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ProfilXpert, Lyon, France
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Department of Pathology, Groupement Hospitalier EST, Hospices Civils de Lyon, University of Lyon, Lyon, France
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Department of Pathology, Groupement Hospitalier EST, Hospices Civils de Lyon, University of Lyon, Lyon, France
Department of Endocrinology, Reference Center for Rare Pituitary Disease (HYPO), Groupement Hospitalier EST, Hospices Civils de Lyon, University of Lyon, Lyon, France
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-Cruz Biotechnology), P-Smad2 (Rabbit, Chemicon International, USA), cleaved caspase3 (Rabbit, Cell Signaling Technology). Phase contrast and fluorescence images were acquired on an Eclipse-NiE NIKON microscope and analysed using NIS-Elements Software. ALK7 expression
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Regional Hospital Cosenza, Italy
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Regional Hospital Cosenza, Italy
Endocrinology Department of Health, University Magna Graecia of Catanzaro, Catanzaro, Italy
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Regional Hospital Cosenza, Italy
Endocrinology Department of Health, University Magna Graecia of Catanzaro, Catanzaro, Italy
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Regional Hospital Cosenza, Italy
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6000 Advanced Fluorescence Imaging System supported by the quantification and image processing software Leica Application Suite Advanced Fluorescence (Leica Microsystems CMS, GbH Mannheim, Germany) were used for evaluation of experiments. Migration
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microscope slide and coverslip with 50% glycerol in water. For TEM, grids were unmounted, washed in Milli-Q water and incubated for 5 min in 0.4% uranyl acetate and 1.8% methylcellulose. Fluorescence images were obtained using a FluoView FV 1200 microscope
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International 2109 – 2117 . ( https://doi.org/10.1046/j.1523-1755.2001.00042.x ) Cui L Gao Y Yu H Li M Wang B Zhou T Hu Q 2017 Intraoperative parathyroid localization with near-infrared fluorescence imaging using indocyanine green during
Center for Neuroendocrine and Endocrine Tumors, University Hospital Basel, Basel Switzerland
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Clinic of Radiology and Nuclear Medicine, University Hospital, Basel, Switzerland
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. Nuklearmedizin 58 124 . ( https://doi.org/10.1055/s-0039-1683525 ) Brand C Abdel-Atti D Zhang Y Carlin S Clardy SM Keliher EJ Weber WA Lewis JS Reiner T 2014 In vivo imaging of GLP-1R with a targeted bimodal PET/fluorescence imaging
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concentrations of ATR-101 for 20 h is shown. The inserts show fluorescence images of cells cultured in the presence of the indicated concentrations of ATR-101 followed by SYTOX staining. (D) Reversibility of membrane permeability and ATP depletion following ATR
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Department of Anatomy and Structural Science, Yamagata University Faculty of Medicine, Yamagata, Japan
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that were re-plated in Matrigel droplets, all as previously described ( Cox et al. 2019 , Vennekens et al. 2021 ; and above). Brightfield and fluorescence images were acquired using an Axiovert 40 CFL microscope (Zeiss, Jena, Germany
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Institute of Biomedicine, University of Eastern Finland, Kuopio, Finland
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. Live cell fluorescence imaging All the above-mentioned assays are valuable tools to characterize the action of TFs. However, they suffer from two major drawbacks; the assays average signals across populations of heterogeneous cells and rely on dead