Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Yong-ping Liu"'
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 179, Iss , Pp 117374- (2024)
Cardiovascular disease (CVD) has now become the leading cause of death worldwide, and its high morbidity and mortality rates pose a great threat to society. Although numerous studies have reported the pathophysiology of CVD, the exact pathogenesis of
Externí odkaz:
https://doaj.org/article/6a9f7442394d42dfb45a89521e3aa067
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 164, Iss , Pp 114931- (2023)
Sirtuins (SIRTs) are a nicotinic adenine dinucleotide (+) -dependent histone deacetylase that regulates critical signaling pathways in prokaryotes and eukaryotes. Studies have identified seven mammalian homologs of the yeast SIRT silencing message re
Externí odkaz:
https://doaj.org/article/b0b5ba84872242148e3f1804d5a94c8a
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 12 (2022)
Sepsis, a life-threatening organ dysfunction caused by a dysregulated host response to infection, is a leading cause of death in intensive care units. The development of sepsis-associated organ dysfunction (SAOD) poses a threat to the survival of pat
Externí odkaz:
https://doaj.org/article/6f6fcf9268a24d4d8feb625f50a42a20
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-12 (2020)
Abstract Background The CACNA1C gene was defined as a risk gene for schizophrenia in a large genome-wide association study of European ancestry performed by the Psychiatric Genomics Consortium. Previous meta-analyses focused on the association betwee
Externí odkaz:
https://doaj.org/article/fb680fcc14d74faebe096140a7aa183f
Autor:
Yong-ping Liu, Mei Ding, Xi-cen Zhang, Yi Liu, Jin-feng Xuan, Jia-xin Xing, Xi Xia, Jun Yao, Bao-jie Wang
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background Schizophrenia is a severe neurodevelopmental disorder with a complex genetic and environmental etiology. Abnormal glutamate ionotropic N-methyl-D-aspartate receptor (NMDA) type subunit 1 (NR1) may be a potential cause of schizophr
Externí odkaz:
https://doaj.org/article/21eaef9f44d747669452b6dae9d7bcd4
Publikováno v:
Journal of International Medical Research, Vol 48 (2020)
Objective Schizophrenia is a severe neurodevelopmental disorder with a complex genetic and environmental etiology. The gene encoding EF-hand domain-containing protein D2 ( EFHD2 ) may be a genetic risk locus for schizophrenia. Methods We genotyped fo
Externí odkaz:
https://doaj.org/article/050e3bde1c2f4c34be8db8f6c373b558
Autor:
Zhi-xin Yang, Jia-hong Xie, Yong-ping Liu, Guang-xin Miao, Ying-han Wang, Sheng-mei Wu, Yuan Li
Publikováno v:
Neural Regeneration Research, Vol 10, Iss 4, Pp 583-588 (2015)
OBJECTIVE: To systematically evaluate the long-term effect and safety of Xingnao Kaiqiao needling method in ischemic stroke treatment. DATA RETRIEVAL: We retrieved relevant random and semi-random controlled trials that used the Xingnao Kaiqiao needli
Externí odkaz:
https://doaj.org/article/6483f18487d5481c95bbd574d6cd0c36
Autor:
Shan‐Yan Gao, Yong‐Ping Liu, Ri Wen, Xin‐Mei Huang, Ping Li, Yu‐Hang Yang, Ni Yang, Tie‐Ning Zhang
Publikováno v:
The FASEB Journal. 37
Publikováno v:
Neuropsychiatric Disease and Treatment. 16:2361-2370
Purpose Abnormal expression of the NR1 subunit of the N-methyl-d-aspartate (NMDA) receptor may potentially increase the susceptibility to neuropsychiatric diseases. The purpose of this study was to investigate the functional sequence of the 3'UTR of
Autor:
Jia-xin Xing, Bao-jie Wang, Yong-ping Liu, Feng-ling Xu, Ya Li, Meng Gao, Kuo Zeng, Jin-feng Xuan, Jun Yao, Xi Xia
Publikováno v:
Neuropsychiatric Disease and Treatment. 16:1519-1532
Background Epidemiological studies have shown that genetic factors are among the causes of schizophrenia. Galanin receptor 1 is an inhibitory receptor of galanin that is widely distributed in the central nervous system. This study mainly explored the