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Frontiers in Neuroscience
|
August 15, 2024
<i>In vitro</i> study of <i>ATP1A3</i> p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism
Dan-Dan Ruan, Jing Zou, Li-Sheng Liao, et al.
Scientific Reports
|
September 10, 2024
Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation
Dan-Dan Ruan, Xing-Lin Ruan, Ruo-Li Wang, et al.
Zoological Research
|
June 10, 2026
First identification of an amphibian-derived peptide with anti-vascular aging activity
Xin Liu, Jie Liu, Bin Li, et al.
Medscience
|
February 24, 2026
Differential genetic analysis of ectrodactyly in a Fanconi anemia pedigree with FANCA mutations
Jian-Hui Zhang, Zi-Yan Xu, Hong-Ping Yu, et al.
Gene
|
September 25, 2025
Genetic analysis of a family with skeletal muscle ion channelopathy and hereditary spastic paraplegia type 7 caused by SCN4A and SPG7 double mutations
Hong-Ping Yu, Zi-Yan Xu, Meng-Qian Wu, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
March 17, 2026
Phosphoproteomics elucidates the functional impact of the PTPN11 p.Asn308Ser variant in a Noonan syndrome pedigree
Wei-Jing Xu, Li-Jun Xie, Wen-Jun Chen, et al.
Gene
|
November 16, 2025
De novo PKD1 splicing and missense variants in two familial ADPKD: Molecular characterization and genetic counseling implications
Juan Zhu, Zi-Yan Xu, Hong-Ping Yu, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
February 15, 2026
Clinical and genetic analysis of an early-onset sitosterolemia family caused by a novel compound heterozygous ABCG5 mutation
Shu-Fang Wu, Zi-Yan Xu, Li-Jun Xie, et al.
Gene
|
December 8, 2025
A de novo INSR variant in Type A insulin resistance syndrome: familial investigation and genetic implications
Xin Lin, Zi-Yan Xu, Li-Jun Xie, et al.
Nature Communications
|
June 3, 2020
Ancient genomes from northern China suggest links between subsistence changes and human migration
Chao Ning, Tianjiao Li, Ke Wang, et al.
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Search research articles
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Showing results (71-80 of 80) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 80 results.
Frontiers in Neuroscience
|
August 15, 2024
<i>In vitro</i> study of <i>ATP1A3</i> p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism
Dan-Dan Ruan, Jing Zou, Li-Sheng Liao, et al.
Scientific Reports
|
September 10, 2024
Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation
Dan-Dan Ruan, Xing-Lin Ruan, Ruo-Li Wang, et al.
Zoological Research
|
June 10, 2026
First identification of an amphibian-derived peptide with anti-vascular aging activity
Xin Liu, Jie Liu, Bin Li, et al.
Medscience
|
February 24, 2026
Differential genetic analysis of ectrodactyly in a Fanconi anemia pedigree with FANCA mutations
Jian-Hui Zhang, Zi-Yan Xu, Hong-Ping Yu, et al.
Gene
|
September 25, 2025
Genetic analysis of a family with skeletal muscle ion channelopathy and hereditary spastic paraplegia type 7 caused by SCN4A and SPG7 double mutations
Hong-Ping Yu, Zi-Yan Xu, Meng-Qian Wu, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
March 17, 2026
Phosphoproteomics elucidates the functional impact of the PTPN11 p.Asn308Ser variant in a Noonan syndrome pedigree
Wei-Jing Xu, Li-Jun Xie, Wen-Jun Chen, et al.
Gene
|
November 16, 2025
De novo PKD1 splicing and missense variants in two familial ADPKD: Molecular characterization and genetic counseling implications
Juan Zhu, Zi-Yan Xu, Hong-Ping Yu, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
February 15, 2026
Clinical and genetic analysis of an early-onset sitosterolemia family caused by a novel compound heterozygous ABCG5 mutation
Shu-Fang Wu, Zi-Yan Xu, Li-Jun Xie, et al.
Gene
|
December 8, 2025
A de novo INSR variant in Type A insulin resistance syndrome: familial investigation and genetic implications
Xin Lin, Zi-Yan Xu, Li-Jun Xie, et al.
Nature Communications
|
June 3, 2020
Ancient genomes from northern China suggest links between subsistence changes and human migration
Chao Ning, Tianjiao Li, Ke Wang, et al.
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of 8