Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Zi-xiong Zhan"'
Autor:
Xin-xin Liao1 xinliao_86@126.com, Zi-xiong Zhan1 zhanzixionh@163.com, Ying-ying Luo1 luoyingying08@gmail.com, Kai Li1 liskai@126.com, Jun-ling Wang1,2 wjling8002@126.com, Ji-feng Guo1,3 guojifeng2003@163.com, Xin-xiang Yan1,3 xxyan1268@126.com, Kun Xia2 xiakun@sklmg.edu.cn, Bei-sha Tang1,2,3 bstang7398@163.com, Lu Shen1,3 shenlu2505@126.com
Publikováno v:
BMC Neurology. 2013, Vol. 13 Issue 1, p1-10. 10p. 3 Charts.
Autor:
Juan Du, Zi-xiong Zhan, Yingying Luo, Kun Xia, Zhengmao Hu, Junling Wang, Yiqiao Hu, Lu Shen, Beisha Tang, Chong Chen
Publikováno v:
Brain Research Bulletin. 97:112-118
Hereditary spastic paraplegias (HSPs) are a group of clinically and genetically heterogeneous monogenic neurodegenerative disorders. The gene screen of hereditary spastic paraplegias patients remains time consuming and costly because of their highly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49793ac7624e99c7717d851432f8484d
https://doi.org/10.1016/j.brainresbull.2013.07.002
https://doi.org/10.1016/j.brainresbull.2013.07.002
Autor:
Mufang Huang, Lu Shen, Juan Du, Zi-xiong Zhan, Beisha Tang, Yingying Luo, Yi-Jing Yang, Zhifan Zhou, Xinxin Liao, Lu Zhou
Publikováno v:
Journal of neurology. 263(10)
Hereditary spastic paraplegias (HSP/SPGs) constitute a clinically and genetically heterogeneous group of neurodegenerative disorders. Inheritance of the disease has been reported to be autosomal dominant (AD), autosomal recessive (AR), or X-linked, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bffa2cb65ca7f2542e7d0c03234e225d
https://pubmed.ncbi.nlm.nih.gov/27553021
https://pubmed.ncbi.nlm.nih.gov/27553021
Autor:
Chen Zheng, Yingying Luo, Elmar H. Pinkhardt, Anette Hall, Hans-Peter Müller, Hans-Jürgen Huppertz, Junling Wang, Hilkka Soininen, Chong Chen, Juan Du, Xinxin Liao, Anne M. Koivisto, Jan Kassubek, Thangiah Geetha, Viljami Väisänen, Johannes Rosskopf, Hong Jiang, Xu Liu, Kun Xia, Lu Shen, Albert C. Ludolph, Satz Mengensatzproduktion, Esa-Heikki Meriläinen, Jeganathan Ramesh Babu, Sanna-Kaisa Herukka, Marjo Laitinen, Beisha Tang, Ruixia Zhu, Qian Pan, Zi-xiong Zhan, Xinxiang Yan, Druckerei Stückle, Zhiyi He, Mikko Hiltunen, Guo-hua Zhao, Ying Zhu, Yin-guang Wang, Zhaoting Hu, Seppo Helisalmi
Publikováno v:
Neurodegenerative Diseases. 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06b5d92bd56b53af94eaf7438fb8af7f
https://doi.org/10.1159/000370326
https://doi.org/10.1159/000370326
Autor:
Xinxin Liao, Lu Shen, Yingying Luo, Qian Pan, Zi-xiong Zhan, Kun Xia, Beisha Tang, Xinxiang Yan, Chong Chen, Junling Wang, Hong Jiang, Zhaoting Hu, Juan Du, Guo-hua Zhao, Yin-guang Wang
Publikováno v:
Neuro-degenerative diseases. 14(4)
Background: Hereditary spastic paraplegias constitute a heterogeneous group of inherited neurodegenerative disorders. To date, there has been no systematic mutation and clinical analysis for a large group of autosomal-dominant hereditary spastic para
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4378bef56667ec817ab07f3b7ba882fe
https://pubmed.ncbi.nlm.nih.gov/25341883
https://pubmed.ncbi.nlm.nih.gov/25341883
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 29(5)
Introduced in 2009, whole-exome sequencing (WES) is a technology in which target capture methods are used to enrich sequences of coding regions of genes from fragmented total genomic DNA, which is followed by high-throughput sequencing of the capture
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::43dc57ba0139d660d275b4f3d3a0cc41
https://pubmed.ncbi.nlm.nih.gov/23042393
https://pubmed.ncbi.nlm.nih.gov/23042393
Autor:
Hong Jiang, Guo-hua Zhao, Kun Xia, Juan Du, Yacen Hu, Beisha Tang, Lu Shen, Chong Chen, Zi-xiong Zhan, Yingying Luo
Publikováno v:
Clinical neurology and neurosurgery. 113(6)
Background Hereditary spastic paraplegia type 6 (SPG6) is caused by mutations in the NIPA1 gene, this is a rare cause of HSP, until now, all the affected individuals reported displayed “pure” spastic paraplegia. Objectives To analyze the genotype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc4f4f152126c8060c00167c7e21ce02
https://pubmed.ncbi.nlm.nih.gov/21419568
https://pubmed.ncbi.nlm.nih.gov/21419568
Autor:
Xinxiang Yan, Yingying Luo, Jifeng Guo, Lu Shen, Kai Li, Beisha Tang, Xinxin Liao, Kun Xia, Junling Wang, Zi-xiong Zhan
Publikováno v:
BMC Neurology
Background Recent studies suggest that epigenetic factors may play an important role in the pathogenesis of Parkinson’s disease (PD). In our previous work, we sequenced the exomes of sixteen patients from eight Chinese PD families using whole exome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad011e9eb3edebf0b1a56bd48719df24
Autor:
Yang, Yi-Jing, Zhou, Zhi-Fan, Liao, Xin-Xin, Luo, Ying-Ying, Zhan, Zi-Xiong, Huang, Mu-Fang, Zhou, Lu, Tang, Bei-Sha, Shen, Lu, Du, Juan
Publikováno v:
Journal of Neurology; Oct2016, Vol. 263 Issue 10, p2136-2138, 3p, 1 Diagram, 1 Chart
Autor:
Xuan YuanShouHu, Babel Novel
An unknown sword with an unknown cultivation technique had achieved a breakthrough to the next realm. It was a useless weapon that could not be cultivated. He had unraveled the secrets of each continent and walked towards the Endless Planes. What kin
