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FZD4 wt Allele

Known as: Fz4, FzE4, Frizzled 4, Seven Transmembrane Spanning Receptor Gene 
Human FZD4 wild-type allele is located in the vicinity of 11q14.2 and is approximately 10 kb in length. This allele, which encodes frizzled-4 protein… Expand
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
Familial exudative vitreoretinopathy (FEVR) is a genetically heterogeneous retinal disorder characterized by abnormal… Expand
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Highly Cited
2010
Highly Cited
2010
Familial exudative vitreoretinopathy (FEVR) is an inherited blinding disorder of the retinal vascular system. Although mutations… Expand
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Highly Cited
2004
Highly Cited
2004
Incomplete retinal vascularization occurs in both Norrie disease and familial exudative vitreoretinopathy (FEVR). Norrin, the… Expand
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Highly Cited
2004
Highly Cited
2004
Familial exudative vitreoretinopathy (FEVR) is an inherited blinding disorder of the retinal vascular system. Autosomal dominant… Expand
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Highly Cited
2004
Highly Cited
2004
Familial exudative vitreoretinopathy (FEVR) is a hereditary eye disorder that affects both the retina and vitreous body… Expand
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Highly Cited
2004
Highly Cited
2004
nt signalling pathways regulate cell proliferation, cell fate and morphogenetic movements. Here, we demonstrate that the Frizzled… Expand
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Review
2004
Review
2004
THE IDENTIFICATION OF mutations in the human lowdensity lipoprotein (LDL) receptor–related protein 5 (LRP5) gene that give rise… Expand
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Highly Cited
2003
Highly Cited
2003
Wnt proteins, regulators of development in many organisms, bind to seven transmembrane–spanning (7TMS) receptors called frizzleds… Expand
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Highly Cited
2002
Highly Cited
2002
Familial exudative vitreoretinopathy (FEVR) is a hereditary ocular disorder characterized by a failure of peripheral retinal… Expand
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Highly Cited
1993
Highly Cited
1993
Familial exudative vitreoretinopathy (FEVR) is a hereditary disorder characterized by an abnormality of the peripheral retina… Expand
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