(Q40250783)

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In contrast to AAV-mediated Cntf expression, AAV-mediated Gdnf expression enhances gene replacement therapy in rodent models of retinal degeneration

scientific article published on 26 July 2006

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scholarly article

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Europe PubMed Central

PubMed publication ID

18 September 2017

In contrast to AAV-mediated Cntf expression, AAV-mediated Gdnf expression enhances gene replacement therapy in rodent models of retinal degeneration (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Robert MacLaren

2

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author name string

Prateek K Buch

1

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Yanaí Durán

3

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Europe PubMed Central

PubMed publication ID

18 September 2017

Kamaljit S Balaggan

4

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Europe PubMed Central

PubMed publication ID

18 September 2017

Angus MacNeil

5

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Europe PubMed Central

PubMed publication ID

18 September 2017

Frank C Schlichtenbrede

6

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Europe PubMed Central

PubMed publication ID

18 September 2017

Alexander J Smith

7

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Europe PubMed Central

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18 September 2017

Robin R Ali

8

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Europe PubMed Central

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18 September 2017

publication date

26 July 2006

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Europe PubMed Central

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18 September 2017

Molecular Therapy

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18 September 2017

14

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18 September 2017

5

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Europe PubMed Central

PubMed publication ID

18 September 2017

700-709

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Europe PubMed Central

PubMed publication ID

18 September 2017

Molecular genetics and prospects for therapy of the inherited retinal dystrophies

1 reference

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7 January 2021

Retinitis pigmentosa: understanding the clinical presentation, mechanisms and treatment options

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

1 reference

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Kinetics of transgene expression in mouse retina following sub-retinal injection of recombinant adeno-associated virus

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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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7 January 2021

Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy.

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7 January 2021

Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIP.

1 reference

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7 January 2021

Long-term preservation of retinal function in the RCS rat model of retinitis pigmentosa following lentivirus-mediated gene therapy

1 reference

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7 January 2021

Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat

1 reference

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7 January 2021

Gene therapy restores vision-dependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosis

1 reference

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7 January 2021

Retinal degeneration slow (rds) in mouse results from simple insertion of a t haplotype-specific element into protein-coding exon II.

1 reference

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7 January 2021

Apoptotic photoreceptor cell death in mouse models of retinitis pigmentosa

1 reference

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7 January 2021

Long-term evaluation of retinal function in Prph2Rd2/Rd2 mice following AAV-mediated gene replacement therapy

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.05.019

7 January 2021

Gene replacement therapy in the retinal degeneration slow (rds) mouse: the effect on retinal degeneration following partial transduction of the retina

1 reference

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7 January 2021

Intraocular gene delivery of ciliary neurotrophic factor results in significant loss of retinal function in normal mice and in the Prph2Rd2/Rd2 model of retinal degeneration

1 reference

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7 January 2021

Effects of adeno-associated virus-vectored ciliary neurotrophic factor on retinal structure and function in mice with a P216L rds/peripherin mutation

1 reference

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7 January 2021

Glial cell line derived neurotrophic factor delays photoreceptor degeneration in a transgenic rat model of retinitis pigmentosa

1 reference

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7 January 2021

High-titer recombinant adeno-associated virus production from replicating amplicons and herpes vectors deleted for glycoprotein H.

1 reference

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7 January 2021

Encapsulated cell-based intraocular delivery of ciliary neurotrophic factor in normal rabbit: dose-dependent effects on ERG and retinal histology

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.05.019

7 January 2021

Adenovirus-mediated gene transfer of ciliary neurotrophic factor can prevent photoreceptor degeneration in the retinal degeneration (rd) mouse

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.05.019

7 January 2021

Intraocular gene transfer of ciliary neurotrophic factor prevents death and increases responsiveness of rod photoreceptors in the retinal degeneration slow mouse

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMTHE.2006.05.019

7 January 2021

Long-term protection of retinal structure but not function using RAAV.CNTF in animal models of retinitis pigmentosa

1 reference

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7 January 2021

Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase I trial of CNTF delivered by encapsulated cell intraocular implants

1 reference

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7 January 2021

Intraputamenal infusion of glial cell line-derived neurotrophic factor in PD: a two-year outcome study.

1 reference

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7 January 2021

Localized striatal delivery of GDNF as a treatment for Parkinson disease

1 reference

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7 January 2021

Long-term glial cell line-derived neurotrophic factor overexpression in the intact nigrostriatal system in rats leads to a decrease of dopamine and increase of tetrahydrobiopterin production

1 reference

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7 January 2021

Regulated delivery of glial cell line-derived neurotrophic factor into rat striatum, using a tetracycline-dependent lentiviral vector

1 reference

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7 January 2021

Protection by synergistic effects of adenovirus-mediated X-chromosome-linked inhibitor of apoptosis and glial cell line-derived neurotrophic factor gene transfer in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease.

1 reference

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7 January 2021

Potential synergistic protection of retinal ganglion cells from axotomy-induced apoptosis by adenoviral administration of glial cell line-derived neurotrophic factor and X-chromosome-linked inhibitor of apoptosis

1 reference

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7 January 2021

Novel functions and signalling pathways for GDNF.

1 reference

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7 January 2021

Functional and structural evaluation after AAV.RPE65 gene transfer in the canine model of Leber's congenital amaurosis

1 reference

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7 January 2021

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10.1016/J.YMTHE.2006.05.019

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Europe PubMed Central

PubMed publication ID

18 September 2017

release_wldfvya6hneunnf2mqx7qq4jxm

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18 September 2017

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