Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Cunjiang Li"'
Autor:
Jingsi Wang, Zhandong Qiu, Dawei Li, Xixi Yang, Yan Ding, Lehong Gao, Aihua Liu, Yang Song, Cunjiang Li, Ran Gao, Lin Wang, Liyong Wu, Longfei Jia, Dongmei Guo, Aihong Zhou, Jianping Jia, Liyuan Huang, Miao Qu, Li Gao, Huiqing Dong, Junwei Hao, Zheng Liu
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundMyelin oligodendrocyte glycoprotein-antibody (MOG-ab)-associated disease (MOGAD) has highly heterogenous clinical and imaging presentations, in which encephalitis is an important phenotype. In recent years, some atypical presentations in MO
Externí odkaz:
https://doaj.org/article/ba6a974738534234b02f1b79e264782c
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Abstract Objective The importance of late-onset cobalamin C (cblC) disorder is underestimated in adults. Improved awareness on its clinical and neuroimaging features helps timely diagnosis and appropriate treatment. Methods Totally 16 late-onset cblC
Externí odkaz:
https://doaj.org/article/3a342ba32157443cbb3f231a16ac6291
Autor:
Zhanjun Wang, Xuying Li, Yue-Shan Piao, Cunjiang Li, Guobin Yuan, Yicong Lin, Xianling Wang, Hai Chen, Chaodong Wang
Publikováno v:
American Journal of Medical Genetics Part A. 188:237-242
Hartnup disease cases were rare, and the genotype-phenotype correlation was not fully understood. Here we reported two unrelated young men diagnosed as Hartnup disease, who carried novel compound heterozygote mutations in the SLC6A19 gene and present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf9c39901fc93d3698a1faf1fcf427f6
https://doi.org/10.1002/ajmg.a.62475
https://doi.org/10.1002/ajmg.a.62475
Autor:
Aihong Zhou, Lin Wang, Aihua Liu, Liyong Wu, Jingsi Wang, Junwei Hao, Xixi Yang, Longfei Jia, Li Gao, Huiqing Dong, Yan Ding, Yang Song, Ran Gao, Zheng Liu, Miao Qu, Cunjiang Li, Lehong Gao, Zhandong Qiu, Liyuan Huang, Dongmei Guo, Jianping Jia, Dawei Li
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Frontiers in Immunology
Frontiers in Immunology
BackgroundMyelin oligodendrocyte glycoprotein-antibody (MOG-ab)-associated disease (MOGAD) has highly heterogenous clinical and imaging presentations, in which encephalitis is an important phenotype. In recent years, some atypical presentations in MO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f4b472d3610963e3cb3dc26f985c40d
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Objective The importance of late-onset cobalamin C (cblC) disorder is underestimated in adults. Improved awareness on its clinical and neuroimaging features helps timely diagnosis and appropriate treatment. Methods Totally 16 late-onset cblC cases we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0ec473c8dfff9eb867d8270e0324e30
http://link.springer.com/article/10.1186/s13023-019-1058-9
http://link.springer.com/article/10.1186/s13023-019-1058-9
Publikováno v:
Pathology oncology research : POR. 26(3)
Norcantharidin is a cantharidin demethylated analog with antitumor effects in many tumors, including cholangiocarcinoma. Autophagy suppression is known to increase chemosensitivity in cholangiocarcinoma. This study aimed to determine whether autophag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e10c9914670ed7017697ea4eea41020
https://pubmed.ncbi.nlm.nih.gov/31612378
https://pubmed.ncbi.nlm.nih.gov/31612378
Table S1. Comparison of allele frequencies of identified mutations between our patients and other reports. (DOC 48 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::244a41b8e21fdc438c41c94eaa714336
Publikováno v:
Chinese Medical Journal
Chinese Medical Journal, Vol 129, Iss 18, Pp 2173-2177 (2016)
Chinese Medical Journal, Vol 129, Iss 18, Pp 2173-2177 (2016)
Background: The brain stem is found to be impaired in multiple system atrophy-cerebellar types (MSA-C). Rapid eye movement (REM) sleep behavior disorder (RBD) is reported as a marker of progressive brain stem dysfunction. Few systematic studies about
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ca663800f2b58dd383d9f1664e64e19
https://doi.org/10.4103/0366-6999.189903
https://doi.org/10.4103/0366-6999.189903
Autor:
Wenbin Wu, Miao Zhang, Yu Fu, Wang Heng, Guoheng Zhang, Dong Liu, Cunjiang Li, Zhang Hui, Shijiang Yang
Publikováno v:
Heart, Lung and Circulation. 23:572-577
Background The Cyclooxygenase-2 (COX-2) rs20417 polymorphism has been implicated in coronary artery disease (CAD) risk, but individually published studies have shown inconsistent results. The aim of this study was to clarify the effects of COX-2 rs20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19c79a9751f1aec3919bddfce8c94857
https://doi.org/10.1016/j.hlc.2014.01.002
https://doi.org/10.1016/j.hlc.2014.01.002
Autor:
Liyong Wu, Lidong Jiao, Chhetri Jagadish Kumar, Xiangbo Wang, Jie Cui, Xianling Wang, Cunjiang Li, Changbiao Chu
Publikováno v:
Chinese Medical Journal
Chinese Medical Journal, Vol 128, Iss 13, Pp 1831-1833 (2015)
Chinese Medical Journal, Vol 128, Iss 13, Pp 1831-1833 (2015)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6825fea6aa55fd9728c07ecac4e34229
https://doi.org/10.4103/0366-6999.159362
https://doi.org/10.4103/0366-6999.159362