Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Zhaoyue Zheng"'
Autor:
Zhaoyue Zheng, Jingya Ye, Mi Leng, Chunmei Gan, Na Tang, Wei Li, C. Alexander Valencia, Biao Dong, Hoi Yee Chow
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2023)
A cell-based transduction inhibition assay (TI) is widely used in clinical trials to detect neutralizing antibody (NAb) titers against recombinant adeno-associated virus (rAAV), one of the most important criteria to exclude patients in gene therapy.
Externí odkaz:
https://doaj.org/article/8e329ca227ff4e4aba82c7b959f9cc20
Autor:
Li Yang, Wenya Du, Zhaoyue Zheng, Li Wang, Lin Xiao, Qingzhe Yang, Qiukui Hao, Jiao Zhou, Jintao Du, Jun Li, C. Alexander Valencia, Birong Dong, Hoi Yee Chow, Xianghui Fu, Biao Dong
Publikováno v:
Molecular Biomedicine, Vol 3, Iss 1, Pp 1-11 (2022)
Abstract MicroRNA-22 (miR-22) was suggested to be important for type 2 diabetes but its functions for this disease remained unclear. Recombinant adeno-associated virus (rAAV)-mediated miR delivery is a powerful approach to study miR functions in vivo
Externí odkaz:
https://doaj.org/article/c41809fd0a524c129af69b32ce4f2e29
Autor:
Rui Tao, Lin Xiao, Lifang Zhou, Zhaoyue Zheng, Jie Long, Lixing Zhou, Minghai Tang, Biao Dong, Shaohua Yao
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 26, Iss , Pp 95- (2022)
Externí odkaz:
https://doaj.org/article/429c85f2e6ad4614bd91c9353cf0decb
Autor:
Rui Tao, Lin Xiao, Lifang Zhou, Zhaoyue Zheng, Jie Long, Lixing Zhou, Minghai Tang, Biao Dong, Shaohua Yao
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 19, Iss , Pp 507-517 (2020)
Phenylketonuria (PKU) is an inherited metabolic disorder caused by mutation within phenylalanine hydroxylase (PAH) gene. Loss-of-function of PAH leads to accumulation of phenylalanine in the blood/body of an untreated patient, which damages the devel
Externí odkaz:
https://doaj.org/article/0946603fe3bb48b394ca938ecd9fd65e
Autor:
Wenman Wu, Lin Xiao, Xi Wu, Xiaoling Xie, Ping Li, Changming Chen, Zhaoyue Zheng, Jiangang Ai, C. Alexander Valencia, Birong Dong, Qiulan Ding, Biao Dong, Xuefeng Wang
Publikováno v:
Haematologica, Vol 106, Iss 1 (2020)
Externí odkaz:
https://doaj.org/article/048ec1ef91904495b77c8c10a6cc896d
Publikováno v:
Abstract and Applied Analysis, Vol 2012 (2012)
By using critical point theory and variational methods, we investigate the subharmonic solutions with prescribed minimal period for a class of second-order impulsive functional differential equations. The conditions for the existence of subharmonic s
Externí odkaz:
https://doaj.org/article/595a60310fda47d09646c2fd20a34de3
Autor:
Jinyuan Luoqian, Wenyong Yang, Xulong Ding, Qing-zhang Tuo, Zheng Xiang, Zhaoyue Zheng, Yu-jie Guo, Li Li, Pengbo Guan, Scott Ayton, Biao Dong, Huiyuan Zhang, Hongbo Hu, Peng Lei
Publikováno v:
Cellular & Molecular Immunology. 19:913-924
While many drugs are effective at reducing the relapse frequency of multiple sclerosis (MS), there is an unmet need for treatments that slow neurodegeneration resulting from secondary disease progression. The mechanism of neurodegeneration in MS has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3175913c10ece40486eeacec0f77453
https://doi.org/10.1038/s41423-022-00883-0
https://doi.org/10.1038/s41423-022-00883-0
Autor:
Shaohua Yao, Lifang Zhou, Jie Long, Minghai Tang, Lixing Zhou, Zhaoyue Zheng, Biao Dong, Rui Tao, Lin Xiao
Publikováno v:
Mol Ther Methods Clin Dev
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 19, Iss, Pp 507-517 (2020)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 19, Iss, Pp 507-517 (2020)
Phenylketonuria (PKU) is an inherited metabolic disorder caused by mutation within phenylalanine hydroxylase (PAH) gene. Loss-of-function of PAH leads to accumulation of phenylalanine in the blood/body of an untreated patient, which damages the devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::214466dc7daddadf63f20adf7b69f68d
https://doi.org/10.1016/j.omtm.2019.12.014
https://doi.org/10.1016/j.omtm.2019.12.014
Autor:
Ping Li, Qiukui Hao, Heng Xu, Lifang Zhou, Zhaoyue Zheng, Yingying Leng, Fengming Qin, Biao Dong, Yu Liu, Lin Xiao, Shaohua Yao
Publikováno v:
Human Gene Therapy. 30:1494-1504
Wilson's disease (WD) is an autosomal recessive disorder of copper metabolism caused by mutations in the ATP7B gene encoding a liver active copper transport enzyme. Gene therapy with adeno-associat...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afab8fa03b1518bdcc4d1a0d4275441d
https://doi.org/10.1089/hum.2019.148
https://doi.org/10.1089/hum.2019.148
Autor:
C. Alexander Valencia, Xi Wu, Biao Dong, Wenman Wu, Lin Xiao, Zhaoyue Zheng, Changming Chen, Xiaoling Xie, Xuefeng Wang, Jiangang Ai, Ping Li, Qiulan Ding, Birong Dong
Publikováno v:
Haematologica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::420d7fce2464aa923e5268e69c6b43ec
http://europepmc.org/articles/PMC7776343
http://europepmc.org/articles/PMC7776343