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Thrombosis Research
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May 2, 2017
Thrombin-activated platelet-derived exosomes regulate endothelial cell expression of ICAM-1 via microRNA-223 during the thrombosis-inflammation response
Jiannan Li, Ming Tan, Qinqin Xiang, et al.
Neurogenetics
|
March 16, 2026
Aberrant RNA splicing caused by variant in DEPDC5 identified in a patient with pharmacoresistant epilepsy
Cong Zhou, Xing Wei, Qinqin Xiang, et al.
Frontiers in Genetics
|
July 24, 2025
Case Report: The nonsense variation of the cardiac transcription factor <i>NKX2-5</i> has been identified in a Chinese family with nonsyndromic congenital heart disease
Haixia Zhang, Jing Chen, He Wang, et al.
BMC Pediatrics
|
February 8, 2022
A novel deletion mutation in the BCOR gene is associated with oculo-facio-cardio-dental syndrome: a case report
Qian Hu, Jingqun Mai, Qinqin Xiang, et al.
ACS Applied Materials & Interfaces
|
April 30, 2026
Precise X-ray Visualization by Double Network Polymeric Gel
Zhihao Wang, Qinqin Xiang, Lei Yu, et al.
Journal of Clinical Laboratory Analysis
|
August 17, 2021
Identification of a novel EXT2 frameshift mutation in a family with hereditary multiple exostoses by whole-exome sequencing
Mei Yang, Hanbing Xie, Bocheng Xu, et al.
Molecular Genetics & Genomic Medicine
|
June 5, 2023
A novel heterozygous PKD1 variant causing alternative splicing in a Chinese family with autosomal dominant polycystic kidney disease
Qianying Zhao, Yu Tan, Xiao Xiao, et al.
Frontiers in Neuroscience
|
June 5, 2023
Case report: A novel
Cong Zhou, Hongmei Zhu, Qinqin Xiang, et al.
Stem Cell Research & Therapy
|
March 23, 2019
Exosomal miR-423-5p mediates the proangiogenic activity of human adipose-derived stem cells by targeting Sufu
Fen Xu, Qinqin Xiang, Jiuzuo Huang, et al.
Frontiers in Genetics
|
April 10, 2023
Case Report: The compound heterozygotes variants in <i>FLT4</i> causes autosomal recessive hereditary lymphedema in a Chinese family
Qinqin Xiang, Jing Chen, Xiao Xiao, et al.
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Search research articles
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Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
Thrombosis Research
|
May 2, 2017
Thrombin-activated platelet-derived exosomes regulate endothelial cell expression of ICAM-1 via microRNA-223 during the thrombosis-inflammation response
Jiannan Li, Ming Tan, Qinqin Xiang, et al.
Neurogenetics
|
March 16, 2026
Aberrant RNA splicing caused by variant in DEPDC5 identified in a patient with pharmacoresistant epilepsy
Cong Zhou, Xing Wei, Qinqin Xiang, et al.
Frontiers in Genetics
|
July 24, 2025
Case Report: The nonsense variation of the cardiac transcription factor <i>NKX2-5</i> has been identified in a Chinese family with nonsyndromic congenital heart disease
Haixia Zhang, Jing Chen, He Wang, et al.
BMC Pediatrics
|
February 8, 2022
A novel deletion mutation in the BCOR gene is associated with oculo-facio-cardio-dental syndrome: a case report
Qian Hu, Jingqun Mai, Qinqin Xiang, et al.
ACS Applied Materials & Interfaces
|
April 30, 2026
Precise X-ray Visualization by Double Network Polymeric Gel
Zhihao Wang, Qinqin Xiang, Lei Yu, et al.
Journal of Clinical Laboratory Analysis
|
August 17, 2021
Identification of a novel EXT2 frameshift mutation in a family with hereditary multiple exostoses by whole-exome sequencing
Mei Yang, Hanbing Xie, Bocheng Xu, et al.
Molecular Genetics & Genomic Medicine
|
June 5, 2023
A novel heterozygous PKD1 variant causing alternative splicing in a Chinese family with autosomal dominant polycystic kidney disease
Qianying Zhao, Yu Tan, Xiao Xiao, et al.
Frontiers in Neuroscience
|
June 5, 2023
Case report: A novel
Cong Zhou, Hongmei Zhu, Qinqin Xiang, et al.
Stem Cell Research & Therapy
|
March 23, 2019
Exosomal miR-423-5p mediates the proangiogenic activity of human adipose-derived stem cells by targeting Sufu
Fen Xu, Qinqin Xiang, Jiuzuo Huang, et al.
Frontiers in Genetics
|
April 10, 2023
Case Report: The compound heterozygotes variants in <i>FLT4</i> causes autosomal recessive hereditary lymphedema in a Chinese family
Qinqin Xiang, Jing Chen, Xiao Xiao, et al.
Page
of 2