Capillary malformation

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Transcriptomics (784)
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Unknown (119)
Metabolomics (9)
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Genomic (1)

Organisms

Homo sapiens (350)
Mus musculus (194)
Caenorhabditis elegans (25)
Rattus norvegicus (23)
Saccharomyces cerevisiae (21)
Drosophila melanogaster (20)
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Organisms

Homo sapiens (7)
Mus musculus (4)

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biostudies-arrayexpress (880)
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Melanocyte (1)
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Disease

Normal (3)
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Invasive lobular carcinoma (1)
Cancer (1)
Obesity (1)
Prostate carcinoma (1)
Sturge-Weber syndrome (1)
Oculocutaneous albinism type VII (1)

Technology Type

Mass spectrometry (8)
Bottom-up proteomics (2)
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Mass spectrometry assay (1)
Data-dependent acquisition (1)

Instrument Platform

Illumina HiSeq 4000 (6)
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N/A (2)
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University College Dublin Animal Research Ethics Committee approval, a licence from the Department of Health (B100/3525) and explicit owner/trainer informed consent were obtained for the use of all horses and procedures in this study. (1)
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Chromium™ Next GEM Single Cell 3′ Kit v3.1 (10X Genomics, PN-1000269) (1)
Bioinformatics Core Facility, Centre for Molecular Medicine, CEITEC Masaryk University (1)
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(Make:PerkinElmer,Model:ScanArray 4000XL) (1)
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Illumina HiSeq 1500 (1)
NextSeq 550 (1)

Publication Date

2013 (215)
2014 (200)
2012 (166)
2011 (92)
2015 (48)
2010 (44)
2016 (17)
2007 (17)
2008 (16)
2005 (12)
2009 (10)
2022 (9)
2026 (8)
2025 (8)
2023 (7)
2024 (6)
2006 (6)
2018 (5)
2021 (4)
2019 (4)
2017 (4)
2020 (4)
2004 (2)
2003 (2)

CHEBI ID

CHEBI:17351 (5)
CHEBI:28842 (4)
CHEBI:15756 (4)
CHEBI:18186 (3)
CHEBI:16411 (3)
CHEBI:15843 (3)
CHEBI:28044 (3)
CHEBI:48131 (3)
CHEBI:7916 (3)
CHEBI:30746 (3)
CHEBI:22470 (3)
CHEBI:18183 (3)
CHEBI:28867 (3)
CHEBI:15428 (3)
CHEBI:16737 (3)
CHEBI:17884 (3)
CHEBI:17368 (3)
CHEBI:27432 (3)
CHEBI:28941 (3)
CHEBI:28822 (3)
CHEBI:28716 (3)
CHEBI:28875 (3)
CHEBI:30805 (3)
CHEBI:15672 (2)
CHEBI:36946 (2)
CHEBI:48429 (2)
CHEBI:34799 (2)
CHEBI:28212 (2)
CHEBI:20000 (2)
CHEBI:5355 (2)

Metabolite Name

Cytosine (3)
L-Proline (3)
Creatinine (3)
Hypoxanthine (3)
Adenosine (3)
Riboflavin (3)
20-Hydroxy-PGF2a (2)
Glycocholic acid (2)
Nb-Palmitoyltryptamine (2)
(6S)-dehydrovomifoliol (2)
Quebrachidine (2)
N-Nitrosoproline (2)
13-Heptadecyn-1-ol (2)
1H-Pyrrole-2-carboxaldehyde (2)
LysoPC(22:4(7Z,10Z,13Z,16Z)) (2)
LysoPC(22:5(4Z,7Z,10Z,13Z,16Z)) (2)
Coixinden B (2)
Hydrocortisone cypionate (2)
Alpha-Chaconine (2)
Erythritol (2)
Ginkgolide A (2)
Dodecanoic acid (2)
Dioscorine (2)
Proline betaine (2)
LysoPC(20:4(5Z,8Z,11Z,14Z)) (2)
Tetradecanoylcarnitine (2)
Stearoylethanolamide (2)
5-Oxo-2(5H)-isoxazolepropanenitrile (2)
Symmetric dimethylarginine (2)
13S-hydroxyoctadecadienoic acid (2)

First Public Date

2026 (3)
2024 (3)
2023 (2)
2022 (2)
2025 (1)
2021 (1)
2020 (1)
2019 (1)

Study type

Transcription profiling by array (542)
RNA-seq of coding RNA (87)
ChIP-seq (86)
ChIP-chip by tiling array (31)
RNA-seq of non coding RNA (24)
Comparative genomic hybridization by array (20)
Methylation profiling by high throughput sequencing (19)
Transcription profiling by tiling array (18)
Other (17)
Methylation profiling by array (12)
Transcription profiling by RT-PCR (6)
RNA-seq of coding RNA from single cells (3)
Unknown experiment type (2)
Human - High-throughput sequencing (2)
Genotyping by array (2)
MicroRNA profiling by array (2)
DNA-seq (2)
RNA-seq of total RNA (2)
Transcription profiling by SAGE (1)
Cell line - High-throughput sequencing (1)
ATAC-seq (1)

Release Date

2013 (222)
2014 (205)
2012 (171)
2011 (95)
2015 (52)
2010 (48)
2022 (23)
2016 (22)
2007 (18)
2019 (16)
2008 (16)
2023 (15)
2009 (14)
2005 (12)
2025 (11)
2021 (11)
2020 (11)
2018 (8)
2017 (8)
2024 (6)
2006 (6)
2026 (4)
2003 (3)
2004 (2)

Lab affiliation

Amsterdam UMC, University of Amsterdam, Department of Medical Biochemistry, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands. (1)
School of Biochemistry, Faculty of Life Sciences, University of Bristol (1)

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Expression data: Venous malformation-causative TIE2-mutations mediate an AKT-dependent decrease in PDGFB

Comparison of transcriptional profiles of human umbilical vein endothelial cells (HUVECs) expressing wild-type vs. VM-causative mutant forms of TIE2/TEK. The effects of the most common Venous Malformation-causative mutations in the endothelial cell tyrosine kinase receptor: R849W and L914F, were tes...

ORGANISM(S): Homo sapiens

2013-06-04 | E-GEOD-46684 | biostudies-arrayexpress

Immune-interacting lymphatic endothelial subtype at capillary terminals drives lymphatic malformation

PRJNA833469 | ENA

Integrated chromatin accessibility and transcriptomic profiling reveals inflammation-associated endothelial remodeling in capillary malformation iECs

Integrated bulk ATAC-seq and RNA-seq profiling of induced endothelial cells (iECs) derived from capillary malformation (CM) lesion-derived and control induced pluripotent stem cells (iPSCs). Differential chromatin accessibility, gene expression, transcription factor activity, and candidate peak-to-g...

ORGANISM(S): Homo sapiens

2026-09-30 | GSE343411 | GEO

The microcephaly-capillary malformation syndrome.

Not available

S-EPMC3428374 | biostudies-literature

Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations.

Not available

S-EPMC1180390 | biostudies-literature

Prenatal Clinical Findings in RASA1-Related Capillary Malformation-Arteriovenous Malformation Syndrome.

Not available

S-EPMC10048332 | biostudies-literature

Efficacy and safety of endovascular embolization for capillary malformation-arteriovenous malformation of the auricular and periauricular region in pediatric patients.