"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 |
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1994 | 5 | 4 | 9 |
1995 | 5 | 12 | 17 |
1996 | 5 | 7 | 12 |
1997 | 8 | 4 | 12 |
1998 | 10 | 7 | 17 |
1999 | 9 | 8 | 17 |
2000 | 9 | 12 | 21 |
2001 | 9 | 8 | 17 |
2002 | 9 | 12 | 21 |
2003 | 13 | 13 | 26 |
2004 | 5 | 7 | 12 |
2005 | 4 | 11 | 15 |
2006 | 20 | 10 | 30 |
2007 | 11 | 12 | 23 |
2008 | 8 | 12 | 20 |
2009 | 11 | 10 | 21 |
2010 | 10 | 12 | 22 |
2011 | 10 | 11 | 21 |
2012 | 11 | 11 | 22 |
2013 | 10 | 9 | 19 |
2014 | 7 | 18 | 25 |
2015 | 12 | 7 | 19 |
2016 | 13 | 10 | 23 |
2017 | 7 | 9 | 16 |
2018 | 5 | 9 | 14 |
2019 | 3 | 4 | 7 |
2020 | 6 | 9 | 15 |
2021 | 5 | 14 | 19 |
2022 | 0 | 7 | 7 |
2023 | 0 | 6 | 6 |
2024 | 0 | 2 | 2 |
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Below are the most recent publications written about "Translocation, Genetic" by people in Profiles.
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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.
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Constitutional balanced translocations involving SMARCB1: A rare cause of rhabdoid tumor predisposition syndrome. Genes Chromosomes Cancer. 2024 Jan; 63(1):e23195.
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From the archives of MD Anderson Cancer Center: Sporadic Burkitt lymphoma with a complex karyotype and SOX11 expression. Ann Diagn Pathol. 2023 Oct; 66:152182.
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Autologous Stem Cell Transplantation for Patients with Multiple Myeloma with Translocation (4;14): The MD Anderson Cancer Center Experience. Transplant Cell Ther. 2023 04; 29(4):260.e1-260.e6.
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Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences. J Med Genet. 2023 06; 60(6):547-556.
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PPP1R7 Is a Novel Translocation Partner of CBFB via t(2;16)(q37;q22) in Acute Myeloid Leukemia. Genes (Basel). 2022 07 29; 13(8).