Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Jinqiu Jiang"'
Autor:
Shi Yan, Xuege Wu, Jinqiu Jiang, Shijuan Yu, Xiao Fang, Huan Yang, Xiaoming Bai, Hua Wang, Xiaoyan Luo
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
BackgroundNetherton syndrome is a rare, life-threatening autosomal recessive genetic disorder with no effective treatment yet. Skin barrier dysfunction caused by SPINK5 gene mutations is a hallmark of the disease. Antigen penetration through the defe
Externí odkaz:
https://doaj.org/article/f855f769d8914a7aa8311a88abe251e0
Autor:
Jinqiu Jiang, Tao Qin, Liang Zhang, Qiao Liu, Jiabin Wu, Rongxin Dai, Lina Zhou, Qin Zhao, Xiaoyan Luo, Hua Wang, Xiaodong Zhao
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Mutations in human DOCK8 cause a combined immunodeficiency syndrome characterized by allergic diseases such as asthma and food allergy. However, the underlying mechanism is unclear. Regulatory B (Breg) cells that produce IL-10 exert potent immunosupp
Externí odkaz:
https://doaj.org/article/49b6f7f19bb44b6da39bf8023be1b23e
Autor:
Jinqiu Jiang, Shi Yan, Xiaoying Zhou, Jinghua Zhou, Xiaoming Bai, Qi Tan, Yunqiu Xia, Hua Wang, Xiaoyan Luo
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Atopic dermatitis (AD) in early childhood is often the initial manifestation of allergic disease associated with high IgE. Accumulating evidences show that follicular helper T (Tfh) cells play a critical role in promoting B cell differentiation and I
Externí odkaz:
https://doaj.org/article/2e4f6ee7ca72448996c5197a6557f81b
Autor:
Xianze Luo, Qing Liu, Jinqiu Jiang, Wenjing Tang, Yuan Ding, Lina Zhou, Jie Yu, Xuemei Tang, Yunfei An, Xiaodong Zhao
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
DNA ligase IV (LIG4) deficiency is an extremely rare autosomal recessive primary immunodeficiency disease caused by mutations in LIG4. Patients suffer from a broad spectrum of clinical problems, including microcephaly, growth retardation, development
Externí odkaz:
https://doaj.org/article/b530485007734e72aa227fd3cf93ac67
Publikováno v:
Journal of Human Hypertension. 31:438-443
We aimed to evaluate the performance of blood pressure-to-height ratio (BPHR) and establish their optimal thresholds for elevated blood pressure (BP) among children aged 6 to 17 years in Chongqing, China. Data were collected from 11 029 children and
Publikováno v:
Clinical Immunology. 163:75-83
DNA ligase IV (LIG4) deficiency is an extremely rare autosomal recessive primary immunodeficiency disease caused by the LIG4 mutation. To date, fewer than 30 cases of patients have been reported worldwide. No reversion mutations have been previously
Autor:
Jiabin Wu, Liang Zhang, Qiao Liu, Tao Qin, Jinqiu Jiang, Xiaodong Zhao, Jihong Dai, Suqian Zhang
Publikováno v:
Biochemical and biophysical research communications. 501(1)
Patients with DOCK8 deficiency are at increased susceptibility to develop allergic diseases such as food allergy and asthma. Here, we aimed to analyze the pathogenesis of asthma in DOCK8-deficient patients. In our mouse model, DOCK8-knockout (KO) mic
Autor:
Li Cheng, Xuan Zhai, Jinqiu Jiang, Li Jiang, Xiaojie Song, Tianyi Li, Hengsheng Chen, Jiannan Ma, Wei Han, Lingling Xie
Publikováno v:
Brain research. 1657
Recent studies have reported microglia that are activated in the central nervous system (CNS) in patients with temporal lobe epilepsy and animal models of epilepsy. However, limited data are available on the dynamic changes of the proportions of vari
Publikováno v:
Zhonghua er ke za zhi = Chinese journal of pediatrics. 53(12)