Zobrazeno 1 - 10
of 99
pro vyhledávání: '"Sijun, Li"'
Publikováno v:
Neurology and Therapy, Vol 13, Iss 3, Pp 763-784 (2024)
Abstract Introduction Most current treatment strategies and investigations on cryptococcal meningitis (CM) focus primarily on the central nervous system (CNS), often overlooking the complex interplay between the CNS and the peripheral system. This st
Externí odkaz:
https://doaj.org/article/47c39bdec331462d860d17901c84b83d
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-16 (2023)
Abstract Background Seizures are associated with a decrease in γ-aminobutyric type A acid receptors (GABAaRs) on the neuronal surface, which may be regulated by enhanced internalization of GABAaRs. When interactions between GABAaR subunit α-1 (GABR
Externí odkaz:
https://doaj.org/article/8b55ba7abecc47e2b1425f981fb53c18
Publikováno v:
Journal of Integrative Neuroscience, Vol 23, Iss 8, p 158 (2024)
Background: Most acute cerebral infarctions (ACI) may develop vascular dementia (VD), which involves almost all types of cognitive impairment. Unfortunately, there is currently no effective treatment for VD. Most patients exhibit mild cognitive impai
Externí odkaz:
https://doaj.org/article/c1462a8b802c42e6abb8e6ae13fa3ae2
Autor:
Zhuangzhi Zhang, Sijun Li, Zheng Zhang, Zhou Chen, Hua Wang, Xianguang Meng, Wenquan Cui, Xiwei Qi, Jiacheng Wang
Publikováno v:
Carbon Energy, Vol 6, Iss 2, Pp n/a-n/a (2024)
Abstract Electrochemical C–C and C–N coupling reactions with the conversion of abundant and inexpensive small molecules, such as CO2 and nitrogen‐containing species, are considered a promising route for increasing the value of CO2 reduction pro
Externí odkaz:
https://doaj.org/article/6ed8e8f2d22244768af8708395601c34
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Histones have a vital function as components of nucleosomes, which serve as the fundamental building blocks of chromatin. Histone deacetylases (HDACs), which target histones, suppress gene transcription by compacting chromatin. This implies that HDAC
Externí odkaz:
https://doaj.org/article/37169dfacb4e435b83584ac3f8fa193c
Publikováno v:
Advanced Energy & Sustainability Research, Vol 5, Iss 1, Pp n/a-n/a (2024)
Compared to the Haber–Bosch (H–B) process for ammonia synthesis with massive emission of greenhouse CO2 and necessary harsh reaction conditions, the electrocatalytic NO3− reduction (NO3RR) for ammonia synthesis under ambient temperature and pre
Externí odkaz:
https://doaj.org/article/b03a668e97224be9aedc01e0a84fb1f9
Autor:
Sijun Li, Mengyao Qin, Shuang Mao, Lingyun Mei, Xinzhang Cai, Yong Feng, Chufeng He, Jian Song
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-14 (2022)
Abstract Background Waardenburg syndrome (WS) is the most common form of syndromic deafness with phenotypic and genetic heterogeneity in the Chinese population. This study aimed to clarify the clinical characteristics and the genetic cause in eight C
Externí odkaz:
https://doaj.org/article/4f5f78041b61473cb8fd3850a8800cf4
Autor:
Honghua Shao, Sijun Li
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
The human immunodeficiency virus (HIV) infection can cause damage to multiple systems within the body, and the interaction among these various organ systems means that pathological changes in one system can have repercussions on the functions of othe
Externí odkaz:
https://doaj.org/article/06326bce74514198aa2ca9edad64539b
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
BackgroundTuberculosis (TB) is an infectious disease caused by Mycobacterium tuberculosis (Mtb) infection. Cuproptosis is a novel cell death mechanism correlated with various diseases. This study sought to elucidate the role of cuproptosis-related ge
Externí odkaz:
https://doaj.org/article/4c402e94f08c4aa58480d58f3d841f69
Autor:
Xianlin Liu, Jie Wen, Xuezhong Liu, Anhai Chen, Sijun Li, Jing Liu, Jie Sun, Wei Gong, Xiaoming Kang, Zhili Feng, Chufeng He, Lingyun Mei, Jie Ling, Yong Feng
Publikováno v:
PLoS ONE, Vol 18, Iss 9, p e0288640 (2023)
The ELMOD3 gene is implicated in causing autosomal recessive/dominant non-syndromic hearing loss in humans. However, the etiology has yet to be completely elucidated. In this study, we generated a patient-derived iPSC line carrying ELMOD3 c.512A>G mu
Externí odkaz:
https://doaj.org/article/adce9d9495d24721b446265975dd91ca