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.
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Year | Major Topic | Minor Topic | Total |
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1994 | 2 | 1 | 3 |
1995 | 0 | 1 | 1 |
1996 | 0 | 2 | 2 |
1997 | 2 | 1 | 3 |
1998 | 3 | 2 | 5 |
1999 | 5 | 3 | 8 |
2000 | 1 | 1 | 2 |
2001 | 2 | 1 | 3 |
2002 | 3 | 0 | 3 |
2003 | 2 | 4 | 6 |
2004 | 0 | 1 | 1 |
2005 | 5 | 1 | 6 |
2006 | 0 | 1 | 1 |
2007 | 2 | 0 | 2 |
2008 | 2 | 4 | 6 |
2009 | 1 | 3 | 4 |
2010 | 1 | 0 | 1 |
2011 | 1 | 4 | 5 |
2012 | 1 | 1 | 2 |
2013 | 0 | 3 | 3 |
2014 | 0 | 2 | 2 |
2015 | 1 | 2 | 3 |
2016 | 2 | 1 | 3 |
2017 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 13" by people in Profiles.
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Two Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry. J Natl Cancer Inst. 2017 08 01; 109(8).
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First-line therapy for young patients with CLL. Hematology Am Soc Hematol Educ Program. 2016 Dec 02; 2016(1):146-148.
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Outcome of Patients with Multiple Myeloma and CKS1B Gene Amplification after Autologous Hematopoietic Stem Cell Transplantation. Biol Blood Marrow Transplant. 2016 12; 22(12):2159-2164.
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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.
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Refractory Kaposiform Hemangioendothelioma Associated with the Chromosomal Translocation t(13;16)(q14;p13.3). Pediatr Dev Pathol. 2016 Sep/Oct; 19(5):417-420.
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Genomic and Clinicopathologic Features of Primary Myelofibrosis With Isolated 13q Deletion. Clin Lymphoma Myeloma Leuk. 2015 Aug; 15(8):496-505.e1-2.
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High fluorescence in situ hybridization percentage of deletion 11q in patients with chronic lymphocytic leukemia is an independent predictor of adverse outcome. Am J Hematol. 2015 Jun; 90(6):471-7.
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Fluorescent in situ hybridization of human sperm: diagnostics, indications, and therapeutic implications. Fertil Steril. 2014 Dec; 102(6):1534-9.
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Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans. Hum Mol Genet. 2014 Dec 15; 23(24):6607-15.
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Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center. Ultrasound Obstet Gynecol. 2014 Mar; 43(3):254-64.