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排名必读论文期刊顶会热点AI 简史溯源树小脉星探人才迁徙塔尖人才国防情报追踪开源工具智慧手语
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论文共 93 篇作者统计合作学者相似作者

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Congenital disorder of glycosylation type Ia in a Chinese family: Function analysis of a novel PMM2 complex heterozygosis mutation
Dan Zhong, Xiujuan Huang, Taoshan Feng,Jieqing Zeng,Shanshan Gu,Fan Ning,Yue Yang, Jinyuan Zhu,Yajun Wang,Riling Chen,Guoda Ma
MOLECULAR GENETICS AND METABOLISM REPORTS (2024): 101067-101067
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Emerging roles of SIRT1 activator, SRT2104, in disease treatment
Ning Chang, Junyang Li, Sufen Lin,Jinfeng Zhang, Weiqiang Zeng,Guoda Ma,Yajun Wang
Scientific Reportsno. 1 (2024): 1-20
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Pan-cancer integrated analysis of ANKRD1 expression, prognostic value, and potential implications in cancer
Xusan Xu, Dan Zhong, Xiaoxia Wang,Fei Luo, Xiaomei Zheng, Taoshan Feng,Riling Chen,Yisen Cheng,Yajun Wang,Guoda Ma
Scientific Reportsno. 1 (2024): 1-17
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A syndrome featuring developmental disorder of the nervous system induced by a novel mutation in the TCF20 gene, rarely concurrent immune disorders: a case report
Si Huang, Jiaxin Xu,Yiyang Li, Wenhui Mo, Xiuwen Lin,Yajun Wang, Fujian Liang, Yan Bai, Guochun Huang, Jing Chen, Jing Xin,Guoda Ma
Frontiers in genetics (2023): 1192668
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The contribution of a novel PHEX gene mutation to X-linked hypophosphatemic rickets: a case report and an analysis of the gene mutation dosage effect in a rat model
Xiaoming Chen, Cijing Cai,Shaocong Lun,Qiuli Ye,Weiyuan Pan, Yushi Chen, Yuexuan Wu, Taoshan Feng, Faming Su, Choudi Ma, Jiaxin Luo,Meilian Liu,
FRONTIERS IN ENDOCRINOLOGY (2023): 1251718-1251718
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