Genetic susceptibility to retinopathy of prematurity: the evidence from clinical and experimental animal studies - Wikidata - awgldk - TriplyDB

Genetic susceptibility to retinopathy of prematurity: the evidence from clinical and experimental animal studies

Genetic susceptibility to retinopathy of prematurity: the evidence from clinical and experimental animal studies

http://www.wikidata.org/entity/Q36172256

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)Gene expression microarray analysis of early oxygen-induced retinopathy in the rat Retinopathy of prematurity promising newer modalities of treatment.Risk factors for retinopathy of prematurity: insights from outlier infants.Genetic screening of Wnt signaling factors in advanced retinopathy of prematurity Associations of VEGF/VEGF-receptor and HGF/c-Met promoter polymorphisms with progression/regression of retinopathy of prematurity.The genetic control of avascular area in mouse oxygen-induced retinopathy Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity.Inhibition of retinopathy of prematurity in rat by intravitreal injection of sorafenib.Retinopathy of prematurity screening criteria in Iran: new screening guidelines.Complex genetics of familial exudative vitreoretinopathy and related pediatric retinal detachments.Genomics and proteomics of retinopathy of prematurity: DNA-based prevention and treatment.Genetic polymorphisms of vascular endothelial growth factor and risk for retinopathy of prematurity in South of Iran.The role of the human leukocyte antigen system in retinopathy of prematurity: a pilot study.Influence of polymorphisms in , , and genes on the susceptibility to retinopathy of prematurity among Chinese infants

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P2860

Genetic susceptibility to retinopathy of prematurity: the evidence from clinical and experimental animal studies

http://www.wikidata.org/entity/Q36172256

description

2007 nî lūn-bûn

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British Journal of Ophthalmology

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Genetic susceptibility to reti ...... nd experimental animal studies

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Douglas J Coster

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Gerd Holmström

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Keryn A Williams

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Peter van Wijngaarden

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P2860

Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy

General involvement of hypoxia-inducible factor 1 in transcriptional response to hypoxia

Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.

Vascular development in the retina and inner ear: control by Norrin and Frizzled-4, a high-affinity ligand-receptor pair

Histopathology and vascular endothelial growth factor in untreated and diode laser-treated retinopathy of prematurity.

Revised indications for the treatment of retinopathy of prematurity: results of the early treatment for retinopathy of prematurity randomized trial.

A different retinal glia response to optic nerve injury/lipopolysaccharide administration in hooded and albino rats.

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.

Linkage and candidate gene analysis of X-linked familial exudative vitreoretinopathy.

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10.1136/BJO.2007.117283

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2095497

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