About: The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo

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About: The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo Goto Sponge NotDistinct Permalink

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scientific journal article

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rdf:type	Item
description	artículu científicu espublizáu en 1997 (ast) vědecký článek publikovaný v roce 1997 (cs) 1997 թուականի Ապրիլին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована у квітні 1997 (uk) مقالة علمية (نشرت في أبريل 1997) (ar) 1997 թվականի ապրիլին հրատարակված գիտական հոդված (hy) vedecký článok (publikovaný 1997/04/01) (sk) article scientifique publié en 1997 (fr) wetenschappelijk artikel (gepubliceerd op 1997/04/01) (nl) scientific journal article (en) im April 1997 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28591300-466085CA-311C-40C2-8F52-C79B3A93A02A
publication date	1997-04-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q28591300-D183332A-3ADA-42BD-BEC0-ACE5CD437DA5 wds:Q28591300-D90A1531-9834-4956-8AB4-02521575A45D wds:Q28591300-E69E622C-74E3-431D-BBC2-9D19F75D7E52
author name string	B. L. Hogan G. E. Winnier L. Hargett
rdfs:label	The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo (en) The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo (nl) The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo (ast)
skos:prefLabel	The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo (en) The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo (nl) The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo (ast)
name	The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo (en) The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo (nl) The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo (ast)
title	wds:Q28591300-BC588073-E6AF-4548-BA26-808D34838D80
title	The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo (en)
page(s)	wds:Q28591300-B667D3A6-5DD4-46D2-A2FA-69707D151C23
page(s)	926–940
instance of	wds:Q28591300-6F242693-703C-4A85-A2FA-74B84036B12A
instance of	scholarly article
main subject	wds:Q28591300-0E031DD3-CB3D-4C25-B8BD-4BC21B71DD27
main subject	Forkhead box C2
PubMed ID	wds:Q28591300-42544CAB-8E5F-44C9-90FD-8E56F37E157C
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9106663
PubMed ID	9106663
published in	wds:Q28591300-7DC92F58-6CF9-4A61-8E90-C89C4E76081A
published in	Genes & Development
issue	wds:Q28591300-17468D84-68A9-4E01-83E4-4A25F7DE7D8D
volume	wds:Q28591300-BFEB1E7C-8654-4604-9294-FFC0EB4DCB62
issue	7
volume	11
DOI	wds:Q28591300-FCD5C4AF-852D-4759-9C38-0DFD4409E69B
DOI	http://dx.doi.org/10.1101/GAD.11.7.926
DOI	10.1101/GAD.11.7.926
ResearchGate publication ID	wds:Q28591300-FA1E0135-CEC9-4546-A168-1E747BF8D3E8
ResearchGate publication ID	14110461
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28591300
is cites work of	Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes. Foxc2 over-expression in bone marrow mesenchymal stem cells stimulates osteogenic differentiation and inhibits adipogenic differentiation. Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance Lack of endothelial cell survivin causes embryonic defects in angiogenesis, cardiogenesis, and neural tube closure Defective valves and abnormal mural cell recruitment underlie lymphatic vascular failure in lymphedema distichiasis. 2,3,7,8-Tetrachlorodibenzo-p-dioxin upregulates FoxQ1b in zebrafish jaw primordium. FAST-2 is a mammalian winged-helix protein which mediates transforming growth factor beta signals Regulation of the FoxO family of transcription factors by phosphatidylinositol-3 kinase-activated signaling FHX.L and FHX.S, two isoforms of the human fork-head factor FHX (FOXJ2) with differential activity The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis NKX2.1 regulates transcription of the gene for human bone morphogenetic protein-4 in lung epithelial cells Inhibition of NF-kappaB activity results in disruption of the apical ectodermal ridge and aberrant limb morphogenesis. FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain Foxc2 is a common mediator of insulin and transforming growth factor beta signaling to regulate plasminogen activator inhibitor type I gene expression Lymphatic vasculature development Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer The forkhead genes, Foxc1 and Foxc2, regulate paraxial versus intermediate mesoderm cell fate Forkhead transcription factor HFH-4 expression is temporally related to ciliogenesis The role of Bapx1 (Nkx3.2) in the development and evolution of the axial skeleton Why increased nuchal translucency is associated with congenital heart disease: a systematic review on genetic mechanisms. The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus Ciliogenesis and left-right axis defects in forkhead factor HFH-4-null mice Cell biology of normal and abnormal ciliogenesis in the ciliated epithelium Id1 and Id3 are required for neurogenesis, angiogenesis and vascularization of tumour xenografts Identification of novel craniofacial regulatory domains located far upstream of SOX9 and disrupted in Pierre Robin sequence The Ptch1(DL) mouse: a new model to study lambdoid craniosynostosis and basal cell nevus syndrome-associated skeletal defects Akt-FOXO3a signaling affects human endothelial progenitor cell differentiation Extensive brain hemorrhage and embryonic lethality in a mouse null mutant of CREB-binding protein Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defects Minimal phenotype of mice homozygous for a null mutation in the forkhead/winged helix gene, Mf2. MFH-1 is required for bone morphogenetic protein-2-induced osteoblastic differentiation of C2C12 myoblasts Expression of the mouse Fkh1/Mf1 and Mfh1 genes in late gestation embryos is restricted to mesoderm derivatives. The human forkhead protein FREAC-2 contains two functionally redundant activation domains and interacts with TBP and TFIIB Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs Hedgehog signaling in the neural crest cells regulates the patterning and growth of facial primordia The mouse forkhead gene Foxc1 is required for primordial germ cell migration and antral follicle development Forkhead box F1 is essential for migration of mesenchymal cells and directly induces integrin-beta3 expression Cooperative activity of noggin and gremlin 1 in axial skeleton development Shh establishes an Nkx3.2/Sox9 autoregulatory loop that is maintained by BMP signals to induce somitic chondrogenesis. The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development Cross-talk in kidney development Myogenic stem cell function is impaired in mice lacking the forkhead/winged helix protein MNF Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome Indian hedgehog signaling from endothelial cells is required for sclera and retinal pigment epithelium development in the mouse eye Sclerotome induction and differentiation. The mouse notches up another success: understanding the causes of human vertebral malformation. Abnormal skeletogenesis occurs coincident with increased apoptosis in the Splotch (Sp2H) mutant: putative roles for Pax3 and PDGFRalpha in rib patterning

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