Chunyan Wang

Shanghai, 201102, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 11 publications

Vitamin D Deficiency Activates Gdnf-Ret-pErk1/2 Signal and Induces Kidney Malformations in Mice.

Vitamin D Deficiency Activates Gdnf-Ret-pErk1/2 Signal and Induces Kidney Malformations in Mice.

Journal: International journal of molecular sciences

Published: February 01, 2026

Renal Tubule-Specific Deletion of Nephrocystin 3 (Nphp3) Causes Infantile Nephronophthisis-like Phenotypes in Mice.

Renal Tubule-Specific Deletion of Nephrocystin 3 (Nphp3) Causes Infantile Nephronophthisis-like Phenotypes in Mice.

Journal: International journal of molecular sciences

Published: January 18, 2026

Effect of Donor-recipient Size on Graft Growth in Pediatric Donor-to-pediatric Recipient Kidney Transplantation.

Effect of Donor-recipient Size on Graft Growth in Pediatric Donor-to-pediatric Recipient Kidney Transplantation.

Journal: Transplantation direct

Published: November 13, 2025

Stem Cell Factors BAM1 and WOX1 Suppressing Longitudinal Cell Division of Margin Cells Evoked by Low-Concentration Auxin in Young Cotyledon of Arabidopsis.

Stem Cell Factors BAM1 and WOX1 Suppressing Longitudinal Cell Division of Margin Cells Evoked by Low-Concentration Auxin in Young Cotyledon of Arabidopsis.

Journal: International journal of molecular sciences

Published: March 28, 2025

Correlation between polymorphisms of the aquaporin-1 gene and peritoneal function in children on chronic peritoneal dialysis.

Correlation between polymorphisms of the aquaporin-1 gene and peritoneal function in children on chronic peritoneal dialysis.

Journal: Pediatric nephrology (Berlin, Germany)

Published: March 03, 2025

Risk factors and outcome of BK polyomavirus infection in pediatric kidney transplantation.

Risk factors and outcome of BK polyomavirus infection in pediatric kidney transplantation.

Journal: Pediatric nephrology (Berlin, Germany)

Published: May 09, 2024

Protein-losing enteropathy as a new phenotype in atypical hemolytic uremic syndrome caused by CD46 gene mutation.

Protein-losing enteropathy as a new phenotype in atypical hemolytic uremic syndrome caused by CD46 gene mutation.

Journal: Pediatric nephrology (Berlin, Germany)

Published: March 05, 2024

The emerging role of clinical genetics in pediatric patients with chronic kidney disease.

The emerging role of clinical genetics in pediatric patients with chronic kidney disease.

Journal: Pediatric nephrology (Berlin, Germany)

Published: February 06, 2024

Overexpression of long noncoding RNA 4933425B07Rik leads to renal hypoplasia by inactivating Wnt/β-catenin signaling pathway.

Overexpression of long noncoding RNA 4933425B07Rik leads to renal hypoplasia by inactivating Wnt/β-catenin signaling pathway.

Journal: Frontiers in cell and developmental biology

Published: August 10, 2023

Diagnosis and Treatment for Shiga Toxin-Producing Escherichia coli Associated Hemolytic Uremic Syndrome.

Diagnosis and Treatment for Shiga Toxin-Producing Escherichia coli Associated Hemolytic Uremic Syndrome.

Journal: Toxins

Published: November 04, 2022

Diagnostic and clinical utility of genetic testing in children with kidney failure.

Diagnostic and clinical utility of genetic testing in children with kidney failure.

Journal: Pediatric nephrology (Berlin, Germany)

Published: March 02, 2021

Showing 1-11 of 11

Last Updated: 09/26/2026