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Renal Failure|August 8, 2025
Identification of novel pathogenic mutations in ATP6V0A4 associated with distal renal tubular acidosis and analysis of wild-type expression in glomerular diseaseYaru Jiang, Menglu Ren, Chun Gan, et al.International Journal of Biological Macromolecules|October 5, 2024
Aberrant serum-derived FN1 variants bind to integrin β1 on glomerular endothelial cells contributing to thin basement membrane nephropathyXindi Zhou, Wanbing Chen, Chun Gan, et al.Journal of Translational Medicine|May 8, 2026
Duration-dependent hippocampal structural changes in focal epilepsy: multicenter neuroimaging evidenceYuxin Wu, Zaiyu Zhang, Baohui Yang, et al.Journal of Biomechanics|March 23, 2023
Roles of irregularity of pore morphology in osteogenesis of Voronoi scaffolds: From the perspectives of MSC adhesion and mechano-regulated osteoblast differentiationTeng Lu, Zhongwei Sun, Cunwei Jia, et al.Genes & Diseases|September 26, 2022
Whole-exome sequencing of a multicenter cohort identifies genetic changes associated with clinical phenotypes in pediatric nephrotic syndromeJia Jiao, Li Wang, Fenfen Ni, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 23, 2026
Novel immune-related susceptibility loci associated with pediatric steroid-sensitive nephrotic syndrome identified by a transethnic genome-wide association studyXueying Yang, Zijian Tian, Xueting Chen, et al.Pageof 5