Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Lianfu Ji"'
Autor:
Xiaoxu Chen, Mingyue Chen, Yuqing Zhu, Haifeng Sun, Yue Wang, Yuan Xie, Lianfu Ji, Cheng Wang, Zhibin Hu, Xuejiang Guo, Zhengfeng Xu, Jun Zhang, Shiwei Yang, Dong Liang, Bin Shen
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-11 (2023)
Abstract Pathogenic mutations in mitochondrial DNA cause severe and often lethal multi-system symptoms in primary mitochondrial defects. However, effective therapies for these defects are still lacking. Strategies such as employing mitochondrially ta
Externí odkaz:
https://doaj.org/article/f37332210d6142babcb847a44f5f05aa
Autor:
Zhongman Zhang, Kangkang Xu, Lianfu Ji, Han Zhang, Jie Yin, Ming Zhou, Chunli Wang, Shiwei Yang
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundThe nebulin-related-anchoring protein (NRAP) gene encodes actin-associated ankyrin. Few studies reported the association of the NRAP gene with cardiomyopathy. Thus, the genetic role of this gene in cardiomyopathy remains to be investigated.
Externí odkaz:
https://doaj.org/article/66b7a015e209443fb89772a785b50a7d
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Restrictive cardiomyopathy (RCM) is a rare form of heart muscle disease with poor prognosis. Its primary manifestations were caused by systemic or pulmonary circulation congestion. Here, we reported a case of RCM with ventricular fibrillation as init
Externí odkaz:
https://doaj.org/article/bd48ae9c34944b34a26fc812585fcc5f
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Abernethy malformation is a rare abnormality of the hepatic portal vein system with non-specific and diverse clinical manifestations. Here, we described a case of abernethy malformation with hepatopulmonary syndrome in a 10-year-old girl. On physical
Externí odkaz:
https://doaj.org/article/c8af0df200ad42f28e2573a3a7f0302a
Autor:
Lianfu Ji, Fan Yang, Xuan Chen, Jinlong Chen, Xueying Cheng, Jie Yin, Yuming Qin, Shiwei Yang
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Iliac vein compression syndrome (IVCS) or May–Thurner syndrome occurs predominantly in young to middle-aged women. Here we reported a case of IVCS in a 5-year-old boy. The child was admitted to our vasculocardiology department with left lower extre
Externí odkaz:
https://doaj.org/article/d00bce67e38b4a20be5cc075cb202bf4
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0152177 (2016)
Enterovirus 71 (EV71) causes hand-foot-and-mouth disease, which can lead to fatal neurological complications in young children and infants. Few gastrointestinal symptoms are observed clinically, suggesting the presence of a unique immunity to EV71 in
Externí odkaz:
https://doaj.org/article/9f2776ffd3144442b947b7b04d626a90
Publikováno v:
Virus Research. 330:199108
Publikováno v:
Viral Immunology. 34:218-226
The nuclear factor-kappa B (NF-κB) signaling network constitutes a first line of defense against the invading viruses. However, viruses also adopted multiple strategies to interfere with NF-κB activation. Enterovirus 71 (EV71), in the family Picorn
Autor:
Yuming Qin, Fan Yang, Xueying Cheng, Xuan Chen, Lianfu Ji, Jinlong Chen, Shiwei Yang, Jie Yin
Publikováno v:
Frontiers in Pediatrics
Frontiers in Pediatrics, Vol 9 (2021)
Frontiers in Pediatrics, Vol 9 (2021)
Iliac vein compression syndrome (IVCS) or May–Thurner syndrome occurs predominantly in young to middle-aged women. Here we reported a case of IVCS in a 5-year-old boy. The child was admitted to our vasculocardiology department with left lower extre
Publikováno v:
Viral immunology. 34(4)
The nuclear factor-kappa B (NF