About: Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development

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rdf:type	Item
description	artículu científicu espublizáu en 2002 (ast) vědecký článek publikovaný v roce 2002 (cs) 2002 թվականի ապրիլին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована у квітні 2002 (uk) 2002 թուականի Ապրիլին հրատարակուած գիտական յօդուած (hyw) vedecký článok (publikovaný 2002/04/05) (sk) مقالة علمية (نشرت في 5-4-2002) (ar) wetenschappelijk artikel (gepubliceerd op 2002/04/05) (nl) article publié dans la revue scientifique Journal of Biological Chemistry (fr) im April 2002 veröffentlichter wissenschaftlicher Artikel (de) scientific journal article (en)
publication date	wds:Q28587688-6C7D84FE-8DB7-44BA-8232-1D127A02BA2A
publication date	2002-04-05 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28587688-52DE6380-787C-4087-8AF0-CE11979A285C
language of work or name	English
author name string	wds:Q28587688-0A073262-699B-4EE9-9DF2-7A59F8FD4CCF wds:Q28587688-28C8F329-6126-4A11-8993-7070D8783005 wds:Q28587688-3C522F74-E940-49AE-830F-9CA04BA60F95 wds:Q28587688-54C2272A-A941-4D28-944F-2C9453D20F4B wds:Q28587688-69954D7B-52DE-4ECA-8AAD-0CFA50F0CEB1 wds:Q28587688-77C05D6C-5E3B-46A9-948A-48A510C65252 wds:Q28587688-CA457ED7-F053-4BE1-B71E-AE9026FCC31D
OpenCitations bibliographic resource ID	wds:Q28587688-0BE01B2C-1784-4937-B0AB-05F30D24A78E
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/5081507
author name string	Yan Zhou Robert H. Costa Wooram Kim Dibyendu Bhattacharyya Brian Shin Vladimir V. Kalinichenko Kalyani Bambal
OpenCitations bibliographic resource ID	5081507
rdfs:label	Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development (en) Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development (nl) Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development (ast)
skos:prefLabel	Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development (en) Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development (nl) Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development (ast)
name	Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development (en) Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development (nl) Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development (ast)
title	wds:Q28587688-395EF459-3CA4-48E5-BB6D-4ED636E8C036
title	Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development (en)
page(s)	wds:Q28587688-DCCE5A60-9FED-407B-A85A-5B10F4EC5CC8
page(s)	12369–12374
instance of	wds:Q28587688-EEC650E7-FC37-44FE-842F-F1A28571C722
instance of	scholarly article
main subject	wds:Q28587688-323DA368-B9FC-4511-B44D-62DACD95B67E wds:Q28587688-E1AE7C41-5705-42A3-8745-0CF6FA38CB2C
main subject	haploinsufficiency Forkhead box F1
PubMed ID	wds:Q28587688-D4867A89-597C-4D75-9C6B-ACC5E9D83EF9
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11809759
PubMed ID	11809759
published in	wds:Q28587688-EB51E252-6255-4674-B2F6-725D8A5E596D
published in	Journal of Biological Chemistry
issue	wds:Q28587688-93EAF4EB-7A85-4ADE-8DF9-696636A720EA
volume	wds:Q28587688-4E301CDA-3DEF-4B3B-9DD4-EBFF8FAB9624
issue	14
volume	277
DOI	wds:Q28587688-CF588818-9EBD-45B8-BAA3-11F77E522336
DOI	http://dx.doi.org/10.1074/JBC.M112162200
DOI	10.1074/JBC.M112162200
ResearchGate publication ID	wds:Q28587688-2A92C80D-51AF-4CE5-8C50-9D903A7E05B3
ResearchGate publication ID	11549155
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28587688
is cites work of	Histology atlas of the developing mouse hepatobiliary system with emphasis on embryonic days 9.5-18.5. The forkhead box m1 transcription factor is essential for embryonic development of pulmonary vasculature Endothelial cell-specific deletion of transcription factor FoxM1 increases urethane-induced lung carcinogenesis Defective development of the gall bladder and cystic duct in Lgr4- hypomorphic mice. The forkhead box F1 transcription factor is expressed in brain and head mesenchyme during mouse embryonic development Transcriptional profiling of bovine intervertebral disc cells: implications for identification of normal and degenerate human intervertebral disc cell phenotypes The mouse Forkhead Box m1 transcription factor is essential for hepatoblast mitosis and development of intrahepatic bile ducts and vessels during liver morphogenesis Development of the biliary tract Regulatory phases of early liver development: paradigms of organogenesis Pulmonary mastocytosis and enhanced lung inflammation in mice heterozygous null for the Foxf1 gene Vertebrate endoderm development and organ formation Transcriptional networks in liver and intestinal development Peutz-Jeghers LKB1 mutants fail to activate GSK-3beta, preventing it from inhibiting Wnt signaling Development of the bile ducts: essentials for the clinical hepatologist Differences in the embryonic expression patterns of mouse Foxf1 and -2 match their distinct mutant phenotypes Forkhead box F1 is essential for migration of mesenchymal cells and directly induces integrin-beta3 expression Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature Sonic hedgehog signaling regulates Gli3 processing, mesenchymal proliferation, and differentiation during mouse lung organogenesis Smooth muscle function and dysfunction in gallbladder disease Epigenetic inactivation of the potential tumor suppressor gene FOXF1 in breast cancer Identification of intramural epithelial networks linked to peribiliary glands that express progenitor cell markers and proliferate after injury in mice Sox17 haploinsufficiency results in perinatal biliary atresia and hepatitis in C57BL/6 background mice Embryonic development of the liver Septum transversum-derived mesothelium gives rise to hepatic stellate cells and perivascular mesenchymal cells in developing mouse liver. Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene. Foxf1haploinsufficiency reduces Notch-2 signaling during mouse lung development Functional characterization of evolutionarily conserved DNA regions in forkhead box f1 gene locus. A Molecular atlas of Xenopus respiratory system development Use of transgenic mice to study lung morphogenesis and function Myocardium defects and ventricular hypoplasia in mice homozygous null for the Forkhead Box M1 transcription factor. Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite Cytoplasmic mislocalization of overexpressed FOXF1 is associated with the malignancy and metastasis of colorectal adenocarcinomas A familial case of alveolar capillary dysplasia with misalignment of pulmonary veins supports paternal imprinting of FOXF1 in human

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