Rufeng Dai

No.399 WanYuan Road
Minhang, 201102, China

Last Updated: 09/26/2026

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Found 30 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

Urinary ANGPTL3: a novel noninvasive biomarker for podocyte injury in pediatric glomerular diseases.

Urinary ANGPTL3: a novel noninvasive biomarker for podocyte injury in pediatric glomerular diseases.

Journal: Journal of translational medicine

Published: December 30, 2025

From mutation to symptoms: a multi-center study on HNF1B-related nephropathy in Chinese children.

From mutation to symptoms: a multi-center study on HNF1B-related nephropathy in Chinese children.

Journal: BMC nephrology

Published: July 16, 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

Genitourinary defects, anxiety and aggressive-like behavior and glucose metabolism disorders in Zmym2 mutant mice with inserted piggyBac transposon.

Genitourinary defects, anxiety and aggressive-like behavior and glucose metabolism disorders in Zmym2 mutant mice with inserted piggyBac transposon.

Journal: Frontiers in cell and developmental biology

Published: November 20, 2024

Noninvasive genetic testing for type IV collagen nephropathy using oral mucosa DNA sampling in children with haematuria.

Noninvasive genetic testing for type IV collagen nephropathy using oral mucosa DNA sampling in children with haematuria.

Journal: Renal failure

Published: November 14, 2024

Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.

Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: July 08, 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

GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tract.

GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tract.

Journal: Human genomics

Published: October 15, 2023

Prioritization of Monogenic Congenital Anomalies of the Kidney and Urinary Tract Candidate Genes with Existing Single-Cell Transcriptomics Data of the Human Fetal Kidney.

Prioritization of Monogenic Congenital Anomalies of the Kidney and Urinary Tract Candidate Genes with Existing Single-Cell Transcriptomics Data of the Human Fetal Kidney.

Journal: Nephron

Published: January 04, 2023

Angiopoietin-like protein 3: a novel potential biomarker for nephrotic syndrome in children.

Angiopoietin-like protein 3: a novel potential biomarker for nephrotic syndrome in children.

Journal: Frontiers in pediatrics

Published: December 01, 2022

Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.

Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.

Journal: European urology open science

Published: August 10, 2022

Showing 1-12 of 30

Last Updated: 09/26/2026