日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Comparison of efficacy of exosomes derived from human umbilical cord blood mesenchymal stem cells in treating mouse acute lung injury via different routes.

比较人脐带血间充质干细胞来源的外泌体通过不同途径治疗小鼠急性肺损伤的疗效

期刊:Frontiers in Pediatrics
影响因子:2
doi:10.3389/fped.2025.1560915
Chen Jing, Liu Shuang, Zou Jizhen, Wang Yi, Ge Haiyan, Hui Yi, Huang Siyuan, Li Wei, Na Weilan, Huang Xiaolan, Bai Lin, Huang Yiying, Qu Dong
发育与干细胞
细胞生物学
Human
Mouse
外泌体
发表日期：2025
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A mosaic karyotype of 45,X/46,X,psu idic(Y)(q12) in a ten-year-old boy: integrating high-throughput sequencing with cytogenetic technique for precise diagnosis and genetic counselling

一名十岁男孩的嵌合核型为45,X/46,X,psuidic(Y)(q12)：结合高通量测序和细胞遗传学技术进行精准诊断和遗传咨询

期刊:BMC Pediatrics
影响因子:2
doi:10.1186/s12887-023-03872-y
Yin, Hui; Xie, Hua; Zou, Jizhen; Ye, Xue; Liu, Ying; He, Cai; Shangguan, Shaofang; Liu, Haoran; Chen, Xiaoli; Chen, Xiaobo
细胞生物学
发表日期：2023
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Quantitative Measurement of PARD3 Copy Number Variations in Human Neural Tube Defects

人类神经管缺陷中PARD3拷贝数变异的定量测量

期刊:Cellular and Molecular Neurobiology
影响因子:4.8
doi:10.1007/s10571-017-0506-0
Gao, Yonghui; Wang, Jianhua; Shangguan, Shaofang; Bao, Yihua; Lu, Xiaoli; Zou, Jizhen; Dai, Yaohua; Liu, Junling; Zhang, Ting
Human
发表日期：2018
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Sporadic Hirschsprung Disease: Mutational Spectrum and Novel Candidate Genes Revealed by Next-generation Sequencing

散发性先天性巨结肠：新一代测序揭示的突变谱和新的候选基因

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-017-14835-6
Zhang, Zhen; Li, Qi; Diao, Mei; Liu, Na; Cheng, Wei; Xiao, Ping; Zou, Jizhen; Su, Lin; Yu, Kaihui; Wu, Jian; Li, Long; Jiang, Qian
发表日期：2017
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Detection of copy number variants reveals association of cilia genes with neural tube defects

拷贝数变异的检测揭示了纤毛基因与神经管缺陷的关联

期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0054492
Chen, Xiaoli; Shen, Yiping; Gao, Yonghui; Zhao, Huizhi; Sheng, Xiaoming; Zou, Jizhen; Lip, Va; Xie, Hua; Guo, Jin; Shao, Hong; Bao, Yihua; Shen, Jianliang; Niu, Bo; Gusella, James F; Wu, Bai-Lin; Zhang, Ting
发表日期：2013
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The maternal folate hydrolase gene polymorphism is associated with neural tube defects in a high-risk Chinese population

母体叶酸水解酶基因多态性与中国高危人群的神经管缺陷相关

期刊:
影响因子:
doi:10.1007/s12263-012-0309-3
Guo, Jin; Xie, Hua; Wang, Jianhua; Zhao, Huizhi; Wang, Fang; Liu, Chi; Wang, Li; Lu, Xiaolin; Bao, Yihua; Zou, Jizhen; Wang, Guoliang; Niu, Bo; Zhang, Ting
发表日期：2013
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PCMT1 gene polymorphisms, maternal folate metabolism, and neural tube defects: a case-control study in a population with relatively low folate intake

PCMT1基因多态性、母体叶酸代谢与神经管缺陷：一项针对叶酸摄入量相对较低的人群的病例对照研究

期刊:
影响因子:
doi:10.1007/s12263-013-0355-5
Wang, Fang; Wang, Jianhua; Guo, Jin; Chen, Xiaoli; Guan, Zhen; Zhao, Huizhi; Xie, Hua; Liu, Chi; Bao, Yihua; Zou, Jizhen; Niu, Bo; Zhang, Ting
代谢
发表日期：2013
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