Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Xiu-Feng Gong"'
Autor:
Xin Zhang, Ci-Xiang Zhou, Di-Fei Wang, Lulu Wo, Cheng-Ning Ma, Chen-Long Wang, Jing-Chi Li, Xiu-Feng Gong, Ming He, Qian Zhao
Publikováno v:
RNA Biol
The adaptation of tumour cells to hypoxic microenvironment is one of the most significant characteristics of many malignant tumour diseases including hepatocarcinoma. Recently, long non-coding RNAs (lncRNAs) have been reported to play important roles
Autor:
Jun Tang, Qian Zhao, An-Lu Yu, Chen-Long Wang, Jianrong He, Guo-Qiang Chen, Ming He, Xiu-Feng Gong, Ci-Xiang Zhou
Publikováno v:
Experimental Cell Research. 362:378-385
MicroRNAs (miRNAs) play critical roles in breast cancer cell biological processes, including proliferation and apoptosis by inhibiting the expression of their target genes. Herein, we reported that miR-630 overexpression initiates apoptosis, blocks c
Autor:
Jun Tang, Meng-Na Zhan, Qiu-Yu Wang, Ming-Ming He, Qian-Qian Yin, Chen-Long Wang, An-Lu Yu, Ci-Xiang Zhou, Qian Zhao, Xiu-Feng Gong, Jianrong He, Guo-Qiang Chen
Publikováno v:
Oncotarget
MicroRNAs have been integrated into tumorigenic programs as either oncogenes or tumor suppressor genes. The miR-630 was reported to be deregulated and involved in tumor progression of several human malignancies. However, its expression regulation sho
Autor:
Xiu-Feng Gong, Albrecht Bindereif, Xing Fu, Li-Juan Cao, Monika Heiner, Wen-Juan Wei, Shi-Rong Mu, Jingyi Hui
Publikováno v:
Nucleic Acids Research
The human Y box-binding protein-1 (YB-1) is a deoxyribonucleic acid (DNA)/ribonucleic acid (RNA)-binding protein with pleiotropic functions. Besides its roles in the regulation of transcription and translation, several recent studies indicate that YB
Autor:
Jianrong He, Chen-Long Wang, Xiao-Ting Yu, Ming He, Qian-Qian Yin, Meng-Na Zhan, Qian Zhao, Jun Tang, Xiu-Feng Gong, Guo-Qiang Chen, Ci-Xiang Zhou
Publikováno v:
Cell Death & Disease
MicroRNA (miRNA) is involved in the progression and metastasis of diverse human cancers, including breast cancer, as strong evidence has been found that miRNAs can act as oncogenes or tumor suppressor genes. Here, we show that miR-494 is decreased in