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Peng Yin

Boston
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Articles

Carbon/Ceramic Composite Nanofillers Derived From Solid Carburizing for Enhancing High-Temperature Insulation Properties of Polymer Dielectrics

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By Shuimiao Xia, Peng Yin, Qingyang Tang
| Wiley Online Library Verified
, , , et al. “Carbon/Ceramic Composite Nanofillers Derived From Solid Carburizing for Enhancing High-Temperature Insulation Properties of Polymer Dielectrics.” Advanced Functional Materials (2026): e76595. https://doi.org/10.1002/adfm.76595 Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement The data that support the findings of this study are available from the corresponding author upon reasonable request.
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Effect of Wire Feed Speed on Microstructure and Mechanical Properties of 205C Aluminum Alloy in CMT+P-Based Arc Additive Manufacturing

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By Peng Yin, Zekai Wang, Ningbo Sub-academy
| Wiley Online Library Verified
Peng, Wang Zekai, Wang Lin, Effect of Wire Feed Speed on Microstructure and Mechanical Properties of 205C Aluminum Alloy in CMT+P-Based Arc Additive Manufacturing, Advanced Engineering Materials2026, 0, e70982. Yin https://doi.org/10.1002/adem.70982 Conflicts of Interest The authors declare no conflicts of interest Data Availability Statement The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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Caspase-4 transgenic mice exhibit cytoplasmic TDP-43 accumulation and age-dependent neuropathology

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By Qingqing Jia, Longhong Zhu, Dandan Li, Junqi Hou, Yue Zhao, Gaolu Zhu, Kaili Ou, Mingwei Guo, Xiangyi Liu, Xiao-Xin Yan, Su Yang, Dongsheng Fan, Shihua Li, Xiao-Jiang Li, Peng Yin, Zhenchun Nan, Huajie Dui, Li’an Huang
| Nature Verified
Abstract TAR DNA-binding protein (TDP-43) is a multifunctional protein that binds DNA and RNA within the nucleus. In neurodegenerative diseases like Amyotrophic Lateral Sclerosis (ALS), TDP-43 is mislocalized to the cytoplasm, forming inclusions. Current TDP-43 transgenic mouse models generally fail to exhibit significant cytoplasmic accumulation and loss of nuclear TDP-43, which hampers the investigation of cytoplasmic TDP-43 pathology.
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