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Ying Lei

Showing results (481-490 of 594) with videos related to

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Human Genetics|July 23, 2020
Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart diseaseFang Fu, Ru Li, Ting-Ying Lei, et al.
Blood|June 11, 2021
Single-cell analysis of ploidy and the transcriptome reveals functional and spatial divergency in murine megakaryopoiesisShu Sun, Chen Jin, Jia Si, et al.
Acta Pharmacologica Sinica|September 12, 2020
SAF-189s, a potent new-generation ROS1 inhibitor, is active against crizotinib-resistant ROS1 mutant-driven tumorsZong-Jun Xia, Yin-Chun Ji, De-Qiao Sun, et al.
Molecular Cell|June 24, 2025
BAG2 releases SAMD4B upon sensing of arginine deficiency to promote tumor cell survivalMeng-Ying Chen, Chun-Yu Sun, Ru Zhao, et al.
Genomics, Proteomics & Bioinformatics|February 5, 2022
Single-cell Transcriptomic Analysis Reveals the Cellular Heterogeneity of Mesenchymal Stem CellsChen Zhang, Xueshuai Han, Jingkun Liu, et al.
Journal of Immunology Research|February 10, 2023
House Dust Mite and Cat Dander Extract Induce Asthma-Like Histopathology with an Increase of Mucosal Mast Cells in a Guinea Pig ModelPatricia Ramos-Ramírez, Jielu Liu, Sofia Mogren, et al.
Journal of Thrombosis and Haemostasis : JTH|March 27, 2024
SET domain containing 2 promotes megakaryocyte polyploidization and platelet generation through methylation of α-tubulinLei Chen, Jingkun Liu, Kunying Chen, et al.
Cellular Signalling|May 30, 2015
The BARD1 BRCT domain contributes to p53 binding, cytoplasmic and mitochondrial localization, and apoptotic functionVarsha Tembe, Estefania Martino-Echarri, Kamila A Marzec, et al.
Journal of Cellular Biochemistry|January 22, 2020
All-trans-retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3β signaling pathwayFang Fu, Lu-Shan Li, Ru Li, et al.
Bioorganic & Medicinal Chemistry Letters|December 27, 2011
The discovery of potent antagonists of NPBWR1 (GPR7)F Anthony Romero, Nicholas B Hastings, Remond Moningka, et al.
Pageof 60

Showing results (481-490 of 594) with videos related to

Sort By:
Pageof 60
Human Genetics|July 23, 2020
Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart diseaseFang Fu, Ru Li, Ting-Ying Lei, et al.
Blood|June 11, 2021
Single-cell analysis of ploidy and the transcriptome reveals functional and spatial divergency in murine megakaryopoiesisShu Sun, Chen Jin, Jia Si, et al.
Acta Pharmacologica Sinica|September 12, 2020
SAF-189s, a potent new-generation ROS1 inhibitor, is active against crizotinib-resistant ROS1 mutant-driven tumorsZong-Jun Xia, Yin-Chun Ji, De-Qiao Sun, et al.
Molecular Cell|June 24, 2025
BAG2 releases SAMD4B upon sensing of arginine deficiency to promote tumor cell survivalMeng-Ying Chen, Chun-Yu Sun, Ru Zhao, et al.
Genomics, Proteomics & Bioinformatics|February 5, 2022
Single-cell Transcriptomic Analysis Reveals the Cellular Heterogeneity of Mesenchymal Stem CellsChen Zhang, Xueshuai Han, Jingkun Liu, et al.
Journal of Immunology Research|February 10, 2023
House Dust Mite and Cat Dander Extract Induce Asthma-Like Histopathology with an Increase of Mucosal Mast Cells in a Guinea Pig ModelPatricia Ramos-Ramírez, Jielu Liu, Sofia Mogren, et al.
Journal of Thrombosis and Haemostasis : JTH|March 27, 2024
SET domain containing 2 promotes megakaryocyte polyploidization and platelet generation through methylation of α-tubulinLei Chen, Jingkun Liu, Kunying Chen, et al.
Cellular Signalling|May 30, 2015
The BARD1 BRCT domain contributes to p53 binding, cytoplasmic and mitochondrial localization, and apoptotic functionVarsha Tembe, Estefania Martino-Echarri, Kamila A Marzec, et al.
Journal of Cellular Biochemistry|January 22, 2020
All-trans-retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3β signaling pathwayFang Fu, Lu-Shan Li, Ru Li, et al.
Bioorganic & Medicinal Chemistry Letters|December 27, 2011
The discovery of potent antagonists of NPBWR1 (GPR7)F Anthony Romero, Nicholas B Hastings, Remond Moningka, et al.
Pageof 60