Department of Pediatric Cardiology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China
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among their peripheral blood mononuclear cells (PBMCs) than healthy individuals. To reveal the mechanism of the increase in peripheral B cells, we studied the lncRNA and mRNA profiles of peripheral B cells from patients with GD by microarray analysis. We
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microarray assay. Endometrium collection and mRNA extraction Mouse uterus was longitudinally dissected and scraped using the back of a scalpel into RNA Later on ice. Total RNA was extracted using an RNeasy Mini-kit (Qiagen) according to the
Department of Nutrition, School of Public Health, Sun Yat-Sen University, Guangzhou, People’s Republic of China
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Guangdong Provincial Key Laboratory of Food, Nutrition and Health, Guangzhou, People’s Republic of China
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Guangdong Provincial Key Laboratory of Food, Nutrition and Health, Guangzhou, People’s Republic of China
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clarified. In the past few years, liver transcriptome technology including microarray and RNA-seq has been widely used for gene expression profiling in the liver tissues from NAFLD patients. However, inconsistencies exist in these studies and some datasets
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cord vein blood from normal pregnancy and GDM-induced macrosomia groups to a microarray. The results were deposited in NCBI’s Gene Expression Omnibus (accession number GSE65737) ( http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE65737 ) ( 13 ). Of
Shanghai National Clinical Research Center for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission of the PR China, Shanghai National Center for Translational Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
Guangdong Geriatric Institute, Guangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China
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Shanghai National Clinical Research Center for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission of the PR China, Shanghai National Center for Translational Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
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Shanghai National Clinical Research Center for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission of the PR China, Shanghai National Center for Translational Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
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Reproductive Medicine Center, Guangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China
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Shanghai National Clinical Research Center for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission of the PR China, Shanghai National Center for Translational Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
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Division of Endocrinology, Department of Internal Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China
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Shanghai National Clinical Research Center for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission of the PR China, Shanghai National Center for Translational Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
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or without T 3 (Sigma-Aldrich) for 24 h or 7 days. After 24 h and 7 days, the cells were harvested, and RNA was extracted for qRT-PCR analysis. lncRNA microarray Three initial GD patients CD4+ T cells and three age- and sex- matched healthy
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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hydroxymethylation and the expression of the demethylation machinery in previously published microarray data from several tissues to find an explanation for the methylome alterations in our patients. Materials and methods Patients and samples Peripheral
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study, we have used microarray analysis of mouse adrenal tissue to gain a comprehensive picture of transcriptional control processes affecting cell signalling, cholesterol supply and cell turnover in response to chronic stimulation of corticosterone
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within the lncRNA have more activity ( 15 ). However, we found very few studies that have identified an association between insulin resistance in GDM and lncRNAs via high-throughput methods (i.e. microarray and RNA-seq). In this study, lncRNA is
Berlin Institute of Health (BIH), Berlin, Germany
Department of Nephrology, School of Medicine, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany
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Core Unit Bioinformatics, Berlin Institute of Health, Berlin, Germany
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Core Unit Bioinformatics, Berlin Institute of Health, Berlin, Germany
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Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany
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Berlin Institute of Health (BIH), Berlin, Germany
Department of Nephrology, School of Medicine, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany
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-stage Benjamini, Krieger and Yekutieli FDR procedure was used. Gene expression microarray Six nonresistant and six mitotane-resistant clones were thawed and cultured to confluence without mitotane. Cells were seeded on a six-well plate (1 × 10 6 cells per
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. In this study, we first identified circRNAs expressed in GD patients using a circRNA microarray. Subsequently, enrichment analysis was carried out to detect the potential function of differentially expressed circRNAs (DECs). To gain further