Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Longxu Xie"'
Autor:
Yingxuan Zhang, Wei Qing, Wenyu Mo, Rongdan Chen, Zuyi Zhou, Yi Hou, Yiya Shi, Cancan Qi, Jinxia Ou, Longxu Xie, CALM 2004 Study Group, Yifeng Wang, Hongwei Zhou, Muxuan Chen
Publikováno v:
BMC Infectious Diseases, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background Ureaplasma spp. can be classified into different serovars. It is unknown whether distinct serovars are associated with clinical signs and symptoms. Methods We conducted a multicentre cross-sectional study. U. parvum serovars were
Externí odkaz:
https://doaj.org/article/903ce7d807ab4d61b5a741f33d23b55a
Autor:
Xin-sheng Yu, Shaoying Tan, Wanting Tang, Fang-fang Zhao, Jie Ji, Jianwei Lin, Han-jie He, Youxin Gu, Jia-Jian Liang, Meng Wang, Yequn Chen, Jiancheng Yang, Longxu Xie, Qian Wang, Mengyu Liu, Yang He, Lan Chen, Ya Xing Wang, Zhaoxiong Wu, Gang Zhao, Yi Liu, Yun Wang, Dongning Hao, Jingyun Cen, Shi-Qi Yao, Dan Zhang, Lifang Liu, David Chien Lye, Zhifeng Hao, Tien Yin Wong, Ling-Ping Cen
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
BackgroundChina exited strict Zero-COVID policy with a surge in Omicron variant infections in December 2022. Given China’s pandemic policy and population immunity, employing Baidu Index (BDI) to analyze the evolving disease landscape and estimate t
Externí odkaz:
https://doaj.org/article/b314dafdbd744d6b8ef4954a55146b43
Autor:
Chun-Ho (Charlie) Ma, Liejun Li, Shuheng Cai, Pei Lin, Wing-Ki (Kristy) Lam, Tsz-Him (Ronald) Lee, Tsz-Kin (Ryan) Kwok, Longxu Xie, Tit-Sang (Tom) Kun, Ben-Zhong Tang
Publikováno v:
Molecules, Vol 27, Iss 20, p 7036 (2022)
Genetic mutations can cause life-threatening diseases such as cancers and sickle cell anemia. Gene detection is thus of importance for disease-risk prediction or early diagnosis and treatment. Apart from genetic defects, gene detection techniques can
Externí odkaz:
https://doaj.org/article/6a3450578ac746a887509294c7ebe757
Autor:
Yingmu Cai, Mengyu Liu, Zhiyuan Wu, Cuihong Tian, Song Qiu, Zhen Li, Feng Xu, Wei Li, Yan Zheng, Aijuan Xu, Longxu Xie, Xuerui Tan
Publikováno v:
The EPMA journal.
Background To date, most countries worldwide have declared that the pandemic of COVID-19 is over, while the WHO has not officially ended the COVID-19 pandemic, and China still insists on the personalized dynamic COVID-free policy. Large-scale nucleic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::125949d002945b68a6c1375daa270718
https://pubmed.ncbi.nlm.nih.gov/36540610
https://pubmed.ncbi.nlm.nih.gov/36540610
Publikováno v:
Annals of Hematology
Chinese Gγ+(Aγδβ)0-thalassemia and SEA-HPFH are the most common types of β-globin gene cluster deletion in Chinese population. The aim of the study was to analyze clinical features of deletional Chinese Gγ+(Aγδβ)0-thalassemia and Southeast A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09f4a65537d59912ad5f9afbaaf1cac2
https://doi.org/10.1007/s00277-020-04252-7
https://doi.org/10.1007/s00277-020-04252-7
Autor:
Cidan Huang, Yuchang Zhuang, Jiafu Lin, Xinghui Nie, Li Qiu, Longxu Xie, Nansong Liu, Lin Zou, Hui Xi, Jie Zou, Jin Zhou, Shuodan Huang, Yajun Chen
Publikováno v:
International journal of laboratory hematologyREFERENCES. 44(1)
Introduction Newborn screening is an important supplement to thalassemia control and prevention. Capillary electrophoresis (CE) technology has several advantages for thalassemia screening but with low sensitivity, especially for thalassemia carriers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c4f17422544b122237ed128b5ce8d91
https://pubmed.ncbi.nlm.nih.gov/34505740
https://pubmed.ncbi.nlm.nih.gov/34505740
Autor:
Meijuan Li, Guiying Hu, Yu He, Longxu Xie, Tingyan Liu, Ling-zhi Mao, Ganfeng Luo, Huachun Zou, Xiaoli Sun, Xiping Luo, Lingmei Yan
Publikováno v:
Journal of Medical Virology. 91:1856-1865
Our study aimed to analyze genotype-specific, age-specific prevalence, and year-on-year trend of cervical human papillomavirus (HPV) detection among women in Guangdong, China 2008 to 2017. A total of 199 963 women attending the gynecological departme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecf256087c25ee7d8cc0da20f43d3789
https://doi.org/10.1002/jmv.25520
https://doi.org/10.1002/jmv.25520
Autor:
Fen, Lin, Liye, Yang, Min, Lin, Xiangbian, Zheng, Min, Lu, Meilan, Qiu, Liejun, Li, Longxu, Xie
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 34(6)
To detect rare types of thalassemia mutations among southern Chinese population.Peripheral blood samples from 327 patients from various regions of southern China were collected. The patients were suspected as rare-type thalassemia for their inconsist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc7279553c7ab55ba980376940bb7501
https://pubmed.ncbi.nlm.nih.gov/29188602
https://pubmed.ncbi.nlm.nih.gov/29188602