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Shiyu Luo

Showing results (21-30 of 107) with videos related to

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Frontiers in Oncology|January 30, 2026
Fish bone foreign body causing rectal, uterine, and bladder perforation: a rare case reportShiyu Luo, Bo Gou, Tengyu Zeng, et al.
Drug Discovery Today|April 3, 2025
Covalent inhibitors possessing autophagy-modulating capabilities: charting novel avenues in drug design and discoveryYutong Wang, Shiyu Luo, Hongbao Sun, et al.
Circulation. Genomic and Precision Medicine|April 2, 2021
Homozygous <i>SPEG</i> Mutation Is Associated With Isolated Dilated CardiomyopathyMohammed Almannai, Shiyu Luo, Eissa Faqeih, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|July 24, 2015
Decreased expression of MicroRNA-200 family in human breast cancer is associated with lymph node metastasisFeng Xu, Hua He, Wen Huang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 1, 2016
[Analysis of CGG repeat instability in germline cells from two male fetuses affected with fragile X syndrome]Ranhui Duan, Shiyu Luo, Wen Huang, et al.
International Journal of Molecular Sciences|August 23, 2020
Correction: Li, et al. LncRNA NEAT1 Silenced miR-133b Promotes Migration and Invasion of Breast Cancer Cells. <i>Int. J. Mol. Sci.</i> 2019, <i>20</i>, 3616Xinping Li, Siwei Deng, Xinyao Pang, et al.
Molecular Genetics & Genomic Medicine|June 2, 2015
Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese populationWen Huang, Qiuping Xia, Shiyu Luo, et al.
International Journal of Molecular Sciences|July 27, 2019
LncRNA NEAT1 Silenced miR-133b Promotes Migration and Invasion of Breast Cancer CellsXinping Li, Siwei Deng, Xinyao Pang, et al.
BMC Medical Genetics|November 26, 2014
Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case reportShiyu Luo, Wen Huang, Qiuping Xia, et al.
Scientific Reports|April 13, 2017
The Phosphatidylcholine Transfer Protein Stard7 is Required for Mitochondrial and Epithelial Cell HomeostasisLi Yang, Cheng-Lun Na, Shiyu Luo, et al.
Pageof 11

Showing results (21-30 of 107) with videos related to

Sort By:
Pageof 11
Frontiers in Oncology|January 30, 2026
Fish bone foreign body causing rectal, uterine, and bladder perforation: a rare case reportShiyu Luo, Bo Gou, Tengyu Zeng, et al.
Drug Discovery Today|April 3, 2025
Covalent inhibitors possessing autophagy-modulating capabilities: charting novel avenues in drug design and discoveryYutong Wang, Shiyu Luo, Hongbao Sun, et al.
Circulation. Genomic and Precision Medicine|April 2, 2021
Homozygous <i>SPEG</i> Mutation Is Associated With Isolated Dilated CardiomyopathyMohammed Almannai, Shiyu Luo, Eissa Faqeih, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|July 24, 2015
Decreased expression of MicroRNA-200 family in human breast cancer is associated with lymph node metastasisFeng Xu, Hua He, Wen Huang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 1, 2016
[Analysis of CGG repeat instability in germline cells from two male fetuses affected with fragile X syndrome]Ranhui Duan, Shiyu Luo, Wen Huang, et al.
International Journal of Molecular Sciences|August 23, 2020
Correction: Li, et al. LncRNA NEAT1 Silenced miR-133b Promotes Migration and Invasion of Breast Cancer Cells. <i>Int. J. Mol. Sci.</i> 2019, <i>20</i>, 3616Xinping Li, Siwei Deng, Xinyao Pang, et al.
Molecular Genetics & Genomic Medicine|June 2, 2015
Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese populationWen Huang, Qiuping Xia, Shiyu Luo, et al.
International Journal of Molecular Sciences|July 27, 2019
LncRNA NEAT1 Silenced miR-133b Promotes Migration and Invasion of Breast Cancer CellsXinping Li, Siwei Deng, Xinyao Pang, et al.
BMC Medical Genetics|November 26, 2014
Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case reportShiyu Luo, Wen Huang, Qiuping Xia, et al.
Scientific Reports|April 13, 2017
The Phosphatidylcholine Transfer Protein Stard7 is Required for Mitochondrial and Epithelial Cell HomeostasisLi Yang, Cheng-Lun Na, Shiyu Luo, et al.
Pageof 11