Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

GNPS C. elegans OAC mutants metabolomics in negative polarity

ABSTRACT: negative polarity of metabolomic data of C. elegans OAC mutants

INSTRUMENT(S): Q Exactive HF

ORGANISM(S): Caenorhabditis Elegans (ncbitaxon:6239)

SUBMITTER: Frank Schroeder

PROVIDER: MSV000088210 | GNPS | Mon Oct 11 11:37:00 BST 2021

REPOSITORIES: GNPS

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
		Other

Items per page:

1 - 1 of 1

Similar Datasets

C. elegans OAC mutants metabolomics in negative polarity

Project description:negative polarity of metabolomic data of C. elegans OAC mutants

2021-10-11 | MSV000088210 | MassIVE

Sequencing of Caenorhabditis elegans overexpression mutants.

Project description:Sequencing of Caenorhabditis elegans overexpression mutants.

| PRJNA434681 | ENA

Gene expression under short-term moderate hypoxia and in the HIF-1 negative regulator mutants in Caenorhabditis elegans

Project description:Hypoxia inducible transcription factor HIF is the master regulator of hypoxia response in metazoans. The stability and activity of HIF are tightly regulated. In the model organism C. elegans, the homolog of HIF is HIF-1. The stability and activity of HIF-1 are negatively regulated by vhl-1, egl-9, rhy-1 and swan-1 when HIF-1 is stabilized by vhl-1 mutation. Here, we are using Affymetrix microarray to measure the immediate gene expression changes under short-term hypoxia treatment (2 hours of 0.5% oxygen treatment). We also want to understand whether the HIF-1 acvitity negative regulators function in common pathway(s) to regulate HIF-1 activity or not. We find that gene expression patterns in these HIF-1 activity negative regulator mutants are extraordinarily similar, which supports the model that they function in common pathway(s) to regulate HIF-1 activity.

2023-04-15 | GSE228851 | GEO

Histone marks in C. elegans IKB mutants

Project description:Our study focuses in undersatnding the chromatin-associated function of the c. elegans IKB homologues nfki-1 and ikb-1. We this objective, we have generated different worm mutant strains and then analyzed by ChIP-seq possible changes in H3K36me3 and H3K27me3 marks in the WT , nfki-1, ikb-1 and double c elegans mutants.

2020-06-27 | GSE101495 | GEO

Transcriptomic Analysis of pnp-1 mutants in C. elegans

Project description:We used RNA-seq to identify gene expression changes in C. elegans pnp-1 mutants

2021-04-14 | GSE165786 | GEO

Transcriptomic analysis of pals-22 and pals-25 mutants in C. elegans

Project description:We used RNA-seq to identify gene expression changes in C. elegans pals-22 mutants, pals-22 pals-25 double mutants, and pals-25 mutants

2022-09-02 | GSE212552 | GEO

Spike-in SILAC MS of C. elegans CPEB homolog mutants.

Project description:Comparative proteomic study between C. elegans wild-type N2 and CPEB homolog mutants: fog-1, cpb-2, and cpb-3.

2017-08-02 | PXD004104 | Pride

Expression data from C. elegans wdr-23 mutants

Project description:The WDR-23 protein regulates the transcription factor SKN-1 directly. C. elegans wdr-23 mutants have highly active SKN-1 and are stress resistant, long-lived, small, and reproduce poorly. We used microarrays to measure global gene expression in wdr-23 mutants and to indentify genes regulated by SKN-1.

2020-09-01 | GSE73101 | GEO

Transcriptomic analysis of ddi-1(icb156) mutants in C. elegans

Project description:We used RNA-seq to identify gene expression changes in C. elegans ddi-1(icb156) mutants

2023-09-30 | GSE241087 | GEO

Transcriptomic analysis of pals-25(icb98gf) mutants in C. elegans

Project description:We used RNA-seq to identify gene expression changes in C. elegans pals-25(icb98gf) mutants

2022-09-02 | GSE206756 | GEO