Foxm1 expression in prostate epithelial cells is essential for prostate carcinogenesis.
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Regulatory functional territory of PLK-1 and their substrates beyond mitosis.SPDEF inhibits prostate carcinogenesis by disrupting a positive feedback loop in regulation of the Foxm1 oncogene.Forkhead box F2 regulation of platelet-derived growth factor and myocardin/serum response factor signaling is essential for intestinal developmentFoxm1 regulates resolution of hyperoxic lung injury in newborns.Forkhead Box M1 Is Essential for Nuclear Localization of Glioma-associated Oncogene Homolog 1 in Glioblastoma Multiforme Cells by Promoting Importin-7 Expression.FOXM1 is a therapeutic target for high-risk multiple myeloma.FOXM1 promotes the progression of prostate cancer by regulating PSA gene transcription.Plk1 Regulates the Repressor Function of FoxM1b by inhibiting its Interaction with the Retinoblastoma ProteinO-GlcNAcylation in Cancer Biology: Linking Metabolism and Signaling.Cross-species regulatory network analysis identifies a synergistic interaction between FOXM1 and CENPF that drives prostate cancer malignancyIncreased FoxM1 expression is associated with clinicopathological features and confers a poor prognosis in human hepatocellular carcinoma.The Emerging Roles of Forkhead Box (FOX) Proteins in Osteosarcoma.The tumour hypoxia marker pimonidazole reflects a transcriptional programme associated with aggressive prostate cancer.FoxM1 is associated with metastasis in colorectal cancer through induction of the epithelial-mesenchymal transition.Treatment with docetaxel in combination with Aneustat leads to potent inhibition of metastasis in a patient-derived xenograft model of advanced prostate cancer.The transcription factor FOXF1 promotes prostate cancer by stimulating the mitogen-activated protein kinase ERK5.FOXF1 maintains endothelial barrier function and prevents edema after lung injury.UBE2C Is a Transcriptional Target of the Cell Cycle Regulator FOXM1.FOXF1 Inhibits Pulmonary Fibrosis by Preventing CDH2-CDH11 Cadherin Switch in Myofibroblasts.FoxM1 repression during human aging leads to mitotic decline and aneuploidy-driven full senescence
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Foxm1 expression in prostate epithelial cells is essential for prostate carcinogenesis.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 17 June 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Foxm1 expression in prostate epithelial cells is essential for prostate carcinogenesis.
@en
Foxm1 expression in prostate epithelial cells is essential for prostate carcinogenesis.
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type
label
Foxm1 expression in prostate epithelial cells is essential for prostate carcinogenesis.
@en
Foxm1 expression in prostate epithelial cells is essential for prostate carcinogenesis.
@nl
prefLabel
Foxm1 expression in prostate epithelial cells is essential for prostate carcinogenesis.
@en
Foxm1 expression in prostate epithelial cells is essential for prostate carcinogenesis.
@nl
P2093
P2860
P356
P1476
Foxm1 expression in prostate epithelial cells is essential for prostate carcinogenesis
@en
P2093
Andrea Hiller
Andrew M Paluch
David Balli
Logan Fulford
Susan Kasper
Tanya V Kalin
Vinko Misetic
Vladimir Ustiyan
Yufang Zhang
P2860
P304
22527-22541
P356
10.1074/JBC.M113.455089
P407
P577
2013-06-17T00:00:00Z