"Karyotyping" 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.
Mapping of the KARYOTYPE of a cell.
Descriptor ID |
D007621
|
MeSH Number(s) |
E01.370.225.500.385.315 E05.200.500.385.315 E05.242.385.315 E05.393.285.475
|
Concept/Terms |
Karyotyping- Karyotyping
- Karyotypings
- Karyotype Analysis Methods
- Analysis Method, Karyotype
- Analysis Methods, Karyotype
- Karyotype Analysis Method
- Method, Karyotype Analysis
- Methods, Karyotype Analysis
|
Below are MeSH descriptors whose meaning is more general than "Karyotyping".
Below are MeSH descriptors whose meaning is more specific than "Karyotyping".
This graph shows the total number of publications written about "Karyotyping" by people in this website by year, and whether "Karyotyping" 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 |
---|
1995 | 0 | 2 | 2 |
1996 | 0 | 5 | 5 |
1997 | 0 | 2 | 2 |
1998 | 1 | 8 | 9 |
1999 | 0 | 1 | 1 |
2000 | 0 | 4 | 4 |
2001 | 0 | 4 | 4 |
2002 | 0 | 1 | 1 |
2003 | 1 | 5 | 6 |
2004 | 0 | 2 | 2 |
2005 | 0 | 3 | 3 |
2006 | 0 | 2 | 2 |
2007 | 0 | 3 | 3 |
2009 | 0 | 1 | 1 |
2010 | 0 | 1 | 1 |
2011 | 0 | 2 | 2 |
2013 | 0 | 1 | 1 |
2017 | 1 | 0 | 1 |
2018 | 0 | 1 | 1 |
2021 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Karyotyping" by people in Profiles.
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Establishment and genomic characterization of a sporadic malignant peripheral nerve sheath tumor cell line. Sci Rep. 2021 03 11; 11(1):5690.
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Complex karyotype in patients with mantle cell lymphoma predicts inferior survival and poor response to intensive induction therapy. Cancer. 2018 06 01; 124(11):2306-2315.
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Predictable phenotypic, but not karyotypic, evolution of populations with contrasting initial history. Sci Rep. 2017 04 19; 7(1):913.
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Rapid and efficient reprogramming of human fetal and adult blood CD34+ cells into mesenchymal stem cells with a single factor. Cell Res. 2013 May; 23(5):658-72.
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In vitro modeling of ryanodine receptor 2 dysfunction using human induced pluripotent stem cells. Cell Physiol Biochem. 2011; 28(4):579-92.
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Membrane proteomic signatures of karyotypically normal and abnormal human embryonic stem cell lines and derivatives. Proteomics. 2011 Jun; 11(12):2515-27.
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Laboratory guideline for Turner syndrome. Genet Med. 2010 Jan; 12(1):52-5.
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Single-agent laromustine, a novel alkylating agent, has significant activity in older patients with previously untreated poor-risk acute myeloid leukemia. J Clin Oncol. 2010 Feb 10; 28(5):815-21.
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Autism spectrum disorder, Klinefelter syndrome, and chromosome 3p21.31 duplication: a case report. MedGenMed. 2007 Dec 18; 9(4):60.
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The genetics of bladder cancer: a cytogeneticist's perspective. Cytogenet Genome Res. 2007; 118(2-4):177-81.