"Chromosome Inversion" 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.
An aberration in which a chromosomal segment is deleted and reinserted in the same place but turned 180 degrees from its original orientation, so that the gene sequence for the segment is reversed with respect to that of the rest of the chromosome.
| Descriptor ID |
D007446
|
| MeSH Number(s) |
C23.550.210.190 G05.365.590.175.190 G05.365.590.770.500 G05.558.805.500
|
| Concept/Terms |
Chromosome Inversion- Chromosome Inversion
- Chromosome Inversions
- Inversions, Chromosome
- Inversion, Chromosome
- Inversion, Chromosomal
- Chromosomal Inversion
- Chromosomal Inversions
- Inversions, Chromosomal
|
Below are MeSH descriptors whose meaning is more general than "Chromosome Inversion".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Inversion".
This graph shows the total number of publications written about "Chromosome Inversion" by people in this website by year, and whether "Chromosome Inversion" 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 |
|---|
| 1994 | 0 | 1 | 1 |
| 1995 | 1 | 2 | 3 |
| 1997 | 0 | 1 | 1 |
| 1999 | 1 | 0 | 1 |
| 2000 | 0 | 1 | 1 |
| 2001 | 1 | 1 | 2 |
| 2002 | 2 | 2 | 4 |
| 2003 | 1 | 1 | 2 |
| 2004 | 3 | 0 | 3 |
| 2005 | 1 | 0 | 1 |
| 2006 | 2 | 0 | 2 |
| 2007 | 1 | 1 | 2 |
| 2009 | 0 | 1 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 0 | 1 | 1 |
| 2014 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosome Inversion" by people in Profiles.
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Genomic architecture and introgression shape a butterfly radiation. Science. 2019 11 01; 366(6465):594-599.
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Chromosomal inversion differences correlate with range overlap in passerine birds. Nat Ecol Evol. 2017 Oct; 1(10):1526-1534.
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Complex or monosomal karyotype and not blast percentage is associated with poor survival in acute myeloid leukemia and myelodysplastic syndrome patients with inv(3)(q21q26.2)/t(3;3)(q21;q26.2): a Bone Marrow Pathology Group study. Haematologica. 2014 May; 99(5):821-9.
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inv(16)/t(16;16) acute myeloid leukemia with non-type A CBFB-MYH11 fusions associate with distinct clinical and genetic features and lack KIT mutations. Blood. 2013 Jan 10; 121(2):385-91.
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Sequencing papaya X and Yh chromosomes reveals molecular basis of incipient sex chromosome evolution. Proc Natl Acad Sci U S A. 2012 Aug 21; 109(34):13710-5.
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Homoplastic microinversions and the avian tree of life. BMC Evol Biol. 2011 May 25; 11:141.
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Immunophenotypic features of acute myeloid leukemia with inv(3)(q21q26.2)/t(3;3)(q21;q26.2). Leuk Res. 2010 May; 34(5):594-7.
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Expression of a uniquely regulated extracellular polysaccharide confers a large-capsule phenotype to Bacteroides fragilis. J Bacteriol. 2008 Feb; 190(3):1020-6.
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Methylation-independent silencing of the tumor suppressor INK4b (p15) by CBFbeta-SMMHC in acute myelogenous leukemia with inv(16). Cancer Res. 2007 Feb 01; 67(3):992-1000.
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Adverse prognostic significance of KIT mutations in adult acute myeloid leukemia with inv(16) and t(8;21): a Cancer and Leukemia Group B Study. J Clin Oncol. 2006 Aug 20; 24(24):3904-11.