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Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
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Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
Steno Diabetes Center Copenhagen, Gentofte, Denmark
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course with the alpha-glucosidase inhibitor, acarbose, on GM profiles (evaluated by 16S rRNA gene-based high-throughput sequencing) in Caucasian individuals with metformin-treated T2D. Materials and methods Ethics and study approvals This
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), anthranilic acid (AA), 3-hydroxyanthranilic acid (HAA), 5-hydroxyindole-3-acetic acid (HIAA), indole-3-lactic acid (ILA), indole-3-acetic acid (IAA) and indole-3-propionic acid (IPA). Gut microbiome Stool specimens for 16S rRNA-based gut microbiome
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‘Research of Age and Age-Associated Conditions’ Department, Laboratory of Bioinformatics, The ‘Russian Clinical Research Center for Gerontology’, ‘Chronic Noncommunicable Diseases Primary Prevention in the Healthcare System’ Department, Moscow Institute of Physics and Technology, National Research Centre for Preventive Medicine, National Research Centre for Preventive Medicine, Building 10, Petroverigskiy Lane, Moscow RF 101000, Russian Federation
‘Research of Age and Age-Associated Conditions’ Department, Laboratory of Bioinformatics, The ‘Russian Clinical Research Center for Gerontology’, ‘Chronic Noncommunicable Diseases Primary Prevention in the Healthcare System’ Department, Moscow Institute of Physics and Technology, National Research Centre for Preventive Medicine, National Research Centre for Preventive Medicine, Building 10, Petroverigskiy Lane, Moscow RF 101000, Russian Federation
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then thawed; the DNA was extracted from each sample; sequencing of the variable V3–V4 16S rRNA gene regions was performed (after the total DNA isolation and library preparation) by using an MiSeq Reagent Kit v2 (300 cycles) and MiSDefault (Illumina, San
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extraction kit, and the quality of the extracted DNA was detected using a Qubit dsDNA HS Assay Kit (Carlsbad, CA, USA). After eliminating the samples that did not meet the test standard, the V3–V4 variable region of the 16S rRNA was specifically amplified by
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clustered using the RDP classifier ( http://rdp.cme.msu.edu/ ) and compared with Silva database (SSU128/16s bacteria) at 70% comparison threshold. Bioinformatics analysis Silva database was selected for comparison with threshold of 70% to obtain the
Department of Endocrinology, Zunyi Medical University, Zunyi, China
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targets, and sample-specific barcode sequences were used for PCR amplification of the variable regions of the 16S rRNA gene (Q5 HiFi DNA polymerase; NEB, Ipswich, MA, USA). The amplification products were subjected to 2% agarose gel electrophoresis, and
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.01 vs NFD group. # P < 0.05, ## P < 0.01 vs HGD group. Effects of HGD on the gut microbiota The composition of the gut microbiota was analyzed by bacterial 16S rRNA sequencing of the intestinal feces. After dereplication of unqualified
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were evaluated by a Nanodrop 2000 (Wilmington, DE, USA), and RNA integrity was assessed by native agarose gel electrophoresis by inspecting the 28S and 18S rRNA bands. High-throughput circular RNA sequencing After removal of rRNA and
Aix Marseille University, INSERM, INRA, C2VN, Marseille, France
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Research Unit EA 3279 and Department of Public Health, Aix-Marseille University, Marseille, France
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Research Unit EA 3279 and Department of Public Health, Aix-Marseille University, Marseille, France
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Nutrition, Metabolic Diseases and Endocrinology Department, AP-HM, La Conception Hospital, Marseille, France
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Aix-Marseille University, CNRS, CRMBM, Marseille, France
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Nutrition, Metabolic Diseases and Endocrinology Department, AP-HM, La Conception Hospital, Marseille, France
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. We used 18S rRNA as a normalization control. Gene expression changes were evaluated using the LIVAK method ( 26 ). Primer designs can be provided on request. For the differentiation markers in culture, real-time PCR assays were run on a StepOne
Medical Research Laboratories, Department of Endocrinology and Diabetes, Department of Pediatrics, Department of Endocrinology and Diabetes, Institute of Clinical Medicine, Aarhus University, Norrebrogade 44, DK-8000 Aarhus C, Denmark
Medical Research Laboratories, Department of Endocrinology and Diabetes, Department of Pediatrics, Department of Endocrinology and Diabetes, Institute of Clinical Medicine, Aarhus University, Norrebrogade 44, DK-8000 Aarhus C, Denmark
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Medical Research Laboratories, Department of Endocrinology and Diabetes, Department of Pediatrics, Department of Endocrinology and Diabetes, Institute of Clinical Medicine, Aarhus University, Norrebrogade 44, DK-8000 Aarhus C, Denmark
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Medical Research Laboratories, Department of Endocrinology and Diabetes, Department of Pediatrics, Department of Endocrinology and Diabetes, Institute of Clinical Medicine, Aarhus University, Norrebrogade 44, DK-8000 Aarhus C, Denmark
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Medical Research Laboratories, Department of Endocrinology and Diabetes, Department of Pediatrics, Department of Endocrinology and Diabetes, Institute of Clinical Medicine, Aarhus University, Norrebrogade 44, DK-8000 Aarhus C, Denmark
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inspection of the two rRNAs, 18S and 28S , on an agarose gel. cDNA was synthesized with the Verso cDNA kit AB 1453 (Thermo Fisher Scientific, Inc.) using random hexamers. Real-time PCR for target gene was done with β2-microglobulin levels as internal