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Molybdenum disulfide (MoS2) is a typical two-dimensional material, which is widely used in many fields because of its excellent electrical and optical properties. In recent years, the high-quality growth of MoS2 has attracted more and more attention from researchers. Many studies have reported a two-step method for the production of MoS2 by pre-deposition of molybdenum (Mo) source and then vulcanization, which is cumbersome and time-consuming, and the preparation temperature is mostly above 800 °C, increasing energy consumption and experimental risk. In this paper, S source and Mo source can be distinguished by double temperature zone tube furnace to prepare MoS2 material in one-step method. The temperatures of S and Mo sources were designed separately, and the effect of each temperature on the quality of MoS2 was investigated. And the monolayer MoS2 with high crystalline quality was obtained at a S source temperature of 165 °C and a Mo source temperature of 680 °C. We produce MoS2 in one-step method at low temperature, which provides a reference for the synthesis of high-quality monolayer MoS2. [ABSTRACT FROM AUTHOR]

Objective: The G‐allele of the ‐1019C/G (rs6295) promoter polymorphism of the serotonin receptor 1A (HTR1A) gene has been implicated in anxiety; however, the underlying neurophysiological processes are still not fully understood. Recent evidence indicates that low parasympathetic (vagal) tone is predictive of anxiety. We thus conducted a structural equation model (SEM) to examine whether the HTR1A rs6295 variant can affect anxiety by altering parasympathetic nervous activity. Method: A sample of 1141 drug‐free healthy Han Chinese was recruited for HTR1A genotyping. Autonomic nervous function was assessed by short‐term spectral analysis of heart rate variability (HRV). Anxiety and stress levels were evaluated by the Beck Anxiety Inventory (BAI) and the Perceived Stress Scale (PSS) respectively. Results: The number of the HTR1A G allele was inversely correlated with high‐frequency power (HF), a parasympathetic index of HRV. The HF index was negatively associated with BAI scores. Furthermore, the good‐fitting SEM, adjusting for confounding variables (e.g., age and PSS levels), revealed a significant pathway linking rs6295 variant to BAI scores via HF index modulation. Conclusion: These results are the first to show that HTR1A ‐1019C/G polymorphism influences anxiety levels by modulating parasympathetic tone, providing a neurophysiological insight into the role of HTR1A in human anxiety. [ABSTRACT FROM AUTHOR]

Molybdenum disulfide (MoS2) is a typical two-dimensional material, which is widely used in many fields because of its excellent electrical and optical properties. In recent years, the high-quality growth of MoS2 has attracted more and more attention from researchers. Many studies have reported a two-step method for the production of MoS2 by pre-deposition of molybdenum (Mo) source and then vulcanization, which is cumbersome and time-consuming, and the preparation temperature is mostly above 800 °C, increasing energy consumption and experimental risk. In this paper, S source and Mo source can be distinguished by double temperature zone tube furnace to prepare MoS2 material in one-step method. The temperatures of S and Mo sources were designed separately, and the effect of each temperature on the quality of MoS2 was investigated. And the monolayer MoS2 with high crystalline quality was obtained at a S source temperature of 165 °C and a Mo source temperature of 680 °C. We produce MoS2 in one-step method at low temperature, which provides a reference for the synthesis of high-quality monolayer MoS2. [ABSTRACT FROM AUTHOR]

Recent studies have revealed that the inflammatory process plays a role in the pathogenesis of osteoarthritis (OA). The S100 family and receptor for advanced glycation end products (RAGE) participate in regulating inflammation, even in the production of matrix metalloproteinases (MMPs). MMP-1 degrades cartilage, which may result in OA development. Moreover, polymorphisms in RAGE, S100A8, and MMP-1 have a marked effect on ligand binding and transcription regulating. In this study, we investigated the potential genetic contribution of the RAGE, S100A8, and MMP-1 genes to OA. We performed a matched case-control association study and genotyped OA patients and healthy controls, who were analyzed by polymerase chain reaction-restriction fragment length polymorphism assays. A total of 207 patients were diagnosed with knee OA and underwent total knee replacement. The control group included 207 individuals who had standard X-rays of the knee joints to confirm K/L < 2 and were matched by age and gender. Single-nucleotide polymorphisms in RAGE (-429T/C, -374T/A, and 557G/A), S100A8 (rs3795391A/G), and MMP-1 (-1607 1G/2G, -755G/T, and -519A/G) were evaluated. RAGE -374T/A, S100A8 rs3795391A/G, MMP-1 -1607 1G/2G, -755G/T, and -519A/G showed no significant difference between OA patients and healthy controls. RAGE -429T/C and 557G/A showed a significant association between OA patients and healthy controls (P = 0.016 and 0.047, respectively). In haplotype analyses, no RAGE and MMP-1 haplotypes showed associations with OA. Our results suggest that the investigated polymorphism in the RAGE gene play a role in OA in the Han Chinese population.