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Wenke Yang

Showing results (31-40 of 68) with videos related to

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Orphanet Journal of Rare Diseases|November 26, 2024
Novel biallelic variants in IREB2 cause an early-onset neurodegenerative disorder in a Chinese pedigreeZhenglong Guo, Dawei Huo, Yingying Shao, et al.
Biochemical and Biophysical Research Communications|November 4, 2021
d-mannose attenuates lipopolysaccharide-induced osteolysis via CPT1A-Mediated lipid metabolic regulation in macrophagesZhenzhen Zhang, Xueman Zhou, Jiaqi Liu, et al.
Frontiers in Aging|March 16, 2026
Ectoine attenuates H<sub>2</sub>O<sub>2</sub>-Induced cellular senescence in human keratinocytes and endothelial cells by modulating the p53/p21 and p16 pathwaysMeini Li, Jingyue Zhang, Wenke Yang, et al.
Frontiers in Cell and Developmental Biology|February 16, 2026
The D826V point mutation in <i>IREB2</i> induces lipogenesis in adipose tissuesYibing Lv, Chunyu Wu, Junyi Xiao, et al.
Frontiers in Medicine|May 14, 2025
Corrigendum: Pregnancy outcomes of 4,200 fetuses with increased nuchal translucency in Henan, ChinaZhenglong Guo, Wenke Yang, Qiongrui Zhao, et al.
Frontiers in Medicine|April 17, 2025
Pregnancy outcomes of 4,200 fetuses with increased nuchal translucency in Henan, ChinaZhenglong Guo, Wenke Yang, Qiongrui Zhao, et al.
Science Bulletin|January 19, 2023
Ultrasensitive strain sensor based on superhydrophobic microcracked conductive Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> MXene/paper for human-motion monitoring and E-skinYibing Bu, Taoyu Shen, Wenke Yang, et al.
Scientific Reports|December 19, 2025
Pan-cancer analysis of DTX3L as a potential prognostic and immunological biomarkerYunfeng Zhang, Jingyi Mu, Yue Lu, et al.
Journal of Molecular Neuroscience : MN|March 27, 2024
Competing Endogenous RNAs Crosstalk in Hippocampus: A Potential Mechanism for Neuronal Developing Defects in Down SyndromeHuiru Zhao, Guiyu Lou, Yupu Shao, et al.
Biological Research|December 9, 2023
Integration of ATAC-seq and RNA-seq identifies MX1-mediated AP-1 transcriptional regulation as a therapeutic target for Down syndromeZhenglong Guo, Yongchang Zhu, Hai Xiao, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
Orphanet Journal of Rare Diseases|November 26, 2024
Novel biallelic variants in IREB2 cause an early-onset neurodegenerative disorder in a Chinese pedigreeZhenglong Guo, Dawei Huo, Yingying Shao, et al.
Biochemical and Biophysical Research Communications|November 4, 2021
d-mannose attenuates lipopolysaccharide-induced osteolysis via CPT1A-Mediated lipid metabolic regulation in macrophagesZhenzhen Zhang, Xueman Zhou, Jiaqi Liu, et al.
Frontiers in Aging|March 16, 2026
Ectoine attenuates H<sub>2</sub>O<sub>2</sub>-Induced cellular senescence in human keratinocytes and endothelial cells by modulating the p53/p21 and p16 pathwaysMeini Li, Jingyue Zhang, Wenke Yang, et al.
Frontiers in Cell and Developmental Biology|February 16, 2026
The D826V point mutation in <i>IREB2</i> induces lipogenesis in adipose tissuesYibing Lv, Chunyu Wu, Junyi Xiao, et al.
Frontiers in Medicine|May 14, 2025
Corrigendum: Pregnancy outcomes of 4,200 fetuses with increased nuchal translucency in Henan, ChinaZhenglong Guo, Wenke Yang, Qiongrui Zhao, et al.
Frontiers in Medicine|April 17, 2025
Pregnancy outcomes of 4,200 fetuses with increased nuchal translucency in Henan, ChinaZhenglong Guo, Wenke Yang, Qiongrui Zhao, et al.
Science Bulletin|January 19, 2023
Ultrasensitive strain sensor based on superhydrophobic microcracked conductive Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> MXene/paper for human-motion monitoring and E-skinYibing Bu, Taoyu Shen, Wenke Yang, et al.
Scientific Reports|December 19, 2025
Pan-cancer analysis of DTX3L as a potential prognostic and immunological biomarkerYunfeng Zhang, Jingyi Mu, Yue Lu, et al.
Journal of Molecular Neuroscience : MN|March 27, 2024
Competing Endogenous RNAs Crosstalk in Hippocampus: A Potential Mechanism for Neuronal Developing Defects in Down SyndromeHuiru Zhao, Guiyu Lou, Yupu Shao, et al.
Biological Research|December 9, 2023
Integration of ATAC-seq and RNA-seq identifies MX1-mediated AP-1 transcriptional regulation as a therapeutic target for Down syndromeZhenglong Guo, Yongchang Zhu, Hai Xiao, et al.
Pageof 7