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Cancer Biology and Therapeutics Laboratory, UCD Conway Institute of Biomolecular and Biomedical Science, University College Dublin, Belfield, Dublin, Ireland
Systems Biology Ireland, University College Dublin, Belfield, Dublin, Ireland
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mM dithiothreitol at 37°C for 30 min before being diluted 20-fold in dilution buffer and proceeding with the second ChIP. Antibodies CREB (Cell Signaling Technology, 9197), CREB phospho-Ser133 (Cell Signaling Technology, 9198), ERα (Santa Cruz
Section on Endocrinology and Genetics, School of Health and Biosciences, Department of Pharmacology and Physiology, Laboratory of Genomics and Molecular Biology, Department of Pathology, Department of Statistics, Program on Developmental Endocrinology and Genetics (PDEGEN) and Pediatric Endocrinology Inter‐institute Training Program, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD 20892, USA
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Section on Endocrinology and Genetics, School of Health and Biosciences, Department of Pharmacology and Physiology, Laboratory of Genomics and Molecular Biology, Department of Pathology, Department of Statistics, Program on Developmental Endocrinology and Genetics (PDEGEN) and Pediatric Endocrinology Inter‐institute Training Program, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD 20892, USA
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Section on Endocrinology and Genetics, School of Health and Biosciences, Department of Pharmacology and Physiology, Laboratory of Genomics and Molecular Biology, Department of Pathology, Department of Statistics, Program on Developmental Endocrinology and Genetics (PDEGEN) and Pediatric Endocrinology Inter‐institute Training Program, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD 20892, USA
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knowledge of the origin of the tissue. Tissues from only two patients with low number of PDE variants were available. Therefore they were not included for the statistical analysis. We studied the expression of cAMP-responsive element binding protein (CREB
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University of the Chinese Academy of Sciences, Beijing, China
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overexpressed in pNEN tissues and was positively correlated with H19 expression to promote cancer progression. Moreover, higher VGF expression was markedly related to poor differentiation and advanced stage. RNA sequence analysis revealed that H19 activates PI3K/Akt/CREB
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University of the Chinese Academy of Sciences, Beijing, China
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primary cultured MEC. We also show that Src- or extracellular signal-regulated kinase (ERK)-dependent cAMP-responsive element-binding protein (CREB) activation is required for the aromatase induction in p53-inactivated MEC. Materials and methods Materials
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polyclonal anti-EGFR antibodies were obtained from Santa Cruz Biotechnology. The polyclonal anti-phospho-AKT, anti-AKT, anti-phospho-CREB1, and anti-CREB1 antibodies were obtained from Cell Signaling Technology (Danvers, MA, USA). The HRP-conjugated goat anti
Institute of Endocrinology e Experimental Oncology, Department of Biology and Cellular, Department of Pharmaceutical Sciences, National Institute of Digestive Diseases, CNR, Via Pansini 5, 80131 Naples, Italy
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transcription factor CRE-binding protein (CREB protein; Bosier et al . 2008 ). In this study, we observed that the activation of CB1 receptor by 2-methyl-2′-F-anandamide (Met-F-AEA) inhibited the HMG-CoA reductase activity due to the decrease of HMG
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Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Neurosurgery Unit, Milan, Italy
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Department of Biomedical Sciences, Humanitas University, Milan, Italy
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Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Endocrinology Unit, Milan, Italy
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Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Endocrinology Unit, Milan, Italy
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-binding protein (CREB) have been encountered in USP8-mutated corticotropinomas as well ( Weigand et al. 2019 ). Interestingly, Sesta and colleagues have recently found that POMC is subject to ubiquitination, regardless of USP8 sequence status ( Sesta et al
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Department of Medicine, Department of Applied Biomedical Science, Neuroendocrine Clinic, Faculty of Medicine and Surgery, Mater Dei Hospital, University of Malta, Block A, Level 0, Msida MSD2080, Malta
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to the well-characterised CRE in its promoter region and the fact that a number of studies have similarly used Id1 expression as an indication of CREB transcription factor activity ( Zhang et al . 2005 , Ohta et al . 2008 , San-Marina et al
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Foundation for Advanced Biomedical Research, Veneto Institute of Molecular Medicine (VIMM), Padova, Italy
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Department of Molecular Medicine, University of Pavia, Pavia, Italy
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intracellular cAMP levels ( Szecówka et al. 1982 ) and consequently, PKA-CREB-dependent signal transduction. In addition, GIP/GIPR signaling exerts pro-proliferative and antiapoptotic effects through the activation of mitogen-activated protein kinase (MAPK