Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Sui-Jun Tong"'
A Pathogenic Variant p.Phe177Val in PSEN1 Causes Early-Onset Alzheimer’s Disease in a Chinese Family
Autor:
Bin Jiang, Min Bi, Jun Li, Qi Liu, Nai-An Xiao, Jie Fang, Man-Yi Shi, Zi-Wen Yu, Qi-Lin Ma, Sui-Jun Tong, Kun-Mu Zheng
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Familial Alzheimer’s disease (FAD) present as a positive family history of cognitive decline, with early onset and an autosomal dominant inheritance pattern. FAD is mainly caused by the mutations in the genes encoding for amyloid precursor protein
Externí odkaz:
https://doaj.org/article/808c3657ce574fceb94a3c337aefecd3
Autor:
Wen-Qing Huang, Hui-Ming Ye, Liang-Liang Cai, Qi-Lin Ma, Cong-Xia Lu, Sui-Jun Tong, Chi-Meng Tzeng, Qing Lin
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Background: Leukoaraiosis (LA) is shown as white matter hyperintensities on T2-weighted magnetic resonance imaging brain scans. Together with candidate gene association studies (CGAS), multiple genome-wide association studies (GWAS) have reported lar
Externí odkaz:
https://doaj.org/article/85d1b9c995bf4264a1da1ef61de19836
Publikováno v:
Proceedings of the VLDB Endowment. 12:1782-1785
To meet the challenge of analyzing rapidly growing graph and network data created by modern applications, a large number of specialized graph databases have emerged, such as Neo4j, JanusGraph, and Sqlg. At the same time, RDBMSs and SQL continue to su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53c48bfc9a2c17df24de4375d8879cfb
https://doi.org/10.14778/3352063.3352065
https://doi.org/10.14778/3352063.3352065
Autor:
Enliang Xu, Md. Shahidul Haque Apu, Yuanyuan Tian, Wen Sun, Thomas Kolanko, Wei Zhao, Sui Jun Tong, Huijuan Peng, Mir Hamid Pirahesh
Publikováno v:
SIGMOD Conference
To meet the challenge of analyzing rapidly growing graph and network data created by modern applications, a large number of graph databases have emerged, such as Neo4j and JanusGraph. They mainly target low-latency graph queries, such as finding the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb092c57495a9b6603f95b1a18e96a38
https://doi.org/10.1145/3318464.3386138
https://doi.org/10.1145/3318464.3386138
Autor:
Bin, Jiang, Min, Bi, Jun, Li, Qi, Liu, Nai-An, Xiao, Jie, Fang, Man-Yi, Shi, Zi-Wen, Yu, Qi-Lin, Ma, Sui-Jun, Tong, Kun-Mu, Zheng
Publikováno v:
Frontiers in Genetics
Familial Alzheimer’s disease (FAD) present as a positive family history of cognitive decline, with early onset and an autosomal dominant inheritance pattern. FAD is mainly caused by the mutations in the genes encoding for amyloid precursor protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::142ba2436bb6d166c3b2ccae41790f05
https://pubmed.ncbi.nlm.nih.gov/32754199
https://pubmed.ncbi.nlm.nih.gov/32754199
Publikováno v:
Studies in health technology and informatics. 264
Collection and management of clinical data for administration and analysis is a time-consuming and complex task, especially when multiple data providers been involved. Even if people are willing to take on the burden for it, there is still no mature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0688e3a585a2c471629c339d3c6b414e
https://pubmed.ncbi.nlm.nih.gov/31438042
https://pubmed.ncbi.nlm.nih.gov/31438042
Autor:
Sui-jun Tong, Yikang Wang, Bi Min, Ran Yao, Bin Jiang, Li Jianpeng, Shijie Duan, Yi-dan Zhang
Publikováno v:
Journal of the Anatomical Society of India. 69:1
Introduction: Matrix metalloproteinase-9 (MMP9) plays a key role in blood–spinal cord barrier dysfunction. MMP9 blockade leads to improved injured locomotor recovery. However, it is still unknown whether MMP9 deficiency affects gene expression or s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37d2f98a585a135b66aed61cda1c2177
https://doi.org/10.4103/jasi.jasi_76_19
https://doi.org/10.4103/jasi.jasi_76_19
Autor:
Sui-Jun Tong, Yilong Wang, Yongjun Wang, Jing Xue, Shi-Ming Cui, Li Ma, Xiaoling Liao, Yan Lin, Xiao-Chun Wang, Peiyi Gao, Mei-Li Liu, Yu-Ming Zhou, Lan Yu, Yuan-Liang Huang
Publikováno v:
Neurological Research. 31:355-361
We investigated whether baseline vessel status evaluated by magnetic resonance angiography (MRA) can be the foremost factor to classify acute ischemic stroke patients into subgroups for thrombolytic therapy within 3-6 hours of symptom onset.Acute isc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80bab61f811b6fb3e2d3c77de2c95322
https://doi.org/10.1179/174313209x444044
https://doi.org/10.1179/174313209x444044
Autor:
Qi-Lin Ma, Bin Cai, Sui-Jun Tong, Wei Wei, Yi-Hong Zhan, Ling Fang, Yi Lin, Ning Wang, Cong-Xia Lu
Recently, CELSR1 was identified by genome-wide association studies (GWAS) as a susceptibility gene for ischaemic stroke (IS) in Japanese individuals.The goal was to examine whether CELSR1 variants are associated with IS in the Chinese Han population.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a407bb6e661812aaccade3e34180f89a
Publikováno v:
Medinfo; 2019, p839-842, 4p