Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Yimeng Qiao"'
Autor:
Zheng Qi, PhD, Ye Cheng, PhD, Yu Su, PhD, Yimeng Qiao, PhD, Jin Zhang, PhD, Jian-jun Yang, MD, Qinghe Xing, PhD
Publikováno v:
World Allergy Organization Journal, Vol 17, Iss 1, Pp 100854- (2024)
Background: Perioperative anaphylaxis (POA) can lead to severe consequences. Identifying clinical risk factors and genetic loci associated with POA through pre-prescription screening may help reduce its incidence. Methods: Using univariate regression
Externí odkaz:
https://doaj.org/article/11b9d5f06457403d87885b3092ad5e5c
Autor:
Dan Wang, Juan Song, Ye Cheng, Yiran Xu, Lili Song, Yimeng Qiao, Bingbing Li, Lei Xia, Ming Li, Jin Zhang, Yu Su, Ting Wang, Jian Ding, Xiaoyang Wang, Sujuan Wang, Changlian Zhu, Qinghe Xing
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2023)
BackgroundCerebral palsy (CP) is a neurodevelopmental disorder characterized by motor impairment. In this study, we aimed to describe the characteristics of amino acids (AA) in the plasma of children with CP and identify AA that could play a potentia
Externí odkaz:
https://doaj.org/article/3a94c1882a754dc09449994b405cef2d
Autor:
Yimeng Qiao, Yangong Wang, Yiran Xu, Jin Zhang, Yu Su, Ye Cheng, Dan Bi, Juan Song, Lei Xia, Ming Li, Xiaoli Zhang, Dengna Zhu, Ting Wang, Jian Ding, Xiaoyang Wang, Changlian Zhu, Qinghe Xing
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-8 (2022)
Abstract Background Cerebral palsy (CP), the most common physical disability of childhood, is a nonprogressive movement disorder syndrome. Eighty percent of cases are considered idiopathic without a clear cause. Evidence has shown that cytokine abnor
Externí odkaz:
https://doaj.org/article/85bf702066b04fb1bed592e17c8f35b3
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Neuronal ceroid lipofuscinoses (NCLs) are among the most common progressive encephalopathies of childhood. Neuronal ceroid lipofuscinosis 7 (CLN7), one of the late infantile-onset NCLs, is an autosomal recessive disorder caused by mutations in the MF
Externí odkaz:
https://doaj.org/article/a2d3243ef4b54932aa4f1754d3543138
Autor:
Yangong Wang, Yiran Xu, Yangyi Fan, Dan Bi, Juan Song, Lei Xia, Qing Shang, Chao Gao, Xiaoli Zhang, Dengna Zhu, Yimeng Qiao, Yu Su, Xiaoyang Wang, Changlian Zhu, Qinghe Xing
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
Background: Cerebral palsy (CP) is a syndrome of non-progressive motor dysfunction caused by early brain development injury. Recent evidence has shown that immunological abnormalities are associated with an increased risk of CP.Methods: We recruited
Externí odkaz:
https://doaj.org/article/b2d4cf52f93445389ec77a7114b61066
Autor:
Lei Xia, Jianhua Xu, Juan Song, Yiran Xu, Bohao Zhang, Chao Gao, Dengna Zhu, Chongchen Zhou, Dan Bi, Yangong Wang, Xiaoli Zhang, Qing Shang, Yimeng Qiao, Xiaoyang Wang, Qinghe Xing, Changlian Zhu
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 13 (2019)
Cerebral palsy (CP) is a group of non-progressive motor impairment syndromes that are secondary to brain injury in the early stages of brain development. Numerous etiologies and risk factors of CP have been reported, and genetic contributions have re
Externí odkaz:
https://doaj.org/article/cec68d2bb011426e9b092bf3dff6e559
Publikováno v:
Proceedings of the ACM Web Conference 2023.
Autor:
Qinghe Xing, Yangong Wang, Xiaoli Zhang, Hongwei Li, Yu Su, Ye Cheng, Juan Song, Yiran Xu, Changlian Zhu, Jun Wang, Chao Gao, Dengna Zhu, Yimeng Qiao, Tianxiang Tang, Qing Shang, Xiaoyang Wang, Lili Song, Lingling Zhang
Publikováno v:
Journal of Genetics and Genomics. 48:1134-1138
Autor:
Qinghe Xing, Ye Cheng, Yiran Xu, Hongwei Li, Yimeng Qiao, Yangong Wang, Yu Su, Jin Zhang, Xiaoyang Wang, Changlian Zhu
Cerebral palsy (CP) is the most common physical disability in childhood that results from the interaction of environmental and genetic factors. Yet in many patients, the etiology remains unknown. We identified significant association at rs3131787 wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26204d9d1c778813180c0a4e58a8c975
https://doi.org/10.21203/rs.3.rs-2368855/v1
https://doi.org/10.21203/rs.3.rs-2368855/v1
Autor:
Yimeng Qiao, Baiyun Chen, Yanqiang Han, Yangong Wang, Jin Zhang, Yu Su, Ye Cheng, Ting Wang, Jian Ding, Simin Ye, Nan Lv, Jinjin Li, Qing Shang, Qinghe Xing
Background Developmental delay (DD) and intellectual disability (ID) represent one of the biggest medical and social challenges in our society with a prevalence of 1 ~ 3% worldwide. Currently, at least 50% of DD/ID cases remained unexplained. Mental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a97b7c24ab6c42f47b9fef54652dcc14
https://doi.org/10.21203/rs.3.rs-2091600/v1
https://doi.org/10.21203/rs.3.rs-2091600/v1