Ming Li

发表

Combined effect between CHRNB3-CHRNA6 region gene variant (rs6474412) and smoking in psoriasis vulgaris severity.

C. Quan, Chi Zhang, K. Zhu, 2014, Gene.

Genome Sequence of a Novel Recombinant Coxsackievirus A6 Strain from Shanghai, China, 2013

Xiaoling Zhang, Yun-wen Hu, Ming Li, 2015, Genome Announcements.

A novel recombinant lineage’s contribution to the outbreak of coxsackievirus A6-associated hand, foot and mouth disease in Shanghai, China, 2012-2013

Xiaoling Zhang, Yun-wen Hu, Ming Li, 2015, Scientific Reports.

Identification of two novel mutations in the PLCD1 gene in Chinese patients with hereditary leukonychia

Xiuli Wang, U. Keyal, Shuzhan Shen, 2021, Molecular medicine reports.

Novel small‐insertion mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis

Ming Li, R. Cheng, H. Lv, 2020, The Journal of dermatology.

Lidocaine inhibits staphylococcal enterotoxin-stimulated activation of peripheral blood mononuclear cells from patients with atopic dermatitis

Honglin Wang, Ming Li, Hui Zhang, 2013, Archives of Dermatological Research.

Netherton syndrome caused by compound heterozygous mutation, c.80A>G mutation in SPINK5 and large‐sized genomic deletion mutation, and successful treatment of intravenous immunoglobulin

Ming Li, Z. Yao, Zhen Zhang, 2021, Molecular genetics & genomic medicine.

Novel mutations in Chinese hypotrichosis simplex patients associated with LSS gene

Ming Li, Yu Ding, Jia Zhang, 2020, The Journal of dermatology.

Prevalence of Atopic Dermatitis in Chinese Children aged 1–7 ys

Jian-ping Tang, H. Gu, Xinghua Gao, 2016, Scientific Reports.

A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis.

Guolong Zhang, A. Sandilands, Ming Li, 2018, The Journal of investigative dermatology.

Effects of lidocaine on regulatory T cells in atopic dermatitis.

Ming Yan, Honglin Wang, Ming Li, 2016, The Journal of allergy and clinical immunology.

Atopic Dermatitis-like Genodermatosis: Disease Diagnosis and Management

Ming Li, C. Pan, Anqi Zhao, 2022, Diagnostics.

The first case of a mosaic superficial epidermolytic ichthyosis diagnosed by Ultra‐Deep Sequence

Ming Li, Z. Yao, R. Cheng, 2020, Molecular genetics & genomic medicine.

Known and novel mutations responsible for epidermolysis bullosa simplex cases in a Chinese population

Ming Li, Z. Yao, Yu Ding, 2019, Experimental and therapeutic medicine.

A novel KRT5 mutation associated with generalized severe epidermolysis bullosa simplex in a 2-year-old Chinese boy

Ming Yan, Ming Li, Z. Yao, 2016, Experimental and therapeutic medicine.

A novel mutation in TRPV3 gene causes atypical familial Olmsted syndrome

Ming Yan, Ming Li, Z. Yao, 2016, Scientific Reports.

Common FLG Mutation K4671X Not Associated with Atopic Dermatitis in Han Chinese in a Family Association Study

W. Liao, Ming Li, Hui Zhang, 2012, PloS one.

Prevalent and rare mutations in IL-36RN gene in Chinese patients with generalized pustular psoriasis and psoriasis vulgaris.

Jian-Wen Han, Ming Li, Chengyao Zhu, 2013, The Journal of investigative dermatology.

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

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

Factors associated with persistence of early-onset atopic dermatitis up to the age of 12 years: a prospective cohort study in China

Ming Li, Hui Zhang, Z. Yao, 2021, European Journal of Dermatology.

Identification of a PTPN11 hot spot mutation in a child with atypical LEOPARD syndrome.

Ming Li, Z. Yao, R. Cheng, 2016, Molecular medicine reports.

The clinical efficacy and safety of anti‐IgE therapy in recessive dystrophic epidermolysis bullosa

Ming Li, Z. Yao, Yifeng Guo, 2021, Clinical genetics.

Severe dermatitis, multiple allergies and metabolic wasting (SAM) syndrome caused by de novo mutation in the DSP gene misdiagnosed as generalized pustular psoriasis and treatment of acitretin with gabapentin

Ming Li, Z. Yao, Zhen Zhang, 2019, The Journal of dermatology.

Expansion of the genotypic and phenotypic spectrum of xeroderma pigmentosum in Chinese population

Ming Li, Z. Yao, R. Cheng, 2017, Photodermatology, photoimmunology & photomedicine.

Molecular screening strategies for NF1-like syndromes with café-au-lait macules

Ming Li, Z. Yao, Jia Zhang, 2016, Molecular medicine reports.

Gentamicin induces COL17A1 nonsense mutation readthrough in junctional epidermolysis bullosa

Ming Li, Z. Yao, Jianying Liang, 2020, The Journal of dermatology.

Two Novel Mutations in the ERCC8 Gene in a Patient with Ultraviolet-sensitive Syndrome.

Ming Li, Z. Yao, Fuying Chen, 2019, Acta dermato-venereologica.

LUMBAR syndrome: A case manifesting as cutaneous infantile hemangiomas of the lower extremity, perineum and gluteal region, and a review of published work

Ming Li, Z. Yao, Jia Zhang, 2017, The Journal of dermatology.

Expanding mutational spectrum of HRAS by a patient with Schimmelpenning–Feuerstein–Mims syndrome

Ming Li, W. Guan, Jia Zhang, 2021, The Journal of dermatology.

Clinical profiles of pediatric patients with GPP alone and with different IL36RN genotypes.

Ming Yan, Peichen Huang, Ming Li, 2017, Journal of dermatological science.

Next‐generation sequencing through multigene panel testing for the diagnosis of hereditary epidermolysis bullosa in Chinese population

Ming Li, Z. Yao, Jia Zhang, 2020, Clinical genetics.

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.

Mutations in POFUT1, encoding protein O-fucosyltransferase 1, cause generalized Dowling-Degos disease.

F. Hao, Heng Yan, Ming Li, 2013, American journal of human genetics.

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

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

Editorial: The genetics of human Mendelian skin disorders

Yiran Guo, W. Yap, Ming Li, 2022, Frontiers in Genetics.

Next‐generation sequencing through multi‐gene panel testing for diagnosis of hereditary ichthyosis in Chinese

X. Kong, Ming Li, Z. Yao, 2020, Clinical genetics.

Molecular Characterization of NF1 and Neurofibromatosis Type 1 Genotype-Phenotype Correlations in a Chinese Population

Furen Zhang, Hong Liu, Yong Zhang, 2015, Scientific Reports.

A novel point mutation at donor splice-site in intron 18 of ATP2A2 gene resulting in the insertion of 27 nucleotides into the mature mRNA in a Chinese patient with severe Darier's disease.

Shu-dong Yang, H. Mu, Ming Li, 2011, Journal of dermatological science.

Halo‐like phenomenon in neurofibromatosis type 1: A potential new diagnostic criterion

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

Novel and recurrent PHGDH and PSAT1 mutations in Chinese patients with Neu-Laxova syndrome

Ming Li, Z. Yao, R. Cheng, 2019, European Journal of Dermatology.

Damaged Keratin Filament Network Caused by KRT5 Mutations in Localized Recessive Epidermolysis Bullosa Simplex

Ming Li, Z. Yao, Jia Zhang, 2021, Frontiers in Genetics.

Mutations in IL36RN are associated with geographic tongue

Peichen Huang, Jie Chen, Ming Li, 2016, Human Genetics.

Genetic spectrum of dyschromatosis symmetrica hereditaria in Chinese patients including a novel nonstop mutation in ADAR1 gene

Zhixiu Li, Xiuli Wang, Guolong Zhang, 2016, BMC Medical Genetics.

Family of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis caused by a novel FAM111B mutation

Ming Li, Z. Yao, Zhen Zhang, 2019, The Journal of dermatology.

Mutation in FAM111B Causes Hereditary Fibrosing Poikiloderma with Tendon Contracture, Myopathy, and Pulmonary Fibrosis.

Ming Li, Z. Yao, Hua-guo Li, 2019, Acta dermato-venereologica.

Effect of Gentamicin Ointment in Patients with Nagashima-type Palmoplantar Keratosis: A Double-blind Vehicle-controlled Study

Ming Li, Z. Yao, Xia Yu, 2021, Acta dermato-venereologica.

Andrographolide suppresses thymic stromal lymphopoietin in phorbol myristate acetate/calcium ionophore A23187-activated mast cells and 2,4-dinitrofluorobenzene-induced atopic dermatitis-like mice model

Ming Li, Hui Zhang, Z. Yao, 2016, Drug design, development and therapy.

A novel 5-bp deletion mutation in AAGAB gene in a Chinese family with punctate palmoplantar keratoderma.

Ming Li, Z. Yao, R. Cheng, 2014, Acta dermato-venereologica.

Three novel mutations in the SLCO2A1 gene in two Chinese families with primary hypertrophic osteoarthropathy.

Yingjia Yao, Ming Li, Chunfang Gao, 2013, European journal of dermatology : EJD.

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.

S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis‐like syndrome

Shenmin Zhang, Yiran Guo, A. Slavotinek, 2022, EMBO molecular medicine.

Nagashima-type palmoplantar keratosis in a Chinese Han population

Guolong Zhang, Ming Li, Z. Yao, 2016, Molecular medicine reports.

Understanding the Pathogenesis of Generalized Pustular Psoriasis Based on Molecular Genetics and Immunopathology

Ming Li, Anqi Zhao, A. Zhao, 2022, International Journal of Dermatology and Venereology.

Coinheritance of generalized pustular psoriasis and familial Behçet‐like autoinflammatory syndrome with variants in IL36RN and TNFAIP3 in the heterozygous state

X. Kong, Ming Li, Hui Zhang, 2019, The Journal of dermatology.

Detection and characterization of low‐level mosaicism among clinically unaffected parents of ‘sporadic’ epidermolysis bullosa simplex cases

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

An Excellent Response to Topical Therapy of Four CHILD Syndrome Patients with an Increased Concentration of Simvastatin Ointment.

Ming Li, Z. Yao, Zhouwei Wu, 2019, Journal of the European Academy of Dermatology and Venereology : JEADV.

Tumor necrosis factor –238A is associated with pediatric‐onset generalized pustular psoriasis in Han patients in Eastern China

Qianqiu Wang, Ming Li, Chang Sun, 2019, The Journal of dermatology.

Two new mutations of the ADAR1 gene associated with dyschromatosis symmetrica hereditaria

Ming Li, Xiulian Xu, P. Cui, 2010, Archives of Dermatological Research.

Filaggrin Gene Mutations in Asian Races

Ming Li, Hui Zhang, Z. Yao, 2014 .

[Mutation analysis of FLG gene in 10 Chinese families with ichthyosis vulgaris].

Guolong Zhang, Ming Li, M. Shao, 2013, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

An excellent response to topical therapy of four congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome patients with an increased concentration of simvastatin ointment

Z. Yang, Y. Gu, Ming Li, 2019, Journal of the European Academy of Dermatology and Venereology : JEADV.

Deep-intronic and frameshift DSG1 variants associated with atypical severe dermatitis, multiple allergies and metabolic wasting (SAM) syndrome in a Chinese family

Mingzhu Zhao, Hongmei Li, Ming Li, 2021, European Journal of Dermatology.

Report of Chinese family with severe dermatitis, multiple allergies and metabolic wasting syndrome caused by novel homozygous desmoglein‐1 gene mutation

Ming Yan, Ming Li, Z. Yao, 2016, The Journal of dermatology.

Clinical profiles of pediatric patients with GPP alone and with different IL36RN genotypes.

Ming Yan, Peichen Huang, Ming Li, 2017, Journal of dermatological science.