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methods In vitro primary GC culture Primary GC culture was performed as previously described ( 15 ). For testing the effects of fatty acids, the media (supplemented α-MEM) were replaced after 48 h with the same media containing different
Centro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI-CONICET), Haya de la Torre y Medina Allende, Ciudad Universitaria, Córdoba (X5000HUA), Argentina
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Instituto de Investigaciones en Ciencias de la Salud (INICSA-CONICET), Av. Enrique Barros y Enfermera Gordillo, Ciudad Universitaria, Córdoba, Argentina
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Centro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI-CONICET), Haya de la Torre y Medina Allende, Ciudad Universitaria, Córdoba (X5000HUA), Argentina
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approved by the Ethical Committee of Hospital Nacional de Clínicas, Universidad Nacional de Córdoba. Cells were cultured in high glucose DMEM media (HG-DMEM; Sigma Aldrich) or RPMI 1640 media (Gibco; Life Technologies) supplemented with 10% v/v fetal bovine
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Doctoral School of Health Sciences, University of Debrecen, Debrecen, Hungary
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Doctoral School of Health Sciences, University of Debrecen, Debrecen, Hungary
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women were aware of the health importance of iodine, mainly learning this fact from the health visitor (30/73; 30% of all), the gynaecologist (24/73; 24% of all) or from the media (22/73; 22% of all). The health visitor system was introduced in 1915 and
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no significant difference in sex composition, age, and TG, HDL-C, FBG, HbA1c, AST and ALT levels between the two groups. Blood pressure, BMI, carotid intima–media thickness and TC, LDL-C, GGT, ALP, and ET-1 levels were higher in patients with
Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Adelaide, South Australia, Australia
Department of Medicine, Faculty of Health and Medical Sciences, University of Adelaide, South Australia, Australia
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St Vincent’s Institute of Medical Research, Fitzroy, Victoria, Australia
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Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Adelaide, South Australia, Australia
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Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Adelaide, South Australia, Australia
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Future Industries Institute, University of South Australia, Mawson Lakes, South Australia, Australia
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School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, South Australia, Australia
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Transplantation Immunology Group, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia
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Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria, Australia
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Cooperative Research Centre for Cell Therapy Manufacturing (CRC-CTM), Adelaide, South Australia, Australia
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next morning, control islets were transferred into a 1.7 mL screw-cap microfuge tube. Tubes were filled with complete media before sealing. This is representative of shipping human islets in 50 mL Falcon tubes, a practice that is widely used in many
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DMEM/F12 media supplemented with 10% fetal bovine serum and 1% streptomycin/penicillin (E490-20ML, VWR, Radnor, PA, USA). Cells were subcultured separately into four groups (control, 1-h Dex-treated, 24-h Dex-treated, and 48-h Dex-treated) using six
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Department of Neurosurgery, Technical University Munich (TMU), Munich, Germany
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Medizinische Klinik Und Poliklinik III, University Hospital Carl Gustav Carus, Dresden, Germany
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Centre for Endocrinology, Diabetes and Metabolism, Birmingham Health Partners, Birmingham, UK
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Centre for Endocrinology, Diabetes and Metabolism, Birmingham Health Partners, Birmingham, UK
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( 33 ) and more recently developed MUC-1 ( 34 ), CU-ACC1 and CU-ACC2 cells ( 35 ). NCI-H295R cells were cultured in Dulbecco’s modified eagle medium (DMEM)/F12, HEPES media) (Gibco, 11330032), supplemented with 2.5% Nu-Serum growth media supplement
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insufficient in the case of PCOS. Several studies were published exploring the influence of public media coverage of other health issues ( 107 , 108 , 109 ). However, the only study exploring how digital (online) teen and women’s magazines portray women with
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Maebashi Hirosegawa Clinic, Maebashi, Gunma, Japan
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treatment. The areas within the internal elastic lamina and between the internal and external elastic lamina were defined as the neointima and media, and the perimeter of the external elastic lamina was defined as the artery perimeter ( 22 ). Sections with
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Section Endocrinology, Department of Medicine, Erasmus MC, Rotterdam, The Netherlands
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cardiovascular disease when analysed as a combination reflecting different pathophysiologic pathways, to reveal underlying patterns or clusters of dysmetabolic development ( 18 ). In addition, vascular ultrasound measurements, such as carotid intima media