Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Ruofan Xu"'
Autor:
Lingbing Meng, Ruofan Xu, Jianyi Li, Jiabin Hu, Hongxuan Xu, Dishan Wu, Xing Hu, Xuezhai Zeng, Qiuxia Zhang, Juan Li, Deping Liu
Publikováno v:
BMC Geriatrics, Vol 24, Iss 1, Pp 1-14 (2024)
Abstract Background Chronic diseases, such as heart disease, cancer, and diabetes, are the leading causes of death and disability. Loneliness is linked to a greater risk of chronic disease. However, the lack of loneliness may change this relationship
Externí odkaz:
https://doaj.org/article/0651f2821c3b4cd49c95c680868ccc31
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-15 (2024)
Abstract The performance of platform flexible employees is a core element that contributes to the rapid growth of the sharing economy platform. It is crucial to explore strategies to improve employees' performance with the growing competition among t
Externí odkaz:
https://doaj.org/article/6c16786929d54633bad3bd263bdc4516
Autor:
Wei Shi, Ruofan Xu, Changjiang Han, Bingxiang Sun, Jin Chai, Jiachang Liu, Xuewen Jiao, Jiale Xiong, Yinghao Li
Publikováno v:
Batteries, Vol 10, Iss 7, p 231 (2024)
The mechanical pressure that arises from the external structure of the automotive lithium battery module and its fixed devices can give rise to the concentration and damage of the internal stress inside the battery and increase the risks of battery d
Externí odkaz:
https://doaj.org/article/74e2646b29f04abca2f52c139e1a4f89
Autor:
Cuiting Peng, Haixia Zhang, Jun Ren, Han Chen, Ze Du, Tong Zhao, Aiping Mao, Ruofan Xu, Yulin Lu, He Wang, Xinlian Chen, Shanling Liu
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract Thalassemia is a group of common hereditary anemias that cause significant morbidity and mortality worldwide. However, precisely diagnosing thalassemia, especially rare thalassemia variants, is still challenging. Long-range PCR and long-mole
Externí odkaz:
https://doaj.org/article/c43ac6845daa4781bdaad4ccd8bb067e
Autor:
Ruofan Xu, Le Yang, Zhewen Zhang, Yuxuan Liao, Yao Yu, Dawei Zhou, Jiahao Li, Haoyu Guan, Wei Xiao
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
IntroductionGastric cancer (GC) remains the major constituent of cancer-related deaths and a global public health challenge with a high incidence rate. Helicobacter pylori (HP) plays an essential role in promoting the occurrence and progression of GC
Externí odkaz:
https://doaj.org/article/811630c84aee45ed8da6d45490dfb9a2
Autor:
Guoxing Zhong, Zeyan Zhong, Zhiyang Guan, Dina Chen, Zhiyong Wu, Kunxiang Yang, Dan Chen, Yinyin Liu, Ruofan Xu, Jianhong Chen
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Thalassemia was the most common monogenic diseases worldwide, which was caused by mutations, deletions or duplications in human globin genes which disturbed the synthesis balance between α- and β-globin chains of hemoglobin. There were
Externí odkaz:
https://doaj.org/article/0563b26d05db44d38b669767cc815ab8
Autor:
Sisi Ning, Yudi Luo, Yi Liang, Yuling Xie, Yinghong Lu, Binrong Meng, Jinjie Pan, Ruofan Xu, Yinyin Liu, Yunrong Qin
Publikováno v:
Clinica Chimica Acta. 535:7-12
Autor:
Zeyan Zhong, Guoxing Zhong, Zhiyang Guan, Dina Chen, Zhiyong Wu, Kunxiang Yang, Dan chen, Yinyin Liu, Ruofan Xu, Jianhong Chen
Publikováno v:
Clinical Biochemistry. 108:46-49
Autor:
Zhenrui Liu, Puqiao Wen, Shuxing Wang, Yuxuan Liao, Dawei Zhou, Hongyi Wang, Ruofan Xu, Yiwei Chen
Homeobox B2 (HOXB2) is a transcription factor that belongs to the homeobox family. Previous investigations have demonstrated that tumor prognosis was strongly linked to aberrant HOXB2 expression. However, the mechanism linking HOXB2 to the tumor micr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::203b975ec199482f8bd5eae1dc1a9816
https://doi.org/10.21203/rs.3.rs-2898626/v1
https://doi.org/10.21203/rs.3.rs-2898626/v1
Autor:
Jianlong, Zhuang, Chunnuan, Chen, Wanyu, Fu, Yuanbai, Wang, Qianmei, Zhuang, Yulin, Lu, Tiantian, Xie, Ruofan, Xu, Shuhong, Zeng, Yuying, Jiang, Yingjun, Xie, Gaoxiong, Wang
Publikováno v:
Archives of Pathology & Laboratory Medicine. 147:208-214
Context.— Identification of rare thalassemia variants requires a combination of multiple diagnostic technologies. Objective.— To investigate a new approach of comprehensive analysis of thalassemia alleles based on third-generation sequencing (TGS