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Roles of Infection in Psoriasis

International journal of molecular sciences, 2022-06, Vol.23 (13), p.6955

2022

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Immune cell trafficking: a novel perspective on the gut-skin axis

Inflammation and Regeneration, 2024-04, Vol.44 (1), p.21-21, Article 21

2024

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Hyperpigmentation in an Elderly Patient with Atopic Dermatitis: A Quiz

Acta dermato-venereologica, 2023-09, Vol.103, p.adv13351

2023

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A Case of Familial Cold Autoinflammatory Syndrome with De Novo NLRP3 Mutation

Annals of Dermatology, 2021, 33(2), , pp.198-200

2021

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Exploring causal correlations between circulating cytokines and atopic dermatitis: a bidirectional two-sample Mendelian randomization study

Frontiers in immunology, 2024-07, Vol.15, p.1367958

2024

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Mutations in POFUT1, Encoding Protein O-fucosyltransferase 1, Cause Generalized Dowling-Degos Disease

American journal of human genetics, 2013-06, Vol.92 (6), p.895-903

2013

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

Scientific reports, 2016-07, Vol.6 (1), p.29751-29751, Article 29751

2016

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Topical Simvastatin Improves Lesions of Diffuse Normolipemic Plane Xanthoma by Inhibiting Foam Cell Pyroptosis

Frontiers in immunology, 2022-05, Vol.13, p.865704-865704

2022

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

Journal of dermatology, 2022-04, Vol.49 (4), p.463-468

2022

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Comparison of the efficacy and safety between a low-fluence 1064-nm Q-switched neodymium-doped yttrium aluminum garnet laser and a conventional Q-switched 532-nm laser for the treatment of cafe-au-lait macules in 40 Chinese children: a prospective, randomized, parallel-controlled, evaluator-blinded trial

Lasers in medical science, 2022-02, Vol.37 (1), p.279-286

2022

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Sensory ASIC3 channel exacerbates psoriatic inflammation via a neurogenic pathway in female mice

Nature communications, 2024-06, Vol.15 (1), p.5288-16, Article 5288

2024

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Gentamicin induces COL17A1 nonsense mutation readthrough in junctional epidermolysis bullosa

Journal of dermatology, 2020-03, Vol.47 (3), p.e82-e83

2020

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Woolly hair nevus caused by somatic mutation and Costello syndrome caused by germline mutation in HRAS: Consider parental mosaicism in prenatal counseling

Journal of dermatology, 2022-01, Vol.49 (1), p.161-164

2022

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Transglutaminase 3 regulates cutaneous squamous carcinoma differentiation and inhibits progression via PI3K-AKT signaling pathway-mediated Keratin 14 degradation

Cell death & disease, 2024-04, Vol.15 (4), p.252-252, Article 252

2024

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Successfully treated with siltuximab and prednisone in a 7-year-old girl with DOCK8 -deficiency presenting as recurrent wart-like lesions: a case report

Frontiers in immunology, 2024-07, Vol.15, p.1414573

2024

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A novel mutation in TRPV3 gene causes atypical familial Olmsted syndrome

Scientific reports, 2016-02, Vol.6 (1), p.21815-21815, Article 21815

2016

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

EMBO molecular medicine, 2022-05, Vol.14 (5), p.e14904-n/a

2022

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

Acta dermato-venereologica, 2019-06, Vol.99 (7), p.695-696

2019

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

Frontiers in genetics, 2021-11, Vol.12, p.736610-736610

2021

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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

Journal of dermatology, 2019-07, Vol.46 (7), p.622-625

2019

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Simvastatin ointment in the treatment of seven childhood diffuse plane xanthomas

Journal of dermatology, 2021-02, Vol.48 (2), p.223-227

2021

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

Acta dermato-venereologica, 2021-02, Vol.101 (2), p.adv00392-adv00392

2021

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Excellent response to oral clarithromycin in a patient with severe childhood granulomatous periorificial dermatitis with neck involvement

Journal of dermatology, 2020-06, Vol.47 (6), p.e222-e224

2020

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

Scientific reports, 2015-06, Vol.5 (1), p.11700-11700, Article 11700

2015

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

Journal of dermatology, 2019-11, Vol.46 (11), p.1014-1018

2019

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Roles of Infection in Psoriasis

Immune cell trafficking: a novel perspective on the gut-skin axis

Hyperpigmentation in an Elderly Patient with Atopic Dermatitis: A Quiz

A Case of Familial Cold Autoinflammatory Syndrome with De Novo NLRP3 Mutation

Exploring causal correlations between circulating cytokines and atopic dermatitis: a bidirectional two-sample Mendelian randomization study

Mutations in POFUT1, Encoding Protein O-fucosyltransferase 1, Cause Generalized Dowling-Degos Disease

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

Topical Simvastatin Improves Lesions of Diffuse Normolipemic Plane Xanthoma by Inhibiting Foam Cell Pyroptosis

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

Sensory ASIC3 channel exacerbates psoriatic inflammation via a neurogenic pathway in female mice

Gentamicin induces COL17A1 nonsense mutation readthrough in junctional epidermolysis bullosa

Woolly hair nevus caused by somatic mutation and Costello syndrome caused by germline mutation in HRAS: Consider parental mosaicism in prenatal counseling

Transglutaminase 3 regulates cutaneous squamous carcinoma differentiation and inhibits progression via PI3K-AKT signaling pathway-mediated Keratin 14 degradation

Successfully treated with siltuximab and prednisone in a 7-year-old girl with DOCK8 -deficiency presenting as recurrent wart-like lesions: a case report

A novel mutation in TRPV3 gene causes atypical familial Olmsted syndrome

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

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

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

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

Simvastatin ointment in the treatment of seven childhood diffuse plane xanthomas

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

Excellent response to oral clarithromycin in a patient with severe childhood granulomatous periorificial dermatitis with neck involvement

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

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

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