Chromosomes, Human, Pair 5
"Chromosomes, Human, Pair 5" 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.
One of the two pairs of human chromosomes in the group B class (CHROMOSOMES, HUMAN, 4-5).
Descriptor ID |
D002895
|
MeSH Number(s) |
A11.284.187.520.300.280.290 G05.360.162.520.300.280.290
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 5".
- Anatomy [A]
- Cells [A11]
- Cellular Structures [A11.284]
- Chromosomes [A11.284.187]
- Chromosomes, Mammalian [A11.284.187.520]
- Chromosomes, Human [A11.284.187.520.300]
- Chromosomes, Human, 4-5 [A11.284.187.520.300.280]
- Chromosomes, Human, Pair 5 [A11.284.187.520.300.280.290]
- Biological Sciences [G]
- Genetic Phenomena [G05]
- Genetic Structures [G05.360]
- Chromosomes [G05.360.162]
- Chromosomes, Mammalian [G05.360.162.520]
- Chromosomes, Human [G05.360.162.520.300]
- Chromosomes, Human, 4-5 [G05.360.162.520.300.280]
- Chromosomes, Human, Pair 5 [G05.360.162.520.300.280.290]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 5".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 5" by people in this website by year, and whether "Chromosomes, Human, Pair 5" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1994 | 2 | 0 | 2 |
1995 | 1 | 2 | 3 |
1996 | 4 | 2 | 6 |
1997 | 3 | 1 | 4 |
1998 | 0 | 1 | 1 |
1999 | 1 | 1 | 2 |
2000 | 2 | 2 | 4 |
2001 | 2 | 1 | 3 |
2003 | 1 | 1 | 2 |
2004 | 3 | 0 | 3 |
2005 | 3 | 1 | 4 |
2006 | 2 | 1 | 3 |
2007 | 1 | 0 | 1 |
2008 | 1 | 0 | 1 |
2009 | 0 | 1 | 1 |
2010 | 5 | 2 | 7 |
2012 | 1 | 2 | 3 |
2013 | 2 | 0 | 2 |
2014 | 1 | 2 | 3 |
2017 | 0 | 4 | 4 |
2021 | 0 | 1 | 1 |
2023 | 0 | 2 | 2 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 5" by people in Profiles.
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TP53 variant allele frequency and therapy-related setting independently predict survival in myelodysplastic syndromes with del(5q). Br J Haematol. 2024 Apr; 204(4):1243-1248.
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TP53 mutations and variant allele frequency in myelodysplastic syndromes with del(5q): A Mayo-Moffitt study of 156 informative cases. Am J Hematol. 2023 04; 98(4):E76-E79.
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Therapy-related myeloid neoplasms in 109 patients after radiation monotherapy. Blood Adv. 2021 10 26; 5(20):4140-4148.
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Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. Circ Cardiovasc Genet. 2017 Oct; 10(5).
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Therapy-related myeloid neoplasms: when genetics and environment collide. Nat Rev Cancer. 2017 08 24; 17(9):513-527.
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Genetic variants and risk of asthma in an American Indian population. Ann Allergy Asthma Immunol. 2017 07; 119(1):31-36.e1.
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Downregulation of GATA1 drives impaired hematopoiesis in primary myelofibrosis. J Clin Invest. 2017 Apr 03; 127(4):1316-1320.
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Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1. Nat Genet. 2014 Aug; 46(8):886-90.
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Exome sequencing of pleuropulmonary blastoma reveals frequent biallelic loss of TP53 and two hits in DICER1 resulting in retention of 5p-derived miRNA hairpin loop sequences. Oncogene. 2014 Nov 06; 33(45):5295-302.
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Knockdown of Hnrnpa0, a del(5q) gene, alters myeloid cell fate in murine cells through regulation of AU-rich transcripts. Haematologica. 2014 Jun; 99(6):1032-40.