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Jianfan Chen

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

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IEEE Transactions on Pattern Analysis and Machine Intelligence|May 27, 2026
Multi-source Fusion Positioning Revisited by Drawing on Human Thinking ProcessJianfan Chen, Qingquan Li, Ke Dong, et al.
Oncology Letters|January 19, 2018
Anticancer effect of triterpenes from <i>Ganoderma lucidum</i> in human prostate cancer cellsLijun Qu, Sumei Li, Yumin Zhuo, et al.
Canadian Journal of Microbiology|March 30, 2016
Study of the diversity of microbial communities in a sequencing batch reactor oxic-settling-anaerobic process and its modified processLianpeng Sun, Jianfan Chen, Xiange Wei, et al.
Molecular Genetics and Genomics : MGG|February 10, 2021
A female carrier of a novel DMD mutation with slightly skewed X-chromosome inactivation shows a suspected case of Becker muscular dystrophy in a Chinese familyJianfan Chen, Hui Zheng, Zhongju Wang, et al.
Clinical Oral Investigations|October 3, 2020
The gain-of-function FAM83H mutation caused hypocalcification amelogenesis imperfecta in a Chinese familyYingchun Zheng, Ting Lu, Jianfan Chen, et al.
Scientific Reports|February 21, 2025
Comparative study of third-generation sequencing-based CASMA-trio and STR linkage analysis for identifying SMN1 2 + 0 carriersJianchun He, Wenzhi He, Jiajia Xian, et al.
Clinical Science (London, England : 1979)|August 23, 2017
Genetic diagnosis of polycystic kidney disease, Alport syndrome, and thalassemia minor in a large Chinese familyYun Miao, Jun Xiong, Xuelian Zhang, et al.
Oxidative Medicine and Cellular Longevity|October 4, 2022
Pyrocatechol Alleviates Cisplatin-Induced Acute Kidney Injury by Inhibiting ROS ProductionXuexia Xie, Fan Wu, Jiaxin Tian, et al.
BMC Oral Health|May 14, 2026
Identification of a rare missense variant in the gene SPATA31H1 associated with hereditary gingival fibromatosis in a large Chinese familyWanqing Wang, Jialin Xu, Shuning Du, et al.
International Journal of Oral Science|September 26, 2023
Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosisJianfan Chen, Xueqing Xu, Song Chen, et al.
Pageof 1

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

Sort By:
Pageof 1
IEEE Transactions on Pattern Analysis and Machine Intelligence|May 27, 2026
Multi-source Fusion Positioning Revisited by Drawing on Human Thinking ProcessJianfan Chen, Qingquan Li, Ke Dong, et al.
Oncology Letters|January 19, 2018
Anticancer effect of triterpenes from <i>Ganoderma lucidum</i> in human prostate cancer cellsLijun Qu, Sumei Li, Yumin Zhuo, et al.
Canadian Journal of Microbiology|March 30, 2016
Study of the diversity of microbial communities in a sequencing batch reactor oxic-settling-anaerobic process and its modified processLianpeng Sun, Jianfan Chen, Xiange Wei, et al.
Molecular Genetics and Genomics : MGG|February 10, 2021
A female carrier of a novel DMD mutation with slightly skewed X-chromosome inactivation shows a suspected case of Becker muscular dystrophy in a Chinese familyJianfan Chen, Hui Zheng, Zhongju Wang, et al.
Clinical Oral Investigations|October 3, 2020
The gain-of-function FAM83H mutation caused hypocalcification amelogenesis imperfecta in a Chinese familyYingchun Zheng, Ting Lu, Jianfan Chen, et al.
Scientific Reports|February 21, 2025
Comparative study of third-generation sequencing-based CASMA-trio and STR linkage analysis for identifying SMN1 2 + 0 carriersJianchun He, Wenzhi He, Jiajia Xian, et al.
Clinical Science (London, England : 1979)|August 23, 2017
Genetic diagnosis of polycystic kidney disease, Alport syndrome, and thalassemia minor in a large Chinese familyYun Miao, Jun Xiong, Xuelian Zhang, et al.
Oxidative Medicine and Cellular Longevity|October 4, 2022
Pyrocatechol Alleviates Cisplatin-Induced Acute Kidney Injury by Inhibiting ROS ProductionXuexia Xie, Fan Wu, Jiaxin Tian, et al.
BMC Oral Health|May 14, 2026
Identification of a rare missense variant in the gene SPATA31H1 associated with hereditary gingival fibromatosis in a large Chinese familyWanqing Wang, Jialin Xu, Shuning Du, et al.
International Journal of Oral Science|September 26, 2023
Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosisJianfan Chen, Xueqing Xu, Song Chen, et al.
Pageof 1