Mei Daoqi相关文献与解析，生知库 | 链接生命科学的每一步

日期影响因子

Ertugliflozin improves animal behaviours associated with oxidative stress and inflammation in a BTBR T + Itpr3tf/J mouse model of autism.

Ertugliflozin 可改善 BTBR T + Itpr3tf/J 自闭症小鼠模型中与氧化应激和炎症相关的动物行为。

期刊:Brain Communications

影响因子:4.5

doi:10.1093/braincomms/fcag083

Wang Xiaona, Zhao Zhengqin, Sun Limin, Gao Chao, Wang Li, Mei Daoqi, Hao Chanjuan, Zhao Shuai, Yan Xingxue, Liu Jing, Liu Lei, Guo Bin, Zhang Yaodong

Immunology/Inflammation

发表日期：2026

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Somatostatin-expressing interneurons of prefrontal cortex modulate social deficits in the Magel2 mouse model of autism.

前额叶皮层中表达生长抑素的中间神经元可以调节 Magel2 自闭症小鼠模型的社交缺陷

期刊:Molecular Autism

影响因子:5.5

doi:10.1186/s13229-025-00653-5

Wang Xiaona, Chen Mengyuan, Mei Daoqi, Shi Shengli, Guo Jisheng, Gao Chao, Wang Qi, Zhao Shuai, Yan Xingxue, Zhang Huichun, Wang Yanli, Guo Bin, Zhang Yaodong

发表日期：2025

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Spinal muscular atrophy with progressive myoclonic epilepsy: A case report from China with new ASAH1 variants

脊髓性肌萎缩症伴进行性肌阵挛性癫痫：来自中国的一例ASAH1新变异病例报告

影响因子:3.6

doi:10.1016/j.heliyon.2024.e41032

Yin, Xiaojing; Shi, Jinghe; Mei, Daoqi; Guo, Jianmei; Ma, Tingting; Gao, Yuna; Wang, Li; Deng, Jie

发表日期：2025

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Identification of three novel GNAO1 variants in a Chinese cohort with GNAO1 encephalopathy: expanding the clinical and genetic spectrum

在中国GNAO1脑病患者队列中鉴定出三种新的GNAO1变异：拓展了临床和遗传谱。

期刊:Orphanet Journal of Rare Diseases

影响因子:3.5

doi:10.1186/s13023-025-03984-x

Mei, Daoqi; Gu, Yu; Zhang, Bingbing; Mei, Shiyue; Wang, Xiaona; Ma, Yuanning; Deng, Jie; Tang, Jihong

发表日期：2025

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Deficiency of calretinin in prefrontal cortex causes behavioral deficits relevant to autism spectrum disorder in mice.

小鼠前额皮质中钙网蛋白的缺乏会导致与自闭症谱系障碍相关的行为缺陷

期刊:Molecular Brain

影响因子:2.9

doi:10.1186/s13041-025-01233-7

Zhang Yaodong, Zhao Xiaotong, Gao Chao, Shi Shengli, Chen Mengyuan, Guo Bin, Hu Shunan, Mei Daoqi, Duan Xujun, Wang Xiaona

发表日期：2025

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Genetic analysis of four cases of Poirier Bienvenu neurodevelopmental syndrome associated with CSNK2B variant

对四例与CSNK2B变异相关的Poirier-Bienvenu神经发育综合征病例进行基因分析

期刊:BMC Medical Genomics

doi:10.1186/s12920-025-02132-5

Yang, Liu; Mei, Daoqi; Liu, Yanping; Gao, Li

发育与干细胞

发表日期：2025

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Evaluating the relationship between the proportion of X-chromosome deletions and clinical manifestations in children with turner syndrome

评估特纳综合征患儿X染色体缺失比例与临床表现之间的关系

期刊:Frontiers in Endocrinology

影响因子:4.6

doi:10.3389/fendo.2024.1324160

Wang, Gaowei; Liu, Xiaojing; Wang, Meiye; Wang, Jin; Zhang, Zhenhua; Allegaert, Karel; Mei, Daoqi; Zhang, Yaodong; Luo, Shuying; Fang, Yang; Li, Dongxiao; Chen, Yongxing; Wei, Haiyan

发表日期：2024

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Case report: Second report of neuromuscular syndrome caused by biallelic variants in ASCC3

病例报告：ASCC3基因双等位基因变异引起的神经肌肉综合征的第二例报告

期刊:Frontiers in Genetics

影响因子:2.8

doi:10.3389/fgene.2024.1382275

Li, Wang; Li, Zhongliang; Fu, Junhui; Xu, Kaili; Mei, Daoqi; Wang, Xiaona; Li, Taisong; Du, Xilong

发表日期：2024

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Epilepsy in Dravet Syndrome-Current and Future Therapeutic Opportunities

Dravet综合征中的癫痫——当前和未来的治疗机遇

期刊:Journal of Clinical Medicine

影响因子:2.9

doi:10.3390/jcm12072532

Gao, Chao; Pielas, Mikolaj; Jiao, Fuyong; Mei, Daoqi; Wang, Xiaona; Kotulska, Katarzyna; Jozwiak, Sergiusz

发表日期：2023

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Subependymal Giant Cell Astrocytomas in Tuberous Sclerosis Complex-Current Views on Their Pathogenesis and Management

结节性硬化症室管膜下巨细胞星形细胞瘤——其发病机制和治疗的最新观点

期刊:Journal of Clinical Medicine

影响因子:2.9

doi:10.3390/jcm12030956

Gao, Chao; Zabielska, Bernadeta; Jiao, Fuyong; Mei, Daoqi; Wang, Xiaona; Kotulska, Katarzyna; Jozwiak, Sergiusz

细胞生物学

发表日期：2023

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