Wan-qi Wang

Changchun, China

Last Updated: 09/26/2026

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Found 12 publications

A Novel Flavonoid Derivative of Icariside II (YS-10) Improves Erectile Dysfunction in a Diabetic Rat Model by Inhibiting Ferroptosis via Activation of the Nrf2/HO-1/GPX4 Pathway.

A Novel Flavonoid Derivative of Icariside II (YS-10) Improves Erectile Dysfunction in a Diabetic Rat Model by Inhibiting Ferroptosis via Activation of the Nrf2/HO-1/GPX4 Pathway.

Journal: Drug design, development and therapy

Published: February 20, 2025

Retinitis pigmentosa with or without skeletal abnormalities due to homozygous mutations in the CWC27 gene: A case report.

Retinitis pigmentosa with or without skeletal abnormalities due to homozygous mutations in the CWC27 gene: A case report.

Journal: Medicine

Published: December 22, 2023

A case of West syndrome and global developmental delay in a child with a heterozygous mutation in the TBL1XR1 gene: A case report.

A case of West syndrome and global developmental delay in a child with a heterozygous mutation in the TBL1XR1 gene: A case report.

Journal: Medicine

Published: May 12, 2023

Children with infectious pneumonia caused by Ralstonia insidiosa: A case report.

Children with infectious pneumonia caused by Ralstonia insidiosa: A case report.

Journal: World journal of clinical cases

Published: November 08, 2022

Retroperitoneal leiomyoma located in the broad ligament: A case report.

Retroperitoneal leiomyoma located in the broad ligament: A case report.

Journal: World journal of clinical cases

Published: August 04, 2022

Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report.

Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report.

Journal: World journal of clinical cases

Published: April 15, 2022

Two novel mutations in the VPS33B gene in a Chinese patient with arthrogryposis, renal dysfunction and cholestasis syndrome 1: A case report.

Two novel mutations in the VPS33B gene in a Chinese patient with arthrogryposis, renal dysfunction and cholestasis syndrome 1: A case report.

Journal: World journal of clinical cases

Published: April 13, 2022

VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report.

VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report.

Journal: World journal of clinical cases

Published: March 25, 2022

Novel frameshift mutation in the AHDC1 gene in a Chinese global developmental delay patient: A case report.

Novel frameshift mutation in the AHDC1 gene in a Chinese global developmental delay patient: A case report.

Journal: World journal of clinical cases

Published: December 21, 2021

Clinical manifestations and gene analysis of Hutchinson-Gilford progeria syndrome: A case report.

Clinical manifestations and gene analysis of Hutchinson-Gilford progeria syndrome: A case report.

Journal: World journal of clinical cases

Published: November 19, 2021

Novel compound heterozygous variants in the TAF6 gene in a patient with Alazami-Yuan syndrome: A case report.

Novel compound heterozygous variants in the TAF6 gene in a patient with Alazami-Yuan syndrome: A case report.

Journal: World journal of clinical cases

Published: July 15, 2021

Autism with dysphasia accompanied by mental retardation caused by FOXP1 exon deletion: A case report.

Autism with dysphasia accompanied by mental retardation caused by FOXP1 exon deletion: A case report.

Journal: World journal of clinical cases

Published: March 18, 2021

Showing 1-12 of 12

Last Updated: 09/26/2026