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NDP encodes a secreted protein with a cystein-knot motif that activates the Wnt/beta-catenin pathway. Additionally we are shipping Norrie Disease (Pseudoglioma) Antibodies (25) and Norrie Disease (Pseudoglioma) Kits (5) and many more products for this protein.
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These structural, biophysical and cellular data, map Fz4 (show FZD4 Proteins) and putative Lrp5 (show LRP5 Proteins)/6 binding sites to distinct patches on Norrin, and reveal a GAG binding site spanning Norrin and Fz4 (show FZD4 Proteins) cysteine-rich domain.
Genetic evaluation of a case of bilateral leukocoria and asymmetric microphthalmia revealed a previously undescribed mutation in the Norrie disease protein gene.
Norrin may play a role in the regulation of angiogenesis.
Norrin induces the formation of a ternary complex with Fz4 (show FZD4 Proteins) and Lrp5 (show LRP5 Proteins)/6 by binding to their respective extracellular domains
Report of a missense mutation, p.Arg41Ser, in NDP causing Norrie disease in an Indian family.
Multi-functional norrin is a ligand for the LGR4 (show LGR4 Proteins) receptor.
NDP mutations are common cause of Norrie disease but might be rare cause for familial exudative vitreoretinopathy (FEVR) in Chinese.
Norrin has a neuroprotective role for retinal neurons independent from its role on the growth of retinal capillaries.
Mutation screening of the NDP gene identified a novel nonsense mutation, c.343C>T.
A novel Norrin missense mutation, p.Arg41Thr, was identified in two apparently unrelated families with Norrie disease
xNorrin promotes dorsal and anterior neural formation by acting on two major signaling pathways, Wnt (show WNT2 Proteins) and TGF-beta (show TGFB1 Proteins), in opposite ways and is essential for early neuroectoderm specification.
The endogenously expressed Lgr4 (show LGR4 Proteins) may act as an antagonist molecule that helps to fine-tune the R-spondin/norrin-mediated Lgr4 (show LGR4 Proteins)-Wnt (show WNT2 Proteins) signaling during gonadal development.
In this study we demonstrate, for the first time, that Norrin protein is expressed along the retinal blood vessels.
Taken together, we have uncovered a cell autonomous function for Ndp in retinal progenitor proliferation that is independent of its function in the retinal vasculature, which could explain the neural defects associated with Norrie disease
We conclude that constitutive overexpression of Norrin protects photoreceptors from light damage, an effect that is mediated by Wnt (show WNT2 Proteins)/beta-catenin (show CTNNB1 Proteins) and EDN2 (show EDN2 Proteins) signaling and involves neurotrophic activities of BDNF (show BDNF Proteins).
The data reveal both cell-autonomous and cell-nonautonomous effects, and they imply a central role for Norrin/Fz4 (show FZD4 Proteins) signaling in central nervous system vascular development and in the maintenance of the blood brain barrier/blood retina barrier state.
Results suggest that the delayed outgrowth of the SRVP and decreased angiogenic sprouting in Norrin knockout (Ndp(y/-)) mice are direct effects of the reduced proliferation of endothelial cells from the superficial retinal vascular plexus (SRVP).
These observations suggest the possibility that Norrin may have developmental and/or homeostatic functions beyond the retina and cochlea.
Norrin has pronounced neuroprotective properties on retinal neurons. The effects of Norrin involve activation of Wnt (show WNT2 Proteins)/beta-catenin (show CTNNB1 Proteins) signaling and subsequent induction of neurotrophic growth factors in Muller cells.
This gene encodes a secreted protein with a cystein-knot motif that activates the Wnt/beta-catenin pathway. The protein forms disulfide-linked oligomers in the extracellular matrix. Mutations in this gene result in Norrie disease and X-linked exudative vitreoretinopathy.
X-linked exudative vitreoretinopathy 2 protein
, norrie disease protein
, Norrie disease protein
, norrie disease protein homolog
, Norrie disease homolog