(Q40728508)

English

Adenovirus vectors containing chimeric type 5 and type 35 fiber proteins exhibit altered and expanded tropism and increase the size limit of foreign genes

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scholarly article

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Europe PubMed Central

PubMed publication ID

23 September 2017

Adenovirus vectors containing chimeric type 5 and type 35 fiber proteins exhibit altered and expanded tropism and increase the size limit of foreign genes (English)

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Europe PubMed Central

PubMed publication ID

23 September 2017

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Hiroyuki Mizuguchi

1

object named as

Hiroyuki Mizuguchi

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Europe PubMed Central

PubMed publication ID

23 September 2017

author name string

Takao Hayakawa

2

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Europe PubMed Central

PubMed publication ID

23 September 2017

language of work or name

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publication date

1 February 2002

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Europe PubMed Central

PubMed publication ID

23 September 2017

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Europe PubMed Central

PubMed publication ID

23 September 2017

285

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Europe PubMed Central

PubMed publication ID

23 September 2017

1-2

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Europe PubMed Central

PubMed publication ID

23 September 2017

69-77

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Europe PubMed Central

PubMed publication ID

23 September 2017

Adenovirus type 37 uses sialic acid as a cellular receptor

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Dependence of efficient adenoviral gene delivery in malignant glioma cells on the expression levels of the Coxsackievirus and adenovirus receptor

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Adenovirus vectors for gene delivery

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

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An efficient and flexible system for construction of adenovirus vectors with insertions or deletions in early regions 1 and 3.

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Polylysine modification of adenoviral fiber protein enhances muscle cell transduction

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Group D adenoviruses infect primary central nervous system cells more efficiently than those from group C.

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An adenovirus vector with genetically modified fibers demonstrates expanded tropism via utilization of a coxsackievirus and adenovirus receptor-independent cell entry mechanism

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Functional and selective targeting of adenovirus to high-affinity Fcgamma receptor I-positive cells by using a bispecific hybrid adapter

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Adenovirus type 5 and 7 capsid chimera: fiber replacement alters receptor tropism without affecting primary immune neutralization epitopes

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SK HEP-1: a human cell line of endothelial origin

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Necrotizing tubulointerstitial nephritis associated with adenovirus infection

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A simple and efficient method for purification of infectious recombinant adenovirus.

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Efficient gene transfer by fiber-mutant adenoviral vectors containing RGD peptide

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Adenoviral vectors for gene transfer

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Influence of adenoviral fiber mutations on viral encapsidation, infectivity and in vivo tropism

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In vivo gene transfer via intravenous administration of cationic lipid-protamine-DNA (LPD) complexes

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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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A simple method for constructing E1- and E1/E4-deleted recombinant adenoviral vectors

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IRES-dependent second gene expression is significantly lower than cap-dependent first gene expression in a bicistronic vector

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A simplified system for constructing recombinant adenoviral vectors containing heterologous peptides in the HI loop of their fiber knob

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Fatal disseminated adenovirus infection in a renal transplant recipient

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Adenovirus types 11p and 35p show high binding efficiencies for committed hematopoietic cell lines and are infective to these cell lines

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Efficient gene transfer into human CD34(+) cells by a retargeted adenovirus vector

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Selective targeting of human cells by a chimeric adenovirus vector containing a modified fiber protein.

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

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Targeting adenovirus

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

1 reference

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

1 reference

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Biodistribution of an adenoviral vector carrying the luciferase reporter gene following intravesical or intravenous administration to a mouse

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Identifiers

10.1016/S0378-1119(02)00410-9

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

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