(Q37039789)

17 August 2017

1 reference

title

The Wnt signaling pathway in familial exudative vitreoretinopathy and Norrie disease (English)

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exudative vitreoretinopathy

17 August 2017

1 reference

Scott M Warden

1

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17 August 2017

Christopher M Andreoli

series ordinal

2

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17 August 2017

Shizuo Mukai

series ordinal

3

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17 August 2017

language of work or name

English

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publication date

1 October 2007

1 reference

Seminars in Ophthalmology

17 August 2017

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17 August 2017

22

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17 August 2017

4

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17 August 2017

211-217

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Many tumors induced by the mouse mammary tumor virus contain a provirus integrated in the same region of the host genome

17 August 2017

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

The Drosophila homolog of the mouse mammary oncogene int-1 is identical to the segment polarity gene wingless

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Ectopic expression of the proto-oncogene int-1 in Xenopus embryos leads to duplication of the embryonic axis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Maternal wnt11 activates the canonical wnt signaling pathway required for axis formation in Xenopus embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Wnt/beta-catenin signaling in development and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Unexpected complexity of the Wnt gene family in a sea anemone

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

The Wnt signaling pathway in development and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

WNT/Frizzled signaling in eye development and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Wnt proteins are lipid-modified and can act as stem cell growth factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

A new member of the frizzled family from Drosophila functions as a Wingless receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Insights into Wnt binding and signalling from the structures of two Frizzled cysteine-rich domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

An LDL-receptor-related protein mediates Wnt signalling in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

arrow encodes an LDL-receptor-related protein essential for Wingless signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

beta-catenin is a target for the ubiquitin-proteasome pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

beta-Trcp couples beta-catenin phosphorylation-degradation and regulates Xenopus axis formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

The human F box protein beta-Trcp associates with the Cul1/Skp1 complex and regulates the stability of beta-catenin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Association of the APC tumor suppressor protein with catenins

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Association of the APC gene product with beta-catenin

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Armadillo coactivates transcription driven by the product of the Drosophila segment polarity gene dTCF

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Functional interaction of beta-catenin with the transcription factor LEF-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

XTcf-3 transcription factor mediates beta-catenin-induced axis formation in Xenopus embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Fluorescein angiographic findings in familial exudative vitreoretinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

A new locus for autosomal dominant familial exudative vitreoretinopathy maps to chromosome 11p12-13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

X linked exudative vitreoretinopathy: clinical features and genetic linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Norrie's disease--differential diagnosis and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

The ocular pathology of Norrie disease in a fetus of 11 weeks' gestational age

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Ocular findings associated with a Cys39Arg mutation in the Norrie disease gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Mutations in the candidate gene for Norrie disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Norrie disease and peripheral venous insufficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Isolation and characterization of a candidate gene for Norrie disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Isolation of a candidate gene for Norrie disease by positional cloning

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

Mutations of the Norrie gene in Korean ROP infants

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F08820530701745124

10.1080/08820530701745124

21 January 2018

Identifiers

DOI

1 reference

17 August 2017

1 reference