Chromosomes, Human, Pair 13
"Chromosomes, Human, Pair 13" 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 D CHROMOSOMES of the human chromosome classification.
| Descriptor ID |
D002882
|
| MeSH Number(s) |
A11.284.187.520.300.370.375 G05.360.162.520.300.370.375
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 13".
- 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, 13-15 [A11.284.187.520.300.370]
- Chromosomes, Human, Pair 13 [A11.284.187.520.300.370.375]
- 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, 13-15 [G05.360.162.520.300.370]
- Chromosomes, Human, Pair 13 [G05.360.162.520.300.370.375]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 13".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 13" by people in this website by year, and whether "Chromosomes, Human, Pair 13" 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 |
|---|
| 1994 | 0 | 1 | 1 |
| 1998 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2002 | 1 | 0 | 1 |
| 2004 | 2 | 1 | 3 |
| 2006 | 0 | 1 | 1 |
| 2007 | 1 | 0 | 1 |
| 2011 | 0 | 1 | 1 |
| 2014 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2018 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Chromosomes, Human, Pair 13" by people in Profiles.
-
Benign Fibromyxoid Lesion of the Breast: A Distinct Entity From Benign Spindle Cell Tumors of the Mammary Stroma? Int J Surg Pathol. 2018 Sep; 26(6):488-493.
-
Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry. Hum Mol Genet. 2016 Mar 15; 25(6):1203-14.
-
"Low-Fat" Pseudoangiomatous Spindle Cell Lipoma: A Rare Variant With Loss of 13q14 Region. Am J Dermatopathol. 2015 Dec; 37(12):920-3.
-
Mortality and morbidity of VLBW infants with trisomy 13 or trisomy 18. Pediatrics. 2014 Feb; 133(2):226-35.
-
Major chromosomal anomalies among very low birth weight infants in the Vermont Oxford Network. J Pediatr. 2012 May; 160(5):774-780.e11.
-
Expansion of the deletion 13q syndrome phenotype: a case report. J Child Neurol. 2007 Sep; 22(9):1124-7.
-
Familial aggregation and linkage analysis of autoantibody traits in pedigrees multiplex for systemic lupus erythematosus. Genes Immun. 2006 Jul; 7(5):417-32.
-
Systemic lupus erythematosus genome scan: support for linkage at 1q23, 2q33, 16q12-13, and 17q21-23 and novel evidence at 3p24, 10q23-24, 13q32, and 18q22-23. Arthritis Rheum. 2004 Oct; 50(10):3203-10.
-
Effectiveness of cardiac surgery in trisomies 13 and 18 (from the Pediatric Cardiac Care Consortium). Am J Cardiol. 2004 Mar 15; 93(6):801-3.
-
Trisomy 16 in a pigtailed macaque (M. nemestrina) with multiple anomalies and developmental delays. Am J Ment Retard. 2004 Jan; 109(1):9-20.