Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Chunlin, Gao"'
Autor:
Wensheng Xu, Ruixue Tian, Chunlin Gao, Chenghao Wang, Yuxin Chen, Ruifen Wang, Jun Peng, Shengli An, Peizhong Li
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract The catalyst is based on CeO2 cannot be widely used in SCR reaction because of its poor NH3 adsorption performance. In this study, Cu-doped CeTi catalyst was designed. The results show that the CeTiCu0.3 has a wide active temperature window
Externí odkaz:
https://doaj.org/article/4eaed786688741d1b9f5498180158d31
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
De novo inflammatory bowel disease (IBD) in response to rituximab (RTX) has been documented on multiple occasions as a severe adverse effect. However, none of these reports mentioned any genetic variation associated with this complication. We describ
Externí odkaz:
https://doaj.org/article/8289f7a5b1044fc9a63501aa401e4922
Autor:
ZHU Chunlin, GAO Jie
Publikováno v:
Zhongguo quanke yixue, Vol 27, Iss 03, Pp 273-279 (2024)
Coronary microvascular dysfunction (CMD) and metabolic syndrome (MetS) have attracted much attention recently due to the adverse effects on cardiovascular system. CMD is a potential factor leading to myocardial ischemia, which is closely related to t
Externí odkaz:
https://doaj.org/article/f37aa4cabb304642aeac80ad8849990a
Autor:
Tingting Han, Mei Xue, Yafei Guan, Tao Ju, Kaili Shi, Mengzhen Fu, Lili Jia, Chunlin Gao, Zhengkun Xia
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundMinimal change disease (MCD) is one of the most common primary glomerular disorders with high serum IgE levels. This study was aimed to investigate the clinical features of different serum IgE levels in pediatric MCD and evaluate the progno
Externí odkaz:
https://doaj.org/article/dd0b01f715a2498dbecd6674ebe5aba2
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
An eight-year-old girl was admitted with vomiting, gross hematuria, and progressive renal dysfunction. A renal biopsy revealed endocapillary proliferative glomerulopathy and crescent formation. Immunofluorescence staining revealed diffuse granular de
Externí odkaz:
https://doaj.org/article/c2a9d9186135432ebfb44bc12577bec5
Autor:
Yingchao Peng, Banghai Li, Xiaojie Li, Tao Ju, Zhiqiang Zhang, Peipei Wang, Tao Sun, Jiaping Shu, Meiqiu Wang, Xiaoyi Sun, Huangyu Chen, Chunlin Gao, Zhengkun Xia
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionSome patients with primary focal segmental sclerosis (FSGS) demonstrate complement 3 (C3) deposition in glomerular capillary loops (Cap-C3) and/or mesangial area (Mes-C3). The clinicopathological and prognostic significance of C3 depositi
Externí odkaz:
https://doaj.org/article/bab33b423248441792615baf5219df27
Autor:
Tao Ju, Yingchao Peng, Yaqin Wei, Xiaojie Li, Meiqiu Wang, Ren Wang, Xiao Yang, Zhiqiang Zhang, Chunlin Gao, Zhengkun Xia
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundMinimal change disease (MCD) is the most common pathological subtype of pediatric idiopathic nephrotic syndrome (INS). It has been suggested that IgM deposition might predict kidney function deterioration in the course of MCD. However, the
Externí odkaz:
https://doaj.org/article/c40e8b2d6b9347b28f69474572e1ced4
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAVs) are closely associated with neutrophil recruitment and activation, but the impact of the neutrophil apoptosis process in autoimmune disease has been rarely explained. Here, by
Externí odkaz:
https://doaj.org/article/39107a03648e4d08a4455501c3cf96e4
Publikováno v:
Autoimmunity, Vol 54, Iss 6, Pp 343-352 (2021)
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis, a class of systemic autoimmune diseases, results in damage of various critical organs including kidneys, lungs, eyes, and nervous system. MicroRNA-340-5p was confirmed to be downregula
Externí odkaz:
https://doaj.org/article/2c4667279b544646a03c77d00bd8dc65
Autor:
Xiaojie Li, Yaqin Wei, Meiqiu Wang, Lili Jia, Zhuo Shi, Xiao Yang, Tao Ju, Qianhuining Kuang, Zhengkun Xia, Chunlin Gao
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundTRIM8 gene mutations have been reported as the genetic basis of autosomal dominant (AD) neuro-renal syndrome in children, which presents with epileptic encephalopathy, focal segmental glomerulosclerosis (FSGS), developmental delay, and ment
Externí odkaz:
https://doaj.org/article/0588d63f9ca14ee8afb20df18e3cf0ab