Feng Zhao

966 Heng Yu Road
Fuzhou, 350014, China

Last Updated: 09/26/2026

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Found 13 publications

Loss of Nup160 dysregulates Cdc42 in the podocytes of podocyte-specific Nup160 knockout mice.

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.

Podocyte-specific Nup160 knockout mice develop nephrotic syndrome and glomerulosclerosis.

Journal: Human molecular genetics

Published: June 04, 2023

Long-term nephrotic syndrome recurrence risk of kidney transplantation in two siblings with ADCK4-associated glomerulopathy.

Long-term nephrotic syndrome recurrence risk of kidney transplantation in two siblings with ADCK4-associated glomerulopathy.

Journal: Pediatric transplantation

Published: April 17, 2021

A child with painful swollen joints, rash and proteinuria: Answers.

A child with painful swollen joints, rash and proteinuria: Answers.

Journal: Pediatric nephrology (Berlin, Germany)

Published: November 24, 2019

A child with painful swollen joints, rash and proteinuria: Questions.

A child with painful swollen joints, rash and proteinuria: Questions.

Journal: Pediatric nephrology (Berlin, Germany)

Published: November 24, 2019

Mutations in NUP160 Are Implicated in Steroid-Resistant Nephrotic Syndrome.

Mutations in NUP160 Are Implicated in Steroid-Resistant Nephrotic Syndrome.

Journal: Journal of the American Society of Nephrology : JASN

Published: August 01, 2018

Knockdown of NUP160 inhibits cell proliferation, induces apoptosis, autophagy and cell migration, and alters the expression and localization of podocyte associated molecules in mouse podocytes.

Knockdown of NUP160 inhibits cell proliferation, induces apoptosis, autophagy and cell migration, and alters the expression and localization of podocyte associated molecules in mouse podocytes.

Journal: Gene

Published: January 21, 2018

TLR4/MyD88 signaling determines the metastatic potential of breast cancer cells.

TLR4/MyD88 signaling determines the metastatic potential of breast cancer cells.

Journal: Molecular medicine reports

Published: August 23, 2017

Mutations in WT1 in boys with sporadic isolated steroid-resistant nephrotic syndrome.

Mutations in WT1 in boys with sporadic isolated steroid-resistant nephrotic syndrome.

Journal: Genetics and molecular research : GMR

Published: March 18, 2016

Wilms' tumor suppressor gene mutations in girls with sporadic isolated steroid-resistant nephrotic syndrome.

Wilms' tumor suppressor gene mutations in girls with sporadic isolated steroid-resistant nephrotic syndrome.

Journal: Genetics and molecular research : GMR

Published: December 17, 2013

Patients with different or identical genotypes of the WT1 gene present different phenotypes.

Patients with different or identical genotypes of the WT1 gene present different phenotypes.

Journal: European journal of pediatrics

Published: June 16, 2013

AIB1 cooperates with ERα to promote epithelial mesenchymal transition in breast cancer through SNAI1 activation.

AIB1 cooperates with ERα to promote epithelial mesenchymal transition in breast cancer through SNAI1 activation.

Journal: PloS one

Published: January 15, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026