Chromosomes, Human, Pair 1
"Chromosomes, Human, Pair 1" 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 human chromosomes in group A (CHROMOSOMES, HUMAN, 1-3) of the human chromosome classification.
| Descriptor ID |
D002878
|
| MeSH Number(s) |
A11.284.187.520.300.235.240 G05.360.162.520.300.235.240
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 1".
- 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, 1-3 [A11.284.187.520.300.235]
- Chromosomes, Human, Pair 1 [A11.284.187.520.300.235.240]
- 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, 1-3 [G05.360.162.520.300.235]
- Chromosomes, Human, Pair 1 [G05.360.162.520.300.235.240]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 1".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 1" by people in this website by year, and whether "Chromosomes, Human, Pair 1" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 1 | 3 | 4 |
| 2018 | 2 | 0 | 2 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 1" by people in Profiles.
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SARS-CoV-2 orf1b Gene Sequence in the NTNG1 Gene on Human Chromosome 1. In Vivo. 2020 Jun; 34(3 Suppl):1629-1632.
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Human Gene Sequences in SARS-CoV-2 and Other Viruses. In Vivo. 2020 Jun; 34(3 Suppl):1633-1636.
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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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Reduced expression of DNA repair genes and chemosensitivity in 1p19q codeleted lower-grade gliomas. J Neurooncol. 2018 Sep; 139(3):563-571.
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[Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10; 34(6):853-856.
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Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature. Int J Mol Sci. 2017 Sep 17; 18(9).
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T2-FLAIR Mismatch, an Imaging Biomarker for IDH and 1p/19q Status in Lower-grade Gliomas: A TCGA/TCIA Project. Clin Cancer Res. 2017 Oct 15; 23(20):6078-6085.
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MRI features predict survival and molecular markers in diffuse lower-grade gliomas. Neuro Oncol. 2017 06 01; 19(6):862-870.