Jianbo Wang

发表

Focal facial dermal dysplasias type III: Two families with Setleis syndrome in China

Ming Li, Z. Yao, Yali Yang, 2022, The Journal of dermatology.

Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from China

Ming Li, Z. Yao, M. Zeng, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation

Xueli Li, Miao Sun, Naihui Zhou, 2020, BMC Medical Genomics.

AQP5 pathogenic variants induce palmoplantar keratoderma Bothnia type in two Chinese families

Ming Li, Z. Yao, C. Pan, 2022, The Journal of dermatology.

Successful treatment of Netherton syndrome with dupilumab: A case report and review of the literature

Zhenlu Li, Ming Li, Chen Wang, 2021, The Journal of dermatology.

A blood-making lung mass

D. I. Kuperman, Jianbo Wang, 2013, Annals of Hematology.

Haplotype-based non-invasive prenatal diagnosis of recessive dystrophic epidermolysis bullosa via targeted capture sequencing of maternal plasma.

Yiming Wu, Ming Li, J. Dou, 2023, The Journal of dermatology.

Effects of mevalonate kinase interference on cell differentiation, apoptosis, prenylation and geranylgeranylation of human keratinocytes are attenuated by farnesyl pyrophosphate or geranylgeranyl pyrophosphate

W. Min, Naihui Zhou, Q. Qian, 2020, Experimental and therapeutic medicine.

Mesoporous Silica Nanoparticle–Based Combination of NQO1 Inhibitor and 5-Fluorouracil for Potent Antitumor Effect Against Head and Neck Squamous Cell Carcinoma (HNSCC)

Jing Chen, Hongbin Sun, Zhiwei Xu, 2019, Nanoscale Research Letters.

A Novel De novo Mutation of the SASH1 Gene in a Chinese Family with Multiple Lentigines.

Xueli Li, Jia Zhang, Zhexin Wang, 2017, Acta dermato-venereologica.