"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
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MeSH Number(s) |
C23.550.210.190 G05.365.590.175.190 G05.365.590.770.500 G05.558.805.500
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Concept/Terms |
Chromosome Inversion- Chromosome Inversion
- Chromosome Inversions
- Inversions, Chromosome
- Inversion, Chromosome
- Inversion, Chromosomal
- Chromosomal Inversion
- Chromosomal Inversions
- Inversions, Chromosomal
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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.
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Year | Major Topic | Minor Topic | Total |
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1994 | 0 | 2 | 2 |
1997 | 1 | 0 | 1 |
2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Chromosome Inversion" by people in Profiles.
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Biological Impact of a Large-Scale Genomic Inversion That Grossly Disrupts the Relative Positions of the Origin and Terminus Loci of the Streptococcus pyogenes Chromosome. J Bacteriol. 2019 09 01; 201(17).
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Familial eosinophilia: clinical and laboratory results on a U.S. kindred. Am J Med Genet. 1998 Mar 19; 76(3):229-37.
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Molecular analysis of deletion (17)(p11.2p11.2) in a family segregating a 17p paracentric inversion: implications for carriers of paracentric inversions. Am J Hum Genet. 1997 May; 60(5):1184-93.
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Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition. Nucleic Acids Res. 1994 Nov 11; 22(22):4851-68.
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Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition. Nucleic Acids Res. 1994 Sep; 22(17):3511-33.