Chromosomes, Human, Pair 8
"Chromosomes, Human, Pair 8" 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.
A specific pair of GROUP C CHROMOSOMES of the human chromosome classification.
| Descriptor ID |
D002898
|
| MeSH Number(s) |
A11.284.187.520.300.325.340 G05.360.162.520.300.325.340
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 8".
- 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, 6-12 and X [A11.284.187.520.300.325]
- Chromosomes, Human, Pair 8 [A11.284.187.520.300.325.340]
- 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, 6-12 and X [G05.360.162.520.300.325]
- Chromosomes, Human, Pair 8 [G05.360.162.520.300.325.340]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 8".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 8" by people in this website by year, and whether "Chromosomes, Human, Pair 8" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 3 | 2 | 5 |
| 2018 | 2 | 5 | 7 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 8" by people in Profiles.
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Laboratory divergences in concurrent diagnosis of acute myeloid leukemia relapse and COVID-19: A case report. Int J Lab Hematol. 2021 10; 43(5):e264-e265.
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Gastrointestinal Behcet's-like disease with myelodysplastic neoplasms with trisomy 8: a French case series and literature review. Leuk Lymphoma. 2019 07; 60(7):1782-1788.
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Inflammatory disorders associated with trisomy 8-myelodysplastic syndromes: French retrospective case-control study. Eur J Haematol. 2019 Jan; 102(1):63-69.
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Genomic changes of chromosomes 8p23.1 and 1q21: Novel mutations in malignant mesothelioma. Lung Cancer. 2018 12; 126:106-111.
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Relationship of the Interaction Between Two Quantitative Trait Loci with ?-Globin Expression in ß-Thalassemia Intermedia Patients. Hemoglobin. 2018 Mar; 42(2):108-112.
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c-MYC amplification and c-myc protein expression in pancreatic acinar cell carcinomas. New insights into the molecular signature of these rare cancers. Virchows Arch. 2018 Oct; 473(4):435-441.
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Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli ulcer. PLoS Negl Trop Dis. 2018 04; 12(4):e0006429.
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Epigenetic heterogeneity affects the risk of relapse in children with t(8;21)RUNX1-RUNX1T1-rearranged AML. Leukemia. 2018 05; 32(5):1124-1134.
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A Genetic Marker Associated with De Quervain's Tenosynovitis. Int J Sports Med. 2017 Nov; 38(12):942-948.
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A three-miRNA-based expression signature at diagnosis can predict occurrence of relapse in children with t(8;21) RUNX1-RUNX1T1 acute myeloid leukaemia. Br J Haematol. 2018 10; 183(2):298-301.