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Lv Liu

Showing results (11-20 of 41) with videos related to

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Frontiers in Genetics|October 26, 2023
Case report: Identification of a recurrent pathogenic <i>DHDDS</i> mutation in Chinese family with epilepsy, intellectual disability and myoclonusYi Dong, Yi Zhang, Yue Sheng, et al.
Pain Management Nursing : Official Journal of the American Society of Pain Management Nurses|May 17, 2026
Pain and Kidney Disease Risk in Older Adults: CHARLS Longitudinal StudyWang Li, Gao-Hui Cao, Lin-Xia Jiang, et al.
Frontiers in Neuroscience|March 8, 2021
Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13AFang-Mei Luo, Ming-Xing Deng, Rong Yu, et al.
Environmental Toxicology|March 28, 2024
Exploring gene biomarkers and targeted drugs for ferroptosis and cuproptosis in osteosarcoma: A bioinformatic approachYingnan Ji, Lv Liu, Yu Liu, et al.
Molecular Genetics & Genomic Medicine|January 20, 2023
Whole-genome sequencing revealed a novel long-range deletion mutation spanning GNAS in familial pseudohypoparathyroidismYangfan Fei, Lv Liu, Lixia Wu, et al.
Frontiers in Cell and Developmental Biology|March 13, 2026
Whole exome sequencing identified two novel mutations of <i>ACD</i> in Chinese patients with idiopathic pulmonary fibrosisGao-Hui Cao, Hui Yang, Qian Wang, et al.
Molecular Genetics & Genomic Medicine|July 1, 2020
Identification and functional characterization of a novel surfactant protein A2 mutation (p.N207Y) in a Chinese family with idiopathic pulmonary fibrosisLv Liu, Jieli Qin, Ting Guo, et al.
Biomaterials Research|July 21, 2025
Hyaluronic Acid-Functionalized Bismuth Vanadate/Molybdenum Disulfide Nanoheterojunctions Achieve Efficient Phototherapy of Hypoxic TumorYunqing Pang, Jia Guo, Qianlong Ma, et al.
Annals of Medicine|June 9, 2026
Differentiating benign from malignant pulmonary nodules in the context of bronchiectasis: a retrospective studyLin Wang, Danhui Yang, Xianglin Zhou, et al.
Frontiers in Genetics|November 29, 2023
Case report: A novel <i>WASHC5</i> variant altering mRNA splicing causes spastic paraplegia in a patientShan-Yu Gao, Yu-Xing Liu, Yi Dong, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Frontiers in Genetics|October 26, 2023
Case report: Identification of a recurrent pathogenic <i>DHDDS</i> mutation in Chinese family with epilepsy, intellectual disability and myoclonusYi Dong, Yi Zhang, Yue Sheng, et al.
Pain Management Nursing : Official Journal of the American Society of Pain Management Nurses|May 17, 2026
Pain and Kidney Disease Risk in Older Adults: CHARLS Longitudinal StudyWang Li, Gao-Hui Cao, Lin-Xia Jiang, et al.
Frontiers in Neuroscience|March 8, 2021
Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13AFang-Mei Luo, Ming-Xing Deng, Rong Yu, et al.
Environmental Toxicology|March 28, 2024
Exploring gene biomarkers and targeted drugs for ferroptosis and cuproptosis in osteosarcoma: A bioinformatic approachYingnan Ji, Lv Liu, Yu Liu, et al.
Molecular Genetics & Genomic Medicine|January 20, 2023
Whole-genome sequencing revealed a novel long-range deletion mutation spanning GNAS in familial pseudohypoparathyroidismYangfan Fei, Lv Liu, Lixia Wu, et al.
Frontiers in Cell and Developmental Biology|March 13, 2026
Whole exome sequencing identified two novel mutations of <i>ACD</i> in Chinese patients with idiopathic pulmonary fibrosisGao-Hui Cao, Hui Yang, Qian Wang, et al.
Molecular Genetics & Genomic Medicine|July 1, 2020
Identification and functional characterization of a novel surfactant protein A2 mutation (p.N207Y) in a Chinese family with idiopathic pulmonary fibrosisLv Liu, Jieli Qin, Ting Guo, et al.
Biomaterials Research|July 21, 2025
Hyaluronic Acid-Functionalized Bismuth Vanadate/Molybdenum Disulfide Nanoheterojunctions Achieve Efficient Phototherapy of Hypoxic TumorYunqing Pang, Jia Guo, Qianlong Ma, et al.
Annals of Medicine|June 9, 2026
Differentiating benign from malignant pulmonary nodules in the context of bronchiectasis: a retrospective studyLin Wang, Danhui Yang, Xianglin Zhou, et al.
Frontiers in Genetics|November 29, 2023
Case report: A novel <i>WASHC5</i> variant altering mRNA splicing causes spastic paraplegia in a patientShan-Yu Gao, Yu-Xing Liu, Yi Dong, et al.
Pageof 5