About: Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice

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rdf:type	Item
description	article scientifique publié en 2006 (fr) artículu científicu espublizáu en 2006 (ast) vědecký článek publikovaný v roce 2006 (cs) наукова стаття, опублікована в липні 2006 (uk) مقالة علمية (نشرت في يوليو 2006) (ar) 2006 թվականի հուլիսին հրատարակված գիտական հոդված (hy) 2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած (hyw) vedecký článok (publikovaný 2006/07/01) (sk) wetenschappelijk artikel (gepubliceerd op 2006/07/01) (nl) scientific journal article (en) im Juli 2006 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28508475-B057F040-3B43-40E0-98E9-1E0170B94000
publication date	2006-04-04 00:00:00Z (xsd:dateTime)
author name string	wds:Q28508475-44357645-75BF-4528-AE82-CBDF45D2DB90 wds:Q28508475-53F67CC7-58C1-4D78-BC4A-C74A9D40E186 wds:Q28508475-8947AB1D-37D3-4FB3-AF27-F7492E238058 wds:Q28508475-9A60EF57-56DA-47CC-B3A6-D4FB8CC2FA30 wds:Q28508475-E8E18D51-76E4-4A66-A29C-2A0D8ACC5643
author name string	Nigel A Brown Anita Marguerie Margaret E Buckingham Fanny Bajolle Clive Dickson
rdfs:label	Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice (en) Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice (nl) Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice (ast)
skos:prefLabel	Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice (en) Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice (nl) Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice (ast)
name	Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice (en) Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice (nl) Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice (ast)
author	wds:Q28508475-20FBCFA7-8A76-4DEC-8C37-296D588D8568 wds:Q28508475-CDC96ED6-09BD-4681-9015-0D30F2EE0F1A
author	Robert G. Kelly Stéphane Zaffran
title	wds:Q28508475-0C867AEE-AC1A-495E-912B-03C2429AE497
title	Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice (en)
page(s)	wds:Q28508475-642CF472-989E-4272-BB68-81ED048E4248
page(s)	50-60
instance of	wds:Q28508475-6AEF6B61-C7BD-46BC-99F4-356C44D4B5C5
instance of	scholarly article
main subject	wds:Q28508475-B325529D-56C4-4B62-8597-6826FE518501
main subject	Fibroblast growth factor receptor 2
PubMed ID	wds:Q28508475-3B6F011B-6FE8-4D54-AE37-1908749966E0
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16687131
PubMed ID	16687131
published in	wds:Q28508475-16E13EC1-FFE6-4FAB-8F21-B8570B3FABA4
published in	Cardiovascular Research
issue	wds:Q28508475-24F586A7-BB8F-459D-9D9E-4D5626EBEC8F
volume	wds:Q28508475-D98A9317-079B-46B1-8BAF-417B79BF4B9D
issue	1
volume	71
DOI	wds:Q28508475-02DA606B-E115-4D20-B24D-B3F1CE2007AA
DOI	http://dx.doi.org/10.1016/J.CARDIORES.2006.03.021
DOI	10.1016/J.CARDIORES.2006.03.021
ResearchGate publication ID	wds:Q28508475-B330FA0B-ECFD-4615-A40B-F57E357354FD
ResearchGate publication ID	7094392
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28508475
is cites work of	How to make a heart: the origin and regulation of cardiac progenitor cells FGF-10 and specific structural elements of dermatan sulfate size and sulfation promote maximal keratinocyte migration and cellular proliferation Importance of myocyte-nonmyocyte interactions in cardiac development and disease Pluripotent stem cell derived cardiovascular progenitors--a developmental perspective Prokineticin receptor 1 (PKR1) signalling in cardiovascular and kidney functions Cardiac outflow tract anomalies Recombinant neuregulin 1 does not activate cardiomyocyte DNA synthesis in normal or infarcted adult mice. Wnt/beta-catenin signaling promotes expansion of Isl-1-positive cardiac progenitor cells through regulation of FGF signaling Redundant and dosage sensitive requirements for Fgf3 and Fgf10 in cardiovascular development An FGF autocrine loop initiated in second heart field mesoderm regulates morphogenesis at the arterial pole of the heart Genetic modifiers of the physical malformations in velo-cardio-facial syndrome/DiGeorge syndrome Exogenous addition of a C-xylopyranoside derivative stimulates keratinocyte dermatan sulfate synthesis and promotes migration The Fibroblast Growth Factor signaling pathway Role of mesodermal FGF8 and FGF10 overlaps in the development of the arterial pole of the heart and pharyngeal arch arteries Frs2alpha-deficiency in cardiac progenitors disrupts a subset of FGF signals required for outflow tract morphogenesis Identification of downstream genetic pathways of Tbx1 in the second heart field Cellular Mechanisms of Drosophila Heart Morphogenesis. A molecular and genetic outline of cardiac morphogenesis. Brn3a regulates the transition from neurogenesis to terminal differentiation and represses non-neural gene expression in the trigeminal ganglion Wnt5a and Wnt11 inhibit the canonical Wnt pathway and promote cardiac progenitor development via the Caspase-dependent degradation of AKT. Expression and function of fibroblast growth factor 10 and its receptor, fibroblast growth factor receptor 2B, in bovine follicles. Conditional deletion of focal adhesion kinase leads to defects in ventricular septation and outflow tract alignment Fibroblast growth factor-10 promotes cardiomyocyte differentiation from embryonic and induced pluripotent stem cells Visualization of outflow tract development in the absence of Tbx1 using an FgF10 enhancer trap transgene. FGF10/FGFR2b signaling is essential for cardiac fibroblast development and growth of the myocardium ISL1 directly regulates FGF10 transcription during human cardiac outflow formation Programming and reprogramming a human heart cell EvoTol: a protein-sequence based evolutionary intolerance framework for disease-gene prioritization FGF10 promotes regional foetal cardiomyocyte proliferation and adult cardiomyocyte cell-cycle re-entry. Cardiac actions of fibroblast growth factor 23. Role of SDF-1 and Wnt signaling pathway in the myocardial fibrosis of hypertensive rats The functional diversity of essential genes required for mammalian cardiac development. Origins and consequences of congenital heart defects affecting the right ventricle. Increased nuchal translucency origins from abnormal lymphatic development and is independent of the presence of a cardiac defect. FGF/FGFR signaling in health and disease FGF10 Signaling in Heart Development, Homeostasis, Disease and Repair Mutations in fibroblast growth factor (FGF8) and FGF10 identified in patients with conotruncal defects
is cites work of	wds:Q34130162-F1FCE815-F665-49AC-BA20-B2DAEBDBD5BE wds:Q38490104-4E5B6D0F-84B6-4B8D-898E-5005B430B19B wds:Q24317993-82AFDF61-845F-4855-80D5-62CE5C0A4C4D

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