"Microarray Analysis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The simultaneous analysis, on a microchip, of multiple samples or targets arranged in an array format.
Descriptor ID |
D046228
|
MeSH Number(s) |
E05.588.570
|
Concept/Terms |
Microarray Analytical Devices- Microarray Analytical Devices
- Analytical Device, Microarray
- Analytical Devices, Microarray
- Device, Microarray Analytical
- Devices, Microarray Analytical
- Microarray Analytical Device
- Microarray Microchips
- Microarray Microchip
- Microchip, Microarray
- Microchips, Microarray
Nanoarray Analytical Devices- Nanoarray Analytical Devices
- Analytical Device, Nanoarray
- Analytical Devices, Nanoarray
- Device, Nanoarray Analytical
- Devices, Nanoarray Analytical
- Nanoarray Analytical Device
|
Below are MeSH descriptors whose meaning is more general than "Microarray Analysis".
Below are MeSH descriptors whose meaning is more specific than "Microarray Analysis".
This graph shows the total number of publications written about "Microarray Analysis" by people in this website by year, and whether "Microarray Analysis" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2006 | 0 | 1 | 1 |
2007 | 1 | 0 | 1 |
2008 | 0 | 1 | 1 |
2010 | 0 | 1 | 1 |
2011 | 1 | 1 | 2 |
2012 | 0 | 1 | 1 |
2013 | 0 | 2 | 2 |
2015 | 0 | 3 | 3 |
2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Microarray Analysis" by people in Profiles.
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Nine newly identified individuals refine the phenotype associated with MYT1L mutations. Am J Med Genet A. 2020 05; 182(5):1021-1031.
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Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. Nat Genet. 2015 Apr; 47(4):373-80.
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Aberrant NMDA receptor DNA methylation detected by epigenome-wide analysis of hippocampus and prefrontal cortex in major depression. Eur Arch Psychiatry Clin Neurosci. 2015 Jun; 265(4):331-41.
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Thrombin stimulates insulin secretion via protease-activated receptor-3. Islets. 2015; 7(4):e1118195.
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Unique transcriptome signature of mouse microglia. Glia. 2013 Sep; 61(9):1429-42.
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Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. Epilepsia. 2013 Feb; 54(2):256-64.
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CD34+ gene expression profiling of individual children with very severe aplastic anemia indicates a pathogenic role of integrin receptors and the proapoptotic death ligand TRAIL. Haematologica. 2012 Sep; 97(9):1304-11.
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Optimal regulatory strategies for metabolic pathways in Escherichia coli depending on protein costs. Mol Syst Biol. 2011 Jul 19; 7:515.
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Analysis of Affymetrix ChIP-chip data using starr and R/Bioconductor. Cold Spring Harb Protoc. 2011 May 01; 2011(5):pdb.top110.
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WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. Am J Hum Genet. 2010 Oct 08; 87(4):465-79.