The mouse Forkhead Box m1 transcription factor is essential for hepatoblast mitosis and development of intrahepatic bile ducts and vessels during liver morphogenesis
about
Chk2 mediates stabilization of the FoxM1 transcription factor to stimulate expression of DNA repair genesFoxM1, a critical regulator of oxidative stress during oncogenesisThe Forkhead transcription factor Hcm1 regulates chromosome segregation genes and fills the S-phase gap in the transcriptional circuitry of the cell cycleThe Role of Forkhead Box Protein M1 in Breast Cancer Progression and Resistance to TherapyFOXM1, a typical proliferation-associated transcription factorHuman mitochondrial Fis1 links to cell cycle regulators at G2/M transitionThe homeobox gene Hhex is essential for proper hepatoblast differentiation and bile duct morphogenesisThe forkhead box m1 transcription factor is essential for embryonic development of pulmonary vasculaturePostnatal development, maturation and aging in the mouse cochlea and their effects on hair cell regeneration.Deletion of Forkhead Box M1 transcription factor from respiratory epithelial cells inhibits pulmonary tumorigenesis.FoxM1, a forkhead transcription factor is a master cell cycle regulator for mouse mature T cells but not double positive thymocytesGestational diabetes mellitus resulting from impaired beta-cell compensation in the absence of FoxM1, a novel downstream effector of placental lactogen.Non-viral FoxM1 gene delivery to hepatocytes enhances liver repopulation.Pro-proliferative FoxM1 is a target of p53-mediated repression.Expression of Foxm1 transcription factor in cardiomyocytes is required for myocardial development.FoxM1 regulates re-annealing of endothelial adherens junctions through transcriptional control of beta-catenin expression.Increased expression of FoxM1 transcription factor in respiratory epithelium inhibits lung sacculation and causes Clara cell hyperplasiaForkhead box M1 transcription factor is required for macrophage recruitment during liver repairSRp20 is a proto-oncogene critical for cell proliferation and tumor induction and maintenance.Novel interactions between FOXM1 and CDC25A regulate the cell cycle.Despite its strong transactivation domain, transcription factor FOXM1c is kept almost inactive by two different inhibitory domains.Foxa1 and Foxa2 regulate bile duct development in mice.Endothelial cell-specific deletion of transcription factor FoxM1 increases urethane-induced lung carcinogenesis.Multiple faces of FoxM1 transcription factor: lessons from transgenic mouse models.A cell-penetrating ARF peptide inhibitor of FoxM1 in mouse hepatocellular carcinoma treatment.Loss of Foxm1 Results in Reduced Somatotrope Cell Number during Mouse Embryogenesis.The suppression of FOXM1 and its targets in breast cancer xenograft tumors by siRNAFoxm1 regulates resolution of hyperoxic lung injury in newborns.Hypoxia-induced pulmonary arterial smooth muscle cell proliferation is controlled by forkhead box M1.Control of regional decidualization in implantation: Role of FoxM1 downstream of Hoxa10 and cyclin D3Activation of FoxM1 Revitalizes the Replicative Potential of Aged β-Cells in Male Mice and Enhances Insulin Secretion.The p38 MAPK-MK2 axis regulates E2F1 and FOXM1 expression after epirubicin treatment.Foxm1 mediates cross talk between Kras/mitogen-activated protein kinase and canonical Wnt pathways during development of respiratory epitheliumHistology atlas of the developing mouse hepatobiliary system with emphasis on embryonic days 9.5-18.5.Overexpression of FoxM1 is associated with tumor progression in patients with clear cell renal cell carcinoma.In control of biology: of mice, men and FoxesFOXM1b, which is present at elevated levels in cancer cells, has a greater transforming potential than FOXM1c.Optimized adeno-associated virus 8 produces hepatocyte-specific Cre-mediated recombination without toxicity or affecting liver regeneration.Co-targeting of Cyclooxygenase-2 and FoxM1 is a viable strategy in inducing anticancer effects in colorectal cancer cellsBeta-cell proliferation, but not neogenesis, following 60% partial pancreatectomy is impaired in the absence of FoxM1.
P2860
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P2860
The mouse Forkhead Box m1 transcription factor is essential for hepatoblast mitosis and development of intrahepatic bile ducts and vessels during liver morphogenesis
description
2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2004
@ast
im Dezember 2004 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2004/12/01)
@sk
vědecký článek publikovaný v roce 2004
@cs
wetenschappelijk artikel (gepubliceerd op 2004/12/01)
@nl
наукова стаття, опублікована в грудні 2004
@uk
مقالة علمية (نشرت في ديسمبر 2004)
@ar
name
The mouse Forkhead Box m1 tran ...... els during liver morphogenesis
@ast
The mouse Forkhead Box m1 tran ...... els during liver morphogenesis
@en
The mouse Forkhead Box m1 tran ...... els during liver morphogenesis
@nl
type
label
The mouse Forkhead Box m1 tran ...... els during liver morphogenesis
@ast
The mouse Forkhead Box m1 tran ...... els during liver morphogenesis
@en
The mouse Forkhead Box m1 tran ...... els during liver morphogenesis
@nl
prefLabel
The mouse Forkhead Box m1 tran ...... els during liver morphogenesis
@ast
The mouse Forkhead Box m1 tran ...... els during liver morphogenesis
@en
The mouse Forkhead Box m1 tran ...... els during liver morphogenesis
@nl
P2093
P1476
The mouse Forkhead Box m1 tran ...... els during liver morphogenesis
@en
P2093
Galina A. Gusarova
Helena M. Yoder
Hiroaki Kiyokawa
I.-Ching Wang
Katherine Krupczak-Hollis
Klaus H. Kaestner
Margaret B. Dennewitz
Robert H. Costa
Vladimir V. Kalinichenko
Xinhe Wang
P356
10.1016/J.YDBIO.2004.08.022
P407
P577
2004-12-01T00:00:00Z