Postgraduation Program in Medical Sciences: Endocrinology, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil
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Postgraduation Program in Medical Sciences: Endocrinology, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil
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Postgraduation Program in Medical Sciences: Endocrinology, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil
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greater depth the functional involvement of miRNAs in T1DM, we selected those miRNAs that were consistently dysregulated in T1DM-related tissues (PBMCs, serum/plasma and pancreas) and performed bioinformatic analysis to retrieve their putative targets and
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’GGGAAACTGTGGCGTGAT3’ R: 5’GAGTGGGTGTCGCTGTTGA3’ U6(HUMAN) F: 5’AGAGAAGATTAGCATGGCCCCTG3’ F, forward. R, reverse. Cell culture and transfection The aforementioned bioinformatic analysis and RT-qPCR results suggested that the
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N6-methyladenosine (m6A) methylation has been reported to play a role in type 2 diabetes (T2D). However, the key component of m6A methylation has not been well explored in T2D. This study investigates the biological role and the underlying mechanism of m6A methylation genes in T2D. The Gene Expression Omnibus (GEO) database combined with the m6A methylation and transcriptome data of T2D patients were used to identify m6A methylation differentially expressed genes (mMDEGs). Ingenuity pathway analysis (IPA) was used to predict T2D-related differentially expressed genes (DEGs). Gene ontology (GO) term enrichment and the Kyoto Encyclopedia of Genes and Genomes (KEGG) were used to determine the biological functions of mMDEGs. Gene set enrichment analysis (GSEA) was performed to further confirm the functional enrichment of mMDEGs and determine candidate hub genes. The least absolute shrinkage and selection operator (LASSO) regression analysis was carried out to screen for the best predictors of T2D, and RT-PCR and Western blot were used to verify the expression of the predictors. A total of 194 overlapping mMDEGs were detected. GO, KEGG, and GSEA analysis showed that mMDEGs were enriched in T2D and insulin signaling pathways, where the insulin gene (INS), the type 2 membranal glycoprotein gene (MAFA), and hexokinase 2 (HK2) gene were found. The LASSO regression analysis of candidate hub genes showed that the INS gene could be invoked as a predictive hub gene for T2D. INS, MAFA,and HK2 genes participate in the T2D disease process, but INS can better predict the occurrence of T2D.
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), bioinformatics analysis and, in the clinical setting, genetic consultation (19) . Due to its well-characterized genotype–phenotype correlation and the limitations imposed by existing technologies, there is a strong argument for investigating the potential use of
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concentration for fetuin-B was 0.1 μg/mL. And the preparation and operation steps of the reagent were performed strictly in accordance with the instructions. Bioinformatics analysis Protein–protein interaction network construction The Search Tool (v
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prognosis and treatment of thyroid cancer. Methods RNA-seq data and bioinformatics analysis This study used data downloaded from the TCGA database ( https://portal.gdc.cancer.gov ). RNA-seq data from the TCGA–thyroid carcinoma (THCA) project was
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bioinformatics analysis of sheep IGF1 splice variants Based on GenBank and Ensemble sequences of IGF1 splice variants in different species, a conserved region was found by aligning sequences from multiple species. Considering sequence specificity and
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.5. Collection of fecal samples and the extraction, amplification, database construction, and bioinformatics analysis of fecal DNA On the same day as the OGTT was conducted, 2–3 g (or four scoops) of fresh feces were collected with a sampler, soaked in a
Department of Breast Surgery, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China
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Department of Surgery, Second People's Hospital of Guizhou Province, Guiyang, Guizhou, China
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analysis and related experimental analysis. Materials and methods Bioinformatic analysis of the Forkhead box P4 analysis of thyroid cancer Data source This study downloaded The Cancer Genome Atlas Thyroid Cancer (TCGA–THCA) dataset from the
Nanchang University, Nanchang, Jiangxi Province, China
Institute of Neuroscience, Nanchang University, Nanchang, Jiangxi Province, China
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Nanchang University, Nanchang, Jiangxi Province, China
Institute of Neuroscience, Nanchang University, Nanchang, Jiangxi Province, China
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Nanchang University, Nanchang, Jiangxi Province, China
Institute of Neuroscience, Nanchang University, Nanchang, Jiangxi Province, China
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Nanchang University, Nanchang, Jiangxi Province, China
Institute of Neuroscience, Nanchang University, Nanchang, Jiangxi Province, China
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Nanchang University, Nanchang, Jiangxi Province, China
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Department of Urology, the 2nd affiliated hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi Province, China
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Nanchang University, Nanchang, Jiangxi Province, China
Institute of Neuroscience, Nanchang University, Nanchang, Jiangxi Province, China
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in invasive PitNETs remains poorly understood. Thus, this study aimed to address this gap by performing bioinformatics analysis to identify DEGs between invasive and non-invasive PitNETs, with a focus on SLC7A11. Immunohistochemical staining was