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BMC Nephrology|November 9, 2014
Whole exome sequencing reveals novel COL4A3 and COL4A4 mutations and resolves diagnosis in Chinese families with kidney diseaseFujun Lin, Fan Bian, Jun Zou, et al.
Cell Death & Disease|October 19, 2019
SPOP suppresses pancreatic cancer progression by promoting the degradation of NANOGPeng Tan, Yunke Xu, Yichao Du, et al.
Renal Failure|September 22, 2025
Homozygous FAT1 frameshift mutation linked to glomerulotubular nephropathy with impaired cell adhesion and Rap1 signalingYang Fei, Zhouhui Jin, Li He, et al.
Plos One|April 17, 2012
Increased CD45RA+ FoxP3(low) regulatory T cells with impaired suppressive function in patients with systemic lupus erythematosusXiujun Pan, Xiangliang Yuan, Yingxia Zheng, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 19, 2016
A novel COL4A1 frameshift mutation in familial kidney disease: the importance of the C-terminal NC1 domain of type IV collagenDaniel P Gale, D Deren Oygar, Fujun Lin, et al.
Journal of Human Genetics|October 11, 2020
Diagnostic yield of additional exome sequencing after the detection of long continuous stretches of homozygosity (LCSH) in SNP arraysYanjie Fan, Lili Wang, Yu Sun, et al.
Journal of the American Society of Nephrology : JASN|February 1, 2017
Inhibition of Reticulon-1A-Mediated Endoplasmic Reticulum Stress in Early AKI Attenuates Renal Fibrosis DevelopmentYing Fan, Wenzhen Xiao, Kyung Lee, et al.
International Journal of Molecular Sciences|January 21, 2022
Tissue Proteome of 2-Hydroxyacyl-CoA Lyase Deficient Mice Reveals Peroxisome Proliferation and Activation of ω-OxidationYoussef Khalil, Sara Carrino, Fujun Lin, et al.
Frontiers in Immunology|January 1, 2025
A comprehensive immune repertoire signature distinguishes pulmonary infiltration in SARS-CoV-2 Omicron variant infectionXuechuan Li, Hongyi Zhu, Peipei Xu, et al.
Clinical Kidney Journal|October 8, 2025
Age at disease onset and risk of chronic kidney disease in patients with heterozygous disease-causing variants in COL4A3 and COL4A4Ningning Hu, Lei Sun, Xuantong Dai, et al.
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