Gaspar M M MM - OmicsDI

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Unknown (89)
Proteomics (8)
Transcriptomics (2)
Metabolomics (1)

Organisms

Homo sapiens (5)
Lactococcus lactis (1)
Drosophila melanogaster (1)
Escherichia coli (1)
Glycine max (1)
Zea mays (1)

Repository

pride (8)
biostudies-arrayexpress (2)
MetaboLights (1)

Tissue

Root (2)
Cervical adenocarcinoma cell (1)
Cholangiocyte (1)
Embryonic stem cell (1)
Macrophage (1)
Plant cell (1)
Spleen (1)
T cell (1)

Disease

Gaucher's disease (1)
Wounds and Injuries (1)

Technology Type

Mass Spectrometry (8)
Bottom-up proteomics (4)
Shotgun proteomics (4)
Data-independent acquisition (2)
Mass spectrometry (1)
Data-dependent acquisition (1)

Instrument Platform

Q Exactive (1)

Publication Date

2026 (3)
2024 (2)
2016 (2)
2012 (1)
2011 (1)
2025 (1)
2023 (1)

CHEBI ID

CHEBI:10072 (1)
CHEBI:10125 (1)
CHEBI:10362 (1)
CHEBI:131434 (1)
CHEBI:132188 (1)
CHEBI:132477 (1)
CHEBI:132479 (1)
CHEBI:132948 (1)
CHEBI:132966 (1)
CHEBI:132983 (1)
CHEBI:132994 (1)
CHEBI:133005 (1)
CHEBI:133026 (1)
CHEBI:133028 (1)
CHEBI:133032 (1)
CHEBI:133046 (1)
CHEBI:133066 (1)
CHEBI:133077 (1)
CHEBI:133089 (1)
CHEBI:133096 (1)
CHEBI:133101 (1)
CHEBI:133112 (1)
CHEBI:133115 (1)
CHEBI:133119 (1)
CHEBI:133139 (1)
CHEBI:133141 (1)
CHEBI:133144 (1)
CHEBI:133148 (1)
CHEBI:133172 (1)
CHEBI:133176 (1)

Metabolite Name

(R)-3-hydroxybutyrylcarnitine (1)
1,3,7-trimethylurate (1)
1,3-dimethylurate (1)
1,6-anhydroglucose (1)
1,7-dimethylurate (1)
1-(1-enyl-palmitoyl)-2-arachidonoyl-GPC (P-16:0/20:4)* (1)
1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (P-16:0/20:4)* (1)
1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (P-16:0/18:2)* (1)
1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (P-16:0/18:2)* (1)
1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1)* (1)
1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0)* (1)
1-(1-enyl-palmitoyl)-GPE (P-16:0)* (1)
1-(1-enyl-stearoyl)-2-linoleoyl-GPE (P-18:0/18:2)* (1)
1-(1-enyl-stearoyl)-GPE (P-18:0)* (1)
1-arachidonoyl-GPI* (20:4)* (1)
1-lignoceroyl-GPC (24:0) (1)
1-linolenoyl-GPC (18:3)* (1)
1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6)* (1)
1-linoleoyl-GPA (18:2)* (1)
1-linoleoyl-GPC (18:2) (1)
1-linoleoyl-GPE (18:2)* (1)
1-linoleoyl-GPI* (18:2)* (1)
1-methyl-4-imidazoleacetate (1)
1-methyladenosine (1)
1-methylhistidine (1)
1-methylnicotinamide (1)
1-methylurate (1)
1-methylxanthine (1)
1-myristoyl-2-palmitoyl-GPC (14:0/16:0) (1)
1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6)* (1)

Study type

Transcription profiling by array (2)

Release Date

2021 (16)
2025 (11)
2024 (10)
2023 (10)
2019 (10)
2022 (8)
2020 (8)
2018 (5)
2012 (2)
2026 (2)
2017 (2)
2015 (2)
2014 (2)
2011 (1)
2013 (1)
2002 (1)

Lab affiliation

Universidade Estadual do Norte Fluminense Darcy Ribeiro (UENF), Centro de Biociências e Biotecnologia, Laboratório de Química e Função de Proteínas e Peptídeos, Prédio P5, Sala 228, Bairro Parque Califórnia, Campos dos Goytacazes, RS - CEP: 28013-602 (2)
Centro de Investigación del Cáncer, CSIC/Universidad de Salamanca, Spain (1)
Clinical Proteomics Facility, Medical Biochemistry, Academic Medical Center, University of Amsterdam (1)
Department of Biochemistry and Molecular Biology. University of the Basque Country (EHU) (1)
Helmholtz Centre for Environmental Research - UFZ Head of Department for Molecular Systems Biology http://www.ufz.de/index.php?de=17634 Permoserstr. 15 Building 6, R 521 04318 Leipzig GERMANY Tel.: +49-341-235-1211 Fax: +49-341-235-451211 (1)
Mayo Clinic, Rochester, USA (1)
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Lisbon, Portugal. (1)

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A red wine intervention does not modify plasma trimethylamine N-oxide but is associated with broad shifts in the plasma metabolome and gut microbiota composition

BACKGROUND: Gut microbiota profiles are closely related to cardiovascular diseases through mechanisms that include the reported deleterious effects of metabolites, such as trimethylamine N-oxide (TMAO), which have been studied as diagnostic and therapeutic targets. Moderate red ...

2024-05-09 | MTBLS310 | MetaboLights

Proteomic analysis of RRP12-containing complexes in HeLa cells upon RPS19 depletion

This dataset contains a mass spectrometry-based proteomic analysis of RRP12-containing complexes isolated from human HeLa cells. The study was designed to analyze the interactome of the ribosome biogenesis factor RRP12 in the context of RPS19 deficiency, a defect associated with Diamond-Blackfan ane...

ORGANISM(S): Homo sapiens (Human)

2026-06-26 | PXD077805 | Pride