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Frontiers in Immunology|July 24, 2024
Successfully treated with siltuximab and prednisone in a 7-year-old girl with DOCK8-deficiency presenting as recurrent wart-like lesions: a case reportZhe Sun, Ruoqu Wei, Chaolan Pan, et al.The Journal of Dermatology|June 17, 2022
Focal facial dermal dysplasias type III: Two families with Setleis syndrome in ChinaQiaoyu Cao, Shuai Zhang, Jianbo Wang, et al.Human Mutation|September 2, 2025
Optical Genomic Mapping and Next-Generation Sequencing Identified Retrotransposon Insertion and Missense Variant Disrupting PARN Gene in Dyskeratosis CongenitaQiaoyu Cao, Anqi Zhao, Zhoukai Long, et al.Molecules (Basel, Switzerland)|April 28, 2023
A Novel Derivative of Curcumol, HCL-23, Inhibits the Malignant Phenotype of Triple-Negative Breast Cancer and Induces Apoptosis and HO-1-Dependent FerroptosisPeng Zhao, Hui Song, Futian Gao, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|October 26, 2022
Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from ChinaFuying Chen, Ruoqu Wei, Dan Deng, et al.American Journal of Human Genetics|July 9, 2026
Overlapping Xq13.3 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivityQiaoyu Cao, Anqi Zhao, Jianbo Wang, et al.The Journal of Dermatology|January 31, 2024
Mosaic GJB2 mutations in widespread porokeratotic adnexal ostial nevus: Report of two patientsAnqi Zhao, Yumeng Wang, Ning Jia, et al.Journal of Controlled Release : Official Journal of the Controlled Release Society|March 30, 2025
Ultra-high gene transfection efficiency in suspension cells mediated by highly branched-linear poly(β-amino ester)sChenfei Wang, Tao Bo, Chen Wu, et al.Journal of Controlled Release : Official Journal of the Controlled Release Society|April 21, 2024
Superior COL7A1 and TGM1 gene expression in difficult-to-transfect skin cell mediated by highly branched poly(β-amino esters) through stepwise fractionationChaolan Pan, Chenfei Wang, Yitong Zhao, et al.JCI Insight|May 21, 2024
ADAM17 variant causes hair loss via ubiquitin ligase TRIM47-mediated degradationXiaoxiao Wang, Chaolan Pan, Luyao Zheng, et al.Pageof 4