Journal of Investigative Dermatology
ISSN: 0022-202X
eISSN: 1523-1747
Publisher: Elsevier
Publications (36)
Genetic Associations of Non–Major Histocompatibility Complex Susceptibility Loci with Systemic Sclerosis in a Han Chinese Population (2022)
Pu W, Zhang R, Ma Y, Liu Q, Jiang S, Liu J, Zhao Y, et al.
Journal article
Transcriptomes of MPO-deficient patients with generalized pustular psoriasis reveals expansion of CD4+cytotoxic T cells and an involvement of complement system and interferon pathways (2021)
Hüffmeier U, Frey B, Becker I, Atreya I, Berking C, Moessner R, Wilsmann-Theis D, et al.
Conference contribution
Unbound corneocyte lipid envelopes in 12R-lipoxygenase deficiency support a direct role in lipid-protein crosslinking (2021)
Meyer JM, Crumrine D, Schneider H, Dick A, Schmuth M, Gruber R, Radner F, et al.
Conference contribution
CD23 Levels on B Cells Determine Long-Term Therapeutic Response in Patients with Atopic Eczema Treated with Selective IgE Immune Apheresis (2021)
Thomas J, Wang R, Batra R, Boehner A, Garzorz-Stark N, Eberlein B, Theis F, et al.
Journal article
Skin Sodium Accumulates in Psoriasis and Reflects Disease Severity (2021)
Maifeld A, Wild J, Karlsen TV, Rakova N, Wistorf E, Linz P, Jung R, et al.
Journal article
Genetic Analysis of MPO Variants in Four Psoriasis Subtypes in Patients from Germany (2021)
Haskamp S, Horowitz J, Oji V, Philipp S, Sticherling M, Schäkel K, Schuhmann S, et al.
Journal article
Interventions for Actinic Keratosis in Nonscalp and Nonface Localizations: Results from a Systematic Review with Network Meta-Analysis (2020)
Steeb T, Wessely A, Schmitz L, Heppt F, Kirchberger M, Berking C, Heppt M
Journal article
The α7 Nicotinic Acetylcholine Receptor: A Promising Target for the Treatment of Fibrotic Skin Disorders (2020)
Stegemann A, Flis D, Ziolkowski W, Distler J, Steinbrink K, Böhm M
Journal article
Rare Loss-of-Function Mutation in SERPINA3 in Generalized Pustular Psoriasis (2020)
Frey S, Sticht H, Wilsmann-Theis D, Gerschütz A, Wolf K, Löhr S, Haskamp S, et al.
Journal article
Homozygous Biallelic KRT5 Mutations in Epidermolysis Bullosa Simplex, Including a Complete Human Keratin 5 "Knock-Out", in Families with Extensive Consanguinity (2019)
Vahidnezhad H, Youssefian L, Daneshpazhooh M, Mahmoudi H, Kariminejad A, Fischer J, Christiansen J, et al.
Conference contribution