Добірка наукової літератури з теми "MiR-198"
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Статті в журналах з теми "MiR-198"
Ray, Jessica, Christianne Hoey, Xiaoyong Huang, Paul Christopher Boutros, and Stanley K. Liu. "Microrna-198: A novel tumor suppressor in prostate cancer." Journal of Clinical Oncology 36, no. 6_suppl (February 20, 2018): 92. http://dx.doi.org/10.1200/jco.2018.36.6_suppl.92.
Повний текст джерелаLi, Siqi, Junmei Yang, Xiaoting Liu, Rui Guo, and Ruidong Zhang. "circITGA7 Functions as an Oncogene by Sponging miR-198 and Upregulating FGFR1 Expression in Thyroid Cancer." BioMed Research International 2020 (June 22, 2020): 1–8. http://dx.doi.org/10.1155/2020/8084028.
Повний текст джерелаSundaram, Gopinath M., Hisyam M. Ismail, Mohsin Bashir, Manish Muhuri, Candida Vaz, Srikanth Nama, Ghim Siong Ow, et al. "EGF hijacks miR-198/FSTL1 wound-healing switch and steers a two-pronged pathway toward metastasis." Journal of Experimental Medicine 214, no. 10 (August 21, 2017): 2889–900. http://dx.doi.org/10.1084/jem.20170354.
Повний текст джерелаGao, Xueying, Ying Tang, and Yunping Ma. "Bone Marrow Mesenchymal Stem Cells (BMSCs)-Triggered Up-Regulation of miR-198 Impedes the Aggressive Migration and Invasion of Cervical Cancer Cells." Journal of Biomaterials and Tissue Engineering 12, no. 7 (July 1, 2022): 1285–92. http://dx.doi.org/10.1166/jbt.2022.3033.
Повний текст джерелаWu, Shujun, Hui Li, Chunya Lu, Furui Zhang, Huaqi Wang, Xinhua Lu, and Guojun Zhang. "Aberrant expression of hsa_circ_0025036 in lung adenocarcinoma and its potential roles in regulating cell proliferation and apoptosis." Biological Chemistry 399, no. 12 (November 27, 2018): 1457–67. http://dx.doi.org/10.1515/hsz-2018-0303.
Повний текст джерелаLU, JIANXIN, BONNIE CHING-HA KWAN, FERNAND MAC-MOUNE LAI, LAI-SHAN TAM, EDMUND KWOK-MING LI, KAI-MING CHOW, GANG WANG, PHILIP KAM-TAO LI, and CHEUK-CHUN SZETO. "Glomerular and tubulointerstitial miR-638, miR-198 and miR-146a expression in lupus nephritis." Nephrology 17, no. 4 (April 17, 2012): 346–51. http://dx.doi.org/10.1111/j.1440-1797.2012.01573.x.
Повний текст джерелаMarín-Müller, Christian, Dali Li, Jian-Ming Lu, Zhengdong Liang, Osvaldo Vega-Martínez, William Fisher, Changyi Chen, and Qizhi Cathy Yao. "MiR-198 sensitizes pancreatic cancer to gemcitabine treatment through downregulation of VCP-mediated autophagy maturation." Journal of Clinical Oncology 40, no. 16_suppl (June 1, 2022): e16290-e16290. http://dx.doi.org/10.1200/jco.2022.40.16_suppl.e16290.
Повний текст джерелаMarin-Muller, Christian, Dali Li, Jian-Ming Lü, Zhengdong Liang, Osvaldo Vega-Martínez, Sue E. Crawford, Mary K. Estes, William E. Fisher, Changyi Chen, and Qizhi Yao. "Nanoparticle-Mediated Therapy with miR-198 Sensitizes Pancreatic Cancer to Gemcitabine Treatment through Downregulation of VCP-Mediated Autophagy." Pharmaceutics 15, no. 8 (July 28, 2023): 2038. http://dx.doi.org/10.3390/pharmaceutics15082038.
Повний текст джерелаLiu, Man, Yao Meng, Keren He, and Chonglin Luan. "Hsa_circ_0002060 Knockdown Ameliorates Osteoporosis by Targeting MiR-198-5p." Biological and Pharmaceutical Bulletin 44, no. 1 (January 1, 2021): 88–95. http://dx.doi.org/10.1248/bpb.b20-00643.
Повний текст джерелаAbhilasha, A., P. Mitra, S. Suri, I. Saxena, R. K. Shukla, and P. Sharma. "T133 Circulating levels of miR-24-3p and miR-198 in type 2 diabetes mellitus." Clinica Chimica Acta 530 (May 2022): S119. http://dx.doi.org/10.1016/j.cca.2022.04.612.
Повний текст джерелаДисертації з теми "MiR-198"
Elfimova, Natalia [Verfasser]. "Die Rolle der Tumorsuppressor-miR-198 in der hepatozellulären Karzinogenese / Natalia Elfimova." Köln : Deutsche Zentralbibliothek für Medizin, 2013. http://d-nb.info/1046228315/34.
Повний текст джерелаKaushik, Pankhuri. "Investigating the role of miR-198 in oral squamous cell carcinoma pathogenesis." Thesis, 2023. https://etd.iisc.ac.in/handle/2005/6197.
Повний текст джерелаYi-TaTsai and 蔡易達. "The human hepatitis c virus (HCV) core protein has a role in modulating hsa-Let-7b, hsa-miR-122, hsa-miR-199 and hsa-miR-198." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/shtsrd.
Повний текст джерела國立成功大學
分子醫學研究所
102
Summary The hepatitis C virus (HCV) core protein (HCVcore) constitutes the viral nucleocapsid structure, and is involved in viral persistence and pathogenesis possibly by interacting with host factors to modulate viral replication and cellular function. It is known that Dicer is an important component of microRNA processor, and HCVcore is associated with Dicer. These pieces of evidence suggest that HCVcore may modulate microRNA biogenesis or metabolism to regulate HCV infection and tumorigenesis. Because HCVcore may interact with many critical components of microRNA processing complexes, we ask in this study whether the levels of certain microRNAs (i.e., hsa-mir-122, hsa-let-7b, hsa-mir-199 and hsa-mir-198) would be affected by the presence of HCVcore in a Huh7.5 cell lines with replicating HCV. Firstly, we compared the 4 endogenous microRNA levels between Huh7.5 with or without replicating FGR (HCV full-genome replicon) by qPCR. The patterns of hsa-mir-122 and hsa-let-7b expression levels in cells with or without FGR are consistent with others in previous literatures, suggesting that our quantitation methods are reliable. Yet we first point out that HCV infection would increase expression of hsa-mir-199 and hsa-mir-198. Secondly, our result indicated that the structural proteins have roles in the modulation of endogenous microRNA. Finally, our result showed that the presence of HCVcore increases the expression level of hsa-mir-122, hsa-let-7b, hsa-mir-199 and hsa-mir-198. Collectively, our results indicated that HCVcore has an essential role in modulating microRNAs during HCV infection. Keyword: HCV, HCVcore, MicroRNA, hsa-miR-122, hsa-miR-198, hsa-miR-199, hsa-Let-7b
Тези доповідей конференцій з теми "MiR-198"
Yu, X., H. Eischeid-Scholz, M. Schmiel, L. Wang, R. Büttner, and M. Odenthal. "MiR-198 overexpression leads to its vesicular release from hepatocellular carcinoma cells." In 35. Jahrestagung der Deutschen Arbeitsgemeinschaft zum Studium der Leber. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0038-1677242.
Повний текст джерелаOgunwobi, Olorunseun O., Jian Li, Xiangxuan Zhao, Jose Trevino, Thomas George, and Chen Liu. "Abstract 896: miR-198 silencing is a mechanism of gemcitabine resistance in human pancreatic adenocarcinoma." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-896.
Повний текст джерелаYu, X., H. Eischeid, M. Schmiel, R. Büttner, and M. Odenthal. "Overexpression of tumor suppressor miR-198 in hepatoma cells leads to its spontaneous and active export via vesicles." In 36. Jahrestagung der Deutschen Arbeitsgemeinschaft zum Studium der Leber. Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0039-3402225.
Повний текст джерелаMiyake, Keisuke, Takatsugu Ishimoto, Hidetaka Sugihara, Kojiro Eto, Daisuke Izumi, Junji Kurashige, Yukiharu Hiyoshi, et al. "Abstract 198: Helicobacter pylori infection via miR-328 suppression and CD44 expression in gastric mucosa causes gastric cancer initiation and progression." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-198.
Повний текст джерелаHan, Hye Sook, Jieun Yun, and Ok-Jun Lee. "Abstract 4165: Combination of cell-free miR-198, carcinoembryonic antigen, and CYFRA 21-1 as a diagnostic biomarker for lung adenocarcinoma-associated malignant pleural effusion." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-4165.
Повний текст джерелаMurakami, Tomohiro, Hirotoshi Kikuchi, Hisahito Ishimatsu, Sanshiro Kawata, Amane Hirotsu, Tomohiro Matsumoto, Yusuke Ozaki, et al. "Abstract 1067: Tenascin C in colorectal cancer stroma is a predictive marker for liver metastasis and is a potent target of miR-198 as identified by microRNA analysis." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-1067.
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