"Transposases" 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.
Enzymes that recombine DNA segments by a process which involves the formation of a synapse between two DNA helices, the cleavage of single strands from each DNA helix and the ligation of a DNA strand from one DNA helix to the other. The resulting DNA structure is called a Holliday junction which can be resolved by DNA REPLICATION or by HOLLIDAY JUNCTION RESOLVASES.
Descriptor ID |
D019895
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MeSH Number(s) |
D08.811.739.500.667 D08.811.913.696.445.825
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Transposases".
Below are MeSH descriptors whose meaning is more specific than "Transposases".
This graph shows the total number of publications written about "Transposases" by people in this website by year, and whether "Transposases" was a major or minor topic of these publications.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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1999 | 0 | 2 | 2 |
2001 | 0 | 1 | 1 |
2004 | 0 | 1 | 1 |
2006 | 1 | 1 | 2 |
2008 | 1 | 0 | 1 |
2010 | 1 | 2 | 3 |
2011 | 1 | 1 | 2 |
2012 | 1 | 2 | 3 |
2013 | 2 | 2 | 4 |
2015 | 0 | 2 | 2 |
2016 | 2 | 1 | 3 |
2018 | 0 | 1 | 1 |
2019 | 1 | 0 | 1 |
2020 | 0 | 1 | 1 |
2021 | 2 | 0 | 2 |
2022 | 0 | 1 | 1 |
2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Transposases" by people in Profiles.
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Atlas-scale single-cell chromatin accessibility using nanowell-based combinatorial indexing. Genome Res. 2023 02; 33(2):208-217.
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A novel, de novo intronic variant in POGZ causes White-Sutton syndrome. Am J Med Genet A. 2022 07; 188(7):2198-2203.
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Identification of mutations that cooperate with defects in B cell transcription factors to initiate leukemia. Oncogene. 2021 10; 40(43):6166-6179.
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High-content single-cell combinatorial indexing. Nat Biotechnol. 2021 12; 39(12):1574-1580.
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Expanded encyclopaedias of DNA elements in the human and mouse genomes. Nature. 2020 07; 583(7818):699-710.
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Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome). Am J Med Genet A. 2020 01; 182(1):38-52.
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A functional genomics approach to identify pathways of drug resistance in medulloblastoma. Acta Neuropathol Commun. 2018 12 27; 6(1):146.
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Joint single-cell DNA accessibility and protein epitope profiling reveals environmental regulation of epigenomic heterogeneity. Nat Commun. 2018 11 02; 9(1):4590.
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Antitumor activity of CD56-chimeric antigen receptor T cells in neuroblastoma and SCLC models. Oncogene. 2018 07; 37(27):3686-3697.
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Transposase-driven rearrangements in human tumors. Nat Genet. 2017 Jun 28; 49(7):975-977.