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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

Genetic susceptibility to advanced retinopathy of prematurity (ROP)

http://www.wikidata.org/entity/Q21093659

about

Refractive and Visual Outcome after Laser-Treated Retinopathy of Prematurity in Western Romania.Risk factors for retinopathy of prematurity: insights from outlier infants.Association of VEGF gene polymorphisms with advanced retinopathy of prematurity: a meta-analysis.Associations of VEGF/VEGF-receptor and HGF/c-Met promoter polymorphisms with progression/regression of retinopathy of prematurity.Treatment of retinopathy of prematurity: a review of conventional and promising new therapeutic options Genetic and Environmental Influences on Retinopathy of Prematurity.Treatment of type I ROP with intravitreal bevacizumab or laser photocoagulation according to retinal zone.Fzd4 Haploinsufficiency Delays Retinal Revascularization in the Mouse Model of Oxygen Induced Retinopathy Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity.WNT Stimulation Dissociates a Frizzled 4 Inactive-State Complex with Gα12/13.A novel Norrie disease pseudoglioma gene mutation, c.-1_2delAAT, responsible for Norrie disease in a Chinese family.Current update on retinopathy of prematurity: screening and treatment The pathophysiology of retinopathy of prematurity: an update of previous and recent knowledge.Review of the mechanisms and therapeutic avenues for retinal and choroidal vascular dysfunctions in retinopathy of prematurity.Complex genetics of familial exudative vitreoretinopathy and related pediatric retinal detachments.Lack of association of VEGF gene 3'- UTR polymorphisms (C702T, C936T and G1612A) and the risk of developing advanced retinopathy of prematurity (ROP).New insight into the pathogenesis of retinopathy of prematurity: assessment of whole-genome expression.A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease.EEG, brain maturation, and the development of retinopathy of prematurity.Familial cases of Norrie disease detected by copy number analysis.The role of the human leukocyte antigen system in retinopathy of prematurity: a pilot study.Correlation of Retinopathy of Prematurity with Bronchopulmonary Dysplasia.

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P2860

Genetic susceptibility to advanced retinopathy of prematurity (ROP)

http://www.wikidata.org/entity/Q21093659

description

2010 nî lūn-bûn

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2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2010 թվականի օգոստոսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)

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Barkur S Shastry

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Creative Commons Attribution 2.0 Generic

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Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy

TSPAN12 regulates retinal vascular development by promoting Norrin- but not Wnt-induced FZD4/beta-catenin signaling

A model for familial exudative vitreoretinopathy caused by LPR5 mutations

Progressive cerebellar, auditory, and esophageal dysfunction caused by targeted disruption of the frizzled-4 gene

Norrin, frizzled-4, and Lrp5 signaling in endothelial cells controls a genetic program for retinal vascularization.

Vitreoretinal findings similar to retinopathy of prematurity in infants with compound heterozygous protein S deficiency.

Association of genetic polymorphisms of vascular endothelial growth factor and risk for proliferative retinopathy of prematurity.

Lack of association between insulin-like growth factor I receptor G(+3174)A polymorphism and retinopathy of prematurity.

A potential biomarker in the cord blood of preterm infants who develop retinopathy of prematurity.

The clinical role of vascular endothelial growth factor (VEGF) system in the pathogenesis of retinopathy of prematurity.

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