Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Huangqi Xue"'
Autor:
Zhenwei Liu, Fengxia Li, Axiao Pan, Huangqi Xue, Shan Jiang, Chengwei Zhu, Mengmeng Jin, Jinxia Fang, Xiaochun Zhu, Matthew A. Brown, Xiaobing Wang
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Primary Sjögren's syndrome (pSS) is a common chronic autoimmune disease characterized by a high prevalence of autoantibodies and lymphocyte-mediated exocrine gland damage. To enhance our understanding of the mechanisms underlying the progression of
Externí odkaz:
https://doaj.org/article/081464fb19b64f02824858ffcf7bd8a9
Autor:
Jinyu Wu, Shan Jiang, Matthew A. Brown, Qiongdan Wang, Xiaochun Zhu, Bing Zhang, Fengxia Li, Mengmeng Jin, Zhenwei Liu, Xiaobing Wang, Lifeng Du, Huangqi Xue, Yu Zhang
Publikováno v:
Rheumatology. 59:2603-2615
Objectives This study aims to characterize the expression profiles of circRNAs in primary Sjogren’s Syndrome (pSS) and examine the potential of noninvasive circular RNAs (circRNAs) as biomarkers of pSS. Methods We performed RNA sequencing of minor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c42bc276334365553338d9fb15e95bd
https://doi.org/10.1093/rheumatology/keaa163
https://doi.org/10.1093/rheumatology/keaa163
Autor:
Zhenwei, Liu, Fengxia, Li, Axiao, Pan, Huangqi, Xue, Shan, Jiang, Chengwei, Zhu, Mengmeng, Jin, Jinxia, Fang, Xiaochun, Zhu, Matthew A, Brown, Xiaobing, Wang
Publikováno v:
Frontiers in Immunology
Primary Sjögren's syndrome (pSS) is a common chronic autoimmune disease characterized by a high prevalence of autoantibodies and lymphocyte-mediated exocrine gland damage. To enhance our understanding of the mechanisms underlying the progression of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cd892c2f08091e374f57cc2472bf948e
https://pubmed.ncbi.nlm.nih.gov/31068931
https://pubmed.ncbi.nlm.nih.gov/31068931
Autor:
Jinyu Wu, Tao Zhang, Huangqi Xue, Qiongdan Wang, Zhenwei Liu, Na Zhang, Bing Zhang, Xiaomin Chen, Yaoqiang Du, Jing Jin
Publikováno v:
Human mutation. 40(3)
Recent whole-exome sequencing (WES) studies have demonstrated the contribution of de novo mutations (DNMs) to epileptic encephalopathies (EEs). Here, we performed WES on four trios with West syndrome and identified three loss-of-function DNMs in both
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a5cf46428f373bdaf0c3c53bda75702
https://pubmed.ncbi.nlm.nih.gov/30488659
https://pubmed.ncbi.nlm.nih.gov/30488659
Autor:
Denghui Chen, Xueqin Xu, Huangqi Xue, Tao Zhang, Wei Li, Chong Chen, Shaohua Tang, Xinting Liu
Publikováno v:
Neuroscience letters. 685
Intellectual disability (ID) is one of the most prevalent chronic developmental brain disorders or phenotype of syndromic ID, affecting nearly 1-2% of the general population worldwide. Over recent decades, tremendous effort and high-throughput platfo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59b2760019cca41ceb376d4918ba8454
https://pubmed.ncbi.nlm.nih.gov/30144540
https://pubmed.ncbi.nlm.nih.gov/30144540