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Yangfan Qi

Showing results (1-10 of 35) with videos related to

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Frontiers in Medicine|April 2, 2026
A case report of X-linked ichthyosis associated with epilepsy due to an <i>Xp22.31</i> deletion fragmentYangfan Qi, Shuangzhu Lin, Yanqiu Zhou, et al.
Medicine|February 3, 2026
Concurrent 12p trisomy and 4q34.2-q35.2 deletion detected by WES-CNV: Case reportXiaoyu Sun, Shuangzhu Lin, Wanqi Wang, et al.
Frontiers in Pediatrics|November 5, 2025
<i>De novo</i> frameshift mutation in SYNGAP1 resulting in autosomal dominant mental retardation type 5 and autism spectrum disorder: a case reportShuangzhu Lin, Yangfan Qi, Hongyan Xie, et al.
Drug Design, Development and Therapy|June 29, 2026
Tubulin Post-Translational Modifications in Cardiovascular Diseases: Emerging Mechanisms and Therapeutic Modulation by Traditional Chinese MedicineYangfan Qi, Yiyi Zhou, Xinyue Ning, et al.
Frontiers in Pediatrics|November 10, 2025
<i>De novo</i> missense mutation in <i>MYT1l</i> leading to autosomal dominant intellectual disability 39 and autism spectrum disorder: a case reportXin Wang, Shuangzhu Lin, Yang Chen, et al.
Frontiers in Pediatrics|June 1, 2026
Navigating the complexities of dual CNV findings: a case of DEE7 caused by a <i>de novo KCNQ2</i> deletion and a Co-occurring chromosome 13 duplication - a case report and literature reviewYangfan Qi, Shuangzhu Lin, Ying Zhou, et al.
Medicine|January 10, 2026
Cartilage-hair hypoplasia in a patient with compound heterozygous variants in the RMRP gene: A case reportShuangzhu Lin, Qiandui Chen, Yangfan Qi, et al.
Cancer Biotherapy & Radiopharmaceuticals|June 7, 2025
PGC-1α Promotes NSCLC Progression via FOXM1 Interaction and MUC1 UpregulationTianyi Zhang, Zhuoshi Li, Shiqing Wang, et al.
Heliyon|July 7, 2023
Aurora kinase A regulates cancer-associated RNA aberrant splicing in breast cancerSisi Li, Yangfan Qi, Jiachuan Yu, et al.
Medicine|June 16, 2023
A case of Sandhoff disease caused by a novel β-hexosaminidase B (HEXB) mutation c.118delG (p.A40fs*24): A case report from ChinaHongyan Xie, Shuangzhu Lin, Yang Chen, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Frontiers in Medicine|April 2, 2026
A case report of X-linked ichthyosis associated with epilepsy due to an <i>Xp22.31</i> deletion fragmentYangfan Qi, Shuangzhu Lin, Yanqiu Zhou, et al.
Medicine|February 3, 2026
Concurrent 12p trisomy and 4q34.2-q35.2 deletion detected by WES-CNV: Case reportXiaoyu Sun, Shuangzhu Lin, Wanqi Wang, et al.
Frontiers in Pediatrics|November 5, 2025
<i>De novo</i> frameshift mutation in SYNGAP1 resulting in autosomal dominant mental retardation type 5 and autism spectrum disorder: a case reportShuangzhu Lin, Yangfan Qi, Hongyan Xie, et al.
Drug Design, Development and Therapy|June 29, 2026
Tubulin Post-Translational Modifications in Cardiovascular Diseases: Emerging Mechanisms and Therapeutic Modulation by Traditional Chinese MedicineYangfan Qi, Yiyi Zhou, Xinyue Ning, et al.
Frontiers in Pediatrics|November 10, 2025
<i>De novo</i> missense mutation in <i>MYT1l</i> leading to autosomal dominant intellectual disability 39 and autism spectrum disorder: a case reportXin Wang, Shuangzhu Lin, Yang Chen, et al.
Frontiers in Pediatrics|June 1, 2026
Navigating the complexities of dual CNV findings: a case of DEE7 caused by a <i>de novo KCNQ2</i> deletion and a Co-occurring chromosome 13 duplication - a case report and literature reviewYangfan Qi, Shuangzhu Lin, Ying Zhou, et al.
Medicine|January 10, 2026
Cartilage-hair hypoplasia in a patient with compound heterozygous variants in the RMRP gene: A case reportShuangzhu Lin, Qiandui Chen, Yangfan Qi, et al.
Cancer Biotherapy & Radiopharmaceuticals|June 7, 2025
PGC-1α Promotes NSCLC Progression via FOXM1 Interaction and MUC1 UpregulationTianyi Zhang, Zhuoshi Li, Shiqing Wang, et al.
Heliyon|July 7, 2023
Aurora kinase A regulates cancer-associated RNA aberrant splicing in breast cancerSisi Li, Yangfan Qi, Jiachuan Yu, et al.
Medicine|June 16, 2023
A case of Sandhoff disease caused by a novel β-hexosaminidase B (HEXB) mutation c.118delG (p.A40fs*24): A case report from ChinaHongyan Xie, Shuangzhu Lin, Yang Chen, et al.
Pageof 4