Chromosomes, Human, Pair 21
"Chromosomes, Human, Pair 21" 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 G CHROMOSOMES of the human chromosome classification.
| Descriptor ID |
D002891
|
| MeSH Number(s) |
A11.284.187.520.300.505.510 G05.360.162.520.300.505.510
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 21".
- 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, 21-22 and Y [A11.284.187.520.300.505]
- Chromosomes, Human, Pair 21 [A11.284.187.520.300.505.510]
- 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, 21-22 and Y [G05.360.162.520.300.505]
- Chromosomes, Human, Pair 21 [G05.360.162.520.300.505.510]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 21".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 21" by people in this website by year, and whether "Chromosomes, Human, Pair 21" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 1 | 0 | 1 |
| 2008 | 0 | 1 | 1 |
| 2010 | 2 | 0 | 2 |
| 2012 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2020 | 0 | 1 | 1 |
| 2021 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Chromosomes, Human, Pair 21" by people in Profiles.
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Tiegs AW, Titus S, Mehta S, Garcia-Milian R, Seli E, Scott RT. Cumulus cells of euploid versus whole chromosome 21 aneuploid embryos reveal differentially expressed genes. Reprod Biomed Online. 2021 Oct; 43(4):614-626.
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Shahbazi MN, Wang T, Tao X, Weatherbee BAT, Sun L, Zhan Y, Keller L, Smith GD, Pellicer A, Scott RT, Seli E, Zernicka-Goetz M. Developmental potential of aneuploid human embryos cultured beyond implantation. Nat Commun. 2020 08 10; 11(1):3987.
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Marin D, Wang Y, Tao X, Scott RT, Treff NR. Comprehensive chromosome screening and gene expression analysis from the same biopsy in human preimplantation embryos. Mol Hum Reprod. 2017 05 01; 23(5):330-338.
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Scott RT, Treff NR, Stevens J, Forman EJ, Hong KH, Katz-Jaffe MG, Schoolcraft WB. Delivery of a chromosomally normal child from an oocyte with reciprocal aneuploid polar bodies. J Assist Reprod Genet. 2012 Jun; 29(6):533-7.
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Bornstein E, Lenchner E, Donnenfeld A, Jodicke C, Keeler SM, Kapp S, Divon MY. Complete trisomy 21 vs translocation Down syndrome: a comparison of modes of ascertainment. Am J Obstet Gynecol. 2010 Oct; 203(4):391.e1-5.
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Martinoli E, Zuccotti GV, Pogliani L, Volontè M, Venturin M, Fortina P, Ertel A, Redaelli S, Riva P, Dalprà L. A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome. Am J Med Genet A. 2010 Apr; 152A(4):1043-5.
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Annable K, Donnenfeld AE, Fischer RL, Knops J. Prenatal diagnosis of a jumping translocation. Prenat Diagn. 2008 Aug; 28(8):767-9.
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Bornstein E, Barnhard Y, Donnenfeld A, Ferber A, Divon MY. Fetal pyelectasis: does fetal gender modify the risk of major trisomies? Obstet Gynecol. 2006 Apr; 107(4):877-9.
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Kiuru-Kuhlefelt S, El-Rifai W, Sarlomo-Rikala M, Knuutila S, Miettinen M. DNA copy number changes in alveolar soft part sarcoma: a comparative genomic hybridization study. Mod Pathol. 1998 Mar; 11(3):227-31.
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Comeglio P, Saitta B, Pepe G, Chu ML. Identification of a polymorphic CA repeat in the COL6A2 gene on human chromosome 21q22.3. Hum Hered. 1996 Jul-Aug; 46(4):239-40.