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Renal Failure|January 5, 2021
COQ2 mutation associated isolated nephropathy in two siblings from a Chinese pedigreeMin Li, Zhihui Yue, Hongrong Lin, et al.
International Journal of Molecular Epidemiology and Genetics|September 17, 2019
Two Chinese nephronophthisis pedigrees harbored a compound heterozygous deletion with a point mutation in NPHP1Huamu Chen, Hongrong Lin, Zhihui Yue, et al.
International Journal of Molecular Sciences|February 25, 2023
Reducing GEF-H1 Expression Inhibits Renal Cyst Formation, Inflammation, and Fibrosis via RhoA Signaling in NephronophthisisQiulei Hu, Jiayong Lai, Huamu Chen, et al.
Biochemical and Biophysical Research Communications|October 24, 2021
Overexpression of smad7 inhibits the TGF-β/Smad signaling pathway and EMT in NPHP1-defective MDCK cellsXiaohong Wu, Haiyan Wang, Huamu Chen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 20, 2021
Cyclosporine A relieved proteinuria and hypoproteinemia in DGKE nephropathyWenjun Fu, Min Li, Hongrong Lin, et al.
Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University|September 2, 2014
[Establishment of a rat model of acute liver failure by a modified 90% bloodless hepatectomy and by D-galactosamine and lipopolysaccharide injection]Xumeng Gong, Bin Zhou, Huamu Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 21, 2022
[Analysis of SALL1 gene variant in a boy with Townes-Brocks syndrome without anal atresia]Haixia Wei, Liangzhong Sun, Min Li, et al.
Clinical Nephrology|March 4, 2017
WT1 mutation-associated nephropathy: a single-center experienceZhihui Yue, Haiyan Wang, Hongrong Lin, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|December 7, 2025
ZONAB regulates renal cyst formation in nphp1 knockout miceJiayong Lai, Xiaoya Wei, Dantong Li, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 17, 2020
Clinical and pathological features and varied mutational spectra of pathogenic genes in 55 Chinese patients with nephronophthisisZhihui Yue, Hongrong Lin, Min Li, et al.
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