Chick embryo lethal orphan virus can be polymer-coated and retargeted to infect mammalian cells-Reference-Cited by-同舟云学术

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Chick embryo lethal orphan virus can be polymer-coated and retargeted to infect mammalian cells

Published:2005-12-15 Issue:4 Volume:13 Page:356-368
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Stevenson M,Boos E,Herbert C,Hale A,Green N,Lyons M,Chandler L,Ulbrich K,van Rooijen N,Mautner V,Fisher K,Seymour L

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/3302655.pdf

Reference59 articles.

1. Bergelson JM, Cunningham JA, Drouguett G, Kurt-Jones EA, Krithivas A, Hong JS et al. Isolation of a common receptor for coxsackie B viruses and adenoviruses 2 and 5. Science 1997; 275: 1320–1323.

2. Bergelson JM . Receptors mediating adenovirus attachment and internalisation. Biochem Pharmacol 1999; 57: 975–979.

3. Wickham TJ, Mathias P, Cheresh DA, Nemerow GR . Integrins αvβ3 and αvβ5 promote adenovirus internalisation but not virus attachment. Cell 1993; 73: 309–319.

4. Chirmule N, Propert K, Magosin S, Qian Y, Qian R, Wilson J . Immune responses to adenovirus and adeno-associated virus in humans. Gene Therapy 1999; 6: 1574–1583.

5. Stallwood Y, Fisher KD, Gallimore PH, Mautner V . Neutralisation of adenovirus infectivity by ascitic fluid from ovarian cancer patients. Gene Therapy 2000; 7: 637–643.

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1. Genetic and Chemical Capsid Modifications of Adenovirus Vectors to Modulate Vector–Host Interactions;Viruses;2021-07-02

2. Fiber modifications enable fowl adenovirus 4 vectors to transduce human cells;The Journal of Gene Medicine;2021-06-11

3. Retargeting adenoviruses for therapeutic applications and vaccines;FEBS Letters;2020-02-03

4. Polymer-coated viral vectors: hybrid nanosystems for gene therapy;The Journal of Gene Medicine;2018-03-25

5. Preclinical Efficacy and Safety Profile of Allometrically Scaled Doses of Doxycycline Used to Turn “On” Therapeutic Transgene Expression from High-Capacity Adenoviral Vectors in a Glioma Model;Human Gene Therapy Methods;2016-06

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