"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 |
|---|
| 2011 | 0 | 2 | 2 |
| 2016 | 0 | 4 | 4 |
| 2017 | 1 | 3 | 4 |
| 2018 | 0 | 3 | 3 |
| 2019 | 0 | 3 | 3 |
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Below are the most recent publications written about "Karyotype" by people in Profiles.
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Generation of FOS gene knockout lines from a human embryonic stem cell line using CRISPR/Cas9. Stem Cell Res. 2019 08; 39:101479.
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A novel human in vitro papillomavirus type 16 positive tonsil cancer cell line with high sensitivity to radiation and cisplatin. BMC Cancer. 2019 Mar 25; 19(1):265.
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Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene. Stem Cell Res. 2019 04; 36:101416.
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Evolutionary rates of mammalian telomere-stability genes correlate with karyotype features and female germline expression. Nucleic Acids Res. 2018 08 21; 46(14):7153-7168.
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MIPSS70+ Version 2.0: Mutation and Karyotype-Enhanced International Prognostic Scoring System for Primary Myelofibrosis. J Clin Oncol. 2018 06 10; 36(17):1769-1770.
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Relapse and survival after transplantation for complex karyotype acute myeloid leukemia: A report from the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation and the University of Texas MD Anderson Cancer Center. Cancer. 2018 05 15; 124(10):2134-2141.
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Characterization of TP53 mutations in low-grade myelodysplastic syndromes and myelodysplastic syndromes with a non-complex karyotype. Eur J Haematol. 2017 Dec; 99(6):536-543.
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Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjögren's Syndrome. Arthritis Rheumatol. 2017 11; 69(11):2187-2192.
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BMPR1B mutation causes Pierre Robin sequence. Oncotarget. 2017 Apr 18; 8(16):25864-25871.
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Fluid intelligence, traits of personality and personality disorders in a cohort of adult KS patients with the classic 47, XXY karyotype. J Endocrinol Invest. 2017 Nov; 40(11):1191-1199.