Zobrazeno 1 - 10
of 1 025
pro vyhledávání: '"Shan Jian"'
Autor:
Tianyu Zhang, Zhongxun Yu, Sihao Gao, Yuelun Zhang, Changyan Wang, Shan Jian, Lin Wang, Lijuan Gou, Ji Li, Mingsheng Ma, Hongmei Song
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss 1, Pp 1-9 (2023)
Abstract Background Cytomegalovirus (CMV) plays an important role in the pathogenesis of systemic lupus erythematosus (SLE). However, it is not clear whether the anti-CMV treatment has an impact on the prognosis of SLE patients with CMV infection. We
Externí odkaz:
https://doaj.org/article/7ca8091ed080488385080a9aef69533c
Publikováno v:
JCI Insight, Vol 8, Iss 19 (2023)
Pyrin, a protein encoded by the MEFV gene, plays a vital role in innate immunity by sensing modifications in Rho GTPase and assembling the pyrin inflammasome, which in turn activates downstream immune responses. We identified a novel and de novo MEFV
Externí odkaz:
https://doaj.org/article/bdcda9bed79a42c1bdfa66054f4cd1b4
Autor:
Jing Liu, Yuelun Zhang, Zhuo Li, Zhenghong Li, Lejia Zhang, Shan Jian, Changyan Wang, Yuqing Song, Zichao Lv, Xiaoyan Tang, Lijuan Gou, Juan Xiao
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 6, Iss 7, Pp n/a-n/a (2022)
Abstract Background Neonatal‐onset hereditary thrombotic thrombocytopenia purpura (hTTP) is often misdiagnosed due to its rarity. It begins with jaundice, similar to infants with ABO incompatibility. Objective To explore early indicators of neonata
Externí odkaz:
https://doaj.org/article/089ecbef16c14c728506b820c099d421
Autor:
Chao Liu, Ying Wang, Feng Feng, Shan Jian, Hua Meng, Yunlong Zhao, Lijian Pei, Yulin Jiang, Yandong Wei, Xiting Zhu, Xiaochen Bai, Yan Lv, Xiya Zhou, Qingwei Qi, Jingna Li, Lishuang Ma
Publikováno v:
World Journal of Pediatric Surgery, Vol 5, Iss 4 (2022)
Objective Previous studies have shown that ex utero intrapartum therapy (EXIT) is safe and feasible for newborns with congenital diaphragmatic hernia (CDH). This study reports our experience with EXIT in fetuses with CDH in an attempt to explore the
Externí odkaz:
https://doaj.org/article/bd01ebd809fc48a5a0a014a7bc324ab9
Publikováno v:
Water, Vol 15, Iss 11, p 2110 (2023)
Few studies have been conducted to simulate watersheds with insufficient meteorological and hydrological information. The Jiyun River watershed was selected as the study area. A suitable catchment area threshold was determined by combining the river
Externí odkaz:
https://doaj.org/article/31725ce82ea6422ea146eb5bf4ec0c1b
Autor:
Wendao Li, Wei Wang, Linqing Zhong, Lijuan Gou, Changyan Wang, Jingran Ma, Meiying Quan, Shan Jian, Xiaoyan Tang, Yu Zhang, Lin Wang, Mingsheng Ma, Hongmei Song
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
ObjectiveThis study aimed to assess the efficacy and safety of 2 Janus kinase (JAK) inhibitors (jakinibs) tofacitinib and ruxolitinib in the treatment of type I interferonopathies patients including STING-associated vasculopathy with onset in infancy
Externí odkaz:
https://doaj.org/article/aee551c602b14baeb50676862b216560
Autor:
Wei Wang, Tianhao Yao, Tianyi Zhang, Meiying Quan, Changyan Wang, Chen Wang, Lejia Zhang, Xiaoyan Tang, Shan Jian, Hongmei Song
Publikováno v:
Genes and Diseases, Vol 7, Iss 1, Pp 115-121 (2020)
Selective immunoglobulin A deficiency (SIgAD) is considered to be the most common human primary immune-deficiency disease in the world. However, the incidence in China is obviously lower than Caucasian races. The definition of SIgAD has changed over
Externí odkaz:
https://doaj.org/article/c5284c9e9dd64f82bb98cdba4b5004bf
Publikováno v:
Frontiers in Microbiology, Vol 12 (2021)
Sediment is thought to be a vital reservoir for antibiotic resistance genes (ARGs). Often, studies describing and comparing ARGs and their potential hosts in sediment are based on single DNA extractions. To date, however, no study has been conducted
Externí odkaz:
https://doaj.org/article/60d6c5e3f2d14f1aa44985d7485ab3ea
Autor:
Ji Li, Jing-Jing Jiang, Chang-Yan Wang, Shan Jian, Yu Zhou, Ming-Sheng Ma, Xiao-Yan Tang, Lin Wang, Mei-Ying Quan, Yu Zhang, Juan Xiao, Yan-Yan He, Hong-Mei Song
Publikováno v:
Italian Journal of Pediatrics, Vol 45, Iss 1, Pp 1-6 (2019)
Abstract Objective To report the clinical features of patients with systemic lupus erythematosus (SLE) associated with thrombotic thrombocytopenic purpura (TTP). Their diagnosis, treatment, and prognosis were also discussed. Methods A total of 25 TTP
Externí odkaz:
https://doaj.org/article/886b7d44fc0c444fa0996ea410088c98
Publikováno v:
Journal of International Medical Research, Vol 48 (2020)
Bartter syndrome is a rare inherited disease caused by CLCNKB mutation, which results in inactivation of the chloride channel Kb protein. Bartter syndrome is characterized by extreme hypokalemia, hypochloremia, metabolic alkalosis, hyperrenin-induced
Externí odkaz:
https://doaj.org/article/fbc287c29636461b98e8155d8177ad47