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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.
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.
Medical Image Analysis
|
June 26, 2026
Beyond the LUMIR challenge: The pathway to foundational registration models
Junyu Chen, Shuwen Wei, Joel Honkamaa, et al.
IEEE Transactions on Medical Imaging
|
January 1, 2026
Benchmark of Segmentation Techniques for Pelvic Fracture in CT and X-Ray: Summary of the PENGWIN 2024 Challenge
Yudi Sang, Yanzhen Liu, Sutuke Yibulayimu, et al.
International Journal of Radiation Oncology, Biology, Physics
|
May 27, 2023
Operational Ontology for Oncology (O3): A Professional Society-Based, Multistakeholder, Consensus-Driven Informatics Standard Supporting Clinical and Research Use of Real-World Data From Patients Treated for Cancer
Charles S Mayo, Mary U Feng, Kristy K Brock, et al.
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Search research articles
Search
Showing results (211-220 of 218) with videos related to
Sort By:
Page
of 22
You have reached the last page of results.
This site can display upto 218 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.
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.
Medical Image Analysis
|
June 26, 2026
Beyond the LUMIR challenge: The pathway to foundational registration models
Junyu Chen, Shuwen Wei, Joel Honkamaa, et al.
IEEE Transactions on Medical Imaging
|
January 1, 2026
Benchmark of Segmentation Techniques for Pelvic Fracture in CT and X-Ray: Summary of the PENGWIN 2024 Challenge
Yudi Sang, Yanzhen Liu, Sutuke Yibulayimu, et al.
International Journal of Radiation Oncology, Biology, Physics
|
May 27, 2023
Operational Ontology for Oncology (O3): A Professional Society-Based, Multistakeholder, Consensus-Driven Informatics Standard Supporting Clinical and Research Use of Real-World Data From Patients Treated for Cancer
Charles S Mayo, Mary U Feng, Kristy K Brock, et al.
Page
of 22