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Article

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

Cell - 19 Mar 2004

Xu Qiang, Wang Yanshu, Dabdoub Alain, Smallwood Philip M, Williams John, Woods Chad, Kelley Matthew W, Jiang Li, Tasman William, Zhang Kang, Nathans Jeremy

Abstract excerpt

Incomplete retinal vascularization occurs in both Norrie disease and familial exudative vitreoretinopathy (FEVR). Norrin, the protein product of the Norrie disease gene, is a secreted protein of unknown biochemical function. One form of FEVR is caused by defects in Frizzled-4 (Fz4), a presumptive...

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Source

Identifiers

PMID: 15035989
DOI: 10.1016/s0092-8674(04)00216-8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15035989-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Vascular development in the retina and inner ear: control by Norrin and Frizzled-4, a high-affinity ligand-receptor pair.PMID 15035989Read ↗

A novel variant p.Y250C of FZD4 influences Norrine/β-catenin signaling pathway that associates with familial exudative vitreoretinopathy (FEVR).Semantic proximity Read ↗

Mechanisms Underlying Rare Inherited Pediatric Retinal Vascular Diseases: FEVR, Norrie Disease, Persistent Fetal Vascular SyndromeSemantic proximity Read ↗

Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP.Semantic proximity Read ↗

Norrin stimulates cell proliferation in the superficial retinal vascular plexus and is pivotal for the recruitment of mural cellsSemantic proximity Read ↗

Norrin-induced Frizzled4 endocytosis and endo-lysosomal trafficking control retinal angiogenesis and barrier function.Semantic proximity Read ↗

A comprehensive functional analysis on the pathogenesis of novel TSPAN12 and NDP variants in familial exudative vitreoretinopathy.Semantic proximity Read ↗

Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.Semantic proximity Read ↗

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Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy.Semantic proximity Read ↗

Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.Semantic proximity Read ↗

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