 Amino Acyl-tRNA Synthetases
"Amino Acyl-tRNA Synthetases" 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 subclass of enzymes that aminoacylate AMINO ACID-SPECIFIC TRANSFER RNA with their corresponding AMINO ACIDS.
| Descriptor ID |
D000604
|
| MeSH Number(s) |
D08.811.464.263.200
|
| Concept/Terms |
Amino Acyl-tRNA Synthetases- Amino Acyl-tRNA Synthetases
- Acyl-tRNA Synthetases, Amino
- Amino Acyl tRNA Synthetases
- Synthetases, Amino Acyl-tRNA
- Amino Acyl-tRNA Ligases
- Acyl-tRNA Ligases, Amino
- Amino Acyl tRNA Ligases
- Ligases, Amino Acyl-tRNA
- tRNA Synthetase
- Synthetase, tRNA
- Aminoacyl-tRNA Synthetase
- Aminoacyl tRNA Synthetase
- Synthetase, Aminoacyl-tRNA
- Transfer RNA Synthetase
- RNA Synthetase, Transfer
- Synthetase, Transfer RNA
- Amino Acyl T RNA Synthetases
- Aminoacyl Transfer RNA Synthetase
|
Below are MeSH descriptors whose meaning is more general than "Amino Acyl-tRNA Synthetases".
Below are MeSH descriptors whose meaning is more specific than "Amino Acyl-tRNA Synthetases".
This graph shows the total number of publications written about "Amino Acyl-tRNA Synthetases" by people in UAMS Profiles by year, and whether "Amino Acyl-tRNA Synthetases" 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 |
|---|
| 2020 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2003 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Amino Acyl-tRNA Synthetases" by people in Profiles over the past ten years.
-
Riley LG, Rudinger-Thirion J, Frugier M, Wilson M, Luig M, Alahakoon TI, Nixon CY, Kirk EP, Roscioli T, Lunke S, Stark Z, Wierenga KJ, Palle S, Walsh M, Higgs E, Arbuckle S, Thirukeswaran S, Compton AG, Thorburn DR, Christodoulou J. The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy. Hum Mutat. 2020 08; 41(8):1425-1434.
-
Samanta D, Gokden M, Willis E. Clinicopathologic Findings of CARS2 Mutation. Pediatr Neurol. 2018 10; 87:65-69.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|