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Links from GEO DataSets

Items: 20

1.

Major differences between human atopic dermatitis and murine models as determined by global genomic profiling

(Submitter supplied) In this study we applied genomic profiling to evaluate the transcriptomic differences between murine models ot atopic dermatitis. We evaluated the expression data of five models and their respective controls, and one previously published murine dataset (GSE50400). The included models were groupe 1 (Lesional: Flaky tail and FLG mutant; Control: C57BL/6NCrSlc), Group 2 (Lesional: NC/Nga(+mite); Control: NC/Nga(-mite)), Group 3 (Lesional: OVA-ODT 24h; Control: C57BL/6NCrSlc), and Group 4 (Lesional: OXA 2h; Control: BALB/c,Acetone).
Organism:
Mus musculus
Type:
Expression profiling by array; Third-party reanalysis
Platforms:
GPL6246 GPL17400
37 Samples
Download data: CEL, TXT
Series
Accession:
GSE81119
ID:
200081119
2.

Genome-Wide Profiling of Lesional and Non-Lesional Skin from Atopic Dermatitis, Psoriasis, and Contact Dermatitis Skin

(Submitter supplied) Genome-Wide Profiling of Lesional and Non-Lesional Skin from Atopic Dermatitis, Psoriasis, and Contact Dermatitis Skin
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
75 Samples
Download data: TXT
Series
Accession:
GSE153007
ID:
200153007
3.

Distinct transcriptomic profiles of early-onset atopic dermatitis in blood and skin of pediatric patients

(Submitter supplied) Background: Atopic dermatitis (AD) predominantly affects young children, but our understanding of AD pathogenesis is based on skin and blood samples from longstanding adult AD. Genomic biopsy profiling from early pediatric AD showed significant Th2 and Th17/Th22-skewing, without the characteristic adult Th1 up-regulation. Since obtaining pediatric biopsies is difficult, blood gene expression profiling may provide a surrogate for the pediatric skin signature. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
46 Samples
Download data: CEL
Series
Accession:
GSE116486
ID:
200116486
4.

Blocking IL-4Rα with dupilumab (REGN668/SAR231893) rapidly suppresses major pathomechanisms in the skin of severe atopic dermatitis patients

(Submitter supplied) Atopic dermatitis (AD) is the most common inflammatory skin disease, with high unmet need for new therapies that are safe for chronic use. Emerging data suggest that TH2-cytokines play important roles in a variety of allergic and atopic conditions, including asthma and AD. In early phase clinical trials, dupilumab (a fully human monoclonal antibody against IL-4Rα that potently blocks IL-4 and IL-13 signaling) rapidly and markedly improved clinical measures in adults with either asthma (with elevated eosinophil counts) or moderate-to-severe AD. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
40 Samples
Download data: CEL
Series
Accession:
GSE59294
ID:
200059294
5.

RNA-Seq atopic dermatitis transcriptome profiling provides insights into novel disease mechanisms with potential therapeutic implications

(Submitter supplied) Purpose: provide evidence that RNA-seq can add information to transcriptome profiling already discovered by other technologies for atopic dermatitis Methods: mRNA profiles of 20 atopic dermatitis were analyzed to compare lesional and non-lesional skin, then transcriptomes found by reads were compared to Microarray and RT-PCR Results:RNA-seq provided complementary genes to AD transcriptome IL-36 and TREM-1 Conclusions: Our study represents the first analysis of lesional AD tissue by RNA-seq and comparison to microarray and RT-PCR
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL10999
40 Samples
Download data: TXT
Series
Accession:
GSE65832
ID:
200065832
6.

Dust mite potently activates Th17/Th22 pathways and models multiple inflammatory skin conditions in humans

(Submitter supplied) House dust mite/HDM atopy patch test/APT elicits positive reactions in the majority of atopic dermatitis/AD and healthy individuals. Experimental systems for new-onset/chronic AD are needed to support rapid therapeutic development, particularly since animal models representing AD pathology in humans are lacking. HDM APT historically simulated AD, but its suitability to model the emerging AD skin phenotype as Th2/Th22 polarized with Th1 and Th17 components is unknown. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
22 Samples
Download data: CEL
Series
Accession:
GSE95759
ID:
200095759
7.

Ichthyosis molecular fingerprinting shows profound Th17-skewing and a unique barrier genomic signature

(Submitter supplied) The purpose of this study was to analyze the genomic signatures and profiles of skin from ichthyosis (various subtypes) vs. healthy patients. The analysis strategy was to study differentially expressed genes common to the ichthyosis shared phenotype, as well as individual ichthyosis subtypes, and compare and contrast to the genomic profiles of atopic dermatitis and psoriasis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
35 Samples
Download data: CEL
Series
Accession:
GSE108640
ID:
200108640
8.

Atopic Dermatitis, Psoriasis and healthy control RNA-seq cohort

(Submitter supplied) To gain a deeper understanding of the pathophysiology of AD, we conducted a large-scale transcriptomic study of AD with deeply-sequenced RNA-seq samples using long (125b) paired-end reads. By integrating deep sequencing-based skin transcriptome profiling with systems biology analysis, we are able to provide deep characterization for the expression signatures for AD, and by including psoriasis samples in the analysis, we can reveal the distinct molecular features of uninvolved and lesional skin of AD that have not been previously described.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
147 Samples
Download data: TXT
9.

Identification of novel immune and barrier genes in atopic dermatitis by means of laser capture microdissection

(Submitter supplied) This is the first report that establishes robust epidermal and dermal genomic signatures of lesional and nonlesional AD skin and normal skin compared with whole tissues. These data establish the utility of laser capture microdissection to separate different compartments and cellular subsets in patients with AD, allowing localization of key barrier or immune molecules and enabling detection of gene products usually not detected on arrays.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
52 Samples
Download data: CEL
Series
Accession:
GSE120721
ID:
200120721
10.

Molecular profiling of contact dermatitis skin identifies allergen-dependent differences in immune response

(Submitter supplied) Different allergens induce different immune responses
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
47 Samples
Download data: CEL
Series
Accession:
GSE60028
ID:
200060028
11.

Early-onset pediatric atopic dermatitis is characterized by Th2/Th17/Th22- centered inflammation and lipid alterations

(Submitter supplied) Background: While atopic dermatitis (AD) often starts in early childhood, detailed tissue profiling of early-onset AD in children is lacking, hindering therapeutic development for this patient population with a particularly high unmet need of better treatments. Objective: We sought to globally profile the skin of infants with AD compared to adults with AD and healthy controls. Methods: We performed microarray, RT-PCR and fluorescence microscopy studies in infants and young children (<5yo) with early-onset AD (<6mo) compared to age-matched controls and adults with longstanding AD. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
108 Samples
Download data: CEL
Series
Accession:
GSE107361
ID:
200107361
12.

Distinct molecular signatures of mild extrinsic and intrinsic atopic dermatitis

(Submitter supplied) Atopic dermatitis (AD) is a common inflammatory skin disease with underlying defects in epidermal function and immune responses. The goal of this study was to investigate differences in gene expression in lesional skin from patients with mild extrinsic or intrinsic AD compared to skin from healthy controls and from lesional psoriasis skin. The aim was to identify differentially expressed genes involved in skin barrier formation and inflammation, and to compare our results with those reported for patients with moderate and severe AD.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17692
31 Samples
Download data: CEL
Series
Accession:
GSE75890
ID:
200075890
13.

Broad defects in epidermal cornification in atopic dermatitis (AD) identified through genomic analysis

(Submitter supplied) In this study we used genomic profiling to characterize differences in expression of genes related to epidermal growth/differentiation and inflammatory circuits in skin lesions of psoriasis and atopic dermatitis (AD), comparing expression values to normal skin. Skin biopsies were collected from 9 patients with chronic atopic dermatitis, 15 psoriasis patients, and 9 healthy volunteers. Keywords: Genetic-pathology
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL570 GPL571
33 Samples
Download data: CEL, TXT
Series
Accession:
GSE16161
ID:
200016161
14.

Oral JAK/SYK-inhibition (ASN002) suppresses inflammation and improves epidermal barrier markers in atopic dermatitis

(Submitter supplied) We conducted a randomized, double-blind, placebo-controlled trial in adults with moderate-to-severe AD to test the efficacy of JAK/SYK-inhibitor ASN002. ASN002 significantly suppressed key AD inflammatory pathways, corresponding to clinical response, and may be an effective novel therapeutic agent for moderate-to-severe AD.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
111 Samples
Download data: CEL
Series
Accession:
GSE133385
ID:
200133385
15.

Single-cell transcriptome analysis of human skin identifies novel fibroblast subpopulation and enrichment of immune subsets in atopic dermatitis

(Submitter supplied) Background: Atopic dermatitis (AD) is a prevalent inflammatory skin disease with a complex pathogenesis, involving immune cell and epidermal abnormalities. Despite whole tissue biopsy studies that have advanced the mechanistic understanding of AD, single-cell-based molecular alterations are largely unknown. Objective: To construct a detailed, high-resolution atlas of cell populations, and to assess variability in cell composition and cell-specific gene expression in the skin of AD patients versus controls. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
17 Samples
Download data: TXT
Series
Accession:
GSE147424
ID:
200147424
16.

TWEAK mediates inflammation in experimental atopic dermatitis and psoriasis

(Submitter supplied) Atopic dermatitis and psoriasis are driven by alternate type 2 and type 17 immune responses, but some proteins might be critical to both diseases. We show that a deficiency of the TNF superfamily molecule TWEAK (TNFSF12) in mice results in defective maintenance of atopic dermatitis-specific Th2 and psoriasis-specific Th17 cells in the skin, and impaired expression of disease-characteristic chemokines and cytokines, such as CCL17 and TSLP in atopic dermatitis, and CCL20 and IL-19 in psoriasis. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
22 Samples
Download data: TXT
Series
Accession:
GSE96957
ID:
200096957
17.

IL-4/IL-13 Inhibitors for Atopic Dermatitis Induce Psoriatic Rash Transcriptionally Close to Pustular Psoriasis

(Submitter supplied) Dupilumab is an antibody targeting the IL-4/IL-13 receptors indicated for atopic dermatitis patients, but paradoxical psoriasis-like reactions have been reported under treatment. To understand the pathogenesis of DI-Pso, we performed a gene expression profiling study using microarray on skin biopsies of dupilumab-induced psoriasis, plaque psoriasis and AD compared with healthy control skin.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
19 Samples
Download data: CEL, CHP, TXT
Series
Accession:
GSE185764
ID:
200185764
18.

Difamilast treatment inhibits the expression of inflammatory mediators in bone marrow-derived basophils (BMBAs) stimulated by IL-3 + IL-33

(Submitter supplied) In this study, we explored gene expression profiles of IL-3+IL-33-stimulated BMBAs treated with difamilast, a highly selective PDE4B inhibitor. We identified that difamilast-treated basophils showed downregulated expression of inflammaory mediators including Il4, Il6 and Il13.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
9 Samples
Download data: TXT
Series
Accession:
GSE234541
ID:
200234541
19.

ScRNAseq analysis of EC sensitized mouse skin

(Submitter supplied) We performed single-cell RNA-seq to transcriptionally characterize the populations and gene expression in the skin of mice epicutaneously sensitized
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21273
6 Samples
Download data: MTX, TSV
Series
Accession:
GSE194254
ID:
200194254
20.

Genomic profiling of the overlap phenotype between psoriasis and atopic dermatitis

(Submitter supplied) Clinical overlaps between psoriasis and atopic dermatitis are sometimes undiscernible, and there is no consensus whether to treat the overlap phenotype as psoriasis or atopic dermatitis. We enrolled patients diagnosed with either psoriasis or atopic dermatitis, and clinically re-stratified them into classic psoriasis, classic atopic dermatitis, and the overlap phenotype between psoriasis and atopic dermatitis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
75 Samples
Download data: CEL
Series
Accession:
GSE182740
ID:
200182740
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