Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Huanyun Jing"'
Autor:
Weiguo Sui, Qing Gan, Wei Wei Gong, Xiaolian Wei, Minglin Ou, Donge Tang, Huanyun Jing, Hua Lin, Yue Zhang, Yong Dai
Publikováno v:
Translational Medicine Communications, Vol 3, Iss 1, Pp 1-8 (2018)
Abstract Background Down Syndrome (DS) has a very high morbidity, according to statistics, the incidence rate of DS is as high as 1:700 among the new born babies. At present, there are still no effective prevention or treatment methods for the diseas
Externí odkaz:
https://doaj.org/article/b829d3d25cd943d2bc5caff092b24097
Autor:
Jiejing Chen, Qing Gan, Donge Tang, Yaoshuang Zou, Huanyun Jing, Yong Dai, Wen Xue, Ruohan Zhang
Background: Chromosome 22q11.2 deletion (CH22qD) syndrome is the most common human deletion syndrome. Competing endogenous RNAs (ceRNAs) have miRNA binding sites that are capable of competitively binding miRNAs and inhibiting miRNA regulation of targ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1040f4bcd3bceb649f916a914a5db0c6
https://doi.org/10.21203/rs.3.rs-244390/v1
https://doi.org/10.21203/rs.3.rs-244390/v1
Autor:
Minglin Ou, Yufeng Sun, Jiejing Chen, Ming Yang, Hua Lin, Qiupei Tan, Huanyun Jing, Yong Dai, Weiguo Sui, Qiang Yan, Tongxiang Zou, Zhenzhen Cui, Wen Xue, Cao Cuihui, Li Guo
Publikováno v:
International Journal of Molecular Medicine. 35:1467-1479
Systemic lupus erythematosus (SLE) is a chronic, potentially fatal systemic autoimmune disease characterized by the production of autoantibodies against a wide range of self-antigens. To investigate the role of the 5-hmC DNA modification with regard
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::672f2ca6d4992928b4fc360b70e0a768
https://doi.org/10.3892/ijmm.2015.2149
https://doi.org/10.3892/ijmm.2015.2149
Autor:
Wen Xue, Weiwei Gong, Guoping Sun, Hui Guo, Xianliang Hou, Qiupei Tan, Yong Dai, Minglin Ou, Huanyun Jing, Weiguo Sui, Fuhua Liu
Publikováno v:
Gene. 578(2)
Objective Mental retardation is characterized by lower intelligence compared to the average intelligence of persons the same age. These patients have low adaptive capacity acquired by society. The genetic factors of causing MR include monogenic disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd1c4d42c981043ad33c58283103e7c9
https://pubmed.ncbi.nlm.nih.gov/26707211
https://pubmed.ncbi.nlm.nih.gov/26707211
Autor:
WEIGUO SUI, QIUPEI TAN, MING YANG, QIANG YAN, HUA LIN, MINGLIN OU, WEN XUE, JIEJING CHEN, TONGXIANG ZOU, HUANYUN JING, LI GUO, CUIHUI CAO, YUFENG SUN, ZHENZHEN CUI, YONG DAI
Publikováno v:
International Journal of Molecular Medicine; 2015, Vol. 35 Issue 5, p1467-1479, 13p