"Translocation, Genetic" 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 type of chromosome aberration characterized by CHROMOSOME BREAKAGE and transfer of the broken-off portion to another location, often to a different chromosome.
| Descriptor ID |
D014178
|
| MeSH Number(s) |
C23.550.210.870 G05.365.590.175.870 G05.558.860
|
| Concept/Terms |
Translocation, Genetic- Translocation, Genetic
- Genetic Translocation
- Genetic Translocations
- Translocations, Genetic
- Chromosomal Translocation
- Chromosomal Translocations
- Translocations, Chromosomal
- Translocation, Chromosomal
|
Below are MeSH descriptors whose meaning is more general than "Translocation, Genetic".
Below are MeSH descriptors whose meaning is more specific than "Translocation, Genetic".
This graph shows the total number of publications written about "Translocation, Genetic" by people in this website by year, and whether "Translocation, Genetic" 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 |
|---|
| 1995 | 0 | 3 | 3 |
| 1996 | 2 | 3 | 5 |
| 1997 | 6 | 1 | 7 |
| 1998 | 4 | 4 | 8 |
| 1999 | 8 | 1 | 9 |
| 2000 | 2 | 3 | 5 |
| 2001 | 5 | 4 | 9 |
| 2002 | 2 | 9 | 11 |
| 2003 | 4 | 2 | 6 |
| 2004 | 3 | 1 | 4 |
| 2005 | 3 | 3 | 6 |
| 2006 | 6 | 4 | 10 |
| 2007 | 8 | 0 | 8 |
| 2008 | 4 | 4 | 8 |
| 2009 | 4 | 1 | 5 |
| 2010 | 3 | 4 | 7 |
| 2011 | 4 | 5 | 9 |
| 2012 | 2 | 3 | 5 |
| 2013 | 4 | 5 | 9 |
| 2014 | 2 | 6 | 8 |
| 2015 | 4 | 1 | 5 |
| 2016 | 4 | 4 | 8 |
| 2017 | 1 | 3 | 4 |
| 2018 | 1 | 5 | 6 |
| 2019 | 0 | 1 | 1 |
| 2020 | 4 | 3 | 7 |
| 2021 | 2 | 6 | 8 |
| 2022 | 0 | 4 | 4 |
| 2023 | 0 | 1 | 1 |
| 2024 | 1 | 1 | 2 |
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Below are the most recent publications written about "Translocation, Genetic" by people in Profiles.
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MLL oncoprotein levels influence leukemia lineage identities. Nat Commun. 2024 Oct 29; 15(1):9341.
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Optical Genome Mapping for Detection of BCR::ABL1-Another Tool in Our Toolbox. Genes (Basel). 2024 Oct 22; 15(11).
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Brd4::Nutm1 fusion gene initiates NUT carcinoma in vivo. Life Sci Alliance. 2024 Jul; 7(7).
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Childhood and Adolescent Relapsed/Refractory Aggressive B-Cell Lymphomas With t(8;14) and BCL2 Expression, Burkitt Lymphoma Versus Diffuse Large B-Cell Lymphoma: A Diagnostic Challenge. Pediatr Dev Pathol. 2024 Jul-Aug; 27(4):348-353.
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Myeloid neoplasm with <10% blasts and t(3;5)(q25.1;q34)/NPM::MLF1: A classification dilemma. Am J Hematol. 2024 Sep; 99(9):1827-1829.
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ASPSCR1-TFE3 reprograms transcription by organizing enhancer loops around hexameric VCP/p97. Nat Commun. 2024 Feb 07; 15(1):1165.
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The fifth edition of the WHO classification of mature B-cell neoplasms: open questions for research. J Pathol. 2024 03; 262(3):255-270.
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Racial Disparities in MiT Family Translocation Renal Cell Carcinoma. Oncologist. 2023 Nov 02; 28(11):1009-1013.
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Characteristics and clinical outcomes of patients with acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2). Haematologica. 2023 09 01; 108(9):2331-2342.
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Secretory Carcinoma with ETV6-NTRK3 Gene Fusion and Lymph Node Metastasis in Maxillary Gingiva: A Case Report with Pathological and Molecular Correlative Studies. Ann Clin Lab Sci. 2023 Sep; 53(5):800-805.