Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Chunxia Lin"'
Autor:
Jun Zhou, Shengyan Mao, Zhaoping Zheng, Chunxia Lin, Jia Tang, Jie Lin, Jie Ling, Lixi Yang, Zijuan Jiang, Dandan Wu
Publikováno v:
Clinical and Experimental Obstetrics & Gynecology, Vol 51, Iss 4, p 97 (2024)
Background: The objective was to explore the impact of different delivery methods on maternal and infant outcomes in women with a prolonged second stage of labor and a fetus with a persistent occipital posterior position. Methods: 60 women with a fet
Externí odkaz:
https://doaj.org/article/ef3eb91e322947acaa22b7536edce6e7
Autor:
Xuerui Pang, Jing Huang, Chunxia Lin, Yingfang Zhang, Nian Cheng, Wei Zi, Zhu‐Zhu Sun, Zhen Yu, Zhiqiang Zhao
Publikováno v:
Chemistry – A European Journal. 29
Among the factors that lead to the reduction of the efficiency of perovskite solar cell (PSCs), is the difficulty involved in realizing a high-quality film and the efficient charge transfer that take place at the interface between electron-transport
Autor:
Chunlei Wang, Xueying Xu, Yunjiang Li, Chunxia Lin, Tuo Ji, Liming Zhang, Weilin Chen, Ting Wang
Publikováno v:
Materials Chemistry Frontiers. 5:6931-6940
The electron transport layer (ETL) transfers the photogenerated electrons generated by the perovskite layer to the conductive glass substrate, which plays a vital role in the performance of the perovskite-based photodetector. SnO2, as a wide bandgap
Autor:
Xinming Guo, Beilong Zhong, Fangfang Zheng, Chunxia Lin, Chuanxin Zhou, Zhizhong Deng, Yi Guo, Yangbin Guo
Publikováno v:
Journal of Tropical Pediatrics
A 16-month-old boy was admitted with cough for 2 days and fever for 1 day. Chest computed tomography (CT) scan of the child revealed large areas of ground-glass opacities in both lungs. Nucleic acid amplification tests (NAATs) were performed repeated
PurposeThis study aimed to investigate the relationship between miR-204-5p and Nestin in esophageal squamous cell carcinoma (ESCC). MethodsThe expression levels of miR-204-5p and Nestin were tested by quantitative real-time polymerase chain reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b87c9bb524f7194c82898dc5c8338d1f
https://doi.org/10.21203/rs.3.rs-510018/v1
https://doi.org/10.21203/rs.3.rs-510018/v1
Publikováno v:
International Journal of Medical Sciences; 2022, Vol. 19 Issue 3, p472-483, 12p
Autor:
Chunxia Lin, Xiaoyan Hou, Longxuan Li, Bin Zhao, Xia Huang, Yinqin Chen, Weili Tian, Hao Chen, Wen Li, Yusen Chen, Du Feng, Wenxian Wu, Sen-Fang Sui, Wangtao Zhong, Zhe Hu, Liangqing Zhang, Ze-Ming Yan, Haixia Zhuang
Publikováno v:
FEBS Letters. 589:1847-1854
UNC-51 like kinase (ULK1) translocates to dysfunctional mitochondria and is involved in mitophagy, but the mechanisms responsible for ULK1 activation and translocation remain unclear. Here, we found that hypoxia induces phosphorylation of ULK1 at Ser
Autor:
Hao Chen, Chunxia Lin, Haixia Zhuang, Liangqing Zhang, Zhiyi Li, Yue Yang, Du Feng, Wen Li, Zijun Wu, Keng Wu, Yusen Chen, Xiaoyan Hou, Wangtao Zhong, Runmin Guo
Publikováno v:
FEBS letters. 590(6)
The functions of some essential autophagy genes are regulated by microRNAs. However, an ATG3-modulating microRNA has never been reported. Here we show that the transcription of miR-495 negatively correlates with the translation of ATG3 under nutrient
Autor:
Liangqing Zhang, Du Feng, Yue Yang, Hao Chen, Haixia Zhuang, Xingliang Zhang, Sen-Fang Sui, Keng Wu, Xiaojing Wang, Wen Li, Yue Lu, Shupeng Li, Ning Tan, Wenxian Wu, Longxuan Li, Jingjing Zhang, Lei Jiang, Bin Zhao, Chunxia Lin, Runzhi Zhu, Jingjing Wang
Publikováno v:
The EMBO journal. 35(13)
In hypoxic cells, dysfunctional mitochondria are selectively removed by a specialized autophagic process called mitophagy. The ER-mitochondrial contact site (MAM) is essential for fission of mitochondria prior to engulfment, and the outer mitochondri
Autor:
Robert Bähring, Lijuan Ma, Yingxue Dong, Yanzong Yang, Jue Ye, Olaf Pongs, Rutai Hui, Chunxia Lin, Zhi-hu Lin, Vitya Vardanyan, Siyong Teng
Publikováno v:
Journal of Molecular Medicine. 82:189-196
We have found a novel nonsense mutation in the C-terminus of HERG in a four-generation Chinese family with long QT syndrome and investigated the molecular mechanism of this mutation in vitro. Six family members, including the proband, were clinically