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tumor and stromal components using Zeiss PALM MicroBeam IV LCM microscope (Carl Zeiss MicroImaging, GmbH). This resulted in four samples for each patient: tumor cells of primary tumor, tumor cells of mesenteric metastasis, stromal cells of primary tumor
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Green Templeton College, University of Oxford, Oxford, UK
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a transcription-factor based classification, a similar move could be envisaged using positive immunostaining for the TTF-1 transcription factor as a key characteristic of all PPTs. Pituicytomas and the related sellar ependymomas, spindle cell
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and adhesion of diabetic endothelial cells, as well as a relative decrease in VEGF secretion by mesenchymal stem cells and wound fibroblasts, have been observed in diabetic skin ( 9 , 10 ). Finally, adipose stem cells from diabetic mice showed a
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. ( https://doi.org/10.1007/BF02892423 ) 6108645 6 Graffmann N Ring S Kawala MA Wruck W Ncube A Trompeter HI Adjaye J . Modeling nonalcoholic fatty liver disease with human pluripotent stem cell-derived immature hepatocyte-like cells reveals
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://doi.org/10.1128/MCB.25.12.4969-4976.2005 ) 38 Zhu Y Liu Q Zhou Z Ikeda Y . PDX1, neurogenin-3, and MAFA: critical transcription regulators for beta cell development and regeneration . Stem Cell Research and Therapy 2017 8 240. ( https
School of Medicine, Universidad de los Andes, Bogotá, Colombia
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Endocrinology Section, Hospital Universitario Fundación Santa Fe de Bogotá, Bogotá, Colombia
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School of Medicine, Universidad de los Andes, Bogotá, Colombia
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School of Medicine, Universidad de los Andes, Bogotá, Colombia
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DNA demethylation has been actively studied, and recently, a crucial role has been observed for their expression in stem cells and during processes of differentiation and cell reprogramming ( 24 , 25 , 26 , 27 ). In addition to active demethylation
Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, The Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, The Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, The Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, The Netherlands
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Department of Pediatric Neuro-Oncology, Prinses Máxima Centrum, Utrecht, The Netherlands
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Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, The Netherlands
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expressed in the brain. They are members of the nuclear receptor family and act as transcriptional regulators. Activation by cortisol leads to translocation of the receptors from the cytoplasm to the cell nucleus and subsequent interaction with DNA and
School of Medicine, Western Sydney University, Sydney, Australia
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Westmead Clinical School, University of Sydney, Sydney, Australia
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Westmead Clinical School, University of Sydney, Sydney, Australia
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Department of Neurosurgery, Westmead Hospital, Sydney, Australia
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School of Medicine, Western Sydney University, Sydney, Australia
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, mammosomatotroph, acidophil stem cell, and mixed somatotroph and lactotroph tumours ( 2 ). Here we demonstrate that multilineage PIT1 and SF1 PitNETs can also cause acromegaly, express SSTR and respond to SRL. The pattern of SSTR expression in this group of
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Maebashi Hirosegawa Clinic, Maebashi, Gunma, Japan
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the vasoprotective and vasopressor effects of nesfatin-1 at different doses in mouse models of peripheral arterial remodeling. Additionally, we sought to clarify the underlying mechanisms in cultured human vascular endothelial cells (VECs) and vascular
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INSERM Unité 1203 (DEFE), Université de Montpellier, Montpellier, France
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Département d'Endocrinologie et de Gynécologie Pédiatrique, Hôpital Arnaud de Villeneuve, Université de Montpellier, Montpellier, France
INSERM Unité 1203 (DEFE), Université de Montpellier, Montpellier, France
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. Molecular Endocrinology 2015 29 1581 – 1593 . ( https://doi.org/10.1210/me.2015-1200 ) 37 Ye L Li X Li L Chen H & Ge RS . Insights into the development of the adult leydig cell lineage from stem Leydig cells . Frontiers in Physiology 2017 8