Genetic contributions to the development of retinopathy of prematurity - Wikidata - awgldk - TriplyDB

Genetic contributions to the development of retinopathy of prematurity

Genetic contributions to the development of retinopathy of prematurity

http://www.wikidata.org/entity/Q37164288

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Genetic susceptibility to advanced retinopathy of prematurity (ROP)Gene-environment interactions in severe intraventricular hemorrhage of preterm neonates Genes and environment in neonatal intraventricular hemorrhage Refractive and Visual Outcome after Laser-Treated Retinopathy of Prematurity in Western Romania.Wnt signaling pathway in retinal vascularization Studies on the pathogenesis of avascular retina and neovascularization into the vitreous in peripheral severe retinopathy of prematurity (an american ophthalmological society thesis)Blood gases and retinopathy of prematurity: the ELGAN Study.Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants Genomics in the neonatal nursery: Focus on ROP.Hyperglycemia as a risk factor for the development of retinopathy of prematurity Familial exudative vitreoretinopathy and related retinopathies.Genetic and Environmental Influences on Retinopathy of Prematurity.Genetic Contributions to the Development of Complications in Preterm Newborns.The A Allele at rs13419896 of EPAS1 Is Associated with Enhanced Expression and Poor Prognosis for Non-Small Cell Lung Cancer.Genetic variation in CYB5R3 is associated with methemoglobin levels in preterm infants receiving nitric oxide therapy.Intersibling variability of retinopathy of prematurity in twins and its risk factors.The pathophysiology of retinopathy of prematurity: an update of previous and recent knowledge.Algorithms for the prediction of retinopathy of prematurity based on postnatal weight gain.Intraretinal calcium channels and retinal morbidity in experimental retinopathy of prematurity.Abnormal Complement Activation and Inflammation in the Pathogenesis of Retinopathy of Prematurity.Angiotensin II Type 1 receptor (AGTR1) gene polymorphisms are associated with vascular manifestations in patients with systemic sclerosis (SSc).The role of the human leukocyte antigen system in retinopathy of prematurity: a pilot study.The genetics of retinopathy of prematurity: a model for neovascular retinal disease A large-scale replication study for the association of rs17039192 in HIF-2α with knee osteoarthritis

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Genetic contributions to the development of retinopathy of prematurity

http://www.wikidata.org/entity/Q37164288

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on February 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Genetic contributions to the development of retinopathy of prematurity

@en

Genetic contributions to the development of retinopathy of prematurity.

@nl

type

label

Genetic contributions to the development of retinopathy of prematurity

@en

Genetic contributions to the development of retinopathy of prematurity.

@nl

prefLabel

Genetic contributions to the development of retinopathy of prematurity

@en

Genetic contributions to the development of retinopathy of prematurity.

@nl

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Pediatric Research

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Genetic contributions to the development of retinopathy of prematurity

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Ana Alvarado

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Elise Ahrens

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Jeffrey C Murray

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Kendra Schaa

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Margaret E Cooper

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Mary L Marazita

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Endothelial PAS domain protein 1 (EPAS1), a transcription factor selectively expressed in endothelial cells

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

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Complement factor H polymorphism in age-related macular degeneration

Indian hedgehog signaling regulates proliferation and differentiation of chondrocytes and is essential for bone formation

T-box genes in human disorders

Molecular models for vertebrate limb development

Sonic hedgehog regulates branching morphogenesis in the mammalian lung

Expression of Drosophila omb-related T-box genes in the developing human and mouse neural retina.

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

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Tarah T Colaizy

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