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Gene
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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.
Liver International : Official Journal of the International Association for the Study of the Liver
|
July 10, 2022
Clinical implications and biological features of a novel postoperative recurrent HCC classification: A multi-centre study
Lu-Nan Qi, Liang Ma, Fei-Xiang 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.
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.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
November 15, 2025
Genome-wide association study of HBV-related hepatocellular carcinoma identifies a functional variant at the FAM114A1 locus
Hong-Ping Yu, Bang-De Xiang, Ji Qian, et al.
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Showing results (51-60 of 56) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 56 results.
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.
Liver International : Official Journal of the International Association for the Study of the Liver
|
July 10, 2022
Clinical implications and biological features of a novel postoperative recurrent HCC classification: A multi-centre study
Lu-Nan Qi, Liang Ma, Fei-Xiang 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.
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.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
November 15, 2025
Genome-wide association study of HBV-related hepatocellular carcinoma identifies a functional variant at the FAM114A1 locus
Hong-Ping Yu, Bang-De Xiang, Ji Qian, et al.
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of 6