Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Qingnan HE"'
Autor:
Rong HUANG, Qingnan HE, Mingyan HEI, Minghua YANG, Xiaofan ZHU, Jun LU, Xiaojun XU, Tianming YUAN, Rong ZHANG, Xu WANG, Jinping LIU, Jing WANG, Zhili SHAO, Mingyi ZHAO, Jia GUO, Xinyin WU, Jiarui CHEN, Qirong CHEN, Rong GUI, Yongjian GUO
Publikováno v:
Zhongguo shuxue zazhi, Vol 37, Iss 7, Pp 839-844 (2024)
Children and adults differ significantly in physiology, biochemistry and immune function, which leads to significant differences in blood transfusion strategies between children and adults. To guide the clinical transfusion practice of pediatric pati
Externí odkaz:
https://doaj.org/article/33ef1147ef4441358da419a4ce612a90
Publikováno v:
PeerJ, Vol 12, p e18070 (2024)
Background Lupus nephritis (LN) is an autoimmune-related kidney disease with a poor prognosis, however the potential pathogenic mechanism remains unclear and there is a lack of precise biomarkers. Therefore, a thorough screening and identification of
Externí odkaz:
https://doaj.org/article/08248f6399c14f51826dd4606e8d1aad
Autor:
Bingqian Zhou, Ni Gong, Qingnan He, Xinjuan Huang, Jingchi Zhu, Lijun Zhang, Yanyan Huang, Xinyun Tan, Yuanqin Xia, Yu Zheng, Qiuling Shi, Chunxiang Qin
Publikováno v:
BMC Public Health, Vol 23, Iss 1, Pp 1-12 (2023)
Abstract Background The aggregation of lifestyle behaviours and their association with metabolic-associated fatty liver disease (MAFLD) remain unclear. We identified lifestyle patterns and investigated their association with the risk of developing MA
Externí odkaz:
https://doaj.org/article/b98730c5e5da4964bea4d6ea6734d5e4
Publikováno v:
Lipids in Health and Disease, Vol 22, Iss 1, Pp 1-12 (2023)
Abstract Aim We aim to develop and validate a nomogram including readily available clinical and laboratory indicators to predict the risk of metabolic-associated fatty liver disease (MAFLD) in the Chinese physical examination population. Methods The
Externí odkaz:
https://doaj.org/article/df91b2337da1483fad96dc8c3b497ccf
Autor:
Lanlan Tang, Yan Yu, Wenjun Deng, Jiao Liu, Yichun Wang, Fanghua Ye, Rui Kang, Daolin Tang, Qingnan He
Publikováno v:
iScience, Vol 26, Iss 12, Pp 108393- (2023)
Summary: Ferroptosis is a type of regulated cell death characterized by lipid peroxidation and subsequent damage to the plasma membrane. Here, we report a ferroptosis resistance mechanism involving the upregulation of TXNDC12, a thioredoxin domain-co
Externí odkaz:
https://doaj.org/article/9301e413c5cf42c5a77f5365b64f8b24
Autor:
Gui Xiao, Qingnan He, Li Liu, Tingting Zhang, Mengjia Zhou, Xingxing Li, Yijun Chen, Yanyi Chen, Chunxiang Qin
Publikováno v:
Journal of Translational Medicine, Vol 20, Iss 1, Pp 1-11 (2022)
Abstract Background Although anxiety disorders are one of the most prevalent mental disorders, their underlying biological mechanisms have not yet been fully elucidated. In recent years, genetically determined metabolites (GDMs) have been used to rev
Externí odkaz:
https://doaj.org/article/7d9ef0cf15a14083b41ae86837b6bfd9
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundGlobally, chronic kidney disease (CKD) is a growing public health concern. Serum uric acid (SUA) is an easily detectable and readily available biochemical indicator that has long been recognized as an independent risk factor for CKD. In add
Externí odkaz:
https://doaj.org/article/b60b4ee6bf034c87b96eda9da215c367
Autor:
Tingting Zhang, Wei-Ti Chen, Qingnan He, Ying Li, Huiting Peng, Jiaying Xie, Hengfen Hu, Chunxiang Qin
Publikováno v:
Frontiers in Public Health, Vol 11 (2023)
IntroductionMany women experience severe emotional distress (such as grief, depression, and anxiety) following a diagnosis of fetal anomaly. The ability to cope with stressful events and regulate emotions across diverse situations may play a primary
Externí odkaz:
https://doaj.org/article/e456c6d9de854c4a9ea45c42ca95d1bd
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundAlport syndrome (AS) and Wilson's disease (WD) are genetic diseases that could lead to kidney damage. Herein, we report the clinical features and gene variants in a patient with WD and X-linked AS.Case presentationThe proband was a 12-year-
Externí odkaz:
https://doaj.org/article/8f34e9d845124284b4d6d24929d157ca
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundCurrent first-line anti-proteinuric treatments do not produce a satisfactory therapeutic effect in a considerable number of patients with nephrotic syndrome (NS). Interest in adrenocorticotropic hormone (ACTH) for the treatment of NS has re
Externí odkaz:
https://doaj.org/article/392a5d7a8d57430db504e815496b02ab