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1.
Alenius, H.* et al.: The power and potential of BIOMAP to elucidate host-microbiome interplay in skin inflammatory diseases. Exp. Dermatol. 30, 1517-1531 (2021)
2.
Amar, Y.* et al.: Skin microbiome diversity and transcriptome profiling in patients with atopic dermatitis. Exp. Dermatol. 28, E8-E9 (2019)
3.
Effner, R. et al.: Effects of environmental signaling in patients with STAT1/STAT3-dependent primary immunodeficiencies. Exp. Dermatol. 28, E70-E70 (2019)
4.
Gaffal, E.* et al.: 46th annual congress of the "Arbeitsgemeinschaft Dermatologische Forschung" in Munich, Germany. Exp. Dermatol. 28, 1094-1099 (2019)
5.
Gokkaya, M. et al.: Changes in immunoglobulin levels under real-life pollen exposure: Role of nasal IgA and IgG antibodies. Exp. Dermatol. 28, E4-E5 (2019)
6.
Hoelge, I.M.* ; Skabytska, Y.* ; Amar, Y.* ; Traidl-Hoffmann, C. & Biedermann, T.*: Interaction of tight junction downregulation and staphylococci-dominated dysbiosis in the context of atopic dermatitis. Exp. Dermatol. 28, E62-E63 (2019)
7.
Hulpusch, C.* et al.: Effect of skin neutral pH versus basic emollient application on skin microbiome and physiology in atopic dermatitis patients and healthy controls. Exp. Dermatol. 28, E29-E29 (2019)
8.
Jiang, D. et al.: Visualizing scar development in living tissues reveals the collective migration of fibroblasts mediated by N-cadherin. Exp. Dermatol. 28, E13-E13 (2019)
9.
Nussbaumer, T. et al.: microbIEM-Microbiome analysis tool with automated decision making and user-friendly graphical interface. Exp. Dermatol. 28, E30-E30 (2019)
10.
Ranzinger, D.L.* et al.: IL23 differentially regulates cytokine profile of Th17 subsets leading to deviation of protective and pathogenic Th17 cells. Exp. Dermatol. 28, E38-E38 (2019)
11.
Rauer, D. et al.: Nasal microbiome under natural pollen exposure conditions: A time series analysis in allergic rhinitis patients vs. health subjects. Exp. Dermatol. 28, E6-E7 (2019)
12.
Rodriguez, E.* et al.: Exome-wide association study reveals DOK2 as novel atopic dermatitis susceptibility gene harbouring low frequency risk variants. Exp. Dermatol. 28, E46-E46 (2019)
13.
Thomas, J. et al.: Foxo4 and AHR control a stress-induced immune-mediated host protection via secretion of IL-22. Exp. Dermatol. 28, E76-E77 (2019)
14.
Wang, R.* et al.: CD23 is a biomarker of clinical response to IgE-specific immunoadsorption in patients with severe atopic eczema. Exp. Dermatol. 28, E29-E30 (2019)
15.
Baghin, V.* et al.: Predictive models for the natural course of atopic dermatitis in childhood based on serum parameters and clinical attributes. Exp. Dermatol. 27, E17-E17 (2018)
16.
Huelpuesch, C.* ; Reiger, M.* ; Nussbaumer, T. ; Neumann, A.U.* & Traidl-Hoffmann, C.*: Skin microbiome analysis is affected by choice of DNA extraction kit. Exp. Dermatol. 27, E96-E96 (2018)
17.
Huelpuesch, C. et al.: Experimental and computational analysis of contaminants in skin microbiome research. Exp. Dermatol. 27, 40-40 (2018)
18.
Kabashima, K.* & Biedermann, T.: A new era for translational atopic dermatitis research and management. Exp. Dermatol. 27, 313-317 (2018)
19.
Speth, P.* ; Jargosch, M. ; Eyerich, K.* ; Eyerich, S.* & Garzorz-Stark, N.*: The relevance of CMV reactivation in immunocompromised patients suffering from chronic inflammatory skin diseases. Exp. Dermatol. 27, E53-E53 (2018)
20.
Thomas, J. et al.: CD23 is a biomarker of clinical response to IgE-specific immunoadsorption in patients with severe atopic eczema. Exp. Dermatol. 27, 26-27 (2018)
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