Yao Wu

399 Wanyuan Road
Shanghai, China

Last Updated: 09/26/2026

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Found 12 publications

A Splice Site Variation in the TP63 Gene Leads to Mild Atypical EEC3 in a Large Chinese Family.

A Splice Site Variation in the TP63 Gene Leads to Mild Atypical EEC3 in a Large Chinese Family.

Journal: International journal of dermatology

Published: March 31, 2026

Cheilitis in an atopic dermatitis patient associated with co-infection of Staphylococcus pseudintermedius and Staphylococcus aureus.

Cheilitis in an atopic dermatitis patient associated with co-infection of Staphylococcus pseudintermedius and Staphylococcus aureus.

Journal: BMC microbiology

Published: January 07, 2023

Functional analysis of HECA variants identified in congenital heart disease in the Chinese population.

Functional analysis of HECA variants identified in congenital heart disease in the Chinese population.

Journal: Journal of clinical laboratory analysis

Published: June 01, 2022

Inverse association between autoimmunity and elevated IgE among childhood vitiligo.

Inverse association between autoimmunity and elevated IgE among childhood vitiligo.

Journal: International journal of dermatology

Published: July 09, 2021

Small molecule approaches to treat autoimmune and inflammatory diseases (Part III): Targeting cytokines and cytokine receptor complexes.

Small molecule approaches to treat autoimmune and inflammatory diseases (Part III): Targeting cytokines and cytokine receptor complexes.

Journal: Bioorganic & medicinal chemistry letters

Published: May 04, 2021

The improvement of infantile atopic dermatitis during the maintenance period: A multicenter, randomized, parallel controlled clinical study of emollients in Prinsepia utilis Royle.

The improvement of infantile atopic dermatitis during the maintenance period: A multicenter, randomized, parallel controlled clinical study of emollients in Prinsepia utilis Royle.

Journal: Dermatologic therapy

Published: October 08, 2019

The expression profile analysis of NKX2-5 knock-out embryonic mice to explore the pathogenesis of congenital heart disease.

The expression profile analysis of NKX2-5 knock-out embryonic mice to explore the pathogenesis of congenital heart disease.

Journal: Journal of cardiology

Published: August 29, 2014

Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of Fallot.

Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of Fallot.

Journal: Journal of translational medicine

Published: November 16, 2013

MicroRNA deregulation in right ventricular outflow tract myocardium in nonsyndromic tetralogy of fallot.

MicroRNA deregulation in right ventricular outflow tract myocardium in nonsyndromic tetralogy of fallot.

Journal: The Canadian journal of cardiology

Published: April 28, 2013

Expression of Cx43-related microRNAs in patients with tetralogy of Fallot.

Expression of Cx43-related microRNAs in patients with tetralogy of Fallot.

Journal: World journal of pediatrics : WJP

Published: September 28, 2012

LINE-1 methylation status and its association with tetralogy of fallot in infants.

LINE-1 methylation status and its association with tetralogy of fallot in infants.

Journal: BMC medical genomics

Published: January 23, 2012

DNA sequencing of TGFβ2 in sporadic patients with tetralogy of Fallot.

DNA sequencing of TGFβ2 in sporadic patients with tetralogy of Fallot.

Journal: Experimental and therapeutic medicine

Published: October 19, 2011

Showing 1-12 of 12

Last Updated: 09/26/2026