Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Wenjing Ying"'
Autor:
Bijun Sun, Mi Yang, Jia Hou, Wenjie Wang, Wenjing Ying, Xiaoying Hui, Qinhua Zhou, Haili Yao, Jinqiao Sun, Xiaochuan Wang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-15 (2022)
Abstract Background Fever of unknown origin (FUO) has been difficult to diagnose in pediatric clinical practice. With the gradual change in the disease spectrum, genetic factors have received increasing attention. Limited studies have shown an associ
Externí odkaz:
https://doaj.org/article/54dd4bd28e164460acfbaf5f1bce5835
Publikováno v:
IEEE Access, Vol 10, Pp 120752-120764 (2022)
Video frame interpolation is an important technology in digital video processing, which has great impact on users’ viewing experience. In particular, in medical or industrial application scenarios, the accuracy of the frame interpolation algorithm
Externí odkaz:
https://doaj.org/article/662285584e8d47089e0e907c1af9c3ed
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
We aimed to investigate the immunological mechanisms of the Toll-like receptor (TLR) signaling pathways in different types of Epstein-Barr virus (EBV) infection. We retrospectively summarized the clinical data, routine laboratory tests and the immuno
Externí odkaz:
https://doaj.org/article/966dd9c395a448a9b283fcbec2e25602
Autor:
Bijun Sun, Qifan Li, Xiaolong Dong, Jia Hou, Wenjie Wang, Wenjing Ying, Xiaoying Hui, Qinhua Zhou, Haili Yao, Jinqiao Sun, Xiaochuan Wang
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Purpose: Severe glucose-6-phosphate dehydrogenase (G6PD) deficiency can lead to reduced nicotinamide adenine dinucleotide phosphate oxidase activity in phagocytes, resulting in immunodeficiency, with a limited number of reported cases. Here, we aimed
Externí odkaz:
https://doaj.org/article/7b642ac7d5f248fd8fb29cfe33c4c3ca
Autor:
Lipin Liu, Bijun Sun, Wenjing Ying, Danru Liu, Ying Wang, Jinqiao Sun, Wenjie Wang, Mi Yang, Xiaoying Hui, Qinhua Zhou, Jia Hou, Xiaochuan Wang
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 12 (2022)
Talaromyces marneffei (T. marneffei) is an opportunistic pathogen. Patients with inborn errors of immunity (IEI) have been increasingly diagnosed with T. marneffei in recent years. The disseminated infection of T. marneffei can be life-threatening wi
Externí odkaz:
https://doaj.org/article/2c3145da55874e29b22c98946baa0fa6
Autor:
Wenjie Wang, Qing Min, Nannan Lai, Krisztian Csomos, Ying Wang, Luyao Liu, Xin Meng, Jinqiao Sun, Jia Hou, Wenjing Ying, Qinhua Zhou, Bijun Sun, Xiaoying Hui, Boglarka Ujhazi, Sumai Gordon, David Buchbinder, Catharina Schuetz, Manish Butte, Jolan E. Walter, Xiaochuan Wang, Ji-Yang Wang
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
BackgroundActivated phosphoinositide 3 kinase (PI3K) -delta syndrome (APDS) is an inborn error of immunity with variable clinical phenotype of immunodeficiency and immune dysregulation and caused by gain-of-function mutations in PIK3CD. The hallmark
Externí odkaz:
https://doaj.org/article/8c8365988a5549fb8f212dacf50ffa66
Autor:
Qiufang Guo, Ping Zhang, Wenjing Ying, Yaqiong Wang, Jitao Zhu, Gang Li, Huijun Wang, Xiaochuan Wang, Caixia Lei, Wenhao Zhou, Jinqiao Sun, Bingbing Wu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 6, Pp n/a-n/a (2022)
Abstract Background DKC1, the dyskerin encoding gene, functions in telomerase activity and telomere maintenance. DKC1 mutations cause a multisystem disease, dyskeratosis congenita (DC), which is associated with immunodeficiency and bone marrow failur
Externí odkaz:
https://doaj.org/article/47d02e1634474fdf829188857c647f16
Autor:
Wenjie Wang, Luyao Liu, Xiaoying Hui, Ying Wang, Wenjing Ying, Qinhua Zhou, Jia Hou, Mi Yang, Bijun Sun, Jinqiao Sun, Xiaochuan Wang
Publikováno v:
BMC Immunology, Vol 22, Iss 1, Pp 1-9 (2021)
Abstract Background We aimed to report the clinical characteristics, immunological features, and treatment of one patient with a de novo STAT3 gain-of-function mutation identified by next generation sequencing. We investigated the efficacy of tociliz
Externí odkaz:
https://doaj.org/article/61c440be3029403faa4a07ceae0b4e4f
Autor:
Li Lin, Ying Wang, Bijun Sun, Luyao Liu, Wenjing Ying, Wenjie Wang, Qinhua Zhou, Jia Hou, Haili Yao, Liyuan Hu, Jinqiao Sun, Xiaochuan Wang
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 16, Iss 1, Pp 1-10 (2020)
Abstract Background Loss-of-function (LOF) mutations in signal transducer and activator of transcription 3 (STAT3) is one of the causes of STAT3 hyperimmunoglobulin E (IgE) syndrome (STAT3-HIES), while gain-of-function (GOF) mutations in STAT3 lead t
Externí odkaz:
https://doaj.org/article/429a5a35266a4a0d9f1d031b6ed6cf76
Autor:
Bijun Sun, Qiuyu Chen, Ying Wang, Danru Liu, Jia Hou, Wenjie Wang, Wenjing Ying, Xiaoying Hui, Qinhua Zhou, Jinqiao Sun, Xiaochuan Wang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background DNA Ligase IV (LIG4) syndrome is a rare disease with few reports to date. Patients suffer from a broad spectrum of clinical features, including microcephaly, growth retardation, developmental delay, dysmorphic facial features, com
Externí odkaz:
https://doaj.org/article/951dd36bd2e34a639601715eb75f17b6