Abel T T - OmicsDI

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Unknown (862)
Proteomics (19)
Transcriptomics (17)
Genomics (9)
Metabolomics (1)

Organisms

Andropogon gerardi (17)
Bacteria (17)
Canis lupus familiaris (17)
Cnidaria (17)
Cricetulus griseus (17)
Eukaryota (17)
Fasciola (17)
Hepatitis B virus (17)
Human betaherpesvirus 5 (17)
Madurella mycetomatis (17)
Mesocricetus auratus (17)
Miscanthus x giganteus (17)
Mus musculus (17)
Mycobacterium tuberculosis (17)
Orthoflavivirus (17)
Panicum virgatum (17)
Platyhelminthes (17)
Pseudomonas aeruginosa AES-1R (17)
Rattus norvegicus (17)
Rattus rattus (17)
Rhodococcus jostii RHA1 (17)
Saccharomyces cerevisiae (17)
Schizosaccharomyces pombe (17)
Severe acute respiratory syndrome coronavirus 2 (17)
Sorghastrum nutans (17)
Homo sapiens (12)
Mus musculus (9)
Rattus norvegicus (2)
Sinorhizobium fredii (1)
mixed sample (1)

Organisms

Homo sapiens (1)

Repository

biostudies-arrayexpress (18)
pride (17)
EGA (7)
MassIVE (2)
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ENA (1)

Tissue

Heart (3)
Brain (2)
Blood (1)
Breast cancer cell line (1)
Epithelial cell (1)
Leaf (1)
Nucleus pulposus (1)
Prostate cancer cell line (1)
Root (1)

Disease

Breast cancer (1)
Prostate adenocarcinoma (1)

Technology Type

Mass Spectrometry (17)
Shotgun proteomics (9)
Data-dependent acquisition (6)
Bottom-up proteomics (5)
Affinity purification coupled with mass spectrometry proteomics (4)
Illumina HiScanSQ, ILLUMINA (1)
Mass spectrometry (1)
Data-independent acquisition (1)
Gel-based experiment (1)
SRM/MRM (1)

Instrument Platform

Scanning hardware (1)
Illumina HiSeq 2500 (1)
Illumina NovaSeq 6000 (1)
Illumina HiSeq 2000 (1)
LTQ (1)
LTQ Orbitrap Elite (1)
Liquid Chromatography MS - positive - reverse phase (1)

Publication Date

2026 (5)
2023 (5)
2015 (4)
2012 (4)
2024 (3)
2017 (2)
2009 (2)
2008 (2)
2020 (2)
2022 (2)
2019 (1)
2014 (1)
2013 (1)
2007 (1)
2025 (1)
2021 (1)
2016 (1)

Metabolite Name

TG 54:1|TG 18:0_18:0_18:1 (1)
TG 54:0 (1)
TG 56:2|TG 18:0_18:1_20:1 (1)
TG O-51:1 (1)
TG 52:0|TG 16:0_18:0_18:0 (1)
TG 54:2|TG 18:0_18:1_18:1 (1)
TG 50:0 (1)
TG 53:2|TG 16:0_18:1_19:1 (1)
TG 54:3|TG 18:1_18:1_18:1 (1)
TG 52:2|TG 16:0_18:1_18:1 (1)
TG 50:1|TG 16:0_16:0_18:1 (1)
TG 56:5|TG 18:0_18:1_20:4 (1)
TG 53:3|TG 17:1_18:1_18:1 (1)
TG 51:2|TG 16:0_17:1_18:1 (1)
TG 54:4|TG 18:1_18:1_18:2 (1)
TG 52:3|TG 16:1_18:1_18:1 (1)
TG 50:2|TG 16:0_16:1_18:1 (1)
TG 53:4 (1)
TG 56:6|TG 16:0_18:1_22:5 (1)
TG 54:5|TG 16:0_18:1_20:4 (1)
TG 52:4|TG 16:1_18:1_18:2 (1)
TG 56:7|TG 16:0_18:1_22:6 (1)
TG 50:3|TG 16:1_16:1_18:1 (1)
TG 48:2|TG 14:0_16:1_18:1 (1)
TG 54:6|TG 14:0_18:1_22:5 (1)
TG 46:1|TG 14:0_16:0_16:1 (1)
TG 52:5|TG 14:0_16:0_22:5 (1)
TG 50:4|TG 14:0_18:2_18:2 (1)
TG 56:8|TG 16:1_18:1_22:6 (1)
TG 54:7|TG 14:0_18:1_22:6 (1)

First Public Date

2024 (1)

Study type

Transcription profiling by array (13)
RNA-seq of coding RNA (3)
Spatial transcriptomics by high-throughput sequencing (1)
ChIP-seq (1)

Release Date

2023 (104)
2024 (94)
2021 (86)
2022 (84)
2025 (69)
2018 (54)
2015 (49)
2019 (46)
2017 (46)
2016 (46)
2020 (44)
2014 (32)
2013 (23)
2012 (18)
2011 (17)
2026 (16)
2009 (12)
2008 (10)
2007 (10)
2010 (9)
2005 (3)
2006 (2)
2003 (2)
2002 (2)
2004 (1)
2001 (1)

Lab affiliation

Hannover Medical School, Department of Cardiology and Angiology (3)
1- i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Portugal 2- IBMC - Instituto de Biologia Celular e Molecular, Universidade do Porto, Portugal 3- ICBAS - Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, Portugal (1)
1- i3S - Instituto de Investigação e Inovação em Saúde,Universidade do Porto, Portugal 2- IBMC - Instituto de Biologia Celular e Molecular, Universidade do Porto, Portugal 3- ICBAS - Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, Portugal (1)
Boston College (1)
Department of Medical BioSciences, Radboud Institute for Medical Innovation, Radboudumc, Nijmegen, The Netherlands (1)
Glial Cell Biology Lab, i3s - Instituto de Investigação e Inovação em Saúde, Porto, Portugal (1)
Gregor Mendel Institute of Molecular Plant Biology GmbH Dr. Bohr-Gasse 3, 1030 Vienna, Austria Phone: +43 1 79044 9850 http://www.gmi.oeaw.ac.at (1)
Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France; University of Paris, Imagine Institute, Paris, France; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA; Department of Pediatrics, Necker Hospital for Sick Children, AP-HP, Paris, France; Howard Hughes Medical Institute, New York, NY, USA (1)
Microbial Genomic Laboratory Division of Biological and Environmental Sciences and Engineering, Level 4, 4326-WS10, Building 2, King Abdullah University of Science and Technology (KAUST), (1)
School of Life Sciences, Queens Medical Centre, University of Nottingham, Nottingham, NG7 2UH, UK (1)
St. Giles Laboratory of Human Genetics of Infectious Diseases, The Rockefeller University, New York, New York, USA. (1)
University of Southern California (1)
Università degli Studi della Campania Luigi Vanvitelli (1)
i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal INEB - Instituto Nacional de Engenharia Biomédica, Universidade do Porto, Porto, Portugal ICBAS - Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, Porto, Portugal (1)
i3S, Instituto de Investigação e Inovação em Saúde, University of Porto ICBAS, Institute of Biomedical Sciences Abel Salazar, University of Porto (1)

Tags

xref:PubMed:38422122 (1)

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Catch Bonds at T Cell Interfaces: Impact of Surface Reorganization and Membrane Fluctuations.

Not available

S-EPMC5510709 | biostudies-literature

HERPES SIMPLEX VIRUS TYPE 1 IMPAIRS DENDRITIC CELL FUNCTION BY REMODELLING NEUTRAL LIPID METABOLISM AND INDUCING LIPID DROPLET ACCUMULATION

Herpes simplex virus type 1 (HSV-1) infects dendritic cells (DCs), professional antigen-presenting cells that initiate and regulate host antiviral responses. HSV-1 infects DCs limiting their maturation, migration to draining lymph nodes and T cell activation capacity, ultimately promotes their apopt...

2025-04-03 | MTBLS5163 | MetaboLights

Gene expression profiling of CD4+CD25+Foxp3+ regulatory T cells and CD4+CD25-Foxp3- T cells in the course of Plasmodium yoelii infection of BALB/c mice

The objective of the present study was to characterize the phenotype of CD4+CD25+Foxp3+ regulatory T cells (Tregs) in the course of parasitic Plasmodium yoelii (P .yoelii) infection of BALB/c mice. Therefore we performed microarray expression analysis of CD4+CD25+Foxp3+ Tregs isolated by FACS from s...

ORGANISM(S): Mus musculus

2012-04-15 | E-GEOD-34621 | biostudies-arrayexpress

An Innovative In Vivo Model for CAR-T-Cell Therapy Development: Efficacy Evaluation of CD19-Targeting CAR-T Cells on Human Lymphoma, Using the Chicken CAM Assay.

Not available

S-EPMC12841510 | biostudies-literature

Acute Malaria Induces PD1+CTLA4+ Effector T Cells with Cell-Extrinsic Suppressor Function.

Not available

S-EPMC5089727 | biostudies-literature

Cytotoxic T Cell-Derived Granzyme B Is Increased in Severe Plasmodium Falciparum Malaria.

Not available

S-EPMC6918797 | biostudies-literature

Camellia (Camellia oleifera Abel.) seed oil promotes milk fat and protein synthesis-related gene expression in bovine mammary epithelial cells.