Zobrazeno 1 - 10
of 115
pro vyhledávání: '"Liangliang Fan"'
Autor:
Linyao Ke, Nan Zhou, Qiuhao Wu, Yuan Zeng, Xiaojie Tian, Jiahui Zhang, Liangliang Fan, Roger Ruan, Yunpu Wang
Publikováno v:
npj Materials Sustainability, Vol 2, Iss 1, Pp 1-20 (2024)
Abstract The quest for low-carbon alternatives to fossil fuels and the carbon emissions associated with the natural degradation of biomass have accelerated the development of biomass processing technologies. Microwave catalytic pyrolysis is emerging
Externí odkaz:
https://doaj.org/article/6ef593796ddf4f16a3e49a383e85338b
Autor:
Song Yang, Wenjing Li, Xueyuan Bai, Giada Di Nunzio, Liangliang Fan, Yueming Zhao, Limei Ren, Ronghua Zhao, Shuai Bian, Meichen Liu, Yuchi Wei, Daqing Zhao, Jiawen Wang
Publikováno v:
Journal of Nanobiotechnology, Vol 22, Iss 1, Pp 1-24 (2024)
Abstract Inflammatory bowel disease (IBD) is closely linked to the homeostasis of the intestinal environment, and exosomes can be used to treat IBD due to their high biocompatibility and ability to be effectively absorbed by the intestinal tract. How
Externí odkaz:
https://doaj.org/article/788f0561c61d4fbb98e1824e69e94a88
Publikováno v:
Heliyon, Vol 10, Iss 7, Pp e28674- (2024)
Paroxysmal kinesigenic dyskinesia (PKD) represents the most prevalent form of paroxysmal dyskinesia, characterized by recurrent and transient attacks of involuntary movements triggered by a sudden voluntary action. In this study, whole-exome sequenci
Externí odkaz:
https://doaj.org/article/be5a4e563feb4238a07d320d2d063574
Publikováno v:
Cardiovascular Innovations and Applications, Vol 9, Iss 1, p 937 (2024)
Externí odkaz:
https://doaj.org/article/baaa4c97c5124462bdefc037bcd2ccba
Whole-exome sequencing detected a novel AIFM1 variant in a Han-Chinese family with Cowchock syndrome
Publikováno v:
Hereditas, Vol 160, Iss 1, Pp 1-6 (2023)
Abstract Charcot-Marie-Tooth disease(CMT) is a hereditary peripheral neuropathy, characterized by progressive distal hypoesthesia and amyotrophia. CMT is characterized by an X- linked recessive inheritance pattern. The apoptosis-inducing factor mitoc
Externí odkaz:
https://doaj.org/article/cb17eb9f0d63462ead488a2cfeab3f93
Autor:
Yuxing Liu, Yiqiao Hu, Siyuan Zhang, Yadong Guo, Yaqin Chen, Liangliang Fan, Jieyuan Jin, Rong Xiang
Publikováno v:
Cardiovascular Innovations and Applications, Vol 9, Iss 1, p 966 (2024)
Background: Sudden cardiac death (SCD), unexpected death based on sudden cardiac ejection cessation, accounts for 15–20% of unnatural deaths in developed countries. Primary electrical disorders (PEDs), a group of cardiac rhythm abnormalities withou
Externí odkaz:
https://doaj.org/article/e0d0469e8feb45f998d5adf57d2555a6
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2023)
BackgroundCampomelic dysplasia (CD) is an autosomal dominant skeletal dysplasia syndrome characterized by shortness and bowing of lower extremities, and often accompanied by XY sex reversal. Heterozygous pathogenic variants of SOX9 or rearrangement i
Externí odkaz:
https://doaj.org/article/4bbcfbe8d98d48b8ba5894f41977fb94
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Chronic kidney disease, a global public health problem, results in kidney damage or a gradual decline in the glomerular filtration rate. Alport syndrome is commonly characterized by chronic glomerulonephritis caused by a structural disord
Externí odkaz:
https://doaj.org/article/101326d2ea2f479cafb57f5031efd56b
Autor:
Hao Huang, Ling Zhu, Chao Huang, Yi Dong, Liangliang Fan, Lijian Tao, Zhangzhe Peng, Rong Xiang
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
BackgroundClear cell renal cell carcinoma (ccRCC) is a common genitourinary cancer type with a high mortality rate. Due to a diverse range of biochemical alterations and a high level of tumor heterogeneity, it is crucial to select highly validated pr
Externí odkaz:
https://doaj.org/article/a9dc71c4118240b097aafa53c2014cb0
Autor:
Yu-Xing Liu, Ai-Qian Zhang, Fang-Mei Luo, Yue Sheng, Chen-Yu Wang, Yi Dong, Liangliang Fan, Lv Liu
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Idiopathic focal segmental glomerulosclerosis (FSGS) is a relatively frequent kidney disorder that manifest clinically as proteinuria and progressive loss of renal function. Genetic factors play a dominant role in the occurrence of FSGS. CD2-associat
Externí odkaz:
https://doaj.org/article/5ea33cf19f7b4c628b45c3256faac43e