 Uniparental Disomy
"Uniparental Disomy" 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.
The presence in a cell of two paired chromosomes from the same parent, with no chromosome of that pair from the other parent. This chromosome composition stems from non-disjunction (NONDISJUNCTION, GENETIC) events during MEIOSIS. The disomy may be composed of both homologous chromosomes from one parent (heterodisomy) or a duplicate of one chromosome (isodisomy).
| Descriptor ID |
D024182
|
| MeSH Number(s) |
C23.550.210.645.890 G05.365.590.175.935
|
| Concept/Terms |
Uniparental Disomy- Uniparental Disomy
- Disomies, Uniparental
- Uniparental Disomies
- Disomy, Uniparental
Uniparental Heterodisomy- Uniparental Heterodisomy
- Heterodisomies, Uniparental
- Heterodisomy, Uniparental
- Uniparental Heterodisomies
|
Below are MeSH descriptors whose meaning is more general than "Uniparental Disomy".
Below are MeSH descriptors whose meaning is more specific than "Uniparental Disomy".
This graph shows the total number of publications written about "Uniparental Disomy" by people in this website by year, and whether "Uniparental Disomy" 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 |
|---|
| 2008 | 1 | 0 | 1 | | 2009 | 2 | 0 | 2 | | 2016 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Uniparental Disomy" by people in Profiles.
-
Riley CJ, Moore T, Eagelston L, Burkett D, Auerbach S, Ing RJ. Cardiac Failure in a Trisomy 9 Patient Undergoing Anesthesia: A Case Report. Anesth Prog. 2017; 64(1):29-32.
-
Potter H, Granic A, Caneus J. Role of Trisomy 21 Mosaicism in Sporadic and Familial Alzheimer's Disease. Curr Alzheimer Res. 2016; 13(1):7-17.
-
Hamvas A, Nogee LM, Wegner DJ, Depass K, Christodoulou J, Bennetts B, McQuade LR, Gray PH, Deterding RR, Carroll TR, Kammesheidt A, Kasch LM, Kulkarni S, Cole FS. Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genes. J Pediatr. 2009 Dec; 155(6):854-859.e1.
-
Keller MC, McRae AF, McGaughran JM, Visscher PM, Martin NG, Montgomery GW. Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan. Am J Med Genet A. 2009 Aug; 149A(8):1823-6.
-
Walsh CS, Ogawa S, Scoles DR, Miller CW, Kawamata N, Narod SA, Koeffler HP, Karlan BY. Genome-wide loss of heterozygosity and uniparental disomy in BRCA1/2-associated ovarian carcinomas. Clin Cancer Res. 2008 Dec 01; 14(23):7645-51.
-
Tsai AC, Gibby T, Beischel L, McGavran L, Johnson JP. A child with Angelman syndrome and trisomy 13 findings due to associated paternal UPD 15 and segmental UPD 13. Am J Med Genet A. 2004 Apr 15; 126A(2):208-12.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|