Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development
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Pulmonary mastocytosis and enhanced lung inflammation in mice heterozygous null for the Foxf1 geneForkhead box F1 is essential for migration of mesenchymal cells and directly induces integrin-beta3 expressionThe forkhead box m1 transcription factor is essential for embryonic development of pulmonary vasculatureGene expression programs of human smooth muscle cells: tissue-specific differentiation and prognostic significance in breast cancers.Identification of intramural epithelial networks linked to peribiliary glands that express progenitor cell markers and proliferate after injury in mice.Epigenetic inactivation of the potential tumor suppressor gene FOXF1 in breast cancer.Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.Endothelial cell-specific deletion of transcription factor FoxM1 increases urethane-induced lung carcinogenesis.Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatelliteThe p53-p21WAF1 checkpoint pathway plays a protective role in preventing DNA rereplication induced by abrogation of FOXF1 functionDeregulation of the Hippo pathway in soft-tissue sarcoma promotes FOXM1 expression and tumorigenesisUse of transgenic mice to study lung morphogenesis and function.Histology atlas of the developing mouse hepatobiliary system with emphasis on embryonic days 9.5-18.5.Sox17 haploinsufficiency results in perinatal biliary atresia and hepatitis in C57BL/6 background miceCytoplasmic mislocalization of overexpressed FOXF1 is associated with the malignancy and metastasis of colorectal adenocarcinomasA familial case of alveolar capillary dysplasia with misalignment of pulmonary veins supports paternal imprinting of FOXF1 in humanNucleus pulposus phenotypic markers to determine stem cell differentiation: fact or fiction?The transcription factor Foxf1 binds to serum response factor and myocardin to regulate gene transcription in visceral smooth muscle cellsVertebrate endoderm development and organ formationGenetic 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 literatureDevelopment of the bile ducts: essentials for the clinical hepatologist.Transcriptional networks in liver and intestinal development.Rapid hepatocyte nuclear translocation of the Forkhead Box M1B (FoxM1B) transcription factor caused a transient increase in size of regenerating transgenic hepatocytes.Morphogenesis of liver epithelial cells.FOXF1 transcription factor is required for formation of embryonic vasculature by regulating VEGF signaling in endothelial cells.Decreased FOXF1 promotes hepatocellular carcinoma tumorigenesis, invasion, and stemness and is associated with poor clinical outcome.Foxf1 haploinsufficiency reduces Notch-2 signaling during mouse lung development.Transcriptional profiling of bovine intervertebral disc cells: implications for identification of normal and degenerate human intervertebral disc cell phenotypes.A Molecular atlas of Xenopus respiratory system developmentGenomic and Epigenetic Complexity of the FOXF1 Locus in 16q24.1: Implications for Development and Disease.The septum transversum mesenchyme induces gall bladder development.Foxm1 transcription factor is critical for proliferation and differentiation of Clara cells during development of conducting airwaysFoxF1 and FoxF2 transcription factors synergistically promote rhabdomyosarcoma carcinogenesis by repressing transcription of p21Cip1 CDK inhibitor.Septum transversum-derived mesothelium gives rise to hepatic stellate cells and perivascular mesenchymal cells in developing mouse liver.Proteomic Analysis of Nucleus Pulposus Cell-derived Extracellular Matrix Niche and Its Effect on Phenotypic Alteration of Dermal Fibroblasts.Embryonic cholecystitis and defective gallbladder contraction in the Sox17-haploinsufficient mouse model of biliary atresia.Functional characterization of evolutionarily conserved DNA regions in forkhead box f1 gene locus.Functions of the Gallbladder.Long-range enhancers modulate Foxf1 transcription in blood vessels of pulmonary vascular network.FOXF1 maintains endothelial barrier function and prevents edema after lung injury.
P2860
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P2860
Haploinsufficiency of the mouse Forkhead Box f1 gene causes defects in gall bladder development
description
2002 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Journal of Biological Chemistry
@fr
artículu científicu espublizáu en 2002
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im April 2002 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2002/04/05)
@sk
vědecký článek publikovaný v roce 2002
@cs
wetenschappelijk artikel (gepubliceerd op 2002/04/05)
@nl
наукова стаття, опублікована у квітні 2002
@uk
name
Haploinsufficiency of the mous ...... ts in gall bladder development
@ast
Haploinsufficiency of the mous ...... ts in gall bladder development
@en
Haploinsufficiency of the mous ...... ts in gall bladder development
@nl
type
label
Haploinsufficiency of the mous ...... ts in gall bladder development
@ast
Haploinsufficiency of the mous ...... ts in gall bladder development
@en
Haploinsufficiency of the mous ...... ts in gall bladder development
@nl
prefLabel
Haploinsufficiency of the mous ...... ts in gall bladder development
@ast
Haploinsufficiency of the mous ...... ts in gall bladder development
@en
Haploinsufficiency of the mous ...... ts in gall bladder development
@nl
P2093
P3181
P356
P1476
Haploinsufficiency of the mous ...... ts in gall bladder development
@en
P2093
Brian Shin
Dibyendu Bhattacharyya
Kalyani Bambal
Robert H. Costa
Vladimir V. Kalinichenko
Wooram Kim
P304
12369–12374
P3181
P356
10.1074/JBC.M112162200
P407
P577
2002-04-05T00:00:00Z