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Multi-Omics Research Strategies for Psoriasis and Atopic Dermatitis

International journal of molecular sciences, 2023-04, Vol.24 (9), p.8018

2023

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Mitophagy and immune infiltration in vitiligo: evidence from bioinformatics analysis

Frontiers in immunology, 2023-05, Vol.14, p.1164124-1164124

2023

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Crosstalk between cholesterol metabolism and psoriatic inflammation

Frontiers in immunology, 2023-05, Vol.14, p.1124786-1124786

2023

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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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Enhanced debris expelling in high-speed wire electrical discharge machining

International journal of advanced manufacturing technology, 2017-11, Vol.93 (5-8), p.2913-2920

2017

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Super-high-thickness high-speed wire electrical discharge machining

International journal of advanced manufacturing technology, 2018-03, Vol.95 (5-8), p.1805-1818

2018

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Hypermethylation of HLA-C may be an epigenetic marker in psoriasis

Journal of dermatological science, 2016-07, Vol.83 (1), p.10-16

2016

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Inflammatory loop involving Staphylococcus aureus, IL-36γ, and cathepsin S drives immunity disorders in familial acne inversa keratinocytes

Heliyon, 2024-06, Vol.10 (11), p.e31509, Article e31509

2024

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A de novo missense mutation in the NC1 domain of type VII collagen leads to dystrophic epidermolysis bullosa

Postȩpy dermatologii i alergologii, 2022-01, Vol.39 (3), p.623-626

2022

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Hidradenitis suppurativa is treated with low‐dose flutamide

Journal of dermatology, 2019-02, Vol.46 (2), p.e52-e54

2019

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Middle of the breasts pigmentation in a pedigree with POFUT1-related Dowling-Degos disease, expansion of the phenotype

Postȩpy dermatologii i alergologii, 2021-01, Vol.38 (3), p.526-527

2021

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Increased serum interleukin-6 levels in patients with hidradenitis suppurativa

Postȩpy dermatologii i alergologii, 2017-02, Vol.1, p.82-84

2017

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Associations between vitamin D receptor gene polymorphisms and chronic spontaneous urticaria in Chinese Han population

Postȩpy dermatologii i alergologii, 2020-04, Vol.37 (2), p.250-254

2020

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Is SAPHO Syndrome Linked to PASH Syndrome and Hidradenitis Suppurativa by Nicastrin Mutation? A Case Report

Journal of rheumatology, 2018-11, Vol.45 (11), p.1605-1607

2018

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Mutational spectrum of the ADAR1 gene in dyschromatosis symmetrica hereditaria

Archives of Dermatological Research, 2010-08, Vol.302 (6), p.469-476

2010

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An atypical case of incontinentia pigmenti with a hypomorphic variant

Pediatric dermatology, 2024-03, Vol.41 (2), p.351-353

2024

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Advance in Multi-omics Research Strategies on Cholesterol Metabolism in Psoriasis

Inflammation, 2024-06, Vol.47 (3), p.839-852

2024

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Two Cases of Eyelid Leukoderma Associated With Eyelash Extension

Journal of cosmetic dermatology, 2024-09

2024

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Nicastrin/miR-30a-3p/RAB31 Axis Regulates Keratinocyte Differentiation by Impairing EGFR Signaling in Familial Acne Inversa

Journal of investigative dermatology, 2019-01, Vol.139 (1), p.124-134

2019

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PSENEN Mutation Carriers with Co-manifestation of Acne Inversa (AI) and Dowling-Degos Disease (DDD): Is AI or DDD the Subphenotype?

Journal of investigative dermatology, 2017-10, Vol.137 (10), p.2234-2236

2017

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Large taper mechanism of HS-WEDM

International journal of advanced manufacturing technology, 2017-06, Vol.90 (9-12), p.2969-2977

2017

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Proprotein Convertase Furin Regulates Melanogenesis via the Notch Signaling Pathway

Discovery medicine, 2023-04, Vol.35 (175), p.144-156

2023

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Novel keratin 16 mutation in a Chinese family with focal palmoplantar keratoderma

International journal of dermatology, 2021-05, Vol.60 (5), p.e187-e189

2021

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KRT5 mutation regulate melanin metabolism through notch signalling pathway between keratinocytes and melanocytes

Experimental dermatology, 2023-06, Vol.32 (6), p.752-765

2023

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

Journal of investigative dermatology, 2018-01, Vol.138 (1), p.230-233

2018

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Multi-Omics Research Strategies for Psoriasis and Atopic Dermatitis

Mitophagy and immune infiltration in vitiligo: evidence from bioinformatics analysis

Crosstalk between cholesterol metabolism and psoriatic inflammation

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

Enhanced debris expelling in high-speed wire electrical discharge machining

Super-high-thickness high-speed wire electrical discharge machining

Hypermethylation of HLA-C may be an epigenetic marker in psoriasis

Inflammatory loop involving Staphylococcus aureus, IL-36γ, and cathepsin S drives immunity disorders in familial acne inversa keratinocytes

A de novo missense mutation in the NC1 domain of type VII collagen leads to dystrophic epidermolysis bullosa

Hidradenitis suppurativa is treated with low‐dose flutamide

Middle of the breasts pigmentation in a pedigree with POFUT1-related Dowling-Degos disease, expansion of the phenotype

Increased serum interleukin-6 levels in patients with hidradenitis suppurativa

Associations between vitamin D receptor gene polymorphisms and chronic spontaneous urticaria in Chinese Han population

Is SAPHO Syndrome Linked to PASH Syndrome and Hidradenitis Suppurativa by Nicastrin Mutation? A Case Report

Mutational spectrum of the ADAR1 gene in dyschromatosis symmetrica hereditaria

An atypical case of incontinentia pigmenti with a hypomorphic variant

Advance in Multi-omics Research Strategies on Cholesterol Metabolism in Psoriasis

Two Cases of Eyelid Leukoderma Associated With Eyelash Extension

Nicastrin/miR-30a-3p/RAB31 Axis Regulates Keratinocyte Differentiation by Impairing EGFR Signaling in Familial Acne Inversa

PSENEN Mutation Carriers with Co-manifestation of Acne Inversa (AI) and Dowling-Degos Disease (DDD): Is AI or DDD the Subphenotype?

Large taper mechanism of HS-WEDM

Proprotein Convertase Furin Regulates Melanogenesis via the Notch Signaling Pathway

Novel keratin 16 mutation in a Chinese family with focal palmoplantar keratoderma

KRT5 mutation regulate melanin metabolism through notch signalling pathway between keratinocytes and melanocytes

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

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