Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Yuejuan Xu"'
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-16 (2024)
Abstract Background Despite the advancements in heart failure(HF) research, the early diagnosis of HF continues to be a challenging issue in clinical practice. This study aims to investigate the genes related to myocardial fibrosis and conduction blo
Externí odkaz:
https://doaj.org/article/e57560c8205a47559083300a337d3c06
Publikováno v:
Promet (Zagreb), Vol 35, Iss 6, Pp 886-903 (2023)
Dockless bike-sharing (DBS) is an effective solution to the “first and last mile” problem in urban transportation. It can be integrated with urban rail transit (URT) to provide passengers with more convenient travel services. This study focuses o
Externí odkaz:
https://doaj.org/article/189083aeb674477a94fdaa43f035be4b
Publikováno v:
World Electric Vehicle Journal, Vol 15, Iss 7, p 302 (2024)
The power battery is a key component of electric vehicles and its performance is greatly affected by temperature. Battery thermal management systems based on phase change materials can effectively control the battery temperature and at the same time
Externí odkaz:
https://doaj.org/article/2bc5a1635c464c2db1b0849879536004
Autor:
Xin Tan, Yuejuan Xu, Shixin Wang, Jiaxuan Li, Chunxia Hu, Zhouqing Chen, Qingzhang Cheng, Zhong Wang
Publikováno v:
Brain Sciences, Vol 13, Iss 12, p 1627 (2023)
Background: SPN-812 has been approved for attention-deficit/hyperactivity disorder (ADHD) treatment in children and adolescents. Objective: We aimed to analyze the efficacy and safety of different doses of SPN-812 for ADHD pediatric patients of diffe
Externí odkaz:
https://doaj.org/article/61a99b8a792a416d9935274daa4e2227
Autor:
Huan Hu, Zilong Geng, Shasha Zhang, Yuejuan Xu, Qingjie Wang, Sun Chen, Bing Zhang, Kun Sun, Yanan Lu
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Atrioventricular septal defect (AVSD) is a deleterious subtype of congenital heart diseases (CHD) characterized by atrioventricular canal defect. The pathogenic genetic changes of AVSD remain elusive, particularly for copy number variation (CNV), a l
Externí odkaz:
https://doaj.org/article/01e9a933fc914838a5a7e280a73a528f
Autor:
Yongxuan Peng, Jiajun Ye, Yuejuan Xu, Jihong Huang, Yurong Wu, Wei Liu, Kai Bai, Sun Chen, Yanan Lu
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
ObjectiveCoronary artery fistula, defined as communication between a coronary artery and a great vessel or a cardiac chamber, is a relatively rare anomaly with an estimated incidence of 0.002% in the general population. It could be combined with a gi
Externí odkaz:
https://doaj.org/article/0f0bb31b3dbc4e0aa5011b9f54699db9
Autor:
Xuechao Jiang, Tingting Li, Sijie Liu, Qihua Fu, Fen Li, Sun Chen, Kun Sun, Rang Xu, Yuejuan Xu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-14 (2021)
Abstract Background TBX1 (T-box transcription factor 1) is a major candidate gene that likely contributes to the etiology of velo-cardio-facial syndrome/DiGeorge syndrome (VCFS/DGS). Although the haploinsufficiency of TBX1 in both mice and humans res
Externí odkaz:
https://doaj.org/article/0b3a087497624863a7b0a9e234c04a19
Autor:
Rong Jiang, Hongyu Zhang, Jinhua Zhou, Juan Wang, Yuejuan Xu, He Zhang, Yanzheng Gu, Fengqing Fu, Yu Shen, Guangbo Zhang, Lanlan Feng, Xueguang Zhang, Youguo Chen, Fangrong Shen
Publikováno v:
Cell Death and Disease, Vol 12, Iss 2, Pp 1-12 (2021)
Abstract Long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) play critical roles in human diseases. We aimed to clarify the role of lncRNA X-inactive specific transcript (XIST)/miR-149-3p/forkhead box P3 (FOXP3) axis in ovarian cancer (OC) cell gro
Externí odkaz:
https://doaj.org/article/23770bb1a56842e082b76d7eb75bcba5
Publikováno v:
Sensors, Vol 22, Iss 16, p 5982 (2022)
The efficient and accurate prediction of urban travel demand, which is a hot topic in intelligent transportation research, is challenging due to its complicated spatial-temporal dependencies, dynamic nature, and uneven distribution. Most existing for
Externí odkaz:
https://doaj.org/article/11c4ae35b79e464abb7a687506b31358
Autor:
Xin Shi, Tao Huang, Jing Wang, Yulai Liang, Chang Gu, Yuejuan Xu, Jing Sun, Yanan Lu, Kun Sun, Sun Chen, Yu Yu
Publikováno v:
EBioMedicine, Vol 38, Iss , Pp 217-227 (2018)
Background: Total anomalous pulmonary venous connection (TAPVC) is recognized as a rare congenital heart defect (CHD). With a high mortality rate of approximately 80%, the survival rate and outcomes of TAPVC patients are not satisfactory. However, th
Externí odkaz:
https://doaj.org/article/639b8b65321246d6acad8fe4d4fa8fa5