

5

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19 September 2017

Yosuke Kawakami

6

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19 September 2017

Joanne T Douglas

7

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19 September 2017

Kenzaburo Tani

8

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19 September 2017

Joel N Glasgow

10

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19 September 2017

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publication date

3 March 2006

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19 September 2017

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19 September 2017

350

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19 September 2017

1

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Europe PubMed Central

PubMed publication ID

19 September 2017

103-115

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Europe PubMed Central

PubMed publication ID

19 September 2017

CAR-binding ablation does not change biodistribution and toxicity of adenoviral vectors

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Blood clearance rates of adenovirus type 5 in mice

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Modulation of adenovirus vector tropism via incorporation of polypeptide ligands into the fiber protein

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A proposal for a new (third) genus within the family Adenoviridae.

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Characterisation of Australian ovine adenovirus isolates

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Structural analysis of a fiber-pseudotyped adenovirus with ocular tropism suggests differential modes of cell receptor interactions

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Reducing the native tropism of adenovirus vectors requires removal of both CAR and integrin interactions

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Gene therapy in renal diseases.

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Adenovirus type 5 viral particles pseudotyped with mutagenized fiber proteins show diminished infectivity of coxsackie B-adenovirus receptor-bearing cells

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Gene expression by atypical recombinant ovine adenovirus vectors during abortive infection of human and animal cells in vitro

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The therapeutic efficacy of adenoviral vectors for cancer gene therapy is limited by a low level of primary adenovirus receptors on tumour cells

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The coxsackievirus and adenovirus receptor acts as a tumour suppressor in malignant glioma cells

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A novel ex vivo model system for evaluation of conditionally replicative adenoviruses therapeutic efficacy and toxicity

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Reduction of natural adenovirus tropism to mouse liver by fiber-shaft exchange in combination with both CAR- and alphav integrin-binding ablation

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Genetic targeting of an adenovirus vector via replacement of the fiber protein with the phage T4 fibritin

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Canine adenovirus vectors: an alternative for adenovirus-mediated gene transfer

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Biology of ovine adenovirus infection of nonpermissive cells

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Integrin alpha(v)beta1 is an adenovirus coreceptor

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The role of capsid-endothelial interactions in the innate immune response to adenovirus vectors

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Ovine adenovirus vectors mediate efficient gene transfer to skeletal muscle

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Advances in the development of non-human viral DNA-vectors for gene delivery

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Construction, Rescue, and Characterization of Vectors Derived from Ovine Atadenovirus

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The polypeptides of adenovirus. I. Evidence for multiple protein components in the virion and a comparison of types 2, 7A, and 12

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Simultaneous CAR- and alpha V integrin-binding ablation fails to reduce Ad5 liver tropism

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Purine nucleoside phosphorylase and fludarabine phosphate gene-directed enzyme prodrug therapy suppresses primary tumour growth and pseudo-metastases in a mouse model of prostate cancer

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CAR- or alphav integrin-binding ablated adenovirus vectors, but not fiber-modified vectors containing RGD peptide, do not change the systemic gene transfer properties in mice

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Adenoviral-mediated gene transfer to renal tubular cells in vivo

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Reduction of natural adenovirus tropism to the liver by both ablation of fiber-coxsackievirus and adenovirus receptor interaction and use of replaceable short fiber

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Mouse adenovirus (MAV-1) expression in primary human endothelial cells and generation of a full-length infectious plasmid

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10.1016/J.VIROL.2006.01.037

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

ResearchGate publication ID

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