Stable and efficient intraocular gene transfer using pseudotyped EIAV lentiviral vectors-Reference-Cited by-同舟云学术

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Stable and efficient intraocular gene transfer using pseudotyped EIAV lentiviral vectors

Published:2006 Issue:3 Volume:8 Page:275-285
ISSN:1099-498X
Container-title:The Journal of Gene Medicine
language:en
Short-container-title:J. Gene Med.

Author:

Balaggan K. S.,Binley K.,Esapa M.,Iqball S.,Askham Z.,Kan O.,Tschernutter M.,Bainbridge J. W. B.,Naylor S.,Ali R. R.

Publisher

Wiley

Subject

Genetics (clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Reference49 articles.

1. Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector

2. In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector; efficient long-term transduction of corneal endothelium and retinal pigment epithelium

3. Intravitreal Injection of Adeno-associated Viral Vectors Results in the Transduction of Different Types of Retinal Neurons in Neonatal and Adult Rats: A Comparison with Lentiviral Vectors

4. Human immunodeficiency virus type 2 (HIV-2) vector-mediated in vivo gene transfer into adult rabbit retina

5. Activity analysis of housekeeping promoters using self-inactivating lentiviral vector delivery into the mouse retina

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3. Intraocular mRNA delivery with endogenous MmPEG10-based virus-like particles;Experimental Eye Research;2024-06

4. Advancements in ocular gene therapy delivery: vectors and subretinal, intravitreal, and suprachoroidal techniques;Expert Opinion on Biological Therapy;2022-09-02

5. Lentiviral Vectors for Ocular Gene Therapy;Pharmaceutics;2022-07-31

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