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Human Mutation
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November 30, 2018
A de novo pathogenic CSNK1E mutation identified by exome sequencing in family trios with epileptic encephalopathy
Xiaomin 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 hypertension
Jing Luo, Haiyan Li, Zhenwei Liu, et al.
Carbohydrate Polymers
|
August 23, 2021
Biological role of heparan sulfate in osteogenesis: A review
Zhujie 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 China
Qi 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 rice
Zhibin 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 human
Yi Jiang, Zhongshan Li, Zhenwei Liu, et al.
Nanoscale
|
March 17, 2018
<sup>64</sup>Cu-Labeled multifunctional dendrimers for targeted tumor PET imaging
Wenhui 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 knob
Xingui 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 autism
Yaoqiang 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 autism
Yaoqiang Du, Zhongshan Li, Zhenwei Liu, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 117) with videos related to
Sort By:
Page
of 12
Human Mutation
|
November 30, 2018
A de novo pathogenic CSNK1E mutation identified by exome sequencing in family trios with epileptic encephalopathy
Xiaomin 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 hypertension
Jing Luo, Haiyan Li, Zhenwei Liu, et al.
Carbohydrate Polymers
|
August 23, 2021
Biological role of heparan sulfate in osteogenesis: A review
Zhujie 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 China
Qi 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 rice
Zhibin 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 human
Yi Jiang, Zhongshan Li, Zhenwei Liu, et al.
Nanoscale
|
March 17, 2018
<sup>64</sup>Cu-Labeled multifunctional dendrimers for targeted tumor PET imaging
Wenhui 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 knob
Xingui 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 autism
Yaoqiang 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 autism
Yaoqiang Du, Zhongshan Li, Zhenwei Liu, et al.
Page
of 12