"Mosaicism" 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 occurrence in an individual of two or more cell populations of different chromosomal constitutions, derived from a single ZYGOTE, as opposed to CHIMERISM in which the different cell populations are derived from more than one zygote.
Descriptor ID |
D009030
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MeSH Number(s) |
G05.365.590.175.595
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Mosaicism".
Below are MeSH descriptors whose meaning is more specific than "Mosaicism".
This graph shows the total number of publications written about "Mosaicism" by people in this website by year, and whether "Mosaicism" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2003 | 1 | 0 | 1 |
2009 | 1 | 0 | 1 |
2012 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2017 | 0 | 2 | 2 |
2019 | 1 | 0 | 1 |
2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mosaicism" by people in Profiles.
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The rate and spectrum of mosaic mutations during embryogenesis revealed by RNA sequencing of 49 tissues. Genome Med. 2020 05 27; 12(1):49.
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Male infant with paternal uniparental diploidy mosaicism and a 46,XX/46,XY karyotype. Am J Med Genet A. 2019 11; 179(11):2252-2256.
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The maternal uniparental disomy of chromosome 6?(upd(6)mat) "phenotype": result of placental trisomy?6?mosaicism? Mol Genet Genomic Med. 2017 11; 5(6):668-677.
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Maternal uniparental disomy of chromosome 16 [upd(16)mat]: clinical features are rather caused by (hidden) trisomy 16 mosaicism than by upd(16)mat itself. Clin Genet. 2017 Jul; 92(1):45-51.
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A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism. Clin Exp Dermatol. 2015 Oct; 40(7):781-5.
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Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith-Wiedemann syndrome and ovarian steroid cell tumour. Eur J Hum Genet. 2013 Jul; 21(7):788-91.
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Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conception. Mol Hum Reprod. 2010 Sep; 16(9):704-13.
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Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype. Prenat Diagn. 2003 Feb; 23(2):128-33.