Yonghui Yang
966 Heng Yu Road
Fuzhou, 350014, China
Fuzhou, 350014, China
Last Updated: 09/26/2026
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Found 9 publications
Loss of Nup160 dysregulates Cdc42 in the podocytes of podocyte-specific Nup160 knockout mice.
Journal: Human molecular genetics
Published: January 30, 2025
Podocyte-specific Nup160 knockout mice develop nephrotic syndrome and glomerulosclerosis.
Journal: Human molecular genetics
Published: June 04, 2023
Scalp Tumor and Hydroureteronephrosis in Patients with Nephronophthisis and Homozygous NPHP1 Deletion.
Journal: Clinical pediatrics
Published: March 21, 2023
Mutations in NUP160 Are Implicated in Steroid-Resistant Nephrotic Syndrome.
Journal: Journal of the American Society of Nephrology : JASN
Published: August 01, 2018
Mechanism of angioneurins' protective effect against premature brain injury: a summary of research progress
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: March 10, 2016
Mutational analysis of MYO1E in children with sporadic steroid-resistant nephrotic syndrome in Chinese Han ethnic group
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: September 17, 2014
Patients with different or identical genotypes of the WT1 gene present different phenotypes.
Journal: European journal of pediatrics
Published: June 16, 2013
A child with isolated nephrotic syndrome and WT1 mutation presenting as a 46, XY phenotypic male.
Journal: European journal of pediatrics
Published: March 14, 2012
Discordant phenotypes in monozygotic twins with identical de novo WT1 mutation.
Journal: Clinical kidney journal
Published: November 28, 2011
Showing 1-9 of 9
Last Updated: 09/26/2026