Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Ling-jie He"'
Autor:
Nathan P Achilly, Ling-jie He, Olivia A Kim, Shogo Ohmae, Gregory J Wojaczynski, Tao Lin, Roy V Sillitoe, Javier F Medina, Huda Y Zoghbi
Publikováno v:
eLife, Vol 10 (2021)
Rett syndrome is a devastating childhood neurological disorder caused by mutations in MECP2. Of the many symptoms, motor deterioration is a significant problem for patients. In mice, deleting Mecp2 from the cortex or basal ganglia causes motor dysfun
Externí odkaz:
https://doaj.org/article/d3b24f10375f4471b540a38aeb3943f0
Autor:
Da-li Tong, Rui-guo Chen, Yu-lan Lu, Wei-ke Li, Yue-fang Zhang, Jun-kai Lin, Ling-jie He, Ting Dang, Shi-fang Shan, Xiao-Hong Xu, Yi Zhang, Chen Zhang, Ya-Song Du, Wen-Hao Zhou, Xiaoqun Wang, Zilong Qiu
Publikováno v:
Neurobiology of Disease, Vol 130, Iss , Pp 104486- (2019)
Accumulated genetic evidences indicate that the contactin associated protein-like (CNTNAP) family is implicated in autism spectrum disorders (ASD). In this study, we identified genetic mutations in the CNTNAP3 gene from Chinese Han ASD cohorts and Si
Externí odkaz:
https://doaj.org/article/4ad3b1b4e13d42ee8a8928cc06d08bbf
Autor:
Ling-jie He, Jian-wei Zhang, Qing Yang, Shu-jun Cao, Shi-wei Yang, Bin Nie, Xiao-han Xu, Yu-jie Zhou
Publikováno v:
International Journal of Gerontology, Vol 8, Iss 2, Pp 70-73 (2014)
Objective: This study aimed to evaluate the incidence and related factors of acute asymptomatic brain infarcts (aABI) following percutaneous coronary intervention (PCI) in patients with acute myocardial infarction (AMI) via the right radial approach.
Externí odkaz:
https://doaj.org/article/67afdad904e14557b535394c78d094c0
Autor:
Xiangling Meng, Wei Wang, Hui Lu, Ling-jie He, Wu Chen, Eugene S Chao, Marta L Fiorotto, Bin Tang, Jose A Herrera, Michelle L Seymour, Jeffrey L Neul, Fred A Pereira, Jianrong Tang, Mingshan Xue, Huda Y Zoghbi
Publikováno v:
eLife, Vol 5 (2016)
Many postnatal onset neurological disorders such as autism spectrum disorders (ASDs) and intellectual disability are thought to arise largely from disruption of excitatory/inhibitory homeostasis. Although mouse models of Rett syndrome (RTT), a postna
Externí odkaz:
https://doaj.org/article/e9b3e20a7632402da35d66faa9ebbd99
Autor:
Kerstin Ure, Hui Lu, Wei Wang, Aya Ito-Ishida, Zhenyu Wu, Ling-jie He, Yehezkel Sztainberg, Wu Chen, Jianrong Tang, Huda Y Zoghbi
Publikováno v:
eLife, Vol 5 (2016)
The postnatal neurodevelopmental disorder Rett syndrome, caused by mutations in MECP2, produces a diverse array of symptoms, including loss of language, motor, and social skills and the development of hand stereotypies, anxiety, tremor, ataxia, respi
Externí odkaz:
https://doaj.org/article/d6aeea3afa9144a29bfb8adb4ffb6ae6
Autor:
J. Lloyd Holder, Vitaliy V. Bondar, Li Wang, Kaifang Pang, Kihoon Han, Zhandong Liu, Kimberley F. Tolias, Wei Wang, Timothy Palzkill, Carolyn J. Adamski, Ronald Richman, Jason K. Lai, Joseph G. Duman, Patrick Barth, Ling-jie He, Huda Y. Zoghbi
Publikováno v:
Molecular psychiatry
Genome sequencing has revealed an increasing number of genetic variations that are associated with neuropsychiatric disorders. Frequently, studies limit their focus to likely gene-disrupting mutations because they are relatively easy to interpret. Mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04a9285b1517dfe30ebf648221e88fe3
https://doi.org/10.1038/s41380-018-0324-x
https://doi.org/10.1038/s41380-018-0324-x
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e106130 (2014)
OBJECTIVE: To date, no study in the published literature has investigated the role of various serum uric acid (SUA) concentrations in the development of angiographically-proven coronary artery disease (CAD) in premenopausal women. Therefore, the aim
Externí odkaz:
https://doaj.org/article/e5e5afde93044498a738e5de405f99cb
Autor:
Tao Lin, Olivia A. Kim, Huda Y. Zoghbi, Shogo Ohmae, Ling-jie He, Roy V. Sillitoe, Nathan P. Achilly, Gregory J. Wojaczynski, Javier F. Medina
Publikováno v:
eLife
eLife, Vol 10 (2021)
eLife, Vol 10 (2021)
Rett syndrome is a devastating childhood neurological disorder caused by mutations in MECP2. Of the many symptoms, motor deterioration is a significant problem for patients. In mice, deleting Mecp2 from the cortex or basal ganglia causes motor dysfun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6435bfd16413c11e12125f5ff442c15b
https://doi.org/10.7554/elife.64833
https://doi.org/10.7554/elife.64833
Autor:
Nathan P. Achilly, Roy V. Sillitoe, Shogo Ohmae, Ling-jie He, Gregory J. Wojaczynski, Tao Lin, Olivia A. Kim, Huda Y. Zoghbi, Javier F. Medina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79b06262b3ff816d4ce625fbc012c466
https://doi.org/10.7554/elife.64833.sa2
https://doi.org/10.7554/elife.64833.sa2
Autor:
Tao Lin, Nathan P. Achilly, Shogo Ohmae, Ling-jie He, Roy V. Sillitoe, Olivia A. Kim, Gregory J. Wojaczynski, Huda Y. Zoghbi, Javier F. Medina
Rett syndrome is a devastating childhood neurological disorder caused by mutations in MECP2. Of the many symptoms, motor deterioration is a significant problem for patients. In mice, deleting Mecp2 from the cortex or basal ganglia causes motor dysfun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::792444be3ab1e4d154b80a2178f683fc
https://doi.org/10.1101/2020.11.12.380162
https://doi.org/10.1101/2020.11.12.380162