Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Chrysanthemum morifolium white flowers mock and infected with Botrytis cinerea

ABSTRACT: LC-MS/MS files of chrysanthemum morifolium white flowers infected with Botrytis cinerea or mock inoculated samples.

INSTRUMENT(S): Orbitrap Exploris 120

ORGANISM(S): Chrysanthemum X Morifolium (ncbitaxon:41568)

SUBMITTER: Jan van kan

PROVIDER: MSV000100849 | MassIVE | Sat Feb 14 03:07:00 GMT 2026

REPOSITORIES: MassIVE

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
		Other

Items per page:

1 - 1 of 1

Similar Datasets

LS-MS/MS dataset of Chrysanthemum seticuspe flowers and leaves infected with Botrytis cinerea

Project description:The LS-MS/MS dataset comprises of Chrysanthemum seticuspe flowers and leaves infected with Botrytis cinerea at different time-points.

2025-12-13 | MSV000100208 | MassIVE

Porcine macrophages: ASFV-infected vs. mock-infected

Project description:Porcine macrophages: ASFV-infected vs. mock-infected

| PRJNA549440 | ENA

Porcine macrophages: ASFV-infected vs. mock-infected

Project description:Transcriptional profiling of porcine macrophages infected with Afraican swine fever virus (ASFV) infected cells and mock infection was conducted in this experiment.

2019-09-30 | GSE132905 | GEO

Mock or latently infected KSHV cells (BCBL, SLK and HFF)

Project description:[original title] Mock or latently infected KSHV cells (BCBL, SLK and HFF) vs common reference (mixture of RNA from both infected and uninfected cells). Expression profiling of latently infected cells using a custom tiling microarray. SLK and HFF cells were infected and selected for rKSHV.219. Mock infected SLK and HFF cells served as controls for each of these two stably infected cells, respectively. BJAB cells served as uninfected controls for the BCBL-1 cells. Biological replicates were harvested and analyzed.

2010-03-24 | GSE20443 | GEO

Transcription profiling of white clover plants following infection by white clover mosaic virus

Project description:White clover mosaic virus (WCMV) is a major pathogen of white clover (Trifolium repens L.), with significant effects on yield and persistence. Due to the absence of natural sources of WCMV resistance a transgenic strategy has been employed to produce plants constitutively expressing WCMV replicase gene derivatives, designed to inhibit the propagation of WCMV through an RNA silencing mechanism. A 12,000 feature oligonucleotide microarray has been used to identify global changes in host plant, in addition to virus genome-encoded gene expression associated with WCMV infection in non-transgenic and transgenic WCMV-resistant white clover. Pairwise comparison between the transcriptome of mock-inoculated non-transgenic and WCMV-inoculated transgenic plants provides clear evidence for substantial equivalence between these two genotype/treatments, and demonstrate the efficacy of the transgenic strategy. WCMV- inoculated non-transgenic plants exhibit elevated abundance of many virus-encoded, and host immune response-specific transcripts compared to the transgenic resistant plants or mock-inoculated non-transgenic plants. By contrast, relative to inoculated sensitive plants, the majority of significantly up-regulated genes in mock-inoculated non-transgenic plants or WCMV-inoculated transgenic plants are markers of healthy cellular function. These results, and the occurrence of levels of WCMV-encoded transcripts in inoculated transgenic plants equivalent to those in virus-free plants, confirm the validity of the transgenic RNA silencing approach.<br>

2010-06-30 | E-MEXP-1688 | biostudies-arrayexpress

TurboID-G3BP1 proteome identification in Mock infected U2OS

Project description:Identifiy G3BP1 interactome via TurboID labeling in mock or SFV infected U2OS cells

2025-03-10 | PXD061635 |

Transcriptome analysis of HCMV infected and mock-infected Kasumi-3 cells at 24 hours post infection

Project description:Purpose: to compare host gene expression in HCMV infected and mock infected Kasumi-3 cells at 24 hours post infection

2021-03-05 | GSE164839 | GEO

RML Prion and mock-infected murine neuroblastoma cells

Project description:Affymetrix genechip profiling analsysis (MOE430A and MOE430B) of murine neuroblastoma cells infected with either RML prion strain or mock brain homogenate Keywords: Affymetrix gene expression profiling

2008-02-25 | GSE7229 | GEO

Digital gene expression (DGE) of CMV-infected tobacco leaves

Project description:Here we performed a transcriptomic study on complete symptom development process of CMV-infected Nicotiana tabacum using Solexa/Illumina's high-throughput digital gene expression (DGE) system. 12 DGE libraries (from six virus-infected samples and six corresponding mock-inoculated samples) were constructed, and the gene expression variations between the virus-infected sample and the mock-inoculated sample in each symptom stage were compared. Thousands of differentially expressed genes were obtained by the comparison, and KEGG pathway analysis of these genes suggested that many biological processes (such as phtosynthesis, pigment metabolism and plant-pathogen interaction) were related to the symptom development. The authenticity of the DGE data was further confirmed by analyzing real-time RT-PCR using several random-selected genes. We sequenced a cDNA library constructed from mixture of total RNA from six virus-infected samples and six mock-inoculated samples to get gene information for tobacco leaves in different symptom stages, including vein clearing, mosaic, severe chlorosis, partial recovery, total recovery and re-mosaic, and 95,916 Unigenes were obtained

2012-11-09 | GSE30162 | GEO

Transcription profiling of mouse scrapie ME7-infected and mock-infected brains at two important preclinical time points and at terminal stages

Project description:The experiment describes the dynamic transcriptional alterations in brains of ME7- infected, and age-matched, mock-inoculated mice immediatly before inoculation, at two important preclinical time points and at terminal stages.

2007-05-04 | E-MEXP-1005 | biostudies-arrayexpress

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