Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Tingxia Lv"'
Publikováno v:
Journal of Immunology Research, Vol 2023 (2023)
Sepsis is defined as a dysregulated immune response to infection that leads to multiple organ dysfunction. To date, though a growing body of knowledge has gained insight into the clinical risk factors, pathobiology, treatment response, and recovery m
Externí odkaz:
https://doaj.org/article/7f8478e28d0549739226f7272ee8d0eb
Publikováno v:
Journal of Immunology Research, Vol 2021 (2021)
Although antiretroviral therapy effectively controls human immunodeficiency virus (HIV) replication, a residual chronic immune activation/inflammation persists throughout the disease. This aberrant immune activation and inflammation are considered an
Externí odkaz:
https://doaj.org/article/455d4bb3a58640e1a5cdd595600d5a8f
Publikováno v:
International immunopharmacology. 110
Human immunodeficiency virus (HIV) infections induce robust, generalized inflammatory responses and lead to pathological systemic immune activation. This abnormal immune status persists despite successful antiretroviral therapy (ART). Immune modulati
Autor:
Xiaosheng Liu, Ling Lin, Tingxia Lv, Lianfeng Lu, Xiaodi Li, Yang Han, Zhifeng Qiu, Xiaoxia Li, Yanling Li, Xiaojing Song, Wei Cao, Taisheng Li
Publikováno v:
Phytomedicine : international journal of phytotherapy and phytopharmacology. 101
The HIV-1 infected immunological non-responders (INRs) are characterized by poor immune reconstitution after long-term treatment. Tripterygium Wilfordii Hook F (TwHF) pill is a traditional Chinese patent drug with extensive immunosuppressive effects
Publikováno v:
Journal of Immunology Research
Journal of Immunology Research, Vol 2021 (2021)
Journal of Immunology Research, Vol 2021 (2021)
Although antiretroviral therapy effectively controls human immunodeficiency virus (HIV) replication, a residual chronic immune activation/inflammation persists throughout the disease. This aberrant immune activation and inflammation are considered an
Autor:
Yongpeng Chen, Jidong Jia, Xiaojuan Ou, Jiang Long, Xiaojin Li, Xinyan Zhao, Longdong Zhu, Xiaoming Wang, Wei Wang, Rongrong Zhao, Tingxia Lv, Yanmeng Li, Yu Wang, Bei Zhang, Sujun Zheng, Weijia Duan, JiShun Zheng, Lungen Lu, Hong You, Wei Zhang, Anjian Xu, Jian Huang, Qianyi Wang, Hexiang Xu, Yuwei Dong, Donghu Zhou
Publikováno v:
Journal of Medical Genetics. 55:650-660
IntroductionHereditary haemochromatosis (HH) caused by a homozygous p.C282Y mutation in haemochromatosis (HFE) gene has been well documented. However, less is known about the causative non-HFE mutation. We aimed to assess mutation patterns of haemoch
Autor:
Xiaoming Wang, Xinyan Zhao, Sujun Zheng, Siyu Jia, Jian Huang, Jidong Jia, Anjian Xu, Yongpeng Chen, Hong You, Jia Shang, Wei Zhang, Hejing Wang, Tingxia Lv, Xiaojuan Ou, Zhen Wu, Xiaojin Li, Yu Wang, Yanmeng Li, Qianyi Wang, Weijia Duan, Li-Ying Sun, Bei Zhang, Mei Liu, Wei Jiang, Yuemin Nan, Donghu Zhou
Publikováno v:
Human mutation. 40(5)
Wilson disease (WD) is a rare autosomal recessive genetic disorder that is associated with various mutations in the ATP7B gene. Although ATP7B variants are frequently identified, the exact mutation patterns remain unknown because of the absence of pe
Autor:
Jian Huang, Sujun Zheng, Xiaoming Wang, Hejing Wang, Qianyi Wang, Mei Liu, Bei Zhang, Jidong Jia, Anjian Xu, Li-Ying Sun, Jia Shang, Wei Jiang, Siyu Jia, Tingxia Lv, Xiaojuan Ou, Yongpeng Chen, Zhen Wu, Yu Wang, Hong You, Weijia Duan, Yanmeng Li, Donghu Zhou, Yuemin Nan, Xinyan Zhao, Wei Zhang, Xiaojin Li
Publikováno v:
Journal of Hepatology. 70:e593-e594
Autor:
Jian Huang, Ning Zhang, Hai Li, Guangyong Chen, Anjian Xu, Jiang Long, Bei Zhang, Xiaojuan Ou, Xiaojin Li, Zhang Zhao, Wei Zhang, Tingxia Lv
Publikováno v:
Oncology Reports.
Neurofibromatosis type 2 with mutations in the neurofibromin 2 (NF2) gene, encoding the Merlin protein, is an autosomal dominant disorder characterized by enhanced cancer predisposition, particularly tumors of the central nervous system. Recent anima
Publikováno v:
Medicine
Rationale: Hereditary hemochromatosis can be divided into HFE- and non-HFE-related based on genetic mutations in different genes. HFE-related hemochromatosis is the most common inherited genetic disease in European populations but rare in Asia-pacifi