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Genetic screening of Wnt signaling factors in advanced retinopathy of prematurity

author

Hideo Orimo

published in: Molecular Vision

date of publication: 2010-12-05

main subject: retinopathy of prematurity

Cites articles 30

Date

Title

Authors

2010-02-01

Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy

Chris F. Inglehearn, James A Poulter, Alexander Markham, Carmel Toomes, Eric A Pierce, David A. Mackey, Jamie E Craig
2010-02-01

Next-generation sequencing of a 40 Mb linkage interval reveals TSPAN12 mutations in patients with familial exudative vitreoretinopathy

Christian Gilissen, Hans Scheffer, Carmen Ayuso, Peer Arts, Joris A Veltman, Alexander Hoischen, Lies H. Hoefsloot, Nienke Wieskamp, Rob W J Collin, Frans P M Cremers
2010-03-01

Severe retinopathy of prematurity associated with FZD4 mutations

Tom G Sheidow
2009-10-01

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

Harald J Junge, Weilan Ye
2009-04-01

A mutation in the signal sequence of LRP5 in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats

Gudrun Nürnberg, Hülya Kayserili, Christian Kubisch, Peter Nürnberg, Bernd Wollnik
2009-12-01

Clinical presentation and genetic correlation of patients with mutations affecting the FZD4 gene
2007-12-01

Genetic susceptibility to retinopathy of prematurity: the evidence from clinical and experimental animal studies
2007-02-01

Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene.
2006-05-01

The c.43_44insCTG variation in PCSK9 is associated with low plasma LDL-cholesterol in a Caucasian population

Maurizio Averna
2005-07-01

The International Classification of Retinopathy of Prematurity revisited
2005-04-01

Genetic variants of frizzled-4 gene in familial exudative vitreoretinopathy and advanced retinopathy of prematurity

Marcia L E MacDonald
2004-09-02

Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5.
2004-03-01

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

Alain Dabdoub, Jeremy Nathans, Philip M Smallwood
2004-03-11

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

Graeme Black, Chris F. Inglehearn, Carmel Toomes, Richard C Trembath, David A. Mackey, Jamie E Craig
2002-08-12

Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy

Marie-Pierre Dubé, Marcia L E MacDonald, Roshni Singaraja, Randall T. Moon, Michael R. Hayden
2002-06-01

Vascular defects and sensorineural deafness in a mouse model of Norrie disease
2002-07-01

A C597-->A polymorphism in the Norrie disease gene is associated with advanced retinopathy of prematurity in premature Kuwaiti infants
2001-11-16

LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development

Miikka Vikkula, Timothy Cundy, Bruno Dallapiccola, Konrad Oexle, Sergio Roman-Roman, Marcela Votruba, Harald Jüppner
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Insertion and deletion mutations in the dinucleotide repeat region of the Norrie disease gene in patients with advanced retinopathy of prematurity
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An LDL-receptor-related protein mediates Wnt signalling in mice

Jane Brennan
2000-01-01

Risk factors in retinopathy of prematurity. a multivariate statistical analysis
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Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity
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Identification of novel missense mutations in the Norrie disease gene associated with one X-linked and four sporadic cases of familial exudative vitreoretinopathy
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Risk factors associated with retinopathy of prematurity (ROP) in northern Jutland, Denmark 1990-1993.
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Article - wd:Q34396837

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