Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa [rd1-p20_analysis]

ABSTRACT: Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa [rd1-p20_analysis]

PROVIDER: PRJNA675587 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
	SRR13010713_1.fastq.gz	Fastqsanger.gz
	SRR13010713_2.fastq.gz	Fastqsanger.gz
	SRR13010714_1.fastq.gz	Fastqsanger.gz
	SRR13010714_2.fastq.gz	Fastqsanger.gz
	SRR13010715_1.fastq.gz	Fastqsanger.gz

Items per page:

1 - 5 of 56

Similar Datasets

Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa [rd1-p20_p40_analysis]

Project description:Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa [rd1-p20_p40_analysis]

| PRJNA675586 | ENA

Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa [rd1-p40_analysis]

Project description:Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa [rd1-p40_analysis]

| PRJNA675588 | ENA

Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa [rd1-p20_analysis]

Project description:Contribution of Nrf2 overexpression to the rescue of the RPE and/or photoreceptors in the PDEb (rd1) model of retinal degeneration

2021-04-28 | GSE161103 | GEO

Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa [rd1-p40_analysis]

Project description:Contribution of Nrf2 overexpression to the rescue of the RPE and/or photoreceptors in the PDEb (rd1) model of retinal degeneration

2021-04-28 | GSE161104 | GEO

Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa [rd1-p20_p40_analysis]

Project description:Contribution of Nrf2 overexpression to the rescue of the RPE and/or photoreceptors in the PDEb (rd1 and rd10) model of retinal degeneration

2021-04-28 | GSE161102 | GEO

Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa

Project description:Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa

| PRJNA675578 | ENA

Inhibition of JNK ameliorates rod photoreceptor degeneration in a mouse model of retinitis pigmentosa

Project description:Retinitis pigmentosa (RP) is an inherited eye disease that causes progressive vision loss.To investigate the biological processes and molecular changes that occur in different cell types in the retinas in rd1 mice, a mouse model of retinitis pigmentosa, we performed single-cell RNA-seq to examine the transcriptomes of various retinal cells.

2024-06-23 | GSE261060 | GEO

Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa [CD1-p40_analysis]

Project description:Nrf2 overexpression rescues RPE morphology in mouse models of retinitis pigmentosa [CD1-p40_analysis]

| PRJNA675589 | ENA

Retinitis pigmentosa (RP) mouse cone transcriptom change with Txnip treatment

Project description:Purpose: To identifiy mRNA changes in retinitis pigmentosa (RP) cone photoreceptors with Txnip overexpression treatment, which improved RP cone survival and visual acuity. Methods: two RP mouse strains, rd1 and Rho-/-, were injected with AAV-Txnip or AAV-H2BGFP control subretinally at P0. Retinas were dissected out at P21 for rd1 and P90 for Rho-/-. 1,000 H2BGFP labeled cones per retina sample were FACS sorted out, and subject for RNA-sequencing. Results: >1,400 genes in P21 rd1 and >700 genes in Rho-/- were found differentially expressed with Txnip treatment. Conclusions: 25 genes are in common between P21 rd1 and P90 Rho-/- with Txnip treatment. On this list, notably, three mitochondrial Electron Transport Chain (ETC) genes were up-regulated.

2021-01-20 | GSE161622 | GEO

Rod photoreceptors degeneration in the rd1 model of retinitis pigmentosa involves a cascade of events leading to proteasome dysfunction

Project description:Retinitis pigmentosa is an inherited disease with sequential retinal degeneration of rod then cone photoreceptors leading to blindness. As in this human syndrome the rd1 mouse model carries a recessive mutation in the rod-specific cGMP phosphodiesterase beta subunit gene leading to rod followed by cone photoreceptor death. The cascade of early events leading to the induction of rod cell death through apoptosis remains unknown. We report a differential whole-genome expression profiling analysis of the wild-type and rd1 mouse retinal transcriptional program using high-density oligonucleotide microarrays with a time series experiment spanning the entire rod photoreceptor degeneration process. Among the 1252 genes found to be significantly differentially expressed, a key group of 19 loci showed distinct differences in expression early in development, suggesting that these genes of clinical interest may play a fundamental role in the induction of the rod photoreceptor degeneration.

2020-09-25 | GSE62020 | GEO

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data