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Links from GEO DataSets

Items: 20

1.

Integrative small and long RNA-omics analysis of human healing and non-healing wounds discovers cooperating microRNAs as therapeutic targets

(Submitter supplied) Due to microRNAs' (miRs) important functions and high potential for disease diagnosis and therapy, increasing efforts have been put to understand their role in wound repair and identify targetable miRs for wound treatment. However, lack of knowledge about miR-mediated gene expression in human wound tissues hinders the recognition of clinically relevant miRs. Here we profiled genome-wide miR and mRNA expression by RNA-sequencing in the same set of samples from human normal acute wounds and chronic non-healing venous ulcers (VU). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL16791 GPL20301
40 Samples
Download data: TXT
2.

Human skin specific long noncoding RNA HOXC13-AS regulates keratinocyte differentiation by inferfering with Golgi-ER retrograde transport

(Submitter supplied) In an RNAseq analysis, we have identified the HOXC13-AS significantly downregulated in wound biopsies and epidermal cells compared to skin counterparts. To study the genes regulated by HOXC13-AS, we transfected HOXC13-AS siRNA pool into human primary epidermal keratinocytes to knockdown HOXC13-AS and induced cell differentiation for 3 days by 1.5 mM calcium. We performed a global transcriptome analysis of keratinocytes upon the HOXC13-AS knockdown using Affymetrix arrays.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL24324
6 Samples
Download data: CEL
Series
Accession:
GSE206103
ID:
200206103
3.

Integrative small and long RNA-omics analysis of human healing and non-healing wounds discovers cooperating microRNAs as therapeutic targets

(Submitter supplied) We identified pathologically relevant miRs that exhibited abnormal VU expression and displayed their targets enriched explicitly in the VU gene signature. The biological function of these miRNAs in human epidermal keratinocytes or fibroblasts during wound repair remains unclear. To study the genes regulated by miR-96-5p, miR-218-5p, miR-424-5p, miR-450b-5p, miR-516b-5p or miR-7704, we transfected miRNA mimics into human primary epidermal keratinocytes or fibroblasts to overexpress respective miRNA expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL23159
27 Samples
Download data: CEL
Series
Accession:
GSE196773
ID:
200196773
4.

A global transcriptome analysis of human epidermal keratinocytes upon overexpression of microRNA-34a or microRNA-34c

(Submitter supplied) miR-34a and miR-34c were found up-regulated at wound-edges of human venous ulcer compared to nomal wound and the intact skin; however their biological role in keratinocytes during wound repair has not been studied. To study the genes regulated by miR-34a and miR-34c, we transfected miR-34a and miR-34c mimic into human primary epidermal keratinocytes to overexpress them. We performed a global transcriptome analysis of keratinocytes upon overexpression of miR-34a or miR-34c using Affymetrix arrays.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL24324
10 Samples
Download data: CEL
Series
Accession:
GSE117506
ID:
200117506
5.

DLX3 binding sites in Supabasal Keratinocytes

(Submitter supplied) DLX3 is a homeodomain transcription factor involved in epidermal differentiation. Here we investigated the distribution of DLX3 DNA binding sites in suprabasal differentiating keratinocytes using ChIP-seq.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
3 Samples
Download data: BED, BEDGRAPH
Series
Accession:
GSE89884
ID:
200089884
6.

A global transcriptome analysis of human epidermal keratinocytes upon inhibition of lncRNA WAKMAR1

(Submitter supplied) Recent study has revealed that long non-coding RNAs (lncRNAs) perform as important regulators of cellular physiology and pathology, which makes them promising therapeutic and diagnostic entities. We found lncRNA WAKMAR1 is significantly down-regulated in wound-edge keratinocytes from venous ulcer and diabetic foot ulcer compared to the normal wounds. To study the genes regulated by WAKMAR1, we transfected lncRNA GapmeRs into human primary epidermal keratinocytes to inhibit its expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17692
6 Samples
Download data: CEL
Series
Accession:
GSE114908
ID:
200114908
7.

The long non-coding RNA LINC00941 regulates human epidermal homeostasis through interaction with the MTA2/NuRD complex

(Submitter supplied) Numerous long non-coding RNAs (lncRNAs) were shown to have functional impact on cellular processes, such as human epidermal homeostasis, but for only a few the mode of action has been elucidated. Here, we report that lncRNA LINC00941 controls keratinocyte differentiation on a global level through association with the MTA2/NuRD complex, one of the major chromatin remodelers in cells. LINC00941 was found to interact with NuRD-associated MTA2, suppressing the expression of the transcription factor EGR3, a regulator of epidermal differentiation. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL30173
10 Samples
Download data: BED, BW
Series
Accession:
GSE237175
ID:
200237175
8.

A global transcriptome analysis of keratinocytes upon overexpression of microRNA-132

(Submitter supplied) MiR-132 is one of the most upregulated miRNAs in keratinocytes of human skin wounds during the inflammatory phase of healing; however its biological role during skin wound healing has not been studied. To study the genes regulated by miR-132, we transfected miR-132 mimics (pre-miR-132) into primary human keratinocytes to overexpress miR-132. We performed a global transcriptome analysis of keratinocytes upon overexpression of miR-132 using Affymetrix arrays.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
6 Samples
Download data: CEL
Series
Accession:
GSE61139
ID:
200061139
9.

Divergent Functions of Histone Acetyltransferase Paralogs KAT2A and KAT2B in Keratinocyte Stemness and Differentiation

(Submitter supplied) The mammalian epidermis undergoes constant renewal replenished by a pool of stem cells and terminal differentiation of their progeny. This is accompanied by changes in gene expression and morphology orchestrated, in part, by epigenetic modifiers. Here, we defined the role of histone acetyltransferase KAT2A in epidermal homeostasis and provided a comparative analysis that revealed key functional divergence with its paralogue, KAT2B. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
24 Samples
Download data: CSV
Series
Accession:
GSE215244
ID:
200215244
10.

A microarray analysis of human epidermal keratinocytes upon depletion of the long non-coding RNA LOC100130476

(Submitter supplied) The lncRNA LOC100130476 (named as WAKMAR2) was found to be down-regulated in epidermal keratinocytes in human chronic non-healing wounds compared to normal acute wounds and the intact skin. However, its biological role in keratinocytes during wound repair has not been studied. To study the genes regulated by WAKMAR2, we transfected Antisense LNA GapmeR against WAKMAR2 into human primary epidermal keratinocytes to deplete it. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL24324
6 Samples
Download data: CEL
Series
Accession:
GSE114203
ID:
200114203
11.

MicroRNA differential expression in skin and oral mucosal epithelium

(Submitter supplied) While skin and oral mucosa share many morphological similarities, oral mucosal wounds heal more rapidly than skin wounds. Epithelial cells from oral mucosa exhibit increased migratory and proliferative capacities when compared to cells from skin, suggesting that the improved repair of mucosa may involve intrinsic differences in epithelial cells. This is an exploratory experiment to define the differential microRNA expression of baseline unwounded skin and oral mucosa epithelium.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL26081
2 Samples
Download data: TXT
Series
Accession:
GSE125423
ID:
200125423
12.

miR-Seq on paired skin and oral mucosal wound healing

(Submitter supplied) To delineate the role of microRNAs in the site-specific injury response, we compared the microRNAome of skin and oral mucosa both at baseline and throughout the time course of wound healing.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL17021
24 Samples
Download data: XLSX
Series
Accession:
GSE121996
ID:
200121996
13.

Healing human gingiva miRNome

(Submitter supplied) This study is the first to report on the miRNome of healing gingiva and to provide an integrative analysis of mRNA/miRNA expression during human oral wound healing; the results offer novel insights into the participating molecular mechanisms and suggest that miR-124-3p and PXDN could be potential wound healing therapeutic targets.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL17303
18 Samples
Download data: XLSX
Series
Accession:
GSE111466
ID:
200111466
14.

Combined miRNA-mRNA transcriptional profiling in the human skin

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
synthetic construct; Homo sapiens
Type:
Non-coding RNA profiling by array; Expression profiling by array
Platforms:
GPL17586 GPL19117
14 Samples
Download data: CEL
Series
Accession:
GSE145305
ID:
200145305
15.

Combined miRNA-mRNA transcriptional profiling in the human skin [mRNA_PSOR]

(Submitter supplied) mRNA and miRNA transcription changes during epidermal differentiation and between lesional psoriatic skin and normal skin were analysed
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
6 Samples
Download data: CEL
Series
Accession:
GSE145304
ID:
200145304
16.

Combined miRNA-mRNA transcriptional profiling in the human skin [Kera]

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; synthetic construct
Type:
Non-coding RNA profiling by array; Expression profiling by array
Platforms:
GPL16686 GPL19117
18 Samples
Download data: CEL
Series
Accession:
GSE145059
ID:
200145059
17.

Combined miRNA-mRNA transcriptional profiling in the human skin [mRNA_Kera]

(Submitter supplied) mRNA and miRNA transcription changes during epidermal differentiation were analysed using proliferating keratinoctes (pKC), differentiated keratinocytes (dKC) and skin equivalents (SE)
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
9 Samples
Download data: CEL
Series
Accession:
GSE145058
ID:
200145058
18.

Combined miRNA-mRNA transcriptional profiling in the human skin [miRNA_Kera]

(Submitter supplied) mRNA and miRNA transcription changes during epidermal differentiation were analysed using proliferating keratinoctes (pKC), differentiated keratinocytes (dKC) and skin equivalents (SE)
Organism:
synthetic construct; Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL19117
9 Samples
Download data: CEL
Series
Accession:
GSE145056
ID:
200145056
19.

Combined miRNA-mRNA transcriptional profiling in the human skin [miRNA_PSOR]

(Submitter supplied) mRNA and miRNA transcription changes during epidermal differentiation and between lesional psoriatic skin and normal skin were analyzed
Organism:
Homo sapiens; synthetic construct
Type:
Non-coding RNA profiling by array
Platform:
GPL19117
8 Samples
Download data: CEL
Series
Accession:
GSE145054
ID:
200145054
20.

Control of Somatic Tissue Differentiation by the Long Non-Coding RNA TINCR

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL9115 GPL570
11 Samples
Download data: CEL
Series
Accession:
GSE40123
ID:
200040123
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