Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Xiaofang Wen"'
Autor:
Zhiquan Qiu, Jun Ji, Yu Xu, Yan Zhu, Chunfang Gao, Guoqiang Wang, Chengcheng Li, Yuzi Zhang, Jing Zhao, Chenyang Wang, Xiaofang Wen, Zhou Zhang, Bingsi Li, Zhihong Zhang, Shangli Cai, Bin Li, Xiaoqing Jiang
Publikováno v:
BMC Medicine, Vol 20, Iss 1, Pp 1-17 (2022)
Abstract Background DNA methylation-associated studies on biliary tract cancer (BTC), including cholangiocarcinoma (CCA) and gallbladder cancer (GBC), may improve the BTC classification scheme. We proposed to identify the shared methylation changes o
Externí odkaz:
https://doaj.org/article/27bf1618e6e44f23ae8f5d989eab5276
Autor:
Guibin Qiao, Weitao Zhuang, Bo Dong, Chengcheng Li, Jiayue Xu, Guoqiang Wang, Liang Xie, Zihao Zhou, Dan Tian, Gang Chen, Jiming Tang, Haiyu Zhou, Dongkun Zhang, Ruiqing Shi, Rixin Chen, Weiqi Nian, Yuzi Zhang, Jing Zhao, Xiaofang Wen, Yu Xu, Bingsi Li, Zhihong Zhang, Shangli Cai, Xiaosong Ben, Yu Qi
Publikováno v:
BMC Medicine, Vol 19, Iss 1, Pp 1-13 (2021)
Abstract Background Plasma cell-free DNA (cfDNA) methylation has shown promising results in the early detection of multiple cancers recently. Here, we conducted a study to investigate the performance of cfDNA methylation in the early detection of eso
Externí odkaz:
https://doaj.org/article/6efc284080ba465bab0dd1650924e8d3
Autor:
Leilei Liang, Yu Zhang, Chengcheng Li, Yuchen Liao, Guoqiang Wang, Jiayue Xu, Yifan Li, Guangwen Yuan, Yangchun Sun, Rong Zhang, Xiaoguang Li, Weiqi Nian, Jing Zhao, Yuzi Zhang, Xin Zhu, Xiaofang Wen, Shangli Cai, Ning Li, Lingying Wu
Publikováno v:
EBioMedicine, Vol 83, Iss , Pp 104222- (2022)
Summary: Background: Plasma cell-free DNA (cfDNA) methylation has shown the potential in the detection and prognostic testing in multiple cancers. Herein, we thoroughly investigate the performance of cfDNA methylation in the detection and prognosis o
Externí odkaz:
https://doaj.org/article/3eee9305fcda4e7780bd5ed2fa77ac3b
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-5 (2020)
Abstract Background Maturity-onset diabetes of the young (MODY) is a genetically and clinically heterogeneous group of hereditary diabetes, generally caused by one abnormal gene. MODY5 is caused by mutations of the hepatocyte nuclear factor 1 homeobo
Externí odkaz:
https://doaj.org/article/be14303d0dfc4e38acc9cbbcc03ca9dd
Publikováno v:
IEEE Access, Vol 6, Pp 78225-78237 (2018)
Finding clusters in datasets with different distributions and sizes is challenging when clusters are of widely various shapes, sizes, and densities. Based on a similar-to-multiple-point clustering strategy, a novel and simple clustering algorithm nam
Externí odkaz:
https://doaj.org/article/44f9fba92a684539be51553b43bfbc0b
Publikováno v:
Complexity, Vol 2019 (2019)
Community detection is helpful to understand useful information in real-world networks by uncovering their natural structures. In this paper, we propose a simple but effective community detection algorithm, called ACC, which needs no heuristic search
Externí odkaz:
https://doaj.org/article/ef3cfbe19a54485ca7ad1db73d6bccf0
Autor:
Xiaofang Wen, Nan Zeng, Ningbo Zhang, Tingting Ou, Xiaowei Li, Xiaoying Li, Wangen Li, Kang Xu, Tao Du
Publikováno v:
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy. 15:3437-3445
Xiaofang Wen,1,* Nan Zeng,1,* Ningbo Zhang,1,2,* Tingting Ou,1 Xiaowei Li,1 Xiaoying Li,1 Wangen Li,1 Kang Xu,3 Tao Du1 1Department of Endocrinology, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, 510260, People
Publikováno v:
Frontiers in Psychiatry, Vol 15 (2024)
AimOur study utilized the Rasch analysis to examine the psychometric properties of the Autism Behavior Checklist (ABC) in children with autism spectrum disorder (ASD).MethodsA total of 3,319 children (44.77 ± 23.52 months) were included. The Rasch m
Externí odkaz:
https://doaj.org/article/e01ef4b7b52b4a60a045ffdd2e3d2888
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-5 (2020)
BMC Medical Genetics
BMC Medical Genetics
BackgroundMaturity-onset diabetes of the young (MODY) is a genetically and clinically heterogeneous group of hereditary diabetes, generally caused by one abnormal gene. MODY5 is caused by mutations of the hepatocyte nuclear factor 1 homeobox β gene
Publikováno v:
Chemical Research in Chinese Universities. 36:774-780
Superoxide anion, one of the most active reactive oxygen species, is associated with the development of many diseases. So monitoring superoxide anion in living cells is of great significance for the pathological research of many diseases. In this wor