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Yaping Liu

Showing results (381-390 of 572) with videos related to

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Orphanet Journal of Rare Diseases|June 11, 2024
A novel variant in the SLCO2A1 gene in a Chinese patient with chronic gastroenteropathy and primary hypertrophic osteoarthropathyYimin Dai, Miao He, Hui Xu, et al.
Optics Express|May 3, 2018
Weakly-coupled 4-mode step-index FMF and demonstration of IM/DD MDM transmissionTao Hu, Juhao Li, Dawei Ge, et al.
Angewandte Chemie (International Ed. in English)|August 3, 2023
Total Biosynthesis of Melleolides from Basidiomycota Fungi: Mechanistic Analysis of the Multifunctional GMC Oxidase Mld7Mitsunori Fukaya, Shota Nagamine, Taro Ozaki, et al.
Optics Express|May 4, 2026
On-chip electro-optic modulator with solution-processed colloidal In<sub>2</sub>O<sub>3</sub> nanocrystalsPeng Liu, Xiaotong Zhang, Jiaying Tian, et al.
BMC Complementary and Alternative Medicine|February 9, 2017
Antibacterial and antioxidant properties of crude extract, fractions and compounds from the stem bark of Polyscias fulva Hiern (Araliaceae)Guy Sedar Singor Njateng, Zhizhi Du, Donatien Gatsing, et al.
Therapeutic Advances in Respiratory Disease|February 28, 2026
Genetic strategies for negative or variant of uncertain significance findings in exome sequencing in hereditary bronchiectasis: a case seriesWangji Zhou, Yixuan Li, Qiaoling Chen, et al.
Cell Death & Disease|October 6, 2017
Calcium/calmodulin-dependent kinase kinase 2 regulates hematopoietic stem and progenitor cell regenerationLuigi Racioppi, William Lento, Wei Huang, et al.
Orphanet Journal of Rare Diseases|October 17, 2019
Genotypic characteristics of Chinese patients with BHD syndrome and functional analysis of FLCN variantsKeqiang Liu, Wenshuai Xu, Xinlun Tian, et al.
Frontiers of Medicine|July 24, 2021
Novel mutation c.1210-3C > G in cis with a poly-T tract of 5T affects CFTR mRNA splicing in a Chinese patient with cystic fibrosisXinyue Zhao, Keqiang Liu, Wenshuai Xu, et al.
Frontiers of Medicine|September 19, 2023
Lack of CFAP54 causes primary ciliary dyskinesia in a mouse model and human patientsXinyue Zhao, Haijun Ge, Wenshuai Xu, et al.
Pageof 58

Showing results (381-390 of 572) with videos related to

Sort By:
Pageof 58
Orphanet Journal of Rare Diseases|June 11, 2024
A novel variant in the SLCO2A1 gene in a Chinese patient with chronic gastroenteropathy and primary hypertrophic osteoarthropathyYimin Dai, Miao He, Hui Xu, et al.
Optics Express|May 3, 2018
Weakly-coupled 4-mode step-index FMF and demonstration of IM/DD MDM transmissionTao Hu, Juhao Li, Dawei Ge, et al.
Angewandte Chemie (International Ed. in English)|August 3, 2023
Total Biosynthesis of Melleolides from Basidiomycota Fungi: Mechanistic Analysis of the Multifunctional GMC Oxidase Mld7Mitsunori Fukaya, Shota Nagamine, Taro Ozaki, et al.
Optics Express|May 4, 2026
On-chip electro-optic modulator with solution-processed colloidal In<sub>2</sub>O<sub>3</sub> nanocrystalsPeng Liu, Xiaotong Zhang, Jiaying Tian, et al.
BMC Complementary and Alternative Medicine|February 9, 2017
Antibacterial and antioxidant properties of crude extract, fractions and compounds from the stem bark of Polyscias fulva Hiern (Araliaceae)Guy Sedar Singor Njateng, Zhizhi Du, Donatien Gatsing, et al.
Therapeutic Advances in Respiratory Disease|February 28, 2026
Genetic strategies for negative or variant of uncertain significance findings in exome sequencing in hereditary bronchiectasis: a case seriesWangji Zhou, Yixuan Li, Qiaoling Chen, et al.
Cell Death & Disease|October 6, 2017
Calcium/calmodulin-dependent kinase kinase 2 regulates hematopoietic stem and progenitor cell regenerationLuigi Racioppi, William Lento, Wei Huang, et al.
Orphanet Journal of Rare Diseases|October 17, 2019
Genotypic characteristics of Chinese patients with BHD syndrome and functional analysis of FLCN variantsKeqiang Liu, Wenshuai Xu, Xinlun Tian, et al.
Frontiers of Medicine|July 24, 2021
Novel mutation c.1210-3C > G in cis with a poly-T tract of 5T affects CFTR mRNA splicing in a Chinese patient with cystic fibrosisXinyue Zhao, Keqiang Liu, Wenshuai Xu, et al.
Frontiers of Medicine|September 19, 2023
Lack of CFAP54 causes primary ciliary dyskinesia in a mouse model and human patientsXinyue Zhao, Haijun Ge, Wenshuai Xu, et al.
Pageof 58