Xiaoliang Ouyang

1 Minde Road
Nanchang, 330006, China

Last Updated: 09/26/2026

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Found 10 publications

Case Report: A new UBA2 variant in a Chinese family with aplasia cutis congenita.

Case Report: A new UBA2 variant in a Chinese family with aplasia cutis congenita.

Journal: Frontiers in medicine

Published: February 27, 2026

Identification of two novel MVD mutations and one novel FDPS mutation in Chinese patients with porokeratosis.

Identification of two novel MVD mutations and one novel FDPS mutation in Chinese patients with porokeratosis.

Journal: Frontiers in medicine

Published: December 04, 2025

Untargeted Metabolomics Investigating the Intracellular Metabolic Alterations of HaCaT Cells Treated with Isotretinoin.

Untargeted Metabolomics Investigating the Intracellular Metabolic Alterations of HaCaT Cells Treated with Isotretinoin.

Journal: Drug design, development and therapy

Published: November 30, 2025

Two Novel and Two Recurrent Variants of the ADAR1 Gene in Three Chinese Families with Dyschromatosis Symmetrica Hereditaria.

Two Novel and Two Recurrent Variants of the ADAR1 Gene in Three Chinese Families with Dyschromatosis Symmetrica Hereditaria.

Journal: Clinical, cosmetic and investigational dermatology

Published: May 07, 2024

Untargeted Lipidomics Analysis to Discover Lipid Profiles and Biomarkers of Rabbit Acne Model and Reveal Action Mechanism of Isotretinoin.

Untargeted Lipidomics Analysis to Discover Lipid Profiles and Biomarkers of Rabbit Acne Model and Reveal Action Mechanism of Isotretinoin.

Journal: Drug design, development and therapy

Published: May 03, 2024

Alopecia areata following COVID-19 vaccine: a systematic review.

Alopecia areata following COVID-19 vaccine: a systematic review.

Journal: European journal of medical research

Published: January 29, 2024

Two Novel and Three Recurrent Mutations in the Mevalonate Pathway Genes in Chinese Patients with Porokeratosis.

Two Novel and Three Recurrent Mutations in the Mevalonate Pathway Genes in Chinese Patients with Porokeratosis.

Journal: Clinical, cosmetic and investigational dermatology

Published: November 06, 2023

A novel variant with a severe phenotype in a patient with CARD14-associated papulosquamous eruption successfully treated with ixekizumab.

A novel variant with a severe phenotype in a patient with CARD14-associated papulosquamous eruption successfully treated with ixekizumab.

Journal: Clinical and experimental dermatology

Published: September 06, 2023

Two Novel and a Recurrent ATP2C1 Mutations in Chinese Population with Hailey-Hailey Disease.

Two Novel and a Recurrent ATP2C1 Mutations in Chinese Population with Hailey-Hailey Disease.

Journal: Clinical, cosmetic and investigational dermatology

Published: April 19, 2023

A new POLH mutation in a consanguineous Chinese family with xeroderma pigmentosum variant type.

A new POLH mutation in a consanguineous Chinese family with xeroderma pigmentosum variant type.

Journal: Clinical and experimental dermatology

Published: June 25, 2022

Showing 1-10 of 10

Last Updated: 09/26/2026