Achieving high-performance lead sulfide quantum dot (PbS QD)-based photodetectors requires enhanced carrier transfer, which inevitably leads to an increased dark current. Balancing a high photocurrent and low dark current is crucial. In this work, a bridge-trap structure constructed by the atomic layer deposition of dual oxides is proposed to simultaneously enhance photoresponse performance and reduce dark current.
View Article and Find Full Text PDFObjectives: During the COVID-19 pandemic, global health systems faced unprecedented challenges, as well as in maternal and neonatal health, thus this study aims to clarify the impacts of COVID-19 on maternal and neonatal disorders (MNDs), regional variations, and the role of economic support.
Methods: We have developed a counterfactual model integrating Autoregressive Integrated Moving Average and Long Short-Term Memory models to forecast the burden of MNDs from 2020 To et al., 2021, which was compared with the actual burden to quantify the specific impact of the COVID-19 pandemic on MNDs.
Background: The increasing prevalence of myopia among Chinese children and adolescents, especially at younger ages, has emerged as a significant concern in recent years. Pre-myopia is a key period for myopia prevention and control in children and adolescents. Previous studies suggested auricular acupressure (AA) therapy might offer a viable approach to prevent and slow down myopia progression.
View Article and Find Full Text PDFIn the present work, we examined the effects of exogenous abscisic acid (ABA) under ultraviolet B (UV-B) exposure on gibberellin (GA) production, signaling, and antioxidant-related genes in Pall (). Using transcriptomics, acetylated proteomics, and widely targeted metabolomics, the effects of UV-B stress on and the regulatory effects of exogenous ABA on it were revealed from multiple perspectives. The findings revealed that 's antioxidant enzyme genes were differentially expressed by UV-B radiation and were substantially enriched in the glutathione metabolic pathway.
View Article and Find Full Text PDFHutchinson-Gilford progeria syndrome (HGPS) is a pediatric condition characterized by clinical features that resemble accelerated aging. The abnormal accumulation of a toxic form of the lamin A protein known as progerin disrupts cellular functions, leading to various complications, including growth retardation, loss of subcutaneous fat, abnormal skin, alopecia, osteoporosis, and progressive joint contractures. Death primarily occurs as the result of complications from progressive atherosclerosis, especially from cardiac disease, such as myocardial infarction or heart failure, or cerebrovascular disease like stroke.
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