Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Sanchuan, Luo"'
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
BackgroundSHANK2 encodes a postsynaptic scaffolding protein involved in synapse formation, stabilization and homeostasis. Variations or microdeletions in the SHANK2 gene have been linked to a variety of neurodevelopmental disorders, including autism
Externí odkaz:
https://doaj.org/article/34aebce8f9b9415abf38e92b697a1e96
Autor:
Sanchuan Luo, Zhongxiang Li, Xin Dai, Rui Zhang, Zhibing Liang, Wenzhou Li, Ming Zeng, Jinfeng Su, Jun Wang, Xia Liang, Yong Wu, Desheng Liang
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Hemophilia A (HA), a common bleeding disorder caused by a deficiency of coagulation factor VIII (FVIII), has long been considered an attractive target for gene therapy studies. However, full-length F8 cDNA cannot be packaged efficiently by adeno-asso
Externí odkaz:
https://doaj.org/article/4890b39949c045bb81bfa1c23458df65
Autor:
Lu Xia, Yalan Liu, Yaowen Zhang, Rongjuan Zhao, Yu Peng, Taoxi Li, Cenying Liu, Lu Shen, Jingjing Chen, Sanchuan Luo, Kun Xia
Publikováno v:
Journal of Psychiatric Research. 143:113-122
NRXN1 is involved in synaptogenesis and have been implicated in Autism spectrum disorders. However, many rare inherited missense variants of NRXN1 have not been thoroughly evaluated. Here, functional analyses in vitro and in Drosophila of three NRXN1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::120b1db0db6c36d46f0bad18adee6fa8
https://doi.org/10.1016/j.jpsychires.2021.09.013
https://doi.org/10.1016/j.jpsychires.2021.09.013
Autor:
Sanchuan Luo
Publikováno v:
2022 International Conference on Informatics, Networking and Computing (ICINC).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70c665a4f66f08af2d4b3246320018e1
https://doi.org/10.1109/icinc58035.2022.00019
https://doi.org/10.1109/icinc58035.2022.00019
Autor:
Jinfeng Su, Xin Dai, Sanchuan Luo, Zhibing Liang, Desheng Liang, Ming Zeng, Yong Wu, Jun Wang, Zhongxiang Li, Xia Liang, Rui Zhang, Wenzhou Li
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Hemophilia A (HA), a common bleeding disorder caused by a deficiency of coagulation factor VIII (FVIII), has long been considered an attractive target for gene therapy studies. However, full-length F8 cDNA cannot be packaged efficiently by adeno-asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f4774c5cef539a8cc25f4d47797ca40
https://doi.org/10.3389/fcell.2021.672564
https://doi.org/10.3389/fcell.2021.672564
Autor:
Sanchuan, Luo, Zhongxiang, Li, Xin, Dai, Rui, Zhang, Zhibing, Liang, Wenzhou, Li, Ming, Zeng, Jinfeng, Su, Jun, Wang, Xia, Liang, Yong, Wu, Desheng, Liang
Publikováno v:
Frontiers in Cell and Developmental Biology
Hemophilia A (HA), a common bleeding disorder caused by a deficiency of coagulation factor VIII (FVIII), has long been considered an attractive target for gene therapy studies. However, full-length F8 cDNA cannot be packaged efficiently by adeno-asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dc0923960638bf45159f826904db9d66
https://pubmed.ncbi.nlm.nih.gov/34485274
https://pubmed.ncbi.nlm.nih.gov/34485274
Autor:
Sanchuan Luo, Xiaojuan Xu, Xuehong Zhang, Yu Zheng, Jia-Da Li, Kun Xia, Hongliang Yao, Hui Guo, Lusi Zhang, Hao Peng, Zhengmao Hu, Hexiang Peng
Publikováno v:
Gene. 575:363-367
Fabry disease (FD) was an X-linked lysosomal storage disorder resulting from a deficiency in glycosphingolipid catabolism caused by mutations in the α-galactosidase A gene GLA. Variant FD patients did not present with classical symptoms during child
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::244cb038992a07e239da8a898b8cf652
https://doi.org/10.1016/j.gene.2015.09.088
https://doi.org/10.1016/j.gene.2015.09.088
Publikováno v:
2018 13th International Conference on Computer Science & Education (ICCSE).
New media technology promotes the improvement of teaching methods, and the reform of teaching methods inevitably promotes the integration of teaching contents. In this paper, we propose course design of personal information security for general educa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2fb2c8c898e5d6daab9d715c10f5dc9
https://doi.org/10.1109/iccse.2018.8468779
https://doi.org/10.1109/iccse.2018.8468779
Autor:
Qiong Liu, Yalan Liu, Jianjun Ou, Yongcheng Pan, Yu Peng, Jingping Zhao, Lijuan Shi, Zhimin Xiong, Hui Guo, Kun Xia, Yidong Shen, Jingjing Chen, Sanchuan Luo, Tengfei Zhu, Zhengmao Hu
Publikováno v:
Scientific Reports
Autism (MIM 209850) is a complex neurodevelopmental disorder characterized by social communication impairments and restricted repetitive behaviors. It has a high heritability, although much remains unclear. To evaluate genetic variants of GRIN2B in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e26d4967fa3465a666f8f9c406b7efc
https://doi.org/10.1038/srep08296
https://doi.org/10.1038/srep08296
Autor:
Zhengmao Hu, Hao Peng, Zhimin Xiong, Wei Li, Sanchuan Luo, Jinjie Xue, Lusi Zhang, Xiaojuan Xu, Kun Xia, Yanmei Lu, Dengming Chen
Publikováno v:
Journal of Medical Case Reports
Introduction Hutchinson-Gilford progeria syndrome is a rare pediatric genetic syndrome with an incidence of one per eight million live births. The disorder is characterized by premature aging, generally leading to death due to myocardial infarction o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afbf7c3e22e5de0e5a4bbf625df8e7c4
https://doi.org/10.1186/1752-1947-7-63
https://doi.org/10.1186/1752-1947-7-63