Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Henghui Cheng"'
Autor:
Yu Wang, Jun Li, Dong Kuang, Xiaoyan Wang, Yuanli Zhu, Sanpeng Xu, Yaobing Chen, Henghui Cheng, Qiu Zhao, Yaqi Duan, Guoping Wang
Publikováno v:
Cell Communication and Signaling, Vol 21, Iss 1, Pp 1-2 (2023)
Externí odkaz:
https://doaj.org/article/6a9b00c1e35e4f6581f9ed872e746dd1
Autor:
Yuhong Dai, Yongqing Liu, Zhimin Gong, Lilin He, Lei Wang, Wenjie Yang, Ping Qiu, Fangyuan Zhang, Xianglin Yuan, Henghui Cheng, Hong Qiu
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
BackgroundImmune-checkpoint inhibitors (ICIs) combined with chemotherapy have been successfully used in clinical trials to treat advanced gastric cancer. However, the efficacy and safety of first-line immunotherapy combined with chemotherapy in Chine
Externí odkaz:
https://doaj.org/article/c31ec0a361fc4842941a55bdf962b56b
Autor:
Yu Wang, Jun Li, Dong Kuang, Xiaoyan Wang, Yuanli Zhu, Sanpeng Xu, Yaobing Chen, Henghui Cheng, Qiu Zhao, Yaqi Duan, Guoping Wang
Publikováno v:
Cell Communication and Signaling, Vol 16, Iss 1, Pp 1-17 (2018)
Abstract Background Gain-of-function mutations and overexpression of KIT are characteristic features of gastrointestinal stromal tumor (GIST). Dysregulation in miRNA expression may lead to KIT overexpression and tumorigenesis. Methods miRNA microarra
Externí odkaz:
https://doaj.org/article/c90aa7da4c3b463ea655e2441cbd4074
Autor:
Jielin Liu, Henghui Cheng, Menglan Xiang, Lun Zhou, Bingruo Wu, Ivan P Moskowitz, Ke Zhang, Linglin Xie
Publikováno v:
PLoS Genetics, Vol 15, Iss 5, p e1007711 (2019)
Dominant mutations of Gata4, an essential cardiogenic transcription factor (TF), were known to cause outflow tract (OFT) defects in both human and mouse, but the underlying molecular mechanism was not clear. In this study, Gata4 haploinsufficiency in
Externí odkaz:
https://doaj.org/article/902ba0ece0cd48d18357111b3f0fb2d9
Autor:
Jing Cai, Tao Li, Bangxing Huang, Henghui Cheng, Hui Ding, Weihong Dong, Man Xiao, Ling Liu, Zehua Wang
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e95974 (2014)
Quantitative real-time PCR (qPCR) is a powerful and reproducible method of gene expression analysis in which expression levels are quantified by normalization against reference genes. Therefore, to investigate the potential biomarkers and therapeutic
Externí odkaz:
https://doaj.org/article/14e0826fd47848918261bfd12414a652
Autor:
Lindsey Kennedy, Jiangyuan Li, Hui Peng, Huiting Xu, Lin Liu, Naomi McCauley, Mikhail Y. Golovko, Gianfranco Alpini, Ernest C. Lynch, Linglin Xie, Ke Zhang, Henghui Cheng, Yi Zhou
Publikováno v:
Laboratory investigation; a journal of technical methods and pathology
Nonalcoholic fatty liver disease (NAFLD) has a developmental origin and is influenced in utero. We aimed to evaluate if maternal diet intervention before pregnancy would be beneficial to reduce the risk of offspring NAFLD. In our study, female mice w
Autor:
Leya He, Xian Wang, Zehuan Ding, Lin Liu, Henghui Cheng, Donalyn Bily, Chaodong Wu, Ke Zhang, Linglin Xie
Publikováno v:
The Journal of nutritional biochemistry. 111
Gata4 is a member of the zinc finger GATA transcription factor family and is required for liver development during the embryonic stage. Gata4 expression is repressed during NAFLD progression, however how it functions in this situation remains unclear
Autor:
Linglin Xie, Lauren Lawless, Henghui Cheng, Zhen Li, Ernest C. Lynch, Yi Zhou, Jiangyuan Li, Ke Zhang, Lin Liu, Zhimin Liu, Leya He
Publikováno v:
Laboratory investigation; a journal of technical methods and pathology
Odd-skipped related 1 (Osr1) is a novel tumor suppressor gene in several cancer cell lines. Non-alcoholic steatohepatitis (NASH) is considered as a high-risk factor for hepatocellular carcinoma (HCC). This study is aimed to investigate the novel role
Autor:
Jin Xue, Guoping Wang, Yaobin Chen, Yu Wang, Dong Kuang, Henghui Cheng, Shouhua Yang, Yuanli Zhu, Qiurong Ruan, Xiaoyan Wang, Yaqi Duan
Publikováno v:
Oncotarget
// Henghui Cheng 1, 2 , Jin Xue 1, 2 , Shouhua Yang 3 , Yaobin Chen 1, 2 , Yu Wang 1, 2 , Yuanli Zhu 1, 2 , Xiaoyan Wang 1, 2 , Dong Kuang 1, 2 , Qiurong Ruan 1, 2 , Yaqi Duan 1, 2 and Guoping Wang 1, 2 1 Institute of Pathology, Tongji Hospital, Tong
Autor:
Henghui Cheng, Qiang Fu, Yushu Qin, Duohua Chen, Linglin Xie, Huiting Xu, Menglan Xiang, Ke Zhang
Publikováno v:
Hum Mol Genet
Dominant TBX5 mutation causes Holt-Oram syndrome (HOS), which is characterized by limb defects in humans, but the underlying mechanistic basis is unclear. We used a mouse model with Tbx5 conditional knockdown in Hh-receiving cells (marked by Gli1+) d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38e3a19af83a4830bed97bf26cce917f
https://europepmc.org/articles/PMC7268785/
https://europepmc.org/articles/PMC7268785/