Genetic basis of inherited macular dystrophies and implications for stem cell therapy. - Wikidata - awgldk - TriplyDB

Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

http://www.wikidata.org/entity/Q34234455

about

Generation of a foveomacular transcriptome Lab generated retina: realizing the dream.Recent Advances in Retinal Stem Cell Therapy.Cellular regeneration strategies for macular degeneration: past, present and future.

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P2860

Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

http://www.wikidata.org/entity/Q34234455

description

2009 nî lūn-bûn

@nan

2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

@ast

Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

@en

Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

@nl

type

label

Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

@ast

Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

@en

Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

@nl

prefLabel

Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

@ast

Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

@en

Genetic basis of inherited macular dystrophies and implications for stem cell therapy.

@nl

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Genetic basis of inherited macular dystrophies and implications for stem cell therapy

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Carla B Mellough

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David H W Steel

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Majlinda Lako

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Creative Commons Attribution 2.5 Unported

P2860

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

Dominant negative mechanism underlies autosomal dominant Stargardt-like macular dystrophy linked to mutations in ELOVL4

Molecular characterization and functional analysis of phagocytosis by human embryonic stem cell-derived RPE cells using a novel human retinal assay

A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration

The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease

A randomized, placebo-controlled, clinical trial of high-dose supplementation with vitamins C and E, beta carotene, and zinc for age-related macular degeneration and vision loss: AREDS report no. 8

Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration

Complement factor H polymorphism in age-related macular degeneration

Correction of the disease phenotype in the mouse model of Stargardt disease by lentiviral gene therapy

Safety and efficacy of gene transfer for Leber's congenital amaurosis

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2833-2845

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scholarly article

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10.1002/STEM.159

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11

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27

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David H W Steel

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age related macular degeneration

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