Editorial: Structure, function and development of neural circuits by Xiangmin Xu, Xiangmin Xu

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Octodon degus laboratory colony management principles and methods for behavioral analysis for Alzheimer’s disease neuroscience research by B. Maximiliano Garduño, Todd C. Holmes, Todd C. Holmes, Robert M. J. Deacon, Xiangmin Xu, Xiangmin Xu, Xiangmin Xu, Patricia Cogram, Patricia Cogram

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Ion Transport Mechanism in the Sub-Nano Channels of Edge-Capping Modified Transition Metal Carbides/Nitride Membranes by Yinan Li, Xiangmin Xu, Xiaofeng Fang, Fang Li

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Low-Rank Tensor Thresholding Ridge Regression by Kailing Guo, Tong Zhang, Xiangmin Xu, Xiaofen Xing

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Time-Varying ℓ0 Optimization for Spike Inference from Multi-Trial Calcium Recordings by Tong Shen, Mingyu Du, Kevin Johnston, Steven F. Grieco, Rachel Crary, John F. Guzowski, Gyorgy Lur, Xiangmin Xu, Hernando Ombao, Michele Guindani, Zhaoxia Yu

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Characterization of a weak allele of zebrafish cloche mutant. by Ning Ma, Zhibin Huang, Xiaohui Chen, Fei He, Kun Wang, Wei Liu, Linfeng Zhao, Xiangmin Xu, Wangjun Liao, Hua Ruan, Shenqiu Luo, Wenqing Zhang

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A one-base therapeutic insertion in the HBG2 distal promoter reactivates γ-globin expression by Xiuqin Bao, Yuanyi Gao, Xiaoyi Chen, Zhongju Wang, Xiaoqin Feng, Liren Wang, Jing Du, Yuhua Ye, Feijing Chen, Li Du, Aihua Yin, Xiangmin Xu

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A common TBP-binding site mutation elevates fetal hemoglobin levels by competitive globin switching change in β-thalassemia by Mengyang Song, Xiaolei Wei, Hualei Luo, Jueheng Wang, Yuhua Ye, Lang Qin, Chao Niu, Yong Long, Xingmin Wang, Congwen Shao, Miao Yu, Feng Gu, Xinhua Zhang, Xiangmin Xu

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A Chinese pediatric patient with thalassemia traits and compound heterozygous mutations in the PIEZO1 gene suspected of having dehydrated hereditary stomatocytosis by Weijie Chen, Xinyu Li, Huaqing Yang, Chao Niu, Yushan Huang, Lang Qin, Mingyan Fang, Shaofen Lin, Kaimei Wang, Yuan Zhuang, Yuhua Ye, Xin Jin, Jianpei Fang, Xiangmin Xu, Ke Huang, Honggui Xu

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Rewired m6A of promoter antisense RNAs in Alzheimer’s disease regulates neuronal genes in 3D nucleome by Benxia Hu, Yuqiang Shi, Feng Xiong, Yi-Ting Chen, Xiaoyu Zhu, Elisa Carrillo, Xingzhao Wen, Nathan Drolet, Chetan Singh Rajpurohit, Xiangmin Xu, Dung-Fang Lee, Claudio Soto, Sheng Zhong, Vasanthi Jayaraman, Hui Zheng, Wenbo Li

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A missense variant in the SOX5 gene (c.221C > T) is associated with intellectual disability by Xiujuan Yang, Zhongzhi Gan, Xiaoling Guo, Xiang Huang, Juan Liu, Yingchun Zheng, Xiaoqiang Zhou, Jingli Lian, Yue Liu, Tingting Yang, Chao Li, Fenying Chen, Fei He, Xiangmin Xu, Yasi Zhou, Qian Liu, Xingkun Yang, Fu Xiong

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Aggrecan protects against plaque accumulation and is essential for proper microglial responses to plaques by Rocio A. Barahona, Nellie E. Kwang, Aashna R. Kono-Soosaipillai, Giovanna Rubio Salgado, Kristine M. Tran, Yueh-Hao Lu, Siddharth Reddy, Celia da Cunha, Eric Velazquez-Rivera, Joshua D. Crapser, Xiangmin Xu, Lindsay A. Hohsfield, Kim N. Green

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Haplotype‐Resolved Genotyping and Association Analysis of 1,020 β‐Thalassemia Patients by Targeted Long‐Read Sequencing by Yuhua Ye, Chao Niu, Aiping Mao, Lang Qin, Jiahan Zhan, Weijie Chen, Zhentian Liu, Tiantian Xie, Qianqian Zhang, Jiaqi Li, Li Huang, Wanli Meng, Yumeng Liu, Liuhua Liao, Junqin Cai, Riyang Liu, Xinhua Zhang, Lihong Zeng, Yaoyun Li, Bin Lin, Kui Li, Xiaoyun Hua, Binbin Huang, Honggui Qin, Yueyan Huang, Zhijing Huang, Jinquan Lao, Xiang Qu, Juanjuan Chen, Xiaoqin Feng, Qiujun Liu, Wanying Lin, Xiaoman Zhou, Yidan Liang, Xingjiang Long, Jiaofeng Qin, Lixiang Yan, Weijian Zhu, Lian Yu, Chengwu Fan, Deguo Tang, Tianyu Zhong, Jufang Tan, Zhilin Ren, Xiangmin Xu

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