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Viruses rely on host cells for replication, often causing cellular damage and disease. In response, hosts activate defense mechanisms, though many viruses have evolved ways to evade these responses, leading to chronic infections. Identifying host genes that viruses exploit can inform the development of antiviral therapies by targeting specific host pathways. Differential gene expression (DGE) analysis is crucial for detecting genes with altered activity during viral infections. By comparing the RNA levels across different conditions, DGE identifies differentially expressed genes (DEGs) that indicate changes in gene expression in response to infection. Functional enrichment analysis follows DEG identification, grouping DEGs into biological pathways to clarify their roles in the host response. This chapter provides a step-by-step guide for performing DGE analysis on RNA-seq data from virus-infected and uninfected samples, covering data processing, DEG identification using edgeR, and functional enrichment analysis using KEGG and Gene Ontology. The protocol supports the analysis of both in-house RNA-seq data and public datasets from NCBI GEO repository.
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http://dx.doi.org/10.1007/978-1-0716-4546-8_3 | DOI Listing |
In Vitro Cell Dev Biol Anim
September 2025
Department of Stomatology, Air Force Medical Center, Air Force Medical University, 30 Fucheng Road, Beijing, 100142, PR China.
TP53TG1 is a long non-coding RNA related to the TP53 gene, which plays an important role in various biological processes such as tumorigenesis, cell cycle regulation, and DNA damage repair. In recent years, researchers have begun to explore the role of TP53TG1 in dental pulp biology, especially its potential impact on pulpitis and other pulp-related diseases. However, the role of TP53TG1 in human dental pulp stem cells (hDPSCs) remains unclear.
View Article and Find Full Text PDFJ Mol Histol
September 2025
Department of Anatomical Sciences and Cognitive Neuroscience, TMS.C., Islamic Azad University, Tehran, Iran.
Int J Implant Dent
September 2025
Department of Periodontology, Center for Biomedical Education and Research (ZBAF), School of Dentistry, Faculty of Health, Witten/Herdecke University, Witten, Germany.
Background: Guided bone regeneration (GBR) relies on biocompatible membranes to support osteogenesis. 1,4-butanediol diglycidyl ether (BDDE)-crosslinked hyaluronic acid (xHyA) has shown promise in enhancing bone regeneration, yet its mechanisms remain unclear.
Objective: This study evaluates the osteogenic effects of xHyA-functionalized native pericardium collagen membrane (NPCM) and ribose-crosslinked collagen membrane (RCCM) using an airlift culture model with SaOS-2 cells.
Odontology
September 2025
Department of Biomaterials, Hamidiye Institute of Health Sciences, University of Health Sciences Turkey, Istanbul, Turkey.
This study evaluates the cytotoxicity, apoptosis, and expression of stress-related genes (TP53 and NF-κB) in response to gingiva-colored indirect composite resins used for veneering tooth or implant-supported prostheses or characterization of denture bases. A total of 120 disc-shaped specimens (2 mm thick, 10 mm diameter) gingiva-colored indirect composite resin specimens (Group A: Anaxgum-Anaxdent, Group B: Crealing Paste Gum-Bredent, Group G: Gradia Gum-GC, Group N: SR Nexco GUM-Ivoclar Vivadent) were prepared and divided into four groups (n = 10 per group). Surface wettability was assessed using water contact angle (WCA) measurements.
View Article and Find Full Text PDFJ Mol Histol
September 2025
Department of Endocrinology, The Third Affiliated Hospital of Soochow University, No.185 Juqian Road, Changzhou, 213003, China.
Thyroid carcinoma (TC) continues to show concerning rates of metastasis and recurrence, despite an overall favorable prognosis. This study aimed to investigate the characteristics and predictive value of synaptotagmin-like 5 (SYTL5) expression and its association with immune infiltration and potential effects on cell apoptosis and proliferation in TC. Messenger ribonucleic acid expression profiles from 45 TC samples and 37 normal samples in The Cancer Genome Atlas database were analysed.
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