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Links from GEO DataSets

Items: 20

1.
Full record GDS3753

Skin-derived precursors

Analysis of primary passage neonatal skin-derived precursors (SKP) and Sox2-positive hair follicle dermal cells from which SKPs derive. SKPs and Sox2+ dermal precursors share similar function and transcriptional profile. Results provide insight into potential role of SKPs as adult dermal stem cells.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 cell type sets
Platform:
GPL6246
Series:
GSE18690
9 Samples
Download data: CEL, CHP
2.

SKPs derive from hair follicle precursors and exhibit properties of adult dermal stem cells

(Submitter supplied) Global expression analysis of neural crest-like skin-derived precursors (SKPs) and Sox2-positive follicle dermal cells that SKPs originate from. In spite of the remarkable regenerative capacity of mammalian skin, an adult dermal stem cell has not yet been identified. Here, we provide evidence that SKPs, multipotent neural crest-like skin-derived precursors, represent an adult dermal stem cell. When transplanted into adult skin, SKPs can reconstitute the adult dermis, contribute to dermal wound-healing, home to a hair follicle niche, and instruct epidermal cells to make hair follicles. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3753
Platform:
GPL6246
9 Samples
Download data: CEL, CHP
Series
Accession:
GSE18690
ID:
200018690
3.

CONVERGENT GENESIS OF AN ADULT NEURAL CREST-LIKE DERMAL STEM CELL FROM DISTINCT DEVELOPMENTAL ORIGINS

(Submitter supplied) Skin-derived precursors (SKPs) are multipotent dermal stem cells that reside within a hair follicle niche and that share properties with embryonic neural crest precursors. Here, we have asked whether SKPs and their endogenous dermal precursors originate from the neural crest or whether, like the dermis itself, they originate from multiple developmental origins. To do this, we used two different mouse Cre lines that allow us to perform lineage tracing: Wnt1-cre, which targets cells deriving from the neural crest, and Myf5-cre, which targets cells of a somite origin. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL6247
13 Samples
Download data: CEL, CHP
Series
Accession:
GSE23954
ID:
200023954
4.

Expression profile of Gli1-expressing keratinocytes from mouse skin

(Submitter supplied) To assess if Hedgehog (Hh) responding cells in the skin have a unique expression profile, isolated keratinocytes that express the Hh response gene Gli1 were collected by FACS and their gene expression was compared to sorted CD34-expressing cells from the middle bulge region of the hair follicle and to cells from the interfollicular epidermis (IFE) by hybridization of isolated RNA to gene expression microarrays.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
8 Samples
Download data: TXT
Series
Accession:
GSE28108
ID:
200028108
5.

Single-cell RNA-seq of the developing C57/BL6 mouse back skin at E13.5, E16.5 and P0

(Submitter supplied) We performed single-cell RNA seq on C57/BL6 mouse back skin at E13.5, E16.5, and P0 to study embryonic hair follicle development. We analyzed 15,086 single cell transcriptome profiles from E13.5, E16.5 and newborn mice (postnatal day 0, P0) dorsal skin cells across hair follicle induction, organogenesis, cytodifferentiation stage. Based on t-distributed Stochastic Neighbor Embedding (tSNE) clustering, we identified 14 cell clusters from skin cells and delineated their cell identity gene expression profile. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
3 Samples
Download data: TXT
Series
Accession:
GSE131498
ID:
200131498
6.

Comparative gene expression analysis of 2 subpopulations of dermal papilla cells.

(Submitter supplied) Different types of hair follicles can be found in the skin of mice. It is believed that the signals that control hair follicle differentiation arise from cells in a structure called the dermal papilla. Understanding the nature of those signals is of interest for the biology of the normal tissue. We have developed a technique for isolation of dermal cells by enzymatic digestion of intact skin. We have identified two subpopulations of cells that can be separated by FACS. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
9 Samples
Download data: CEL, CHP
Series
Accession:
GSE16801
ID:
200016801
7.

Expression data from Transgenic mice skin expressing deltaNp63alpha

(Submitter supplied) We developed a Tet-inducible system to express deltaNp63alpha isoform under the control of keratin 5 promoter. Transgenic mice, which were Bigenic (BG) developed a severe skin phenotype with abnormal keratinocyte differentiation and defects in hair follicle development and cycling. Skin samples from transgenic animals and wild type animals were analyzed for global transcriptome changes.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE20514
ID:
200020514
8.

Sox2 ablation in the DP alters its gene expression signature

(Submitter supplied) Using Tbx18Cre to target embryonic DP precursors, we ablate Sox2 early and efficiently, resulting in diminished hair shaft outgrowth. Transcriptional profiling of Sox2 null DPs reveals increased Bmp6 and decreased Bmp inhibitor Sostdc1, a direct Sox2 transcriptional target.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
4 Samples
Download data: CEL
Series
Accession:
GSE41597
ID:
200041597
9.

Pioneer factors govern super-enhancer dynamics in stem cell plasticity and lineage choice

(Submitter supplied) Mouse hair follicles undergo synchronized cycles. Cyclical regeneration and hair growth is fueled by hair follicle stem cells (HFSCs) and transit-amplifying cells (TACs). We used ChIP-seq to unfold genome-wide chromatin landscapes of H3K27ac and Med1 to identify super-enhancers and dissect their biological relevance in cell identity and plasticity of HFSCs in vivo and in vitro.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
10 Samples
Download data: WIG
Series
Accession:
GSE61316
ID:
200061316
10.

Gene signature of mouse skin resident macrophages

(Submitter supplied) Skin resident macrophages were isolated by FACS sorting at different ages post natally and RNA was extracted
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
3 Samples
Download data: TXT
Series
Accession:
GSE58098
ID:
200058098
11.

RNA-seq analysis of hair follicle stem cell transcriptome upon loss of the transcription factor FOXC1

(Submitter supplied) We report downstream gene expression changes in stem cells of the adult mouse hair follicle upon conditional ablating of the transcription factor Forkhead Box C1 transcription factor (FOXC1). Hair follicles undergo cycles of rest (telogen; Tel) and regeneration (anagen; Ana). As such, we performed our analysis on these two different stages of hair follicles.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: TXT
Series
Accession:
GSE77256
ID:
200077256
12.

LGR5 is a conserved marker of hair follicle stem cells across species

(Submitter supplied) Using a transgenic pig expressing H2B-GFP under the control of the endogenous LGR5 promoter, we used fluorescence activated cell sorting to isolate LGR5-high and LGR5-negative epidermal cells to generate mRNA profiles of the hair follicle stem cell population, n=2 pigs. Bulk RNAseq samples were prepared from porcine cells, at least 500ng of RNA was extracted from sorted LGR5-GFP-high or LGR5-GFP-negative populations. more...
Organism:
Sus scrofa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22475
4 Samples
Download data: CSV
Series
Accession:
GSE190069
ID:
200190069
13.

Distinct Self-renewal and Differentiation Phases in the Niche of Infrequently Dividing Hair Follicle Stem Cells

(Submitter supplied) In homeostasis of adult vertebrate tissues, stem cells are thought to self-renew by infrequent and asymmetric divisions that generate another stem cell daughter and a progenitor daughter cell committed to differentiate. This model is based largely on in vivo invertebrate or in vitro mammal studies. Here we examine the dynamic behaviour of adult hair follicle stem cells in their normal setting by employing mice with repressible H2B-GFP expression to track cell divisions and Cre inducible mice to perform long-term single cell lineage tracing. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
18 Samples
Download data: CEL
Series
Accession:
GSE16516
ID:
200016516
14.

Single-cell analysis RNA sequencing of whole mouse skin at embryonic day 13.5 and 14.5

(Submitter supplied) A major challenge in delineating molecular and cellular events that precede appendage morphogenesis stems from the inability to distinguish quantitative molecular differences between cells that lack histological distinction. The hair follicle (HF) dermal condensate (DC) is a cluster of cells critical for HF development and regeneration. Events that presage emergence of this distinctive population are poorly understood. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: MTX, TSV
Series
Accession:
GSE122043
ID:
200122043
15.

Architectural niche organization by LHX2 is linked to hair follicle stem cell function

(Submitter supplied) To identify direct LHX2 target genes in HFSCs, we performed chromatin immunoprecipitation and deep sequencing (ChIP-seq) analysis using FACS-isolated HFSCs.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11002
6 Samples
Download data: WIG
Series
Accession:
GSE48068
ID:
200048068
16.

Dermal sheath contraction powers stem cell niche relocation during hair cycle regression

(Submitter supplied) Tissue homeostasis requires the balance of growth by cell production and regression through cellular loss. In the hair cycle during follicle regression, the niche traverses the skin through an unknown mechanism to reach the stem cells and prime regeneration. Here, by cell specific ablation and intravital imaging in live mice, we identify the follicle-lining dermal sheath as the key driver of tissue regression and niche relocation via smooth muscle contractile machinery that generates centripetal constriction force. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: XLSX
Series
Accession:
GSE136996
ID:
200136996
17.

Single-cell transcriptome analysis of cells in mouse hairy melanocytic nevi

(Submitter supplied) Single cell RNA-seq data was obtained from different skin cell types at days P30 or P56, when WT hair follicles are in active state (aka anagen) or resting state (aka telogen), respectively. Cell types include: Bulge stem cells, melanocytes, and myeloid cells. All cells were FACS sorted and only live single cells were collected for RNA extraction.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
605 Samples
Download data: TXT
Series
Accession:
GSE112722
ID:
200112722
18.

Transcriptome analysis of human hairy melanocytic nevi

(Submitter supplied) RNA-seq data was obtained from three individual patients. The whole skin samples were collected for RNA extraction using TRIZOL.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
6 Samples
Download data: TXT
19.

Transcriptome analysis of cells in mouse hairy melanocytic nevi

(Submitter supplied) RNA-seq data was obtained from different skin cell types at two time points: postnatal day P30, when WT dorsal hair follicles are in actively growing state (aka anagen) and P56, when WT hair follicles are in resting state (aka telogen). Cell types include: Bulge stem cells (B), dermal papilla fibroblasts (DP), secondary hair germ cells (HG), melanocytes (Melan), myeloid cells (Myel) and CD45-positive immune cells (I). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
38 Samples
Download data: TXT
Series
Accession:
GSE111999
ID:
200111999
20.

Stem cells expand potency and alter tissue fitness by accumulating diverse epigenetic memories (scRNA-seq)

(Submitter supplied) Immune and tissue stem cells retain an epigenetic memory of inflammation that intensifies sensitivity to future encounters. Here, we address whether and to what consequence stem cells possess and accumulate memories of diverse experiences. Monitoring a choreographed response to wounds, we find that as hair follicle stem cells leave their niche, migrate to repair damaged epidermis and take up long-term foreign residence there, they accumulate long-lasting epigenetic memories of each experience, culminating in post-repair epigenetic adaptations that sustain the epidermal transcriptional program and surface barrier. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
1929 Samples
Download data: CSV
Series
Accession:
GSE165314
ID:
200165314
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