Long-term retinal cone rescue using a capsid mutant AAV8 vector in a mouse model of CNGA3-achromatopsia.

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Retinal Cyclic Nucleotide-Gated Channels: From Pathophysiology to Therapy.

P2860

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Long-term retinal cone rescue using a capsid mutant AAV8 vector in a mouse model of CNGA3-achromatopsia.

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2017年学术文章

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Long-term retinal cone rescue ...... model of CNGA3-achromatopsia.

@en

Long-term retinal cone rescue ...... model of CNGA3-achromatopsia.

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type

Item

label

Long-term retinal cone rescue ...... model of CNGA3-achromatopsia.

@en

Long-term retinal cone rescue ...... model of CNGA3-achromatopsia.

@nl

prefLabel

Long-term retinal cone rescue ...... model of CNGA3-achromatopsia.

@en

Long-term retinal cone rescue ...... model of CNGA3-achromatopsia.

@nl

P1476

Long-term retinal cone rescue ...... model of CNGA3-achromatopsia.

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P2093

Hao Chen

http://www.w3.org/2001/XMLSchema#string

Hua Zhang

http://www.w3.org/2001/XMLSchema#string

Ji-Jing Pang

http://www.w3.org/2001/XMLSchema#string

Muran Wang

http://www.w3.org/2001/XMLSchema#string

Yan Liu

http://www.w3.org/2001/XMLSchema#string

Yangyang Zhang

http://www.w3.org/2001/XMLSchema#string

Ying He

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P2860

Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia

CNGA3 mutations in hereditary cone photoreceptor disorders

Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration

Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 year

AAV-mediated gene therapy in mouse models of recessive retinal degeneration

Gene Augmentation Therapy Restores Retinal Function and Visual Behavior in a Sheep Model of CNGA3 Achromatopsia

Dosage thresholds for AAV2 and AAV8 photoreceptor gene therapy in monkey

Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel

Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia

Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial

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e0188032

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scholarly article

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10.1371/JOURNAL.PONE.0188032

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English

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Xufeng Dai

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2017-11-13T00:00:00Z

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29131863

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5683625

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Long-term retinal cone rescue using a capsid mutant AAV8 vector in a mouse model of CNGA3-achromatopsia.

about

P2860

P2860

Long-term retinal cone rescue using a capsid mutant AAV8 vector in a mouse model of CNGA3-achromatopsia.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932