Zobrazeno 1 - 7
of 7
pro vyhledávání: '"YINGZHONG HE"'
Autor:
Song Li, Xinxing Ouyang, Hongxiang Sun, Jingsi Jin, Yao Chen, Liang Li, Qijun Wang, Yingzhong He, Jiwen Wang, Tongxin Chen, Qing Zhong, Yinming Liang, Philippe Pierre, Qiang Zou, Youqiong Ye, Bing Su
Publikováno v:
Cell Discovery, Vol 10, Iss 1, Pp 1-19 (2024)
Abstract Peripheral CD8+ T cell number is tightly controlled but the precise molecular mechanism regulating this process is still not fully understood. In this study, we found that epilepsy patients with loss of function mutation of DEPDC5 had reduce
Externí odkaz:
https://doaj.org/article/824b50abd9694c4e8e1778931ed140ef
Autor:
Ruen Yao, Yunqing Zhou, Jie Tang, Niu Li, Tingting Yu, Yingzhong He, Cuijin Wang, Jiwen Wang, Jian Wang
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Childhood epilepsy is a considerably heterogeneous neurological condition with a high worldwide incidence. Genetic diagnosis of childhood epilepsy provides the most accurate pathogenetic evidence; however, a large proportion of highly suspected cases
Externí odkaz:
https://doaj.org/article/9da4b224e9494427973784dd4e3544e1
Autor:
Fen Zhao, Xiaoning Sun, Yingyan Wang, Yunqing Zhou, Yingzhong He, Cuijin Wang, Feng Han, Jie Liu, Shao-Yu Tsai, Guanghai Wang, Jiwen Wang
Publikováno v:
Nature and Science of Sleep.
Fen Zhao,1,* Xiaoning Sun,2,* Yingyan Wang,1 Yunqing Zhou,1 Yingzhong He,1 Cuijin Wang,1 Feng Han,1 Jie Liu,1 Shao-Yu Tsai,3 Guanghai Wang,2 Jiwen Wang1 1Department of Pediatric Neurology, Shanghai Childrenâs Medical Center, School of Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e10a51963034a22a8ddde25211655dc
https://www.dovepress.com/sleep-disturbances-in-chinese-children-with-epilepsy-associations-with-peer-reviewed-fulltext-article-NSS
https://www.dovepress.com/sleep-disturbances-in-chinese-children-with-epilepsy-associations-with-peer-reviewed-fulltext-article-NSS
Autor:
Yu, Ding, Qianwen, Zhang, Yingzhong, He, Lei, Zhang, Niu, Li, Guoying, Chang, Yao, Chen, Jian, Wang, Jinjin, Wu, Lijun, Fu, Xiumin, Wang
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 38(2)
To explore the genetic basis for 7 patients with Alström syndrome.DNA was extracted from peripheral blood samples of the patients and their parents. Whole exome sequencing was carried out for the patients. Suspected variant was verified by Sanger se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c483d033f820716fdc904d930d0fa496
https://pubmed.ncbi.nlm.nih.gov/33565060
https://pubmed.ncbi.nlm.nih.gov/33565060
Publikováno v:
Experimental and Therapeutic Medicine
Ectopic expression of microRNA (miRNA) in rheumatoid arthritis (RA) fibroblast-like synoviocyte (RA FLS) is associated with the development of rheumatoid arthritis. The present study aimed to evaluate the effects of miRNA-140-5p (miR-140) on the prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c960df0b1fa4278b911b1685aa50ef5
http://europepmc.org/articles/PMC7792473
http://europepmc.org/articles/PMC7792473
Publikováno v:
Experimental & Therapeutic Medicine; Feb2021, Vol. 21 Issue 2, p1-10, 10p
Autor:
Yingzhong He, Jiwen Wang, Yunqing Zhou, Tingting Yu, Zhiping Wang, Qihua Fu, Niu Li, Jian Wang
Publikováno v:
Clinical neurology and neurosurgery. 154
Objective The study was designed to identify pathogenic TSC1 or TSC2 gene mutations and provide solid evidence for the diagnosis of tuberous sclerosis complex (TSC). Methods 11 unrelated Chinese patients with TSC were investigated in the present stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aa41528ca8c2e1547f099c1279f9f98
https://pubmed.ncbi.nlm.nih.gov/28178598
https://pubmed.ncbi.nlm.nih.gov/28178598