Rui Zhou

Dr. Rui Zhou

Shaanxi Institute for Pediatric Diseases, China
+2

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2015 in Medical Science Monitor
Verified
Journal Article
Open access
PDF file
RZRui Zhou
Rui Zhou
HWHuang Wenjun
Huang Wenjun
WJWen Jing
Wen Jing
LTLi Tao
Li Tao
MLMao Ling
Mao Ling
ZXZeng Xiaorong
Zeng Xiaorong
BACKGROUND:Although puerarin is generally considered as a protective agent for cardio-cerebrovascular diseases, the exact effect on reducing myocardial infarction reperfusion injury (MIRI) is not well understood. This study aimed to pool previous ran...

7 February 2022 in Cardiovascular Toxicology
Verified
Journal Article
Closed access
PDF file
DLDandan Long
Dandan Long
CCChunyue Chen
Chunyue Chen
WLWei Li
Wei Li
WPWanling Peng
Wanling Peng
DLDongmei Li
Dongmei Li
XDXitong Dang
Xitong Dang

28 February 2022 in International Journal of Stem Cells
Verified
Journal Article
Open access
PDF file
FLFeng Liu
Feng Liu
DLDandan Long
Dandan Long
WHWenjun Huang
Wenjun Huang
WPWanling Peng
Wanling Peng
HLHuan Lan
Huan Lan
RZRui Zhou
Rui Zhou
Feng Liu, Dandan Long, Wenjun Huang, Wanling Peng, Huan Lan, Yafei Zhou, Xitong Dang, Rui Zhou. IJSC 2022;15:247-57. https://doi.org/10.15283/ijsc21148

3 October 2022 in Stem Cell Research
Verified
Journal Article
Open access
WHWenjun Huang
Wenjun Huang
YZYafei Zhou
Yafei Zhou
JWJie Wang
Jie Wang
CJCongshan Jiang
Congshan Jiang
YZYanmin Zhang
Yanmin Zhang
RZRui Zhou
Rui Zhou
Pompe disease results from GAA mutations that leads to lysosomal glycogen accumulation and cardiac and skeletal muscle pathology. We have previously generated an infantile-onset Pompe disease patient-derived human-induced pluripotent stem cells (iPSCs) line carrying compound GAA mutations (R608X and E888X). Using his parents' peripheral blood mononuclear cells (PBMCs), we here generated two iPSCs lines which carry mutations of R608X E888X respectively. Both lines show typical cell morphology, high expressed pluripotent and self-renewal markers, normal karyotype, and trilineage differentiation potential. These two lines are valuable re-sources for studying the pathological mechanisms of GAA mutation-caused Pompe disease.

8 January 2024 in Biochemical and Biophysical Research Communications
Verified
Journal Article
Closed access
JHJun He
Jun He
LHLin Hou
Lin Hou
QLQuanwei Liu
Quanwei Liu
RZRui Zhou
Rui Zhou

30 November 2021 in International Journal of Stem Cells
Verified
Journal Article
Open access
PDF file
YLYuanshu Liu
Yuanshu Liu
PZPeng Zhang
Peng Zhang
WHWenjun Huang
Wenjun Huang
FLFeng Liu
Feng Liu
DLDandan Long
Dandan Long
RZRui Zhou
Rui Zhou
Yuanshu Liu,*, Peng Zhang,*, Wenjun Huang, Feng Liu, Dandan Long, Wanling Peng, Xitong Dang, Xiaorong Zeng, Rui Zhou. IJSC 2021;14:410-22. https://doi.org/10.15283/ijsc21051