Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity.
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Genetic susceptibility to advanced retinopathy of prematurity (ROP)Wnt signaling pathway in retinal vascularizationAdopting Western Retinopathy of Prematurity Screening Programs in Eastern Countries, are we Screening Properly?Retinal expression of Wnt-pathway mediated genes in low-density lipoprotein receptor-related protein 5 (Lrp5) knockout mice.Unilateral sporadic retinal dysplasia: results of histopathologic, immunohistochemical, chromosomal, genetic, and VEGF-A analyses.Familial exudative vitreoretinopathy and related retinopathies.Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a family.Retinal Oximetry with Scanning Laser Ophthalmoscope in Infants.Fzd4 Haploinsufficiency Delays Retinal Revascularization in the Mouse Model of Oxygen Induced RetinopathyGenetic susceptibility to retinopathy of prematurity: the evidence from clinical and experimental animal studiesLaminins containing the β2 and γ3 chains regulate astrocyte migration and angiogenesis in the retina.Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVRThe Wnt signaling pathway in familial exudative vitreoretinopathy and Norrie disease.Genetic contributions to the development of retinopathy of prematurityA novel Norrie disease pseudoglioma gene mutation, c.-1_2delAAT, responsible for Norrie disease in a Chinese family.Testing for association of the monoamine oxidase A promoter polymorphism with brain structure volumes in both autism and the fragile X syndrome.Current update on retinopathy of prematurity: screening and treatmentDiagnosis and treatment of coats' disease: a review of the literature.Familial retinal detachment associated with COL2A1 exon 2 and FZD4 mutations.Complex genetics of familial exudative vitreoretinopathy and related pediatric retinal detachments.Wnt signaling mediates pathological vascular growth in proliferative retinopathyScreening for NDP mutations in 44 unrelated patients with familial exudative vitreoretinopathy or Norrie disease.Meta-analysis argues for a female-specific role of MAOA-uVNTR in panic disorder in four European populations.Clinical and next-generation sequencing findings in a Chinese family exhibiting severe familial exudative vitreoretinopathy.A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease.MAOA and mechanisms of panic disorder revisited: from bench to molecular psychotherapy.Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family.Correlation of Retinopathy of Prematurity with Bronchopulmonary Dysplasia.Familial Exudative Vitreoretinopathy.The genetics of retinopathy of prematurity: a model for neovascular retinal diseaseRetinopathy of prematurity: is genetic predisposition an important risk factor?
P2860
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P2860
Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity.
description
2006 nî lūn-bûn
@nan
2006 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Mutations in the NDP gene: con ...... nd retinopathy of prematurity.
@ast
Mutations in the NDP gene: con ...... nd retinopathy of prematurity.
@en
Mutations in the NDP gene: con ...... nd retinopathy of prematurity.
@nl
type
label
Mutations in the NDP gene: con ...... nd retinopathy of prematurity.
@ast
Mutations in the NDP gene: con ...... nd retinopathy of prematurity.
@en
Mutations in the NDP gene: con ...... nd retinopathy of prematurity.
@nl
prefLabel
Mutations in the NDP gene: con ...... nd retinopathy of prematurity.
@ast
Mutations in the NDP gene: con ...... nd retinopathy of prematurity.
@en
Mutations in the NDP gene: con ...... nd retinopathy of prematurity.
@nl
P2093
P2860
P50
P1476
Mutations in the NDP gene: con ...... nd retinopathy of prematurity.
@en
P2093
Abraham Passmore
Catherine M Wheatley
Hector Maclean
Jamie E Craig
Michèle M Sale
Supaporn Tengtrisorn
P2860
P304
P356
10.1111/J.1442-9071.2006.01314.X
P577
2006-09-01T00:00:00Z