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20341por Mohammadzadeh, Nazanin, Zhang, Na, Branton, William G., Zghidi-Abouzid, Ouafa, Cohen, Eric A., Gelman, Benjamin B., Estaquier, Jerome, Kong, Linglong, Power, Christopher“…Analyses of SIV-associated RFs in brains from SIV-infected Chinese rhesus macaques with different ART regimens revealed diminished RF expression among ART-exposed SIV-infected animals, although ART interruption resulted in an induced expression of several RF genes including OAS3, RNASEL, MX2 and MAN1B1. Thus, the brain displays a distinct expression profile of RFs that is associated with the neurological status as well as the brain viral burden. …”
Publicado 2023
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20342por Chechenova, Maria B., Maes, Sara, Oas, Sandy T., Nelson, Cloyce, Kiani, Kaveh G., Bryantsev, Anton L., Cripps, Richard M.Enlace del recurso
Publicado 2017
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20343“…Then, regression analyses indicated that 9 prognostic genes (including ANPEP, OAS1, SCGB1A1, HLA‐A, NPPB, FGB, CCL2, TLR4, and SERPINE1) might play important roles in quercetin for treating UCEC/COVID-19. …”
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20344por Tirone, Nelson Ranieri, Campos, Carolina Guissoni, Ferreira, Kézia Jesus Aguiar, Stark, Léticia Montes, Vieira, Jéssica Ferreira, Murta, Eddie Fernando Cândido, Michelin, Márcia Antoniazi“…The real-time polymerase chain reaction (RT-PCR) technique was used to evaluate the gene expression of IFNR1 , IFNR2 , IFN-α, oligoadenylate synthase (2'5′OAS), cytokine signal suppressor 1 ( SOCS ) 1, SOCS3 , signal transducer and transcription activator 1 ( STAT1 ), and IRF9 from 128 biopsies. …”
Publicado 2021
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20345por Lin, Zhiwei, Xue, Mingshan, Wu, Ziman, Liu, Ze, Yang, Qianyue, Hu, Jiaqing, Peng, Jiacong, Yu, Lin, Sun, Baoqing“…Results: Seven hub genes (IFI44, IFI44L, MX1, OAS3, USP18, IFI27, and ISG15) were potential biomarkers for Omicron infection’s symptomatic diagnosis and treatment. …”
Publicado 2023
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20346por Briney, Bryan“…The AntiRef versioning scheme (current version: v2022.12.14) refers to the date on which sequences were retrieved from OAS.…”
Publicado 2023
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20347por Tsai, Ming-Ju, Jeong, Sohyun, Yu, Fangtang, Chen, Ting-Fu, Li, Peng-Hsuan, Juan, Hsueh-Fen, Huang, Jia-Hsin, Hsu, Yi-Hsiang“…These genes include IFNAR1, IFNAR2, TYK2, IL10RB, CXCR6, CCR9, and OAS1. We performed an extensive molecular docking analysis of these targets using 553 small molecules derived from five therapeutically enriched categories, namely antibacterials, antivirals, antineoplastics, immunosuppressants, and anti-inflammatories. …”
Publicado 2023
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20348por Wang, Ruomeng, Zhuang, Qi, Wang, Jian, Yang, Menghui, Zhang, Xueming, Shen, Jieyan“…Based on the PPI module analysis, we identified that the pro-inflammatory genes, such as OAS1, CXCL10, STAT1 and TLR4, were the hub genes in the PPI modules. …”
Publicado 2020
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20349por Sharma, Sanjay, Neale, Michael H, Di Nicolantonio, Federica, Knight, Louise A, Whitehouse, Pauline A, Mercer, Stuart J, Higgins, Bernard R, Lamont, Alan, Osborne, Richard, Hindley, Andrew C, Kurbacher, Christian M, Cree, Ian A“…Median progression free survival (PFS) was 6.6 months per course of chemotherapy; median overall survival (OAS) for each patient following the start of TCA-directed therapy was 10.4 months (95% confidence interval 7.9–12.8 months). …”
Publicado 2003
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20350por Onomoto, Koji, Morimoto, Shiho, Kawaguchi, Takahisa, Toyoda, Hidenori, Tanaka, Masami, Kuroda, Masahiko, Uno, Kazuko, Kumada, Takashi, Matsuda, Fumihiko, Shimotohno, Kunitada, Fujita, Takashi, Murakami, Yoshiki“…PRINCIPAL FINDINGS: Five IFN related-genes (IFI27, IFI 44, ISG15, MX1, and OAS1) had expression levels significantly higher in nonresponders (NR) than in normal liver (NL) and sustained virological responders (SVR); this high expression was also frequently seen in cases with the minor (TG or GG) IL28B genotype. …”
Publicado 2011
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20351por Choi, Jung Eun, Kwon, Jung Hyun, Kim, Jung-Hee, Hur, Wonhee, Sung, Pil Soo, Choi, Sang Wook, Yoon, Seung Kew“…The mRNA expression levels of myxovirus resistance protein A (MxA), 2'-5'-oligoadenylate synthetase 1 (OAS1), ISG15 ubiquitin-like modifier (ISG15), chemokine C-X-C motif ligand 10 (CXCL10), and ubiquitin-specific protease 18 (USP18) were also accelerated by silencing of DUSP1. …”
Publicado 2015
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20352por Mendoza, L., Piquemal, D., Lejeune, J. P., Vander Heyden, L., Noguier, F., Bruno, R., Sandersen, C., Serteyn, D.“…RESULTS: Relative expression of genes of horses less than 12 months of age showed significant induction of the genes MGAT4A, PRKCG, MHCI, ApoB, ApoB3G, B4GALT6 and a significantly lower expression of the genes OAS3. Horses of 18–24 months of age, showed a significantly higher expression of the genes TBC1D9, MGAT4A, IFIH1, MHCIIa and MMP1. …”
Publicado 2015
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20353por Palma-Ocampo, Helen K., Flores-Alonso, Juan C., Vallejo-Ruiz, Verónica, Reyes-Leyva, Julio, Flores-Mendoza, Lilian, Herrera-Camacho, Irma, Rosas-Murrieta, Nora H., Santos-López, Gerardo“…The reduction of viral titer corresponded with increased ISG mRNA levels (MX1 and OAS1), with the highest inhibition occurring at ISG’s peak expression. …”
Publicado 2015
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20354por Kobylarz, Marek J., Grigg, Jason C., Liu, Yunan, Lee, Mathew S. F., Heinrichs, David E., Murphy, Michael E. P.“…SbnA is a pyridoxal 5′-phosphate (PLP)-dependent enzyme with homology to O-acetyl-l-serine sulfhydrylases; however, SbnA utilizes OPS instead of O-acetyl-l-serine (OAS), and l-glutamate serves as a nitrogen donor instead of a sulfide. …”
Publicado 2016
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20355por Imgenberg-Kreuz, Juliana, Sandling, Johanna K, Almlöf, Jonas Carlsson, Nordlund, Jessica, Signér, Linnea, Norheim, Katrine Braekke, Omdal, Roald, Rönnblom, Lars, Eloranta, Maija-Leena, Syvänen, Ann-Christine, Nordmark, Gunnel“…In minor salivary gland biopsies we observed hypomethylation of the IFN-induced gene OAS2. Pathway and disease analysis resulted in enrichment of antigen presentation, IFN signalling and lymphoproliferative disorders. …”
Publicado 2016
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20356“…The differential expression of selected sets of genes, including interferon-stimulated and tumor suppressor genes of the XAF1 and OAS families, was confirmed by RT-qPCR. In addition, we showed that the over-expression of BNC2 inhibited the proliferation of A549 cells. …”
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20357por Sponchiado, Mariana, Gomes, Nathália Souza, Fontes, Patrícia Kubo, Martins, Thiago, del Collado, Maite, Pastore, Athos de Assumpção, Pugliesi, Guilherme, Nogueira, Marcelo Fábio Gouveia, Binelli, Mario“…Abundance of 12 transcripts was modulated in the Preg endometrium, including classical interferon-stimulated genes (ISG15, MX1, MX2 and OAS1Y), prostaglandin biosynthesis genes (PTGES, HPGD and AKR1C4), water channel (AQP4) and a solute transporter (SLC1A4) and this was in the UTJ and IA mainly. …”
Publicado 2017
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20358por Sambarey, Awanti, Devaprasad, Abhinandan, Baloni, Priyanka, Mishra, Madhulika, Mohan, Abhilash, Tyagi, Priyanka, Singh, Amit, Akshata, JS, Sultana, Razia, Buggi, Shashidhar, Chandra, Nagasuma“…The core comprises 380 genes in which STAT1, phospholipid scramblase 1 (PLSCR1), C1QB, OAS1, GBP2 and PSMB9 are prominent hubs. This network captures the interplay between several biological processes including pro-inflammatory responses, apoptosis, complement signalling, cytoskeletal rearrangement, and enhanced cytokine and chemokine signalling. …”
Publicado 2017
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20359por Dardiotis, Efthimios, Siokas, Vasileios, Garas, Antonios, Paraskevaidis, Evangelos, Kyrgiou, Maria, Xiromerisiou, Georgia, Deligeoroglou, Efthimios, Galazios, Georgios, Kontomanolis, Emmanuel N., Spandidos, Demetrios A., Tsatsakis, Aristidis, Daponte, Alexandros“…In this study, we aimed to evaluate the association of 10 single nucleotide polymorphisms (SNPs) of the Fas cell surface death receptor (FAS), trinucleotide repeat containing 6C (TNRC6C), transmembrane channel like 8 (TMC8), DNA meiotic recombinase 1 (DMC1), deoxyuridine triphosphatase (DUT), sulfatase 1 (SULF1), 2′-5-oligoadenylate synthetase 3 (OAS3), general transcription factor IIH subunit 4 (GTF2H4) and interferon gamma (IFNG) genes with susceptibility to precancerous lesions and cervical cancer. …”
Publicado 2018
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20360por Naumann, Marcel, Hubberten, Hans-Michael, Watanabe, Mutsumi, Hänsch, Robert, Schöttler, Mark Aurel, Hoefgen, Rainer“…This metabolic signature resembles a sulfate deprivation phenotype as corroborated by the fact that O-acetylserine (OAS) accumulated. Further, chlorophyll contents, photosynthetic electron transport, and the contents of carbohydrates such as starch, sucrose, fructose, and glucose were reduced. …”
Publicado 2018
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