Zobrazeno 1 - 7
of 7
pro vyhledávání: '"XiangYe Xu"'
Autor:
Meiwan Cao, Baoling Peng, Huan Chen, Min Yang, Peiyu Chen, Liping Ye, Hongli Wang, Lu Ren, Jing Xie, Jingnan Zhu, Xiangye Xu, Wanfu Xu, Lanlan Geng, Sitang Gong
Publikováno v:
Redox Report, Vol 27, Iss 1, Pp 167-175 (2022)
Background The number of neutrophils is significantly reduced in myelodysplastic syndrome (MDS), but the molecular basis remains unclear. We recently found that miR-34a was significantly increased in MDS neutrophils. Therefore, this study aims to cla
Externí odkaz:
https://doaj.org/article/e4faff7aa9bc455c9f1f62c7839a3b40
Autor:
Meiwan Cao, BaoLing Peng, WanFu Xu, PeiYu Chen, Huan Chen, LiPing Ye, Jing Xie, HongLi Wang, Lu Ren, LiYa Xiong, JingNan Zhu, XiangYe Xu, LanLan Geng, SiTang Gong
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 15, Iss 1 (2023)
Myelodysplastic syndromes (MDS) are a group of heterogeneous myeloid clonal diseases that are characterized by ineffective bone marrow hematopoiesis. Since studies have confirmed the significance of miRNAs in ineffective hematopoiesis in MDS, the cur
Externí odkaz:
https://doaj.org/article/b4d7cc643e11482a9f4ea14a615e90fa
Publikováno v:
Stem Cell Research, Vol 27, Iss , Pp 42-45 (2018)
Turner syndrome (TS) with 45,X/46,XY mosaic karyotype is a rare sex chromosome disorder with an occurrence of 0.15‰ at birth. We report the generation of an induced pluripotent stem cell (iPSC) line from peripheral blood mononuclear cells of a Chin
Externí odkaz:
https://doaj.org/article/25b3889d97ea41f98ae16dc44ef19d56
Autor:
MeiWan Cao, BaoLing Peng, WanFu Xu, PeiYu Chen, HuiWen Li, Yang Cheng, Huan Chen, LiPing Ye, Jing Xie, HongLi Wang, Lu Ren, LiYa Xiong, JingNan Zhu, XiangYe Xu, LanLan Geng, SiTang Gong
Publikováno v:
Mediterranean Journal of Hematology & Infectious Diseases; 2023, Vol. 15 Issue 1, p1-10, 10p
Publikováno v:
Stem Cell Research, Vol 27, Iss, Pp 42-45 (2018)
Turner syndrome (TS) with 45,X/46,XY mosaic karyotype is a rare sex chromosome disorder with an occurrence of 0.15‰ at birth. We report the generation of an induced pluripotent stem cell (iPSC) line from peripheral blood mononuclear cells of a Chin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::281aafae963350e3b49807dc9875ea1a
https://pubmed.ncbi.nlm.nih.gov/29320756
https://pubmed.ncbi.nlm.nih.gov/29320756
Autor:
Ru Zhang, Yao Xue, Liwen Zhu, Meiyun Kang, Xiangye Xu, Jie Huang, Liucheng Rong, Juncheng Dai, Zhibin Hu, Yongjun Fang, Zhaoming Wang
Publikováno v:
Cancer Research. 79:1685-1685
Landscape of pathogenic or likely pathogenic (P/LP) germline mutations in cancer predisposition genes have been well-studied among patients or survivors of childhood cancer in the US. However, little is known for cancer predisposing germline mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bc37461413e78a87c751c2da0f27c84
https://doi.org/10.1158/1538-7445.am2019-1685
https://doi.org/10.1158/1538-7445.am2019-1685
Autor:
Yumei Luo, Yaoyong Chen, Bolan Yu, Yu Gong, Xiaofang Sun, Detu Zhu, Chun Xie, Rong Du, Yong Fan, Xiangye Xu
Publikováno v:
Cell Discovery
The human induced pluripotent stem cell (iPSC) technique promises to provide an unlimited, reliable source of genetically matched pluripotent cells for personalized therapy and disease modeling. Recently, it is observed that cells with ring chromosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::621c6b5b55f1efb57239b90b327428d9
http://europepmc.org/articles/PMC4860828
http://europepmc.org/articles/PMC4860828