Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Croton draco

ABSTRACT: Analysis of the transcriptome of Croton draco.

PROVIDER: PRJNA484499 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
	SRR7644190_1.fastq.gz	Fastqsanger.gz
	SRR7644190_2.fastq.gz	Fastqsanger.gz
	SRR7644191_1.fastq.gz	Fastqsanger.gz
	SRR7644191_2.fastq.gz	Fastqsanger.gz
	SRR7644192_1.fastq.gz	Fastqsanger.gz

Items per page:

1 - 5 of 12

Similar Datasets

Genome-scale deconvolution of RNA structure ensembles

Project description:RNA structure heterogeneity is a major challenge when querying RNA structures with chemical probing. We introduce DRACO, an algorithm for the deconvolution of coexisting RNA conformations from mutational profiling experiments. Analysis of the SARS-CoV-2 genome using dimethyl sulfate mutational profiling with sequencing (DMS-MaPseq) and DRACO, identifies multiple regions that fold into two mutually exclusive conformations, including a conserved structural switch in the 3′ untranslated region. This work may open the way to dissecting the heterogeneity of the RNA structurome.

2020-12-23 | GSE158052 | GEO

MrgprD-expressing neurons maintain cutaneous mast cell homeostasis

Project description:This study shows that croton oil has a specific inflammatory signature involving altered expression of cytokines that is quantitatively altered by long-term LC ablation.

2021-03-23 | GSE143569 | GEO

Croton tiglium

Project description:Croton tiglium overview

| PRJNA509967 | ENA

Apodemus draco

Project description:Apodemus draco overview

| PRJNA182843 | ENA

Project description:Croton tiglium L.

| PRJNA489565 | ENA

Croton tiglium isolate:Marburg

Project description:Croton tiglium Transcriptomes from 5 different tissues

| PRJNA416498 | ENA

Epidermal RelA specifically restricts contact allergen-induced inflammation and apoptosis in skin

Project description:Strong inhibition of NF-kB signaling in the epidermis results in spontaneous skin inflammation in mice and men. Since there is evidence for linkage between polymorphisms within the NF-kB signaling pathway and human inflammatory skin phenotypes, we asked whether partial functional inhibition of NF-kB signaling in epidermal keratinocytes can modulate clinically relevant skin inflammation. We therefore mutated rela specifically in the epidermis of mice (RelAE-MUT mice). These mice show no inflammatory phenotype. Induction of contact allergy, but not croton oil induced irritant dermatitis, resulted in stronger ear swelling and increased epidermal thickness in RelAE-MUT mice. Both contact allergen and croton oil treatment led to increase expression of calgranulins A and B (S100A8/ A9) in RelAE-MUT mice. Epidermal hyperproliferation in RelAE-MUT mice was non-cell autonomous since cultured primary epidermal keratinocytes from RelAE-MUT mice showed reduced proliferation compared to controls. These results demonstrate that epidermal RelA specifically regulates DTH-induced skin inflammation. In addition, we here describe an essential but non- specific function of RelA in the protection of epidermal keratinocytes from apoptosis. Our study identifies new functions of NF-kB signaling in the epidermis and corroborates a specific role of epidermal keratinocytes in the regulation of skin inflammation

2014-12-01 | GSE56067 | GEO

Project description:Gut microbiota of South China field mice (Apodemus draco)

| PRJNA974389 | ENA

Project description:Targeted exon capture of Draco lineatus group flying lizards

| PRJNA943262 | ENA

YA_YAK_RNA_seq

Project description:Transcriptome Analysis

| OEX00021331 | NODE