Publications by authors named "Yuan Jun Liao"

Article Synopsis
  • Older adults are at high risk for femoral neck fractures (FNFs) and may experience significant psychological stress, which could affect their recovery after total hip replacement surgery.
  • The study analyzed data from 120 elderly patients to examine the link between preoperative psychological stress and short-term postoperative outcomes.
  • Results indicated that factors like anxiety, depression, and the quality of FNF reduction were significant predictors of poor recovery outcomes, with moderate correlations observed between mental health scores and overall functional recovery.
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HIV-associated neurocognitive disorders (HAND) are characterized by synaptic damage and neuronal loss in the brain, ultimately leading to progressive decline of cognitive abilities and memory. Chemokine CC motif ligand 2 (CCL2) is elevated in cerebrospinal fluid (CSF), and has been believed to contribute to HAND. Previous studies by our research team have shown that CCL2 enhances N-Methyl-D-aspartate receptor (NMDAR)-mediated excitatory postsynaptic currents (EPSCs) and causes nerve cell damage.

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Article Synopsis
  • CCL2 is a proinflammatory chemokine linked to cognitive impairments in HIV-1 patients, contributing to HIV-associated neurocognitive disorder (HAND).
  • In a study, researchers injected CCL2 into rats to induce cognitive impairment and tested the protective effects of Tanshinone IIA, finding that it significantly improved learning and memory.
  • Tanshinone IIA was shown to reduce oxidative stress, inflammation, and apoptosis in the rats' brains, suggesting its potential as a therapeutic agent for HAND.
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Background: Chemokine C-C motif ligand 2 (CCL2) is one of the most widely recognised proinflammatory chemokines in cognitive disorders. Currently, CCL2-targeting drugs are extremely limited. Thus, this study aimed to explore the neuroprotection afforded by naringin in CCL2-induced cognitive impairment in rats.

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Although nasopharyngeal carcinoma (NPC) and oral squamous cell carcinoma (OSCC) are highly correlated clinical diseases, the underling molecular mechanisms to link the two diseases remain largely unknown. The aim of this study is to identify the shared functional modules for NPC and OSCC by using large-scale transcriptomic data. Gene expression profile datasets of NPC and OSCC were obtained from the GEO database.

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