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Unknown (543)
Proteomics (16)
Transcriptomics (12)
Genomics (11)
Metabolomics (3)

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Homo sapiens (31)
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pride (16)
biostudies-arrayexpress (12)
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Disease

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Instrument Platform

Bruker (1)
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Publication Date

2019 (4)
2022 (4)
2010 (3)
2021 (3)
2016 (2)
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2025 (2)
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2013 (1)
2011 (1)
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2026 (1)
2024 (1)
2018 (1)

CHEBI ID

CHEBI:111173 (1)
CHEBI:133530 (1)
CHEBI:137448 (1)
CHEBI:137450 (1)
CHEBI:137451 (1)
CHEBI:137452 (1)
CHEBI:137453 (1)
CHEBI:141538 (1)
CHEBI:15354 (1)
CHEBI:15366 (1)
CHEBI:15428 (1)
CHEBI:15843 (1)
CHEBI:16393 (1)
CHEBI:16449 (1)
CHEBI:16870 (1)
CHEBI:16919 (1)
CHEBI:16933 (1)
CHEBI:169465 (1)
CHEBI:17234 (1)
CHEBI:172722 (1)
CHEBI:17568 (1)
CHEBI:17822 (1)
CHEBI:17862 (1)
CHEBI:180545 (1)
CHEBI:180546 (1)
CHEBI:180548 (1)
CHEBI:180549 (1)
CHEBI:18086 (1)
CHEBI:18101 (1)
CHEBI:18346 (1)

Metabolite Name

(11Z,14Z)-Eicosadienoic acid (1)
(2S,3S,4R)-2-aminohexadecane-1,3,4-triol (1)
1-Meadoyl-glycero-3-phosphate (1)
1-O-Octadecylglycerol-3-phosphatidylcholine (1)
12-Hydroxystearic acid (1)
15-Hydroxypentadecanoic acid (1)
16(R)-HETE (1)
2,3-Dihydroxypropyl stearate (1)
2,3-Dinor-6-oxoprostaglandin F1alpha (1)
3-(Tert-butyl)-N-(2,3-dihydro-1-benzofuran-5-ylmethyl)-1-methyl-1H-pyrazole-5-carboxamide (1)
3-Dehydrosphinganine (1)
3-dehydro-4-methylzymosterol (1)
4-Hydroxy-16,18-tritriacontanedione (1)
4-Undecylbenzenesulfonic acid (1)
4beta-methylzymosterol-4alpha-carboxylic acid (1)
Arachidonic acid (1)
Boc-D-Asparagine (1)
Dihomo-alpha-linolenic acid (1)
Docosatetraenoic acid (1)
Ethyl eicosapentaenoic acid (1)
Glycidyl Stearate (1)
Hexyl furoate (1)
Linoleamide (1)
Mebutamate (1)
Methyl stearate (1)
PA(14:0/16:1(9Z)) (1)
PA(14:1(9Z)/16:0) (1)
PE(12:0/16:0) (1)
PI(18:0/0:0) (1)
Retinol acetate (1)

First Public Date

2024 (1)

Study type

Transcription profiling by array (10)
Comparative genomic hybridization by array (1)
MicroRNA profiling by array (1)

Release Date

2022 (67)
2021 (60)
2024 (57)
2023 (54)
2025 (47)
2020 (43)
2019 (31)
2018 (29)
2017 (29)
2014 (25)
2015 (24)
2013 (18)
2012 (18)
2016 (17)
2026 (10)
2011 (8)
2010 (6)
2008 (4)
2009 (3)
2006 (2)
2005 (1)
1999 (1)
1998 (1)

Lab affiliation

Chemistry Institute, LADETEC, Proteomics Laboratory, UFRJ, RJ, Brazil. (1)
Computational and Experimental Biology Group NOVA MEDICAL SCHOOL / FACULDADE DE CIÊNCIAS MÉDICASUNIVERSIDADE NOVA DE LISBOARua Câmara Pestana, 6-6A | 1150-082 Lisboa Portugal E-mail: rune.matthiesen@nms.unl.pt | www.nms.unl.pt (1)
Department of Biochemistry, Institute of Chemistry, Federal university of Rio de Janeiro (1)
Dipartimento di Chimica, Sapienza Università di Roma, Roma, Italy (1)
Federal University of Rio de Janeiro (1)
Federal University of Rio de Janeiro, Institute of Chemistry, Proteomics unit (1)
Head of Mass Spectrometry Laboratory, Brazilian Biosciences National Laboratory (LNBio), Brazilian Center for Research in Energy and Materials (CNPEM), Campinas, SP, Brazil. (1)
Instituto de Investigaciones Sanitarios de Santiago de Compostela (1)
Laboratory of Proteomics/LADETEC, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil (1)
NMS, CEDOC, NOVA University Lisbon, Portugal (1)
Obesity and Comorbidities Research Center (OCRC), Department of Structural and Functional Biology, Institute of Biology (IB), University of Campinas (UNICAMP), Campinas, São Paulo, Brazil (1)
Sonia Melo, PhD Principal Investigator Cancer Unit Intercellular Communication and Cancer i3s (http://www.i3s.up.pt) Rua Alfredo Allen, 208 | 4200-135 Porto - Portugal (1)
Unidade Proteômica, Departamento de Bioquímica, Instituto de Química, Universidade Federal do Rio de Janeiro; Laboratório de Proteômica (LabProt), LADETEC, Instituto de Química, Universidade Federal do Rio de Janeiro; Centro de Pesquisa em Medicina de Precisão, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro (1)
Universitätsklinikum Heidelberg Medizinische Klinik - Med.V Im Neuenheimer Feld 410 69120 Heidelberg (1)
i3S - Institute for Research and Innovation in Health, University of Porto, Portugal (1)
i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal Ipatimup - Instituto de Patologia e Imunologia Molecular da Universidade do Porto, Porto, Portugal (1)

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Inhibition of hepatitis C virus using siRNA targeted to the virus and Hsp90.

Not available

S-EPMC5225065 | biostudies-literature

Complete Genome Sequences of Two Bovine Alphaherpesvirus 5 Subtype C Strains from Southeast Brazil.

Not available

S-EPMC8830361 | biostudies-literature

Maize Crops Under Rising Temperatures: Bacterial Influence on Biochemical and Lipidomic Changes Induced by Heat.

Not available

S-EPMC12389081 | biostudies-literature

Multisystem inflammatory syndrome (MIS-C): a systematic review and meta-analysis of clinical characteristics, treatment, and outcomes.

Not available

S-EPMC9432310 | biostudies-literature

Hepatitis C and Human Pegivirus Coinfection in Patients with Chronic Hepatitis C from the Brazilian Amazon Region: Prevalence, Genotypes and Clinical Data.

Not available

S-EPMC10536978 | biostudies-literature

Seroprevalence of meningococcal serogroup C bactericidal antibodies in the Portuguese population, a decade after vaccine introduction in the National Immunisation Programme.

Not available

S-EPMC8049472 | biostudies-literature

Endothelial protein C receptor function in murine and human breast cancer development.

Not available

S-EPMC3621887 | biostudies-literature

Shared prognostic markers in undifferentiated pleomorphic sarcoma and leiomyosarcoma of the extremities

Soft tissue sarcoma diagnostics and prognostics are challenging, particularly in highly malignant and pleomorphic subtypes such as undifferentiated pleomorphic sarcoma (UPS) and leiomyosarcoma (LMS). We applied 32K BAC-arrays and gene expression profiling to 18 extremity soft tissue LMS and 31 extre...

ORGANISM(S): Homo sapiens

2010-10-08 | E-GEOD-13775 | biostudies-arrayexpress

Evaluation of canonical siRNA and Dicer substrate RNA for inhibition of hepatitis C virus genome replication--a comparative study.

Not available

S-EPMC4338191 | biostudies-literature

The CDH1 c.1901C>T Variant: A Founder Variant in the Portuguese Population with Severe Impact in mRNA Splicing.

Not available

S-EPMC8430675 | biostudies-literature