Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Yuanhan, Qin"'
Autor:
Sheng Li, Chao He, Yu Sun, Jie Chen, Yunguang Liu, Zengpo Huang, Weifang Huang, Yongqiu Meng, Wenjing Liu, Xianqiang Lei, Rihong Zhao, Zihui Lin, Chunlin Huang, Fengying Lei, Yuanhan Qin
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-8 (2024)
Abstract Background This study investigated the factors influencing the prognosis of children with steroid-resistant nephrotic syndrome (SRNS) in patients from the Guangxi region. Methods We retrospectively analyzed clinical and pathological data of
Externí odkaz:
https://doaj.org/article/09ba71bafc9b46169baba6427c7e0162
Autor:
Sheng Li, Miaoyue Hu, Chao He, Yu Sun, Weifang Huang, Fengying Lei, Yunguang Liu, Zengpo Huang, Yongqiu Meng, Wenjing Liu, Xianqiang Lei, Yanfang Dong, Zihui Lin, Chunlin Huang, Rihong Zhao, Yuanhan Qin
Publikováno v:
PLoS ONE, Vol 19, Iss 12, p e0304864 (2024)
This study aimed to discuss the pathogenic hereditary factors of children with steroid-resistant nephrotic syndrome (SRNS) in Guangxi, China. We recruited 89 patients with SRNS or infantile NS from five major pediatric nephrology centers in Guangxi,
Externí odkaz:
https://doaj.org/article/24f86cb23bcf429b89509cb76c9a231e
Publikováno v:
PLoS ONE, Vol 19, Iss 3, p e0299509 (2024)
IntroductionObesity has been found to be correlated with numerous health issues, including an elevated risk of albuminuria in adults. However, this correlation is still controversial among children and adolescents, as several recent large-scale cross
Externí odkaz:
https://doaj.org/article/579aa0693eb64656a448e03ae2216b30
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
The Poirier-Bienvenu neurodevelopmental syndrome (POBINDS) is a rare disease caused by mutations in the CSNK2B gene, which is characterized by intellectual disability and early-onset epilepsy. Mosaicism has not been previously reported in CSNK2B gene
Externí odkaz:
https://doaj.org/article/9040995c4c61428689a55cac492c26b6
Autor:
Jinshuang Wei, Junlin Zhang, Junyu Wei, Miaoyue Hu, Xiuqi Chen, Xuankai Qin, Jie Chen, Fengying Lei, Yuanhan Qin
Publikováno v:
PLoS ONE, Vol 18, Iss 2, p e0281439 (2023)
Acute kidney injury (AKI) is a serious and frequently observed disease associated with high morbidity and mortality. Weighted gene co-expression network analysis (WGCNA) is a research method that converts the relationship between tens of thousands of
Externí odkaz:
https://doaj.org/article/3fee9d1ea7874851bc2854831947c144
Autor:
Xiujuan Zhu, Yanqin Zhang, Zihua Yu, Li Yu, Wenyan Huang, Shuzhen Sun, Yingjie Li, Mo Wang, Yongzhen Li, Liangzhong Sun, Qing Yang, Fang Deng, Xiaoshan Shao, Ling Liu, Cuihua Liu, Yuanhan Qin, Shipin Feng, Hongtao Zhu, Fang Yang, Weimin Zheng, Wanqi Zheng, Rirong Zhong, Ling Hou, Jianhua Mao, Fang Wang, Jie Ding
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Steroid-resistant nephrotic syndrome (SRNS) is one of the major causes of end-stage kidney disease (ESKD) in children and young adults. For approximately 30% of children with SRNS results from a genetic cause. In this study, genotype-phenotype correl
Externí odkaz:
https://doaj.org/article/673a215dfd0c4e87afa3a818e55e2a0c
Autor:
Jinshuang Wei, Junlin Zhang, Xiuqi Chen, Jiasen Zou, Junyu Wei, Miaoyue Hu, Shiqun Zhu, Yuanhan Qin, Fengying Lei
Publikováno v:
Pharmacological Research - Modern Chinese Medicine, Vol 3, Iss , Pp 100114- (2022)
Objective: To investigate the molecular mechanism underlying the therapeutic effect of resveratrol for nephrotic syndrome using various online network pharmacology databases. Methods: Genes related to resveratrol and nephrotic syndrome were downloade
Externí odkaz:
https://doaj.org/article/82eb9c08c1384e9698ba9aee1250514c
Publikováno v:
Sensors, Vol 22, Iss 13, p 4955 (2022)
Pavement texture characteristics can reflect early performance decay, skid resistance, and other information. However, most statistical texture indicators cannot express this difference. This study adopts 3D image camera equipment to collect texture
Externí odkaz:
https://doaj.org/article/29687de14b754b60b8b39796e26dac90
Publikováno v:
Transl Pediatr
BACKGROUND: Brain death (BD) is a catastrophic physiological outcome that can occur in individuals with terminal illness and can adversely affect the graft quality after donation of their organs. As BD has no specific symptoms, it can be difficult to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e3290c2e2dd1f52af203141c403b459
https://doi.org/10.21037/tp-21-559
https://doi.org/10.21037/tp-21-559
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2021 (2021)
BioMed Research International, Vol 2021 (2021)
Objectives. This study is aimed at exploring the relationships between miRNAs and mRNAs and to characterize their biological functions in temporal lobe epilepsy (TLE). Methods. Novel clinical significant miRNAs and target genes and their potential un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b39abf0b15472ba6a4e95ecf463c1341
https://doi.org/10.1155/2021/4118216
https://doi.org/10.1155/2021/4118216