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Molecular Cytogenetics
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July 28, 2022
Identification of partial trisomy 13q in two unrelated patients using single-nucleotide polymorphism array and literature overview
Jianlong Zhuang, Chunnuan Chen, Hegan Zhang, et al.
Journal of Colloid and Interface Science
|
July 27, 2020
Non-tubular-biomass-derived nitrogen-doped carbon microtubes for ultrahigh-area-capacity lithium-ion batteries
Gang Yuan, Weicai Zhang, Huimin Li, et al.
Frontiers in Genetics
|
September 12, 2022
Case Report: Novel compound heterozygous variants in <i>CHRNA1</i> gene leading to lethal multiple pterygium syndrome: A case report
Jianlong Zhuang, Junyu Wang, Qi Luo, et al.
Biomed Research International
|
November 17, 2016
Autophagy Promoted the Degradation of Mutant ATXN3 in Neurally Differentiated Spinocerebellar Ataxia-3 Human Induced Pluripotent Stem Cells
Zhanhui Ou, Min Luo, Xiaohua Niu, et al.
Stem Cells and Development
|
April 18, 2018
CRISPR/Cas9-Targeted Deletion of Polyglutamine in Spinocerebellar Ataxia Type 3-Derived Induced Pluripotent Stem Cells
Shuming Ouyang, Yingjun Xie, Zeyu Xiong, et al.
Scientific Reports
|
January 27, 2025
A retrospective analysis on maternal and neonatal outcomes in pSS/AITD pregnancies
Miaoguan Peng, Taizhen Luo, Xiaoshi Weng, et al.
Research in Developmental Disabilities
|
November 6, 2017
Increased stool immunoglobulin A level in children with autism spectrum disorders
Jiaxiu Zhou, Fusheng He, Feng Yang, et al.
Journal of Cellular and Molecular Medicine
|
October 22, 2019
Efficient gene correction of an aberrant splice site in β-thalassaemia iPSCs by CRISPR/Cas9 and single-strand oligodeoxynucleotides
Zeyu Xiong, Yingjun Xie, Yi Yang, et al.
Frontiers in Neuroscience
|
July 2, 2025
Development of patient-specific iPSC-based epilepsy models and identification of differentially expressed genes for disease mechanisms
Jianfeng Wu, Siqi Huang, Lihao Chen, et al.
Archives of Pathology & Laboratory Medicine
|
May 31, 2022
Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare α- and β-Globin Gene Variants in Thalassemia Alleles in the Chinese Population
Jianlong Zhuang, Chunnuan Chen, Wanyu Fu, et al.
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of 9
Search research articles
Search
Showing results (71-80 of 89) with videos related to
Sort By:
Page
of 9
Molecular Cytogenetics
|
July 28, 2022
Identification of partial trisomy 13q in two unrelated patients using single-nucleotide polymorphism array and literature overview
Jianlong Zhuang, Chunnuan Chen, Hegan Zhang, et al.
Journal of Colloid and Interface Science
|
July 27, 2020
Non-tubular-biomass-derived nitrogen-doped carbon microtubes for ultrahigh-area-capacity lithium-ion batteries
Gang Yuan, Weicai Zhang, Huimin Li, et al.
Frontiers in Genetics
|
September 12, 2022
Case Report: Novel compound heterozygous variants in <i>CHRNA1</i> gene leading to lethal multiple pterygium syndrome: A case report
Jianlong Zhuang, Junyu Wang, Qi Luo, et al.
Biomed Research International
|
November 17, 2016
Autophagy Promoted the Degradation of Mutant ATXN3 in Neurally Differentiated Spinocerebellar Ataxia-3 Human Induced Pluripotent Stem Cells
Zhanhui Ou, Min Luo, Xiaohua Niu, et al.
Stem Cells and Development
|
April 18, 2018
CRISPR/Cas9-Targeted Deletion of Polyglutamine in Spinocerebellar Ataxia Type 3-Derived Induced Pluripotent Stem Cells
Shuming Ouyang, Yingjun Xie, Zeyu Xiong, et al.
Scientific Reports
|
January 27, 2025
A retrospective analysis on maternal and neonatal outcomes in pSS/AITD pregnancies
Miaoguan Peng, Taizhen Luo, Xiaoshi Weng, et al.
Research in Developmental Disabilities
|
November 6, 2017
Increased stool immunoglobulin A level in children with autism spectrum disorders
Jiaxiu Zhou, Fusheng He, Feng Yang, et al.
Journal of Cellular and Molecular Medicine
|
October 22, 2019
Efficient gene correction of an aberrant splice site in β-thalassaemia iPSCs by CRISPR/Cas9 and single-strand oligodeoxynucleotides
Zeyu Xiong, Yingjun Xie, Yi Yang, et al.
Frontiers in Neuroscience
|
July 2, 2025
Development of patient-specific iPSC-based epilepsy models and identification of differentially expressed genes for disease mechanisms
Jianfeng Wu, Siqi Huang, Lihao Chen, et al.
Archives of Pathology & Laboratory Medicine
|
May 31, 2022
Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare α- and β-Globin Gene Variants in Thalassemia Alleles in the Chinese Population
Jianlong Zhuang, Chunnuan Chen, Wanyu Fu, et al.
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of 9