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Zhenwei Liu

Showing results (81-90 of 117) with videos related to

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Human Mutation|November 30, 2018
A de novo pathogenic CSNK1E mutation identified by exome sequencing in family trios with epileptic encephalopathyXiaomin Chen, Jing Jin, Qiongdan Wang, et al.
BMC Medical Genomics|June 27, 2020
Integrative analyses of gene expression profile reveal potential crucial roles of mitotic cell cycle and microtubule cytoskeleton in pulmonary artery hypertensionJing Luo, Haiyan Li, Zhenwei Liu, et al.
Carbohydrate Polymers|August 23, 2021
Biological role of heparan sulfate in osteogenesis: A reviewZhujie Xu, Shayang Chen, Dehong Feng, et al.
Frontiers in Public Health|September 23, 2022
Rational medication management mode and its implementation effect for the elderly with multimorbidity: A prospective cohort study in ChinaQi Tang, Litao Wan, Jing Lu, et al.
BMC Genomics|April 19, 2015
Global epigenomic analysis indicates that epialleles contribute to Allele-specific expression via Allele-specific histone modifications in hybrid riceZhibin Guo, Gaoyuan Song, Zhenwei Liu, et al.
Nucleic Acids Research|November 2, 2016
mirDNMR: a gene-centered database of background de novo mutation rates in humanYi Jiang, Zhongshan Li, Zhenwei Liu, et al.
Nanoscale|March 17, 2018
<sup>64</sup>Cu-Labeled multifunctional dendrimers for targeted tumor PET imagingWenhui Ma, Fanfan Fu, Jingyi Zhu, et al.
Emerging Microbes & Infections|December 12, 2018
Broadly neutralizing monoclonal antibodies against human adenovirus types 55, 14p, 7, and 11 generated with recombinant type 11 fiber knobXingui Tian, Ye Fan, Zhenwei Liu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 24, 2019
Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autismYaoqiang Du, Zhongshan Li, Zhenwei Liu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2019
Correction: Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autismYaoqiang Du, Zhongshan Li, Zhenwei Liu, et al.
Pageof 12

Showing results (81-90 of 117) with videos related to

Sort By:
Pageof 12
Human Mutation|November 30, 2018
A de novo pathogenic CSNK1E mutation identified by exome sequencing in family trios with epileptic encephalopathyXiaomin Chen, Jing Jin, Qiongdan Wang, et al.
BMC Medical Genomics|June 27, 2020
Integrative analyses of gene expression profile reveal potential crucial roles of mitotic cell cycle and microtubule cytoskeleton in pulmonary artery hypertensionJing Luo, Haiyan Li, Zhenwei Liu, et al.
Carbohydrate Polymers|August 23, 2021
Biological role of heparan sulfate in osteogenesis: A reviewZhujie Xu, Shayang Chen, Dehong Feng, et al.
Frontiers in Public Health|September 23, 2022
Rational medication management mode and its implementation effect for the elderly with multimorbidity: A prospective cohort study in ChinaQi Tang, Litao Wan, Jing Lu, et al.
BMC Genomics|April 19, 2015
Global epigenomic analysis indicates that epialleles contribute to Allele-specific expression via Allele-specific histone modifications in hybrid riceZhibin Guo, Gaoyuan Song, Zhenwei Liu, et al.
Nucleic Acids Research|November 2, 2016
mirDNMR: a gene-centered database of background de novo mutation rates in humanYi Jiang, Zhongshan Li, Zhenwei Liu, et al.
Nanoscale|March 17, 2018
<sup>64</sup>Cu-Labeled multifunctional dendrimers for targeted tumor PET imagingWenhui Ma, Fanfan Fu, Jingyi Zhu, et al.
Emerging Microbes & Infections|December 12, 2018
Broadly neutralizing monoclonal antibodies against human adenovirus types 55, 14p, 7, and 11 generated with recombinant type 11 fiber knobXingui Tian, Ye Fan, Zhenwei Liu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 24, 2019
Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autismYaoqiang Du, Zhongshan Li, Zhenwei Liu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2019
Correction: Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autismYaoqiang Du, Zhongshan Li, Zhenwei Liu, et al.
Pageof 12