Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.
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Sp1 and KLF15 regulate basal transcription of the human LRP5 geneRegulation of norrin receptor frizzled-4 by Wnt2 in colon-derived cellsExpression patterns of Wnt genes during development of an anterior part of the chicken eyeZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculatureAutosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5.A model for familial exudative vitreoretinopathy caused by LPR5 mutationsThe Norrin/Frizzled4 signaling pathway in retinal vascular development and diseaseWnt/beta-catenin signaling: components, mechanisms, and diseasesThe Wnt-dependent signaling pathways as target in oncology drug discoveryLrp5 controls bone formation by inhibiting serotonin synthesis in the duodenumCritical Endothelial Regulation by LRP5 during Retinal Vascular DevelopmentStructural Basis of Wnt Signaling Inhibition by Dickkopf Binding to LRP5/6LRP5 and LRP6 in development and diseaseWhole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesisWhere Wnts went: the exploding field of Lrp5 and Lrp6 signaling in boneNorrin, frizzled-4, and Lrp5 signaling in endothelial cells controls a genetic program for retinal vascularization.WNT and beta-catenin signalling: diseases and therapiesA biochemical screen for identification of small-molecule regulators of the Wnt pathway using Xenopus egg extracts.Molecular and clinical studies of X-linked deafness among Pakistani families.The mouse retina as an angiogenesis model.A novel signaling pathway regulates colon cancer angiogenesis through Norrin.Phenotypic overlap of familial exudative vitreoretinopathy (FEVR) with persistent fetal vasculature (PFV) caused by FZD4 mutations in two distinct pedigrees.LRP5 is required for vascular development in deeper layers of the retina.Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.Wnt signaling in angiogenesisThe ever-expanding conundrum of primary osteoporosis: aetiopathogenesis, diagnosis, and treatment.exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels.Clinical and molecular findings in osteoporosis-pseudoglioma syndrome.Osteoporosis-pseudoglioma syndrome: description of 9 new cases and beneficial response to bisphosphonatesThe role of the cysteine-rich domain of Frizzled in Wingless-Armadillo signaling.Retinal expression of Wnt-pathway mediated genes in low-density lipoprotein receptor-related protein 5 (Lrp5) knockout mice.Novel mutations in the TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathy.LRP5 sequence and polymorphisms in the baboon.Genetic screening of Wnt signaling factors in advanced retinopathy of prematurityRelating diseases by integrating gene associations and information flow through protein interaction networkWnt/Frizzled signaling in the vasculature: new angiogenic factors in sight.Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity.Regulation of bone mass by Wnt signaling.Genetic evidence that Drosophila frizzled controls planar cell polarity and Armadillo signaling by a common mechanism.An essential role of the cysteine-rich domain of FZD4 in Norrin/Wnt signaling and familial exudative vitreoretinopathy.
P2860
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P2860
Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.
description
2004 nî lūn-bûn
@nan
2004 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մարտին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Mutations in LRP5 or FZD4 unde ...... opathy locus on chromosome 11q
@nl
Mutations in LRP5 or FZD4 unde ...... pathy locus on chromosome 11q.
@ast
Mutations in LRP5 or FZD4 unde ...... pathy locus on chromosome 11q.
@en
Mutations in LRP5 or FZD4 unde ...... pathy locus on chromosome 11q.
@en-gb
type
label
Mutations in LRP5 or FZD4 unde ...... opathy locus on chromosome 11q
@nl
Mutations in LRP5 or FZD4 unde ...... pathy locus on chromosome 11q.
@ast
Mutations in LRP5 or FZD4 unde ...... pathy locus on chromosome 11q.
@en
Mutations in LRP5 or FZD4 unde ...... pathy locus on chromosome 11q.
@en-gb
prefLabel
Mutations in LRP5 or FZD4 unde ...... opathy locus on chromosome 11q
@nl
Mutations in LRP5 or FZD4 unde ...... pathy locus on chromosome 11q.
@ast
Mutations in LRP5 or FZD4 unde ...... pathy locus on chromosome 11q.
@en
Mutations in LRP5 or FZD4 unde ...... pathy locus on chromosome 11q.
@en-gb
P2093
P2860
P50
P921
P3181
P356
P1476
Mutations in LRP5 or FZD4 unde ...... pathy locus on chromosome 11q.
@en
P2093
Cheryl Y Gregory-Evans
Geoffrey Woodruff
Helen M Bottomley
Jamie E Craig
Kang Zhang
Katherine V Towns
Kevin Gregory-Evans
Louise M Downey
Michael J Parker
P2860
P304
P3181
P356
10.1086/383202
P407
P577
2004-03-11T00:00:00Z