Icam1 - OmicsDI

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Unknown (749)
Transcriptomics (167)
Genomics (139)
Proteomics (25)
Other (6)
Metabolomics (3)
Models (2)
Methylation profiling (1)

Organisms

Homo sapiens (103)
Mus musculus (78)
Andropogon gerardi (18)
Bacteria (18)
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synthetic construct (2)
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Organisms

Homo sapiens (63)
Mus musculus (56)
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unidentified (1)

Repository

ENA (134)
geo (120)
biostudies-arrayexpress (59)
pride (18)
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Tissue

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Disease

Melanoma (2)
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Technology Type

Mass Spectrometry (18)
Fluorescence intensity (15)
MEMA (15)
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Bottom-up proteomics (5)
Mass spectrometry (2)
Data-dependent acquisition (2)
Mass spectrometry assay (1)
Affinity proteomics (1)
Affinity purification coupled with mass spectrometry proteomics (1)
All-ion fragmentation (1)
SRM/MRM (1)

Instrument Platform

Illumina HiSeq 2500 (3)
Illumina NovaSeq 6000 (2)
Illumina HiSeq 2000 (2)
Illumina HiSeq 4000 (2)
10x Genomics (1)
Affymetrix GeneChip Scanner 3000 7G (1)
GeneChip Scanner 3000 7G (1)
Q Exactive HF-X (1)
Liquid Chromatography MS - negative - HILIC (1)
Liquid Chromatography MS - positive - HILIC (1)
Liquid Chromatography MS - positive - reverse phase (1)
Liquid Chromatography MS - negative - reverse phase (1)
Liquid Chromatography MS - negative - hilic (1)
Liquid Chromatography MS - positive - hilic (1)

Publication Date

2026 (34)
2025 (24)
2024 (23)
2016 (20)
2023 (14)
2021 (13)
2013 (12)
2018 (9)
2022 (8)
2014 (8)
2011 (8)
2015 (7)
2019 (6)
2012 (6)
2010 (5)
2008 (5)
2020 (5)
2009 (4)
2017 (3)
2007 (2)
2006 (2)
2005 (1)

UNIPROT ID/AC

O75326 (1)
P10914 (1)
Q6ZMJ4 (1)
P20339 (1)
P49747 (1)
P35241 (1)
P27348 (1)
P07996 (1)
Q9NPH9 (1)
Q13568 (1)
Q5D1E8 (1)
Q8N884 (1)
O75131 (1)
O00220 (1)
Q8IUC6 (1)
P19876 (1)
Q9NP97 (1)
P54753 (1)
P08754 (1)
Q16548 (1)
O95760 (1)
Q92974 (1)
O95819 (1)
P24001 (1)
P02778 (1)
O43521 (1)
P17275 (1)
P01911 (1)
O43734 (1)
P35613 (1)

ENSEMBL ID

ENSG00000104432 (1)
ENSG00000168811 (1)
ENSG00000182866 (1)
ENSG00000125347 (1)
ENSG00000157368 (1)
ENSG00000169429 (1)
ENSG00000271503 (1)
ENSG00000106366 (1)
ENSG00000144566 (1)
ENSG00000044574 (1)
ENSG00000105664 (1)
ENSG00000137710 (1)
ENSG00000105974 (1)
ENSG00000006062 (1)
ENSG00000134308 (1)
ENSG00000284565 (1)
ENSG00000109458 (1)
ENSG00000197122 (1)
ENSG00000082701 (1)
ENSG00000124762 (1)
ENSG00000002330 (1)
ENSG00000081041 (1)
ENSG00000137801 (1)
ENSG00000102871 (1)
ENSG00000137693 (1)
ENSG00000065559 (1)
ENSG00000111536 (1)
ENSG00000145386 (1)
ENSG00000128604 (1)
ENSG00000284049 (1)

Metabolite Name

Tripropylamine (2)
Leu-Thr (2)
Agmatine (2)
His-Leu (2)
Glu-Arg (2)
Trigonelline (2)
L-Lysine (2)
Triethanolamine (2)
Piperidine (2)
Acetylcholine (2)
Choline (2)
Ectoine (2)
Val-Ile (2)
PTM_1919 (1)
Trp(dioxidation)-Glu (1)
Trans-1,4-cyclohexanedimethanol (1)
Methyl 5(s),6(r)-7-trihydroxyheptanoate (1)
L-serine methyl ester (1)
L-isoleucine, methyl ester (1)
Guan-fu base y (1)
Ethyl 8-methoxycoumarin-3-carboxylate (1)
7-oxabicyclo[2.2.1]heptane (1)
2,3-dimethyl-3-pentanol (1)
1h-indole-3-ethanamine, 5-methoxy-n-methyl-n-(1-methylethyl)- (1)
1h-indazole-3-carboxamide, n-[1-(aminocarbonyl)-2,2-dimethylpropyl]-1-pentyl- (1)
1,5-hexadien-3-ol (1)
(s)-mephenytoin (1)
.gamma.-nonalactone (1)
.alpha.-santonin (1)
Asperlactone (1)

IsPrivate

False (2)

Submitter Keywords

TransQST (1)

First Public Date

2026 (31)
2024 (24)
2025 (21)
2021 (11)
2014 (11)
2023 (9)
2022 (7)
2020 (4)
2019 (4)
2018 (4)
2017 (3)
2015 (3)
2013 (2)

Modelling Approach

Logical model (2)

Study type

Transcription profiling by array (45)
RNA-seq of coding RNA (8)
Transcription profiling by RT-PCR (2)
RNA-seq of coding RNA from single cells (2)
Proteomic profiling by array (1)
RNA-seq of non coding RNA (1)

Release Date

2025 (94)
2022 (87)
2024 (79)
2023 (79)
2021 (75)
2020 (61)
2019 (49)
2018 (41)
2017 (31)
2013 (30)
2015 (29)
2016 (27)
2012 (23)
2014 (22)
2010 (14)
2011 (11)
2026 (11)
2008 (10)
2009 (9)
2007 (7)
2006 (3)
2005 (1)

Lab affiliation

1Department of Microbiology and Molecular Genetics, Institute for Medical Research Israel-Canada, Faculty of Medicine, The Hebrew University of Jerusalem, Israel. (1)
Aarhus University Department of Biomedicine DK-8000 Aarhus C (1)
Aarhus University Department of Biomedicine DK-8000 Aarhus C (lab head) (1)
Babraham Institute (1)
BioMedizinisches Centrum Walter-Brendel-Zentrum für Experimentelle Medizin Ludwig-Maximilians-Universität München (1)
Department of Anatomy and Developmental BiologyMonash University, Clayton, Victoria, Australia; Development and Stem Cells Program, Monash Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia. Alexander N Combes alex.combes@monash.edu. David J Nikolic-Paterson david.nikolic-paterson@monash.edu. (1)
Department of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong 510120, China. (1)
Department of Hematopoiesis, Sanquin Research, Amsterdam, The Netherlands (1)
Head of Laboratory of Neuro-Oncology, Neurology, Clinical & Cancer Proteomics (1)
Institute for Radiation Biology, Helmholtz Center Munich, German Research Center for Environmental Health GmbH, Neuherberg, Germany (1)
Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow G61 1QH (1)
Keck MS & Proteomics Resource at Yale School of Medicine (1)
Microenvironment and Metastasis Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Center (CNIO), Madrid, Spain. (1)
NKI Proteomics Facility, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, the Netherlands (1)
Proteomics and Metabolomics research program, Basic research department, Children’s Cancer Hospital 57357, Cairo, Egypt (1)
Research Institute for Complex Issues of Cardiovascular Diseases (1)
Sanquin Research, Department of Plasma Proteins, Amsterdam, The Netherlands (1)
Spanish National Cancer Research Centre (CNIO) Address: Melchor Fernández Almagro, 3. 28029 Madrid. SPAIN (1)

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Transcriptional profiling of ICAM-positive and -negative cells from the mouse olfactory epithelium

We used trasncriptional profiling of fluorescent activated cell sorting (FACS) purified ICAM1-positive and negative cells from the olfactory epithelium (OE) of three-week old mice to identify genes enriched in the horizontal basal cells. The olfactory epithelia from P21-P25 CD1 mice (Charles River L...

ORGANISM(S): Mus musculus

2011-12-07 | E-GEOD-31972 | biostudies-arrayexpress

Mechanism of OGT-mediated FASN glycosylation regulating JNK/ICAM1 pathway in Liver cancer stem cell metastasis [ICAM1]

PRJNA1136502 | ENA

Type I IFN Dynamics Orchestrate Protective ICAM1⁺ Neutrophil Heterogeneity as an Early Checkpoint for Survival in Lethal Viral Infection [ICAM1 RNAseq]

PRJNA1378722 | ENA

Development of potent antibody drug conjugates against ICAM1+ cancer cells in preclinical models of cholangiocarcinoma

PRJNA978044 | ENA

ICAM1 expression and associated clinical parameters as predictive biomarkers for acute celluar rejection

PRJNA1425483 | ENA

Mechanism of OGT-mediated FASN glycosylation regulating JNK/ICAM1 pathway in Liver cancer stem cell metastasis [ICAM1]

We performed transcriptome sequencing analysis on LCSCs with different metastatic abilities. KEGG enrichment showed that genes upregulated during LCSC3 metastasis were related to cell membrane pathways. qPCR and flow cytometry confirmed that FASN expression was significantly upregulated during LCSCs...

ORGANISM(S): Homo sapiens

2025-06-13 | GSE272351 | GEO

Musashi-1 Enhances Glioblastoma Migration by Promoting ICAM1 Translation.

Not available

S-EPMC6453839 | biostudies-literature

ICAM1 mRNA Functions Independently of Protein Coding to Inhibit Translation via a dsRNA-ILF2/ILF3 Pathway in Lung Cancer

PRJNA1161413 | ENA

A Rationally Designed ICAM1 Antibody Drug Conjugate for Pancreatic Cancer.

Not available

S-EPMC7740099 | biostudies-literature

Development of potent antibody drug conjugates against ICAM1+ cancer cells in preclinical models of cholangiocarcinoma

We observed an interesting contradictory phenomenon that ICAM1-Dxd showed a very weak cytotoxicity on CCA cell lines in vitro, whereas it mediates more potent tumor attenuation than ICAM1-MMAE in vivo, suggesting the potency of ICAM1-Dxd may arise from its multifaceted biological activities instead ...

ORGANISM(S): Homo sapiens

2023-09-20 | GSE233818 | GEO

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