Zobrazeno 1 - 10
of 2 004
pro vyhledávání: '"Jia Fang"'
Autor:
Jia Fang, Yao Xu, Chenghui Lin, Jiewen Yang, Dongxu Zhai, Qingyuan Zhuang, Wangli Qiu, Yun Wang, Longjuan Zhang
Publikováno v:
BMC Pulmonary Medicine, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background miR-223-3p has been demonstrated as a Pseudomonas aeruginosa colonization-related miRNA in bronchiectasis (BE), but its clinical value in BE has not been revealed, which is of great significance for the clinical diagnosis and moni
Externí odkaz:
https://doaj.org/article/edc1658fd16b40c484e5fea7ea837312
Publikováno v:
Journal of Functional Foods, Vol 120, Iss , Pp 106368- (2024)
Ophiopogonis radix has been used for both food and traditional Chinese medicine in China for millennia. Oligosaccharides of Ophiopogon japonicus (OOJ), the primary bioactive components of Ophiopogonis radix, have significant hypoglycemic and hypolipi
Externí odkaz:
https://doaj.org/article/fa81cf8ea4a64950a293fe4641e7bc3f
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-20 (2024)
Abstract Ignition electrodes have an immense impact on the accurate measurement of the flame propagation spherical radius. In this study, a flame-radius calculation method is designed. The method is able to eliminate effects due to the ignition elect
Externí odkaz:
https://doaj.org/article/6bcc9105ca97494bb6cca315b5f6966a
Publikováno v:
Journal of Transport and Land Use, Vol 17, Iss 1 (2024)
Understanding the connections between the built environment and travel mode choice is a major research topic in transportation. However, existing studies usually examine the relationship through trip-based analyses rather than tour-based approaches.
Externí odkaz:
https://doaj.org/article/9a72a55f5fda487ea2cfb53aefaa11c1
Autor:
Xihua Li, Junlan Lv, Wenhua Zhu, Siqi Hong, Zhiqiang Wang, Xingzhi Chang, Ying Xu Gao, Yangmei Zhou, Caiping Jia, Jia Fang, Terrell A. Patterson
Publikováno v:
The Lancet Regional Health. Western Pacific, Vol 42, Iss , Pp 100944- (2024)
Summary: Background: Duchenne muscular dystrophy (DMD) is a disabling and life-threatening, X-linked recessive disorder caused by mutations in dystrophin. Natural history studies can inform the disease characteristics of DMD, and data from these stud
Externí odkaz:
https://doaj.org/article/8c5a4151318c4a178a77e3922934f78e
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
SCPx deficiency is a rare disorder of peroxisomal beta-oxidation dysfunction, and it has only been documented in two patients thus far. In the previously reported patients, both patients were primarily presented with slowly progressive dystonia or at
Externí odkaz:
https://doaj.org/article/09077b1ccc404605ad113eee3c931fe2
Autor:
Jia Fang, Cho-Lee Wong, Chun-Qin Liu, Hai-Ying Huang, Yi-Shu Qi, Li-Ling Xu, Mei-Xiang Wang, Yan Lin
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundPrevious studies have examined symptom clusters in children with acute leukemia, yet a knowledge gap persists regarding central symptom clusters and their influencing factors. By identifying these central clusters and associated factors, he
Externí odkaz:
https://doaj.org/article/95c27310f74e419a85baa10902608964
Publikováno v:
BMC Anesthesiology, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background Sugammadex is a newer medication used for rapid and reliable reversal of neuromuscular blockade. This study evaluated whether sugammadex could reduce the length of postoperative hospital stay in patients undergoing abdominal surge
Externí odkaz:
https://doaj.org/article/3b5d8fe894794cf09ca7a935e1f2767f
Autor:
Yipeng Yao, Zhiqiang Han, Wei Tian, Xueshun Wu, Yi Wu, Yan Yan, Qi Xia, Jia Fang, Liping Luo, Guy De Weireld
Publikováno v:
Case Studies in Thermal Engineering, Vol 47, Iss , Pp 103099- (2023)
Fouling has limited the evolution of compact heat exchangers (represented by EGR cooler) to smaller and more efficient sizes, an important reason is the unclear mechanism of the effect of exhaust gas condensation on fouling and thermal performance. T
Externí odkaz:
https://doaj.org/article/2cb750702289483589207184a403fe53
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Background HINT1 mutations cause an autosomal recessive axonal neuropathy with neuromyotonia. This is a first case report of coexistence of myasthenia gravis (MG) and HINT1-related motor axonal neuropathy without neuromyotonia. Case presenta
Externí odkaz:
https://doaj.org/article/c887ace3f6474678a32ef51a27999e0a