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Ruixue Zhang

Showing results (221-230 of 250) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|October 8, 2024
Identification of novel variants in hereditary spherocytosis patients by whole-exome sequencingLi Qin, Yujiao Jia, Haoxu Wang, et al.
Cancer Medicine|March 6, 2025
Impact of ASXL1 Gene Alterations on Myelodysplastic Syndrome With Isolated 20q DeletionYanan Chang, Linlin Liu, Chenghua Cui, et al.
Frontiers in Genetics|January 3, 2022
Fine-Mapping of the Major Histocompatibility Complex Region Linked to Leprosy in Northern ChinaRuixue Zhang, Lu Cao, Weiwei Chen, et al.
Scientific Reports|April 11, 2025
Covariation of scleral remodeling and PI3K/Akt signaling pathway in experimental myopiaXiaomeng Li, Xiaojing Liu, Yingxin Yu, et al.
Experimental & Molecular Medicine|July 3, 2025
Single-cell RNA sequencing reveals anterograde trans-synaptic degeneration and exacerbated synaptic remodeling in myopiaRuixue Zhang, Yunxiao Xie, Miao Zhang, et al.
Journal of Animal Physiology and Animal Nutrition|January 25, 2020
Dietary thymol supplementation promotes skeletal muscle fibre type switch in longissimus dorsi of finishing pigsPei Luo, Lv Luo, Weijie Zhao, et al.
Pharmacological Research|May 10, 2021
Food reward depends on TLR4 activation in dopaminergic neuronsYongxiang Li, Lvshuang Chen, Weijie Zhao, et al.
Clinical Rheumatology|July 19, 2022
Rare mutations in NLRP3 and NLRP12 associated with familial cold autoinflammatory syndrome: two Chinese pedigreesShirui Chen, Zhen Li, Xia Hu, et al.
Molecular Genetics & Genomic Medicine|March 30, 2022
Gene interaction analysis of psoriasis in Chinese Han populationQiongqiong Xu, Xiaodong Zheng, Yiwen Mao, et al.
Bioscience Reports|February 10, 2021
Development of a mutation hotspot detection kit for the phenylalanine hydroxylase gene by ARMS-PCR combined with fluorescent probe technologyRong Qiang, Lin Wang, JinHua He, et al.
Pageof 25

Showing results (221-230 of 250) with videos related to

Sort By:
Pageof 25
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 8, 2024
Identification of novel variants in hereditary spherocytosis patients by whole-exome sequencingLi Qin, Yujiao Jia, Haoxu Wang, et al.
Cancer Medicine|March 6, 2025
Impact of ASXL1 Gene Alterations on Myelodysplastic Syndrome With Isolated 20q DeletionYanan Chang, Linlin Liu, Chenghua Cui, et al.
Frontiers in Genetics|January 3, 2022
Fine-Mapping of the Major Histocompatibility Complex Region Linked to Leprosy in Northern ChinaRuixue Zhang, Lu Cao, Weiwei Chen, et al.
Scientific Reports|April 11, 2025
Covariation of scleral remodeling and PI3K/Akt signaling pathway in experimental myopiaXiaomeng Li, Xiaojing Liu, Yingxin Yu, et al.
Experimental & Molecular Medicine|July 3, 2025
Single-cell RNA sequencing reveals anterograde trans-synaptic degeneration and exacerbated synaptic remodeling in myopiaRuixue Zhang, Yunxiao Xie, Miao Zhang, et al.
Journal of Animal Physiology and Animal Nutrition|January 25, 2020
Dietary thymol supplementation promotes skeletal muscle fibre type switch in longissimus dorsi of finishing pigsPei Luo, Lv Luo, Weijie Zhao, et al.
Pharmacological Research|May 10, 2021
Food reward depends on TLR4 activation in dopaminergic neuronsYongxiang Li, Lvshuang Chen, Weijie Zhao, et al.
Clinical Rheumatology|July 19, 2022
Rare mutations in NLRP3 and NLRP12 associated with familial cold autoinflammatory syndrome: two Chinese pedigreesShirui Chen, Zhen Li, Xia Hu, et al.
Molecular Genetics & Genomic Medicine|March 30, 2022
Gene interaction analysis of psoriasis in Chinese Han populationQiongqiong Xu, Xiaodong Zheng, Yiwen Mao, et al.
Bioscience Reports|February 10, 2021
Development of a mutation hotspot detection kit for the phenylalanine hydroxylase gene by ARMS-PCR combined with fluorescent probe technologyRong Qiang, Lin Wang, JinHua He, et al.
Pageof 25