(Q50683565)

17 March 2018

title

Improved retinal transduction in vivo and photoreceptor-specific transgene expression using adenovirus vectors with modified penton base. (English)

1 reference

17 March 2018

main subject

photoreceptor protein

0 references

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Siobhan M Cashman

1

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17 March 2018

Laura McCullough

series ordinal

2

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17 March 2018

Rajendra Kumar-Singh

series ordinal

3

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17 March 2018

publication date

15 May 2007

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17 March 2018

published in

Molecular Therapy

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17 March 2018

volume

15

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17 March 2018

page(s)

1640-1646

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17 March 2018

issue

9

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17 March 2018

Photoreceptor cell rescue in retinal degeneration (rd) mice by in vivo gene therapy

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Adenoviral vector-delivered pigment epithelium-derived factor for neovascular age-related macular degeneration: results of a phase I clinical trial

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Encapsidated adenovirus minichromosomes allow delivery and expression of a 14 kb dystrophin cDNA to muscle cells

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Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboons

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Intercellular trafficking of adenovirus-delivered HSV VP22 from the retinal pigment epithelium to the photoreceptors--implications for gene therapy

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

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Rescue from photoreceptor degeneration in the rd mouse by human immunodeficiency virus vector-mediated gene transfer

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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

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Lentiviral vector-mediated gene transfer in adult mouse photoreceptors is impaired by the presence of a physical barrier

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7 January 2021

Photoreceptor morphogenesis in the human retina: a scanning electron microscopic study.

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Right timing for retina repair

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

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In vivo transduction of photoreceptors or ciliary body by intravitreal injection of pseudotyped adenoviral vectors

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7 January 2021

Efficient gene transfer into retinal cells using adenoviral vectors: dependence on receptor expression

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7 January 2021

Efficient selection for high-expression transfectants with a novel eukaryotic vector

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Participation of the retinal pigment epithelium in the rod outer segment renewal process

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Phagocytosis of rod outer segments by retinal pigment epithelial cells requires alpha(v)beta5 integrin for binding but not for internalization

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7 January 2021

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Recombinant AAV-mediated gene transfer to the retina: gene therapy perspectives

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Humoral response after administration of E1-deleted adenoviruses: immune privilege of the subretinal space

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7 January 2021

Adenoviral-mediated gene transfer to retinal explants during development and degeneration

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7 January 2021

Adenovirus type 5 pseudotyped with adenovirus type 37 fiber uses sialic acid as a cellular receptor

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7 January 2021

Exchange of surface proteins impacts on viral vector cellular specificity and transduction characteristics: the retina as a model

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7 January 2021

Interferon-gamma inhibits transgene expression driven by SV40 or CMV promoters but augments expression driven by the mammalian MHC I promoter

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7 January 2021

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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7 January 2021

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

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7 January 2021

A simplified system for generating recombinant adenoviruses

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7 January 2021

Characterization of 911: a new helper cell line for the titration and propagation of early region 1-deleted adenoviral vectors.

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7 January 2021

Identifiers

DOI

10.1038/SJ.MT.6300203

1 reference

17 March 2018

PubMed ID

17505470

1 reference

17 March 2018