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Items: 15

1.
Histocompatibility Minor 13 (HM13), targeted by miR-760, exerts oncogenic role in breast cancer by suppressing autophagy and activating PI3K-AKT-mTOR pathway
Haiyan Yang, Zhi Li, Zhangwei Wang, Xu Zhang, Xinyuan Dai, Guoren Zhou, Qiang Ding
Cell Death Dis. 2022 Aug; 13(8): 728. Published online 2022 Sep 25. doi: 10.1038/s41419-022-05154-4
PMCID:
PMC9509374
AbstractArticlePDF–6.3M
2.
Mechanism of miR-760 Reversing Lung Cancer Immune Escape by Downregulating IDO1 and Eliminating Regulatory T Cells Based on Mathematical Biology
Hong Ge, Lili Wang, Wenqiang Chen, Lei Wang
Comput Math Methods Med. 2022; 2022: 2960773. Published online 2022 Jul 14. doi: 10.1155/2022/2960773
PMCID:
PMC9303114
AbstractArticlePDF–1.5M
3.
Long Non-Coding RNA KCNQ1OT1 Regulates Protein Kinase CK2 Via miR-760 in Senescence and Calorie Restriction
Yoonsung Lee, Young-Seuk Bae
Int J Mol Sci. 2022 Feb; 23(3): 1888. Published online 2022 Feb 8. doi: 10.3390/ijms23031888
PMCID:
PMC8836653
AbstractArticlePDF–1.5M
4.
Androgen downregulation of miR-760 promotes prostate cancer cell growth by regulating IL6
Shuo Wang, Yong Yang, Yu-Dong Cao, Xing-Xing Tang, Peng Du
Asian J Androl. 2021 Jan-Feb; 23(1): 85–90. Published online 2020 May 15. doi: 10.4103/aja.aja_20_20
PMCID:
PMC7831841
AbstractArticlePDF–1.2M
5.
miR760 regulates ATXN1 levels via interaction with its 5′ untranslated region
Larissa Nitschke, Ambika Tewari, Stephanie L. Coffin, Eder Xhako, Kaifang Pang, Vincenzo A. Gennarino, Jennifer L. Johnson, Francisco A. Blanco, Zhandong Liu, Huda Y. Zoghbi
Genes Dev. 2020 Sep 1; 34(17-18): 1147–1160. doi: 10.1101/gad.339317.120
PMCID:
PMC7462065
AbstractArticlePDF–2.1M
6.
MicroRNA-760 acts as a tumor suppressor in gastric cancer development via inhibiting G-protein-coupled receptor kinase interacting protein-1 transcription
Liang Ge, Yu Wang, Quan-Hong Duan, Song-Shan Liu, Guo-Jing Liu
World J Gastroenterol. 2019 Dec 7; 25(45): 6619–6633. Published online 2019 Dec 7. doi: 10.3748/wjg.v25.i45.6619
PMCID:
PMC6906209
AbstractArticlePDF–8.7M
7.
MiR-760 enhances sensitivity of pancreatic cancer cells to gemcitabine through modulating Integrin β1
Dejun Yang, Zunqi Hu, Jiapeng Xu, Yuan Tang, Yu Wang, Qingping Cai, Zhenxin Zhu
Biosci Rep. 2019 Nov 29; 39(11): BSR20192358. Published online 2019 Nov 19. doi: 10.1042/BSR20192358
PMCID:
PMC6863763
AbstractArticlePDF–1.0M
8.
LncRNA NR_003923 promotes cell proliferation, migration, fibrosis, and autophagy via the miR-760/miR-215-3p/IL22RA1 axis in human Tenon’s capsule fibroblasts
Yang Zhao, Feng Zhang, Zheng Pan, Haomin Luo, Ke Liu, Xuanchu Duan
Cell Death Dis. 2019 Aug; 10(8): 594. Published online 2019 Aug 7. doi: 10.1038/s41419-019-1829-1
PMCID:
PMC6685939
AbstractArticlePDF–2.8M
9.
miR-760 mediates hypoxia-induced proliferation and apoptosis of human pulmonary artery smooth muscle cells via targeting TLR4
Yu-Zhong Yang, Yun-Feng Zhang, Lei Yang, Jing Xu, Xu-Ming Mo, Wei Peng
Int J Mol Med. 2018 Nov; 42(5): 2437–2446. Published online 2018 Sep 7. doi: 10.3892/ijmm.2018.3862
PMCID:
PMC6192785
AbstractArticlePDF–1.9M
10.
Upregulation of miR-760 and miR-186 Is Associated with Replicative Senescence in Human Lung Fibroblast Cells
Young-Hoon Lee, Soo Young Kim, Young-Seuk Bae
Mol Cells. 2014 Aug 31; 37(8): 620–627. Published online 2014 Aug 19. doi: 10.14348/molcells.2014.0157
PMCID:
PMC4145374
AbstractArticlePDF–878K
11.
Plasma miR-601 and miR-760 Are Novel Biomarkers for the Early Detection of Colorectal Cancer
Qifeng Wang, Zhaohui Huang, Shujuan Ni, Xiuying Xiao, Qinghua Xu, Lisha Wang, Dan Huang, Cong Tan, Weiqi Sheng, Xiang Du
PLoS One. 2012; 7(9): e44398. Published online 2012 Sep 6. doi: 10.1371/journal.pone.0044398
PMCID:
PMC3435315
AbstractArticlePDF–419K
12.
miRBase: integrating microRNA annotation and deep-sequencing data
Ana Kozomara, Sam Griffiths-Jones
Nucleic Acids Res. 2011 Jan; 39(Database issue): D152–D157. Published online 2010 Oct 30. doi: 10.1093/nar/gkq1027
PMCID:
PMC3013655
AbstractArticlePDF–5.1M
13.
A Mammalian microRNA Expression Atlas Based on Small RNA Library Sequencing
Pablo Landgraf, Mirabela Rusu, Robert Sheridan, Alain Sewer, Nicola Iovino, Alexei Aravin, Sébastien Pfeffer, Amanda Rice, Alice O. Kamphorst, Markus Landthaler, Carolina Lin, Nicholas D. Socci, Leandro Hermida, Valerio Fulci, Sabina Chiaretti, Robin Foà, Julia Schliwka, Uta Fuchs, Astrid Novosel, Roman-Ulrich Müller, Bernhard Schermer, Ute Bissels, Jason Inman, Quang Phan, Minchen Chien, David B. Weir, Ruchi Choksi, Gabriella De Vita, Daniela Frezzetti, Hans-Ingo Trompeter, Veit Hornung, Grace Teng, Gunther Hartmann, Miklos Palkovits, Roberto Di Lauro, Peter Wernet, Giuseppe Macino, Charles E. Rogler, James W. Nagle, Jingyue Ju, F. Nina Papavasiliou, Thomas Benzing, Peter Lichter, Wayne Tam, Michael J. Brownstein, Andreas Bosio, Arndt Borkhardt, James J. Russo, Chris Sander, Mihaela Zavolan, Thomas Tuschl
Cell. Author manuscript; available in PMC 2009 May 13.
Published in final edited form as: Cell. 2007 Jun 29; 129(7): 1401–1414. doi: 10.1016/j.cell.2007.04.040
PMCID:
PMC2681231
AbstractArticlePDF–2.5M
14.
Many novel mammalian microRNA candidates identified by extensive cloning and RAKE analysis
Eugene Berezikov, Geert van Tetering, Mark Verheul, Jose van de Belt, Linda van Laake, Joost Vos, Robert Verloop, Marc van de Wetering, Victor Guryev, Shuji Takada, Anton Jan van Zonneveld, Hiroyuki Mano, Ronald Plasterk, Edwin Cuppen
Genome Res. 2006 Oct; 16(10): 1289–1298. doi: 10.1101/gr.5159906
PMCID:
PMC1581438
AbstractArticlePDF–521K
15.
miRBase: microRNA sequences, targets and gene nomenclature
Sam Griffiths-Jones, Russell J. Grocock, Stijn van Dongen, Alex Bateman, Anton J. Enright
Nucleic Acids Res. 2006 Jan 1; 34(Database issue): D140–D144. Published online 2005 Dec 28. doi: 10.1093/nar/gkj112
PMCID:
PMC1347474
AbstractArticlePDF–245K

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