Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Haijing Ge"'
Autor:
Tao He, Junxing Pu, Haijing Ge, Tianli Liu, Xintong Lv, Yu Zhang, Jia Cao, Hong Yu, Zhibing Lu, Fen Du
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-18 (2024)
Abstract Atherosclerosis is a leading cause of cardiovascular diseases, characterized by endothelial dysfunction and lipid accumulation. Long non-coding RNAs (lncRNAs) are emerging as key regulators of endothelial cell behavior. This study aimed to i
Externí odkaz:
https://doaj.org/article/3afaf43b182b41f98e39ab7490812eef
Autor:
Leiming Wang, Zhuo Li, Cuicui Liu, Liyan Zhang, Dandan Wang, Haijing Ge, Weiwei Xu, Yongjuan Fu, Yanning Cai, Dehong Lu, Yueshan Piao
Publikováno v:
Glioma, Vol 3, Iss 4, Pp 168-174 (2020)
Background and Aim: Mutations in isocitrate dehydrogenase (IDH), co-deletion of 1p and 19q, loss or expression of the transcription regulator ATRX, and mutations in telomerase reverse transcriptase (TERT) gene promoters are intimately linked with dif
Externí odkaz:
https://doaj.org/article/d7381adc93c94630aab2500bb9b9cde2
Autor:
Hezuo Liu, Xiaorong Chen, Minhui Huang, Xiaomin Yu, Ye Gan, Ji Wang, Qiujin Chen, Zhipeng Nie, Haijing Ge
Publikováno v:
Reviews on Environmental Health.
Objectives The association between screen time and attention deficit hyperactivity disorder (ADHD) has been controversial. This study sheds light on the contentious correlation between screen time and ADHD. Content Until August 2022, electronic searc
Publikováno v:
Neuropathology : official journal of the Japanese Society of NeuropathologyREFERENCES. 41(3)
We investigated the risk factors for diffuse midline gliomas of the spinal cord (DMGSCs). Seventy patients with spinal cord gliomas in two hospitals were analyzed retrospectively. Sixty-nine patients that underwent surgery achieved partial or gross t
Autor:
Haijing Ge, Yanning Cai, De-Hong Lu, Wei-Wei Xu, Leiming Wang, Yong-Juan Fu, Zhuo Li, Dandan Wang, Cuicui Liu, Liyan Zhang, Yue-Shan Piao
Publikováno v:
Glioma, Vol 3, Iss 4, Pp 168-174 (2020)
Background and Aim: Mutations in isocitrate dehydrogenase (IDH), co-deletion of 1p and 19q, loss or expression of the transcription regulator ATRX, and mutations in telomerase reverse transcriptase (TERT) gene promoters are intimately linked with dif