 Microarray Analysis
"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
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| MeSH Number(s) |
E05.588.570
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| 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
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 0 | 1 | 1 | | 2015 | 0 | 3 | 3 | | 2018 | 0 | 1 | 1 | | 2021 | 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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Shi G, Xu J, Barnes SF, Farooqi MS, Luu HS, Gotway G, Park JY. Chromosomal Microarray Reinterpretation: Applications to Pediatric Practice. J Pediatr. 2022 Apr; 243:219-223.
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Cadieux-Dion M, Safina NP, Engleman K, Saunders C, Repnikova E, Raje N, Canty K, Farrow E, Miller N, Zellmer L, Thiffault I. Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report. BMC Med Genet. 2018 03 09; 19(1):41.
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Renaud SJ, Chakraborty D, Mason CW, Rumi MA, Vivian JL, Soares MJ. OVO-like 1 regulates progenitor cell fate in human trophoblast development. Proc Natl Acad Sci U S A. 2015 Nov 10; 112(45):E6175-84.
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Vujkovic M, Attiyeh EF, Ries RE, Horn M, Goodman EK, Ding Y, Kavcic M, Alonzo TA, Gerbing RB, Hirsch B, Raimondi S, Gamis AS, Meshinchi S, Aplenc R. Concordance of copy number alterations using a common analytic pipeline for genome-wide analysis of Illumina and Affymetrix genotyping data: a report from the Children's Oncology Group. Cancer Genet. 2015 Jul-Aug; 208(7-8):408-13.
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Verbitsky M, Sanna-Cherchi S, Fasel DA, Levy B, Kiryluk K, Wuttke M, Abraham AG, Kaskel F, K?ttgen A, Warady BA, Furth SL, Wong CS, Gharavi AG. Genomic imbalances in pediatric patients with chronic kidney disease. J Clin Invest. 2015 May; 125(5):2171-8.
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Williamson DA, Ritchie SR, Roberts SA, Coombs GW, Thomas MG, Hannaford O, Baker MG, Lennon D, Fraser JD. Clinical and molecular epidemiology of community-onset invasive Staphylococcus aureus infection in New Zealand children. Epidemiol Infect. 2014 Aug; 142(8):1713-21.
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Copeland JN, Feng Y, Neradugomma NK, Fields PE, Vivian JL. Notch signaling regulates remodeling and vessel diameter in the extraembryonic yolk sac. BMC Dev Biol. 2011 Feb 25; 11:12.
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Bittel DC, Kibiryeva N, Talebizadeh Z, Driscoll DJ, Butler MG. Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD. Genomics. 2005 Jan; 85(1):85-91.
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