"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
|
| MeSH Number(s) |
D08.811.739.500.667 D08.811.913.696.445.825
|
| Concept/Terms |
|
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,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 0 | 2 | 2 |
| 2001 | 0 | 1 | 1 |
| 2005 | 1 | 0 | 1 |
| 2006 | 1 | 1 | 2 |
| 2010 | 1 | 0 | 1 |
| 2011 | 0 | 1 | 1 |
| 2012 | 0 | 2 | 2 |
| 2013 | 1 | 0 | 1 |
| 2015 | 0 | 2 | 2 |
| 2016 | 1 | 0 | 1 |
| 2019 | 2 | 0 | 2 |
| 2020 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
| 2022 | 0 | 1 | 1 |
| 2023 | 1 | 0 | 1 |
| 2025 | 1 | 1 | 2 |
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Below are the most recent publications written about "Transposases" by people in Profiles.
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MultiSite Assembly of Gateway Induced Clones (MAGIC): a flexible cloning toolbox for use in vertebrate model systems. Development. 2025 Nov 15; 152(22).
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Programmable gene insertion in human cells with a laboratory-evolved CRISPR-associated transposase. Science. 2025 May 15; 388(6748):eadt5199.
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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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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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In vivo CRISPR screening in CD8 T cells with AAV-Sleeping Beauty hybrid vectors identifies membrane targets for improving immunotherapy for glioblastoma. Nat Biotechnol. 2019 Nov; 37(11):1302-1313.
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POGZ truncating alleles cause syndromic intellectual disability. Genome Med. 2016 Jan 06; 8(1):3.
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A genetic toolkit for tagging intronic MiMIC containing genes. Elife. 2015 Jun 23; 4.