"Karyotype" 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 full set of CHROMOSOMES presented as a systematized array of METAPHASE chromosomes from a photomicrograph of a single CELL NUCLEUS arranged in pairs in descending order of size and according to the position of the CENTROMERE. (From Stedman, 25th ed)
| Descriptor ID |
D059785
|
| MeSH Number(s) |
G05.360.162.679
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Karyotype".
Below are MeSH descriptors whose meaning is more specific than "Karyotype".
This graph shows the total number of publications written about "Karyotype" by people in this website by year, and whether "Karyotype" 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 |
|---|
| 2013 | 0 | 1 | 1 |
| 2015 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2019 | 1 | 1 | 2 |
| 2020 | 0 | 1 | 1 |
| 2021 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Karyotype" by people in Profiles.
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Repeat-based holocentromeres influence genome architecture and karyotype evolution. Cell. 2022 Aug 18; 185(17):3153-3168.e18.
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Intellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal study. Am J Med Genet A. 2021 04; 185(4):1216-1221.
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Acquisition of chromosome 1q duplication in parental and genome-edited human-induced pluripotent stem cell-derived neural stem cells results in their higher proliferation rate in vitro and in vivo. Cell Prolif. 2020 Oct; 53(10):e12892.
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Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines. Sci Rep. 2019 10 09; 9(1):14476.
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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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Generation of human induced pluripotent stem cell line from a patient with a long QT syndrome type 2. Stem Cell Res. 2016 Mar; 16(2):304-7.
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Next-generation-sequencing of recurrent childhood high hyperdiploid acute lymphoblastic leukemia reveals mutations typically associated with high risk patients. Leuk Res. 2015 Sep; 39(9):990-1001.
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Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12. Birth Defects Res A Clin Mol Teratol. 2013 Mar; 97(3):133-9.
MeSH information
