Zobrazeno 1 - 10
of 986
pro vyhledávání: '"Jianhua FENG"'
Autor:
Haibo WANG, Jianhui FU, Jincheng ZHONG, Jianhua FENG, Jing ZHAO, Tingting LI, Yinghua SHI, Xinglong ZHANG, Hang LI
Publikováno v:
Shipin gongye ke-ji, Vol 45, Iss 11, Pp 79-85 (2024)
This study was conducted to explore the aging technology of high-grade beef, a total of 12 high-grade fattening Angus longissimus dorsi were selected and aged in dry or wet environment for 3, 5 and 7 d, and the meat basic physicochemical indexes, fre
Externí odkaz:
https://doaj.org/article/0190a4df739b4b5096a5852fc30b424f
Autor:
Xinyi Ge, Lifei Zhang, Qiaolei Zhang, Jianhua Feng, Linlin Yang, Yuxin Tong, Shan Zheng, Yamin Tan
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
BackgroundLeukemia imposes a large healthcare burden both in China and the United States (US). The disease burden differs greatly between the two countries, but related research is limited. We explored the differences in leukemia incidence and mortal
Externí odkaz:
https://doaj.org/article/84d0f2d7cab246dba6929a25ee83aae4
Autor:
Wenji Huang, Ning Ji, Xin Zhao, Jiahong Guo, Jianhua Feng, Kangyong Chen, Yaxin Wu, Junya Wang, Jun Zou
Publikováno v:
Aquaculture and Fisheries, Vol 9, Iss 2, Pp 181-192 (2024)
A cell line, termed ZFIN, was established from the caudal fin of zebrafish and was shown to be susceptible to spring viremia of carp virus (SVCV). The ZFIN cells are epithelial like cells and have a moderate plasmid transfection efficiency of 13.9%.
Externí odkaz:
https://doaj.org/article/c832136ee0204be5881dd19e550dbfd3
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 2, Pp n/a-n/a (2024)
Abstract Background Intellectual disability (ID) refers to a childhood‐onset neurodevelopmental disorder with a prevalence of approximately 1%–3%. Methods We performed whole exome sequencing for the patient with ID. And the splicing variant we fo
Externí odkaz:
https://doaj.org/article/895e750437aa4393a10099f8596f1cc3
Autor:
Pu Miao, Xueying Zhu, Wenqin Jin, Lingyan Yu, Yanfang Li, Ye Wang, Qunyan Su, Sha Xu, Shuang Wang, Jianhua Feng
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 8, Pp 1374-1382 (2023)
Abstract Objective The efficacy of perampanel (PER) in pediatric epilepsy with specific etiologies has not been well established. Here, we investigated outcome and predictors of PER treatment in a pediatric cohort with known and presumed genetic etio
Externí odkaz:
https://doaj.org/article/c65e9ed34cc244179a4802816bfb5c34
Autor:
Kangyong Chen, Qianzi Xiu, Qingyu Min, Xingxing Cheng, Hehe Xiao, Zhao Jia, Jianhua Feng, Yanjie Shi, Qianli Zhuo, Junya Wang, Jun Zou
Publikováno v:
Fish and Shellfish Immunology Reports, Vol 4, Iss , Pp 100090- (2023)
Tumor necrosis factor like ligand 1A (TL1A), a member of TNF superfamily, regulates inflammatory response and immune defense. TL1A homologues have recently been discovered in fish, but their functions have not been studied. In this study, a TL1A homo
Externí odkaz:
https://doaj.org/article/f8dbd95f0ce94055b994d7cb904de3c1
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2023)
Perampanel is a promising option for the treatment of pediatric epilepsy, but its plasma concentration varies among patients. This retrospective study aimed to investigate the initial target attainment of perampanel plasma concentration in pediatric
Externí odkaz:
https://doaj.org/article/1dceb76f1a1f41279b21bb86def1582c
Autor:
Xiaoquan, Chen, Yuting, Lou, Pu, Miao, Haiying, Cheng, Zheng, Wan, Ye, Wang, Fan, Yang, Mengmeng, Liang, Jianhua, Feng
Publikováno v:
In Clinical Neurology and Neurosurgery October 2023 233
Publikováno v:
Stem Cell Research, Vol 71, Iss , Pp 103127- (2023)
Developmental epileptic encephalopathy-47 (DEE47) is a nervous system disease characterized by the onset of intractable seizures that appear the first days or weeks after birth. FGF12 is the disease-causing gene of DEE47 that encodes a small cytoplas
Externí odkaz:
https://doaj.org/article/b80e3ed7173b487aa5a139b47efd7c6e
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2023)
BackgroundDevelopmental and epileptic encephalopathy (DEE) is a condition characterized by severe seizures and a range of developmental impairments. Pathogenic variants in KCNQ2, encoding for potassium channel subunit, cause KCNQ2-related DEE. This s
Externí odkaz:
https://doaj.org/article/10fd095b523f43dc82b5a1705a12021b