Publications by authors named "Xiaoxiao Zang"
Article Synopsis
- Fragile X Syndrome (FXS) is a genetic neurodevelopmental disorder linked to intellectual disabilities and autism, caused by an abnormal expansion of the CGG repeat in the FMR1 gene.
- Over 200 repeats silence the FMR1 gene, resulting in the absence of the Fragile X mental retardation protein (FMRP), which is crucial for normal brain development.
- Recent research highlights the importance of epigenetics in FXS, focusing on how gene expression can be modulated without altering DNA sequences, offering new potential avenues for treatment.
Constructing 3D/2D perovskite heterojunction is a promising approach to integrate the benefits of high efficiency and superior stability in perovskite solar cells (PSCs). However, in contrast to n-i-p architectural PSCs, the p-i-n PSCs with 3D/2D heterojunction have serious limitations in achieving high-performance as they suffer from a large energetic mismatch and electron extraction energy barrier from a 3D perovskite layer to a 2D perovskite layer, and serious nonradiative recombination at the heterojunction. Here a strategy of incorporating a thin passivating dipole layer (PDL) onto 3D perovskite and then depositing 2D perovskite without dissolving the underlying layer to form an efficient 3D/PDL/2D heterojunction is developed.
View Article and Find Full Text PDFBackground: Uterine fibroids(UF) are the most common benign tumors in women, with high incidence and unknown causes. We aimed to explore the correlation between Methylenetetra-hydrofolate reductase () polymorphism and UF.
Methods: This is a retrospective cohort study.