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Jing-Yu Liu

Showing results (61-70 of 130) with videos related to

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Frontiers in Physiology|December 10, 2021
Effects of Evolocumab Added to Moderate-Intensity Statin Therapy in Chinese Patients With Acute Coronary Syndrome: The EMSIACS Trial Study ProtocolJing Gao, Jing-Yu Liu, Peng-Ju Lu, et al.
Phytochemistry|September 24, 2022
Norbisabolane-type sesquiterpenoid derivatives, benzofuran lignans and a phenolic glycoside from the roots of Glochidion wilsonii HutchRuixi Gao, Xuan Xu, Hao Sun, et al.
Journal of Natural Products|March 5, 2020
Amide-Iminoate Isomerism in Antineuroinflammatory Isoquinoline Alkaloids from <i>Stephania cepharantha</i>Jiao Xiao, Jun-Yu Song, Bin Lin, et al.
Gene|October 20, 2011
Mutation p.Leu354Pro in EDA causes severe hypohidrotic ectodermal dysplasia in a Chinese familyYing Liu, Xiaoyan Yu, Lei Wang, et al.
Neuroscience Bulletin|December 5, 2022
The Pathology of Primary Familial Brain Calcification: Implications for TreatmentXuan Xu, Hao Sun, Junyu Luo, et al.
Medicine|September 28, 2017
SCN11A variants may influence postoperative pain sensitivity after gynecological surgery in Chinese Han female patientsJiaoli Sun, Guangyou Duan, Ningbo Li, et al.
Molecular Genetics & Genomic Medicine|April 1, 2021
Severe brain calcification and migraine headache caused by SLC20A2 and PDGFRB heterozygous mutations in a five-year-old Chinese girlHao Sun, Zhijian Cao, Ruixi Gao, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|June 28, 2013
Anti-tumor efficacy of a hepatocellular carcinoma vaccine based on dendritic cells combined with tumor-derived autophagosomes in murine modelsShu Su, Hao Zhou, Meng Xue, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 17, 2010
Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcificationXiaohua Dai, Yong Gao, Zhenping Xu, et al.
BMC Medical Genetics|April 11, 2008
Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese familySu Zhang, Ke Yin, Xiang Ren, et al.
Pageof 13

Showing results (61-70 of 130) with videos related to

Sort By:
Pageof 13
Frontiers in Physiology|December 10, 2021
Effects of Evolocumab Added to Moderate-Intensity Statin Therapy in Chinese Patients With Acute Coronary Syndrome: The EMSIACS Trial Study ProtocolJing Gao, Jing-Yu Liu, Peng-Ju Lu, et al.
Phytochemistry|September 24, 2022
Norbisabolane-type sesquiterpenoid derivatives, benzofuran lignans and a phenolic glycoside from the roots of Glochidion wilsonii HutchRuixi Gao, Xuan Xu, Hao Sun, et al.
Journal of Natural Products|March 5, 2020
Amide-Iminoate Isomerism in Antineuroinflammatory Isoquinoline Alkaloids from <i>Stephania cepharantha</i>Jiao Xiao, Jun-Yu Song, Bin Lin, et al.
Gene|October 20, 2011
Mutation p.Leu354Pro in EDA causes severe hypohidrotic ectodermal dysplasia in a Chinese familyYing Liu, Xiaoyan Yu, Lei Wang, et al.
Neuroscience Bulletin|December 5, 2022
The Pathology of Primary Familial Brain Calcification: Implications for TreatmentXuan Xu, Hao Sun, Junyu Luo, et al.
Medicine|September 28, 2017
SCN11A variants may influence postoperative pain sensitivity after gynecological surgery in Chinese Han female patientsJiaoli Sun, Guangyou Duan, Ningbo Li, et al.
Molecular Genetics & Genomic Medicine|April 1, 2021
Severe brain calcification and migraine headache caused by SLC20A2 and PDGFRB heterozygous mutations in a five-year-old Chinese girlHao Sun, Zhijian Cao, Ruixi Gao, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|June 28, 2013
Anti-tumor efficacy of a hepatocellular carcinoma vaccine based on dendritic cells combined with tumor-derived autophagosomes in murine modelsShu Su, Hao Zhou, Meng Xue, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 17, 2010
Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcificationXiaohua Dai, Yong Gao, Zhenping Xu, et al.
BMC Medical Genetics|April 11, 2008
Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese familySu Zhang, Ke Yin, Xiang Ren, et al.
Pageof 13