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 |
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1995 | 1 | 0 | 1 |
1996 | 1 | 0 | 1 |
1997 | 1 | 0 | 1 |
1999 | 1 | 0 | 1 |
2007 | 0 | 1 | 1 |
2008 | 1 | 0 | 1 |
2009 | 0 | 2 | 2 |
2014 | 0 | 1 | 1 |
2017 | 0 | 1 | 1 |
2018 | 0 | 1 | 1 |
2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 1" by people in Profiles.
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Acquisition of chromosome 1q duplication in parental and genome-edited human-induced pluripotent stem cell-derived neural stem cells results in their higher proliferation rate in vitro and in vivo. Cell Prolif. 2020 Oct; 53(10):e12892.
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Further evidence for complex inheritance of holoprosencephaly: Lessons learned from pre- and postnatal diagnostic testing in Germany. Am J Med Genet C Semin Med Genet. 2018 06; 178(2):198-205.
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Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability. Hum Genet. 2017 07; 136(7):821-834.
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16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy. Hum Mol Genet. 2014 Nov 15; 23(22):6069-80.
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Duffy antigen receptor for chemokines (Darc) polymorphism regulates circulating concentrations of monocyte chemoattractant protein-1 and other inflammatory mediators. Blood. 2010 Jul 01; 115(26):5289-99.
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Variation in genes of the epidermal differentiation complex in German atopic dermatitis patients. Int J Immunogenet. 2009 Aug; 36(4):217-22.
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Left-ventricular non-compaction (LVNC): a clinical feature more often observed in terminal deletion 1p36 than previously expected. Eur J Med Genet. 2008 Nov-Dec; 51(6):685-8.
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Increased radiosensitivity as an indicator of genes conferring breast cancer susceptibility. Strahlenther Onkol. 2007 Dec; 183(12):655-60.
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Genomic structure, 5' flanking sequences, and precise localization in 1P31.1 of the human prostaglandin F receptor gene. Biochem Biophys Res Commun. 1999 Jan 19; 254(2):413-6.
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Cloning and characterization of freac-9 (FKHL17), a novel kidney-expressed human forkhead gene that maps to chromosome 1p32-p34. Genomics. 1997 Nov 15; 46(1):78-85.