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Can Liao

Showing results (211-220 of 262) with videos related to

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Tissue & Cell|June 4, 2025
Inhibition of the NLR pathway alleviates MAPK1 mutation-driven proliferation and differentiation deficits and enhanced apoptosis in P19 cellsTingying Lei, Lei Liu, Fei Guo, et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi|July 2, 2004
[A retrospective analysis on multiple cord blood transplantation in 13 cases]Can Liao, Xi Yang, Zun-Peng Xu, et al.
Human Genomics|February 4, 2026
Genetic architecture and prognostic significance of suspected fetal microcephaly: evidence from prenatal exome sequencing in a large prospective cohortFang Fu, Xing Wei, Chen Chen, et al.
Genes|September 23, 2022
Prenatal Diagnosis and Outcomes in Fetuses with HemivertebraHang Zhou, You Wang, Ruibin Huang, et al.
Molecular Cytogenetics|June 28, 2022
Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysisRuibin Huang, Hang Zhou, Fang Fu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|October 30, 2024
Multipoint Anionic Bridge: Asymmetric Solvation Structure Improves the Stability of Lithium-Ion BatteriesTianle Zheng, Tonghui Xu, Jianwei Xiong, et al.
Italian Journal of Pediatrics|August 21, 2024
Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary centerShujuan Yan, Qiuxia Yu, Hang Zhou, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 8, 2017
Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tractTing-Ying Lei, Fang Fu, Ru Li, et al.
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.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|January 8, 2024
Prenatal diagnosis and outcomes in fetuses with duplex kidneyChunling Ma, Ruibin Huang, Fang Fu, et al.
Pageof 27

Showing results (211-220 of 262) with videos related to

Sort By:
Pageof 27
Tissue & Cell|June 4, 2025
Inhibition of the NLR pathway alleviates MAPK1 mutation-driven proliferation and differentiation deficits and enhanced apoptosis in P19 cellsTingying Lei, Lei Liu, Fei Guo, et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi|July 2, 2004
[A retrospective analysis on multiple cord blood transplantation in 13 cases]Can Liao, Xi Yang, Zun-Peng Xu, et al.
Human Genomics|February 4, 2026
Genetic architecture and prognostic significance of suspected fetal microcephaly: evidence from prenatal exome sequencing in a large prospective cohortFang Fu, Xing Wei, Chen Chen, et al.
Genes|September 23, 2022
Prenatal Diagnosis and Outcomes in Fetuses with HemivertebraHang Zhou, You Wang, Ruibin Huang, et al.
Molecular Cytogenetics|June 28, 2022
Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysisRuibin Huang, Hang Zhou, Fang Fu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|October 30, 2024
Multipoint Anionic Bridge: Asymmetric Solvation Structure Improves the Stability of Lithium-Ion BatteriesTianle Zheng, Tonghui Xu, Jianwei Xiong, et al.
Italian Journal of Pediatrics|August 21, 2024
Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary centerShujuan Yan, Qiuxia Yu, Hang Zhou, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 8, 2017
Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tractTing-Ying Lei, Fang Fu, Ru Li, et al.
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.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|January 8, 2024
Prenatal diagnosis and outcomes in fetuses with duplex kidneyChunling Ma, Ruibin Huang, Fang Fu, et al.
Pageof 27