About: Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice

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About: Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice Goto Sponge NotDistinct Permalink

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scientific journal article

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rdf:type	Item
description	article scientifique publié en 2005 (fr) artículu científicu espublizáu en 2005 (ast) vědecký článek publikovaný v roce 2005 (cs) 2005 թվականի նոյեմբերին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в листопаді 2005 (uk) 2005 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած (hyw) vedecký článok (publikovaný 2005/11/15) (sk) مقالة علمية (نشرت في 15-11-2005) (ar) wetenschappelijk artikel (gepubliceerd op 2005/11/15) (nl) scientific journal article (en) im November 2005 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28507633-DF3010FD-80D2-4673-B85E-9FDEE4B9537F
publication date	2005-11-15 00:00:00Z (xsd:dateTime)
author name string	wds:Q28507633-5EFE3C20-F924-49C0-BC23-6362038820C4 wds:Q28507633-9DB8244D-0ABE-4AF1-B3E0-DD2D89910628 wds:Q28507633-A369D9B7-822C-4E7D-B8D0-17EA801A0623
author name string	Joachim Herz Robert E. Hammer Eric B. Johnson
rdfs:label	Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice (en) Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice (nl) Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice (ast)
skos:prefLabel	Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice (en) Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice (nl) Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice (ast)
name	Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice (en) Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice (nl) Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice (ast)
title	wds:Q28507633-A0BD5706-43C1-42BB-ABFF-D13875751AC8
title	Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice (en)
page(s)	wds:Q28507633-7154D41A-8179-4E0F-80A2-0657692A4B81
page(s)	3523–3538
instance of	wds:Q28507633-455ECA90-C784-4E45-BF1E-8CF53D156DA4
instance of	scholarly article
main subject	wds:Q28507633-132DE6AE-589E-4F92-9306-69D35B0852E9 wds:Q28507633-1C8350CE-0F54-4806-814B-5ABF5B285D89 wds:Q28507633-2D764DAB-A1F0-464B-B871-75E82D94B67F wds:Q28507633-A39BC1C6-C57C-4A6A-9B67-331990FD0AF1 wds:Q28507633-FF196EBE-2E88-426D-8EA2-9107DC187583
main subject	Apical ectodermal ridge polysyndactyly Low density lipoprotein receptor-related protein 1 Low density lipoprotein receptor-related protein 4 Wingless-type MMTV integration site family, member 1
PubMed ID	wds:Q28507633-E2FDBA01-66C5-4A8C-BDD5-1BE2BE0BD18D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16207730
PubMed ID	16207730
published in	wds:Q28507633-EC067CC5-7D08-4EE2-B329-E96FB322FB02
published in	Human Molecular Genetics
issue	wds:Q28507633-8C536272-2421-47A4-9C8F-DD16E9A3F54B
volume	wds:Q28507633-D45C8BFA-CBB9-481D-9A57-31CEF0424193
issue	22
volume	14
DOI	wds:Q28507633-1B5597BB-F6DC-49DB-97BE-8E24A6870993
DOI	http://dx.doi.org/10.1093/HMG/DDI381
DOI	10.1093/HMG/DDI381
Fatcat ID	wds:Q28507633-3DD298B0-A99D-4576-84DB-CAAFB70AF2E8
Fatcat ID	release_aru4shjtnbao7cc5lnejjogsiu
ResearchGate publication ID	wds:Q28507633-849A11E6-9BD6-4114-A42B-AB500B86A6FB
ResearchGate publication ID	7557272
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28507633
is cites work of	SOX9 regulates multiple genes in chondrocytes, including genes encoding ECM proteins, ECM modification enzymes, receptors, and transporters Wnt signaling in neuromuscular junction development To build a synapse: signaling pathways in neuromuscular junction assembly Expanding functions of lipoprotein receptors Defective splicing of Megf7/Lrp4, a regulator of distal limb development, in autosomal recessive mulefoot disease Ectodomains of the LDL receptor-related proteins LRP1b and LRP4 have anchorage independent functions in vivo Apolipoprotein E and its receptors in Alzheimer's disease: pathways, pathogenesis and therapy The LDL receptor-related protein (LRP) family: an old family of proteins with new physiological functions WNT signaling in bone homeostasis and disease: from human mutations to treatments Alternative cell death mechanisms in development and beyond Role of Epiprofin, a zinc-finger transcription factor, in limb development ADAM33 is not essential for growth and development and does not modulate allergic asthma in mice Bone overgrowth-associated mutations in the LRP4 gene impair sclerostin facilitator function Disruption of Lrp4 function by genetic deletion or pharmacological blockade increases bone mass and serum sclerostin levels A Novel Domain-Specific Mutation in a Sclerosteosis Patient Suggests a Role of LRP4 as an Anchor for Sclerostin in Human Bone. Characterization of wise protein and its molecular mechanism to interact with both Wnt and BMP signals Lrp4 modulates extracellular integration of cell signaling pathways in development Lrp4 regulates initiation of ureteric budding and is crucial for kidney formation--a mouse model for Cenani-Lenz syndrome Update on Wnt signaling in bone cell biology and bone disease. Antibody effector mechanisms in myasthenia gravis-pathogenesis at the neuromuscular junction Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes Apolipoprotein E and apolipoprotein E receptors: normal biology and roles in Alzheimer disease LRP4 mutations alter Wnt/beta-catenin signaling and cause limb and kidney malformations in Cenani-Lenz syndrome Anti-LRP4 autoantibodies in AChR- and MuSK-antibody-negative myasthenia gravis Lrp4 is a receptor for Agrin and forms a complex with MuSK LRP4 serves as a coreceptor of agrin Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse Lrp4, a novel receptor for Dickkopf 1 and sclerostin, is expressed by osteoblasts and regulates bone growth and turnover in vivo The development of several organs and appendages is impaired in mice lacking Sp6. LRP5 and bone mass regulation: Where are we now? Grape-seed proanthocyanidin extract as suppressors of bone destruction in inflammatory autoimmune arthritis Birth and death of cells in limb development: a mapping study. The generation and function of soluble apoE receptors in the CNS Lipoprotein receptors--an evolutionarily ancient multifunctional receptor family A role for suppressed incisor cuspal morphogenesis in the evolution of mammalian heterodont dentition LRP4 is critical for neuromuscular junction maintenance A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice Congenital syndactyly in cattle: four novel mutations in the low density lipoprotein receptor-related protein 4 gene (LRP4)

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