Lrp4 regulates initiation of ureteric budding and is crucial for kidney formation--a mouse model for Cenani-Lenz syndrome
about
Apolipoprotein E and apolipoprotein E receptors: normal biology and roles in Alzheimer diseaseKidney regeneration: common themes from the embryo to the adultA secreted BMP antagonist, Cer1, fine tunes the spatial organization of the ureteric bud tree during mouse kidney developmentAnti-LRP4 autoantibodies in AChR- and MuSK-antibody-negative myasthenia gravisLRP4 third β-propeller domain mutations cause novel congenital myasthenia by compromising agrin-mediated MuSK signaling in a position-specific manner.Sall1-dependent signals affect Wnt signaling and ureter tip fate to initiate kidney developmentMore than cholesterol transporters: lipoprotein receptors in CNS function and neurodegenerationDisruption of Lrp4 function by genetic deletion or pharmacological blockade increases bone mass and serum sclerostin levelsLrp4 domains differentially regulate limb/brain development and synaptic plasticityAdvances in the Molecular Genetics of Non-syndromic Syndactyly.A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice.Lipoprotein receptors--an evolutionarily ancient multifunctional receptor family.Polyhydramnios in Lrp4 knockout mice with bilateral kidney agenesis: Defects in the pathways of amniotic fluid clearanceAPP interacts with LRP4 and agrin to coordinate the development of the neuromuscular junction in mice.Antibodies against low-density lipoprotein receptor-related protein 4 induce myasthenia gravis.Multiple modes of Lrp4 function in modulation of Wnt/β-catenin signaling during tooth development.The Lrp4R1170Q Homozygous Knock-In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans.ApoE, ApoE Receptors, and the Synapse in Alzheimer's Disease.Functional Roles of the Interaction of APP and Lipoprotein Receptors.Low-Density Lipoprotein Receptor-Related Proteins in Skeletal Development and Disease.Synaptic plasticity and cognitive function are disrupted in the absence of Lrp4.Fundamental Molecules and Mechanisms for Forming and Maintaining Neuromuscular Synapses.Dentin Dysplasia in Notum Knockout Mice.
P2860
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P2860
Lrp4 regulates initiation of ureteric budding and is crucial for kidney formation--a mouse model for Cenani-Lenz syndrome
description
2010 nî lūn-bûn
@nan
2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Lrp4 regulates initiation of u ...... model for Cenani-Lenz syndrome
@ast
Lrp4 regulates initiation of u ...... model for Cenani-Lenz syndrome
@en
Lrp4 regulates initiation of u ...... odel for Cenani-Lenz syndrome.
@nl
type
label
Lrp4 regulates initiation of u ...... model for Cenani-Lenz syndrome
@ast
Lrp4 regulates initiation of u ...... model for Cenani-Lenz syndrome
@en
Lrp4 regulates initiation of u ...... odel for Cenani-Lenz syndrome.
@nl
prefLabel
Lrp4 regulates initiation of u ...... model for Cenani-Lenz syndrome
@ast
Lrp4 regulates initiation of u ...... model for Cenani-Lenz syndrome
@en
Lrp4 regulates initiation of u ...... odel for Cenani-Lenz syndrome.
@nl
P2093
P2860
P1433
P1476
Lrp4 regulates initiation of u ...... model for Cenani-Lenz syndrome
@en
P2093
Bernd Wollnik
Christian Tennert
Courtney M Karner
Eric B Johnson
Ferda Percin
Joachim Herz
Martin F Dietrich
Natalie Kappesser
Thomas J Carroll
P2860
P304
P356
10.1371/JOURNAL.PONE.0010418
P407
P577
2010-04-29T00:00:00Z