Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Fengyun ZHENG"'
Autor:
Runyi Cao, Rui Zhu, Zhao Sha, Sixian Qi, Zhenxing Zhong, Fengyun Zheng, Yubin Lei, Yanfeng Tan, Yuwen Zhu, Yu Wang, Yi Wang, Fa-Xing Yu
Publikováno v:
Cell Death and Disease, Vol 14, Iss 8, Pp 1-14 (2023)
Abstract WWC1 regulates episodic learning and memory, and genetic nucleotide polymorphism of WWC1 is associated with neurodegenerative diseases such as Alzheimer’s disease. However, the molecular mechanism through which WWC1 regulates neuronal func
Externí odkaz:
https://doaj.org/article/9062e1170c0f4a20a308467ec3089761
Autor:
Shengqiang YUAN, Lirong DOU, Dingsheng CHENG, Fengjun MAO, Chunfu PAN, Fengyun ZHENG, Hong JIANG, Wenzhu PANG, Zaohong LI
Publikováno v:
Petroleum Exploration and Development, Vol 50, Iss 2, Pp 268-280 (2023)
Based on the seismic and drilling data, casting thin sections, geochemical analysis of oil and rock samples, and hydrocarbon generation history simulation, the hydrocarbon accumulation characteristics and exploration direction of Termit superimposed
Externí odkaz:
https://doaj.org/article/1aa83d80ace14a2d80a7a28744e23e05
Autor:
Yinwen Xu, Chenchen Cheng, Fengyun Zheng, Hexige Saiyin, Pingzhao Zhang, Wenjiao Zeng, Xiuping Liu, Guoyuan Liu
Publikováno v:
Heliyon, Vol 9, Iss 9, Pp e19984- (2023)
Perinatal autopsies are essential to establish the cause of stillbirth or neonatal death and improve clinical practice. Limited studies have provided detailed major missed diagnoses of perinatal deaths in current clinical practice. In this retrospect
Externí odkaz:
https://doaj.org/article/416333f4a16b46229d8903afae635b28
Publikováno v:
Petroleum Exploration and Development, Vol 49, Iss 6, Pp 1339-1350 (2022)
Based on seismic and drilling data in the study area, the geological structure and kinematic process of the Termit rift basin were studied using seismic profile interpretation and balanced restoration to find out the dynamic mechanism of the basin. (
Externí odkaz:
https://doaj.org/article/fde5dd360a6f4f43a26485b7af1bace2
Autor:
Yufeng Liu, Hanghang Cheng, Chenchen Cheng, Fengyun Zheng, Zhonghua Zhao, Qi Chen, Wenjiao Zeng, Pingzhao Zhang, Cheng Huang, Wei Jiang, Xiuping Liu, Guoyuan Liu
Publikováno v:
Cancer Medicine, Vol 11, Iss 5, Pp 1269-1280 (2022)
Abstract Background Alteration of DNA methylation is an important event in pathogenesis and progression of hepatocellular carcinoma (HCC). DNA methyltransferase (DNMT) 1, the foremost contributor in DNA methylation machinery, was revealed elevated in
Externí odkaz:
https://doaj.org/article/c935daac1422478f91d4765f523832a6
Publikováno v:
The Journal of Prosthetic Dentistry.
STATEMENT OF PROBLEM Digital light processing (DLP), continuous liquid interface printing (CLIP), and stereolithography (SLA) technologies enable 3-dimensional (3D) printing of surgical guides. However, how their accuracy compares and how accuracy ma
Autor:
Bai-Lin Wu, Zilong Qiu, Guoyuan Liu, Ting Dang, Fengyun Zheng, Meng Wu, Yu An, Qiaowen Chen, Xiangxuan Kong
Publikováno v:
Neurosci Bull
Autor:
Chenggang Zhu, Bilin Ge, Ru Chen, Xiangdong Zhu, Lan Mi, Jiong Ma, Xu Wang, Fengyun Zheng, Yiyan Fei
Publikováno v:
Sensors, Vol 18, Iss 2, p 524 (2018)
Total internal reflection (TIR) is useful for interrogating physical and chemical processes that occur at the interface between two transparent media. Yet prism-coupled TIR imaging microscopes suffer from limited sensing areas due to the fact that th
Externí odkaz:
https://doaj.org/article/35437edcd43f498dbb88ec7eb37bd765
Autor:
Yufeng Liu, Hanghang Cheng, Chenchen Cheng, Fengyun Zheng, Zhonghua Zhao, Qi Chen, Wenjiao Zeng, Pingzhao Zhang, Cheng Huang, Wei Jiang, Xiuping Liu, Guoyuan Liu
Publikováno v:
Cancer medicine. 11(5)
Alteration of DNA methylation is an important event in pathogenesis and progression of hepatocellular carcinoma (HCC). DNA methyltransferase (DNMT) 1, the foremost contributor in DNA methylation machinery, was revealed elevated in HCC and significant
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e54404 (2013)
Velocardiofacial syndrome (VCFS) is a disease in human with an expansive phenotypic spectrum and diverse genetic mechanisms mainly associated with copy number variations (CNVs) on 22q11.2 or other chromosomes. However, the correlations between CNVs a
Externí odkaz:
https://doaj.org/article/922c8484f03b4f35bdf004100f368877