Xiumin Yang

发表

Genetic analyses of Chinese patients with digenic oculocutaneous albinism.

S. Lian, A. Wei, Wei Li, 2013, Chinese medical journal.

Identification of a Novel MLPH Missense Mutation in a Chinese Griscelli Syndrome 3 Patient

Zhan Qi, Tianjiao Zhang, A. Wei, 2022, Frontiers in Medicine.

microRNA-146a-5p affects the inflammatory response and vascular permeability through targeting autophagy related gene 7 (ATG7) via JAK/STAT3 signaling pathway in chronic idiopathic urticaria

Wen-bin Liu, Xiaoju Zhou, Xiumin Yang, 2020 .

Differentiation of Trichophyton rubrum clinical isolates from Japanese and Chinese patients by randomly amplified polymorphic DNA and DNA sequence analysis of the non-transcribed spacer region of the rRNA gene.

M. Takashima, T. Sugita, Ruoyu Li, 2009, Journal of dermatological science.

Rhinofacial conidiobolomycosis caused by Conidiobolus coronatus in a Chinese rice farmer

T. Sugita, Xinxin Lu, Honggang Liu, 2009, Mycoses.

Pathogenicity of Conidiobolus coronatus and Fusarium solani in mouse models

Xiumin Yang, Yuxin Wang, Xiaoqian Zhou, 2017, Mycoses.

Prenatal genotyping of four common oculocutaneous albinism genes in 51 Chinese families.

Wei Li, A. Wei, Xiumin Yang, 2015, Journal of genetics and genomics = Yi chuan xue bao.

Exome sequencing identifies SLC24A5 as a candidate gene for nonsyndromic oculocutaneous albinism.

A. Wei, M. Zhang, Lin Yang, 2013, The Journal of investigative dermatology.

Identification of two Chinese oculocutaneous albinism type 6 patients and mutation updates of the SLC24A5 gene

A. Wei, Yunlan Zhang, Wei Li, 2019, The Journal of dermatology.

Application of multiplex ligation-dependent probe amplification in the genetic testing of oculocutaneous albinism

Zhan Qi, A. Wei, Wei Li, 2019, Chinese medical journal.

NGS‐based 100‐gene panel of hypopigmentation identifies mutations in Chinese Hermansky–Pudlak syndrome patients

A. Wei, Lin Yang, Wei Li, 2016, Pigment cell & melanoma research.

Genetic variants and mutational spectrum of Chinese Hermansky–Pudlak syndrome patients

Zhan Qi, Tianjiao Zhang, A. Wei, 2020, Pigment cell & melanoma research.

Implementation of an optimized strategy for genetic testing of the Chinese patients with oculocutaneous albinism.

Wei Li, S. Lian, A. Wei, 2011, Journal of dermatological science.

Spectrum Analysis of Albinism Genes in A Large Cohort of Chinese Index Patients

Zhan Qi, Tianjiao Zhang, A. Wei, 2021, Journal of Investigative Dermatology.

Instability of BLOC‐2 and BLOC‐3 in Chinese patients with Hermansky‐Pudlak syndrome

Wei Li, Zhan Qi, A. Wei, 2018, Pigment cell & melanoma research.

Se´zary Syndrome Shows Whole Genome Duplication as a Late Event in Tumor Evolution

Zhan Qi, Tianjiao Zhang, A. Wei, 2022 .

"Efficacy and safety of Liangxue Jiedu decoction for the treatment of progressive psoriasis vulgaris: a multicenter, randomized, controlled study".

Wei Zhu, Ping Wang, Dong-mei Zhou, 2020, Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan.

Tazarotene/Betamethasone Dipropionate Cream in Patients with Plaque Psoriasis: Results of a Prospective, Multicenter, Observational Study

Q. Lu, Xiujuan Xia, Linfeng Li, 2020, Dermatology.

Genome-Wide MicroRNA Analysis of Peripheral Blood Mononuclear Cells Reveals Elevated miR-142-3p Expression as a Potential Biomarker for Secondary Syphilis

C. Si, Xiumin Yang, Wei Liu, 2021, BioMed research international.

The first Hermansky–Pudlak syndrome type 9 patient with two novel variants in Chinese population

Zhan Qi, Tianjiao Zhang, A. Wei, 2021, The Journal of dermatology.