Yaowang Zhao
Hunan Key Laboratory Of Medical Genetics, MOE Key Lab Of Rare Pediatric Diseases
Changsha, 410000, China
Changsha, 410000, China
Last Updated: 09/26/2026
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Found 15 publications
The genetic landscape of hypospadias: clinical insights into inherited and de novo risk factors.
Journal: Science China. Life sciences
Published: October 06, 2025
NCYM facilitates cell proliferation and invasion in Wilms tumor by regulating SIX1/β-catenin axis.
Journal: American journal of clinical and experimental urology
Published: August 10, 2025
DNMT1 targets SRD5A2 to induce mitochondrial homeostasis and EMT in urothelial cells of hypospadias.
DNMT1 targets SRD5A2 to induce mitochondrial homeostasis and EMT in urothelial cells of hypospadias.
Journal: Molecular biology reports
Published: January 16, 2025
The safety of cyclosporine and tacrolimus in pediatric nephrotic syndrome patients: a disproportionate analysis based on the FAERS database.
Journal: Frontiers in pediatrics
Published: September 10, 2024
MicroR-1199-5p targeting SRD5A2 promotes the biological behavior and EMT of hypospadias cells.
Journal: Cellular and molecular biology (Noisy-le-Grand, France)
Published: February 04, 2024
Risk-Factor Analysis and Prediction-Model Construction of Urethral Stricture after Hypospadias Surgery in Children: A Single-Centre Retrospective Study.
Journal: Archivos espanoles de urologia
Published: December 06, 2023
Risk factors for postoperative complications following one-stage proximal hypospadias repair involving the disconnection of the urethral plate: a retrospective study.
Journal: BMC pediatrics
Published: August 03, 2023
Clinical characteristics and surgical treatment of children with 45, X/46, XY differences of sex development.
Journal: Journal of pediatric urology
Published: March 17, 2023
Use of whole-exome sequencing to identify novel monogenic gene mutations and genotype-phenotype correlations in Chinese Han children with urolithiasis.
Journal: Frontiers in genetics
Published: December 21, 2022
Genetic and Clinical Analyses of 13 Chinese Families With Cystine Urolithiasis and Identification of 15 Novel Pathogenic Variants in SLC3A1 and SLC7A9.
Journal: Frontiers in genetics
Published: October 09, 2019
Additional data support the role of LINC00673 rs11655237 C>T in the development of neuroblastoma.
Journal: Aging
Published: February 18, 2019
Two Novel AGXT Mutations Cause the Infantile Form of Primary Hyperoxaluria Type I in a Chinese Family: Research on Missed Mutation.
Journal: Frontiers in pharmacology
Published: August 06, 2018
Last Updated: 09/26/2026