Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Ruoyi Gu"'
Autor:
Guixiang Tian, Lili He, Ruoyi Gu, Jingwei Sun, Weicheng Chen, Yanyan Qian, Xiaojing Ma, Weili Yan, Zhenshan Zhao, Ziqing Xu, Meijiao Suo, Wei Sheng, Guoying Huang
Publikováno v:
Molecular Medicine Reports
Tetralogy of Fallot (TOF) is the most common cyanotic congenital heart malformation accounting for ~10% of cases. Although the pathogenesis of TOF is complex and largely unknown, epigenetics plays a huge role, specifically DNA methylation. The protei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8552951856d32856ebfb4cf4fc0faec
http://europepmc.org/articles/PMC8809049
http://europepmc.org/articles/PMC8809049
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Intoeing in children is a common parental concern, but our understanding of the impact of foot progression angle (FPA) in these children leaves remains limited. This study examines the relationship between FPA and plantar loading pattern, as
Externí odkaz:
https://doaj.org/article/7c2c2f841e1c4dca83823a869a23077c
Publikováno v:
Heliyon, Vol 10, Iss 17, Pp e37091- (2024)
Aims: Earlier studies have indicated an association between the TIMP1 polymorphism and the risk of certain autoimmune diseases, as well as a link between higher TIMP1 levels and blood-brain barrier (BBB) disruption in neuromyelitis optica spectrum di
Externí odkaz:
https://doaj.org/article/a63e366e97be4943b100536484e123e6
Autor:
Xiaodi, Li, Ming, Ye, Hongfei, Xu, Yanjie, Zhu, Ruoyi, Gu, Ma, Xiaojing, Wei, Sheng, Guoying, Huang
Publikováno v:
In Biochemical and Biophysical Research Communications 3 September 2020 529(4):1209-1215
Autor:
Ming Ye, Yanjie Zhu, Hongfei Xu, Xiaojing Ma, Wei Sheng, Xiaodi Li, Guoying Huang, Ruoyi Gu, Mingwu Chen
Publikováno v:
Molecular Medicine Reports
Tetralogy of Fallot (TOF) is the most common form of cyanotic congenital heart disease (CHD). Although a lower methylation level of whole genome has been demonstrated in TOF patients, little is known regarding the DNA methylation changes in specific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::976f4663e8d6fffc7e32fd5bd2d98a7b
https://pubmed.ncbi.nlm.nih.gov/33000281
https://pubmed.ncbi.nlm.nih.gov/33000281
Autor:
Hao Huang, Lei Qiang, Minjie Fan, Yihao Liu, Anchun Yang, Dongbiao Chang, Jinsheng Li, Tong Sun, Yiwei Wang, Ruoyi Guo, Hanjie Zhuang, Xiangyu Li, Tailin Guo, Jinwu Wang, Huan Tan, Pengfei Zheng, Jie Weng
Publikováno v:
Bioactive Materials, Vol 31, Iss , Pp 18-37 (2024)
The resection of malignant osteosarcoma often results in large segmental bone defects, and the residual cells can facilitate recurrence. Consequently, the treatment of osteosarcoma is a major challenge in clinical practice. The ideal goal of treatmen
Externí odkaz:
https://doaj.org/article/4de7a5a527764875938db3d43d7a1ef1
Autor:
Hao Huang, Lei Qiang, Minjie Fan, Yihao Liu, Anchun Yang, Dongbiao Chang, Jinsheng Li, Tong Sun, Yiwei Wang, Ruoyi Guo, Hanjie Zhuang, Xiangyu Li, Tailin Guo, Jinwu Wang, Huan Tan, Pengfei Zheng, Jie Weng
Publikováno v:
Bioactive Materials, Vol 35, Iss , Pp 445-446 (2024)
Externí odkaz:
https://doaj.org/article/04f1461eee6243c1bdf19a2ac1bbc909
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Background and ObjectivePost-translational modifications of antibodies, with a specific focus on galactosylation, have garnered increasing attention in the context of understanding the pathogenesis and therapeutic implications of autoimmune diseases.
Externí odkaz:
https://doaj.org/article/efcd8fae05e844158bd61d656b968b14
Autor:
Jun Xu, Wei Sheng, Guoying Huang, Ruoyi Gu, Yixiang Lin, Xiaojing Ma, Duan Ma, Huijun Wang, Jing Zhang
Publikováno v:
Pediatric Research. 80:159-168
Retinoic acid X receptor alpha (RXRα) and Connexin 43 (Cx43) both play a crucial role in cardiogenesis. However, little is known about the interplay mechanism between the RXRα and Cx43. The activations of retinoic acid response element (RARE) in Cx
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd206355c276159db30d55caf4f2a94d
https://doi.org/10.1038/pr.2016.47
https://doi.org/10.1038/pr.2016.47
Autor:
Huijun Wang, Wei Sheng, Shuolin Li, Yixiang Lin, Weicheng Chen, Ruoyi Gu, Jun Xu, Yangliu Song, Guoying Huang, Yinyin Cao, Duan Ma, Yuan Yuan, Jian Li, Xiaojing Ma, Sida Liu
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)
Heterotaxy syndrome (HTX) is characterized by left-right (LR) asymmetry disturbances associated with severe heart malformations. However, the exact genetic cause of HTX pathogenesis remains unclear. The aim of this study was to investigate the pathog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5330ab4e0c53ea642f6eec374e4d9ea2
https://doi.org/10.1038/s41598-018-30204-3
https://doi.org/10.1038/s41598-018-30204-3