"RNA, Transfer, Leu" 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 transfer RNA which is specific for carrying leucine to sites on the ribosomes in preparation for protein synthesis.
| Descriptor ID |
D012356
|
| MeSH Number(s) |
D13.444.735.757.700.500
|
| Concept/Terms |
RNA, Transfer, Leu- RNA, Transfer, Leu
- Transfer RNA, Leu
- Leu Transfer RNA
- RNA, Leu Transfer
- tRNA(Leu)
- tRNALeu
- Leucine-Specific tRNA
- Leucine Specific tRNA
- tRNA, Leucine-Specific
|
Below are MeSH descriptors whose meaning is more general than "RNA, Transfer, Leu".
Below are MeSH descriptors whose meaning is more specific than "RNA, Transfer, Leu".
This graph shows the total number of publications written about "RNA, Transfer, Leu" by people in this website by year, and whether "RNA, Transfer, Leu" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2005 | 2 | 0 | 2 |
| 2006 | 1 | 0 | 1 |
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Below are the most recent publications written about "RNA, Transfer, Leu" by people in Profiles.
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Kirino Y, Yasukawa T, Marjavaara SK, Jacobs HT, Holt IJ, Watanabe K, Suzuki T. Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect. Hum Mol Genet. 2006 Mar 15; 15(6):897-904.
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Kirino Y, Goto Y, Campos Y, Arenas J, Suzuki T. Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease. Proc Natl Acad Sci U S A. 2005 May 17; 102(20):7127-32.
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Kirino Y, Suzuki T. Human mitochondrial diseases associated with tRNA wobble modification deficiency. RNA Biol. 2005 Apr; 2(2):41-4.
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Kirino Y, Yasukawa T, Ohta S, Akira S, Ishihara K, Watanabe K, Suzuki T. Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease. Proc Natl Acad Sci U S A. 2004 Oct 19; 101(42):15070-5.
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Park H, Davidson E, King MP. The pathogenic A3243G mutation in human mitochondrial tRNALeu(UUR) decreases the efficiency of aminoacylation. Biochemistry. 2003 Feb 04; 42(4):958-64.