RNA, Transfer
"RNA, Transfer" 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.
The small RNA molecules, 73-80 nucleotides long, that function during translation (TRANSLATION, GENETIC) to align AMINO ACIDS at the RIBOSOMES in a sequence determined by the mRNA (RNA, MESSENGER). There are about 30 different transfer RNAs. Each recognizes a specific CODON set on the mRNA through its own ANTICODON and as aminoacyl tRNAs (RNA, TRANSFER, AMINO ACYL), each carries a specific amino acid to the ribosome to add to the elongating peptide chains.
Descriptor ID |
D012343
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MeSH Number(s) |
D13.444.735.757
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "RNA, Transfer".
Below are MeSH descriptors whose meaning is more specific than "RNA, Transfer".
This graph shows the total number of publications written about "RNA, Transfer" by people in this website by year, and whether "RNA, Transfer" 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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1991 | 2 | 1 | 3 | 1994 | 1 | 1 | 2 | 1996 | 0 | 1 | 1 | 1997 | 1 | 1 | 2 | 1998 | 1 | 0 | 1 | 2000 | 1 | 3 | 4 | 2001 | 2 | 2 | 4 | 2002 | 0 | 1 | 1 | 2003 | 1 | 0 | 1 | 2004 | 1 | 1 | 2 | 2006 | 1 | 1 | 2 | 2007 | 1 | 2 | 3 | 2008 | 1 | 1 | 2 | 2009 | 1 | 1 | 2 | 2010 | 1 | 2 | 3 | 2011 | 1 | 1 | 2 | 2012 | 2 | 1 | 3 | 2013 | 1 | 1 | 2 | 2014 | 2 | 3 | 5 | 2015 | 1 | 4 | 5 | 2016 | 2 | 1 | 3 | 2017 | 0 | 3 | 3 | 2018 | 1 | 2 | 3 | 2019 | 2 | 1 | 3 | 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "RNA, Transfer" by people in Profiles.
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Ontiveros RJ, Shen H, Stoute J, Yanas A, Cui Y, Zhang Y, Liu KF. Coordination of mRNA and tRNA methylations by TRMT10A. Proc Natl Acad Sci U S A. 2020 04 07; 117(14):7782-7791.
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Narula A, Ellis J, Taliaferro JM, Rissland OS. Coding regions affect mRNA stability in human cells. RNA. 2019 12; 25(12):1751-1764.
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Yanas A, Liu KF. RNA modifications and the link to human disease. Methods Enzymol. 2019; 626:133-146.
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Ontiveros RJ, Stoute J, Liu KF. The chemical diversity of RNA modifications. Biochem J. 2019 04 26; 476(8):1227-1245.
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Friederich MW, Timal S, Powell CA, Dallabona C, Kurolap A, Palacios-Zambrano S, Bratkovic D, Derks TGJ, Bick D, Bouman K, Chatfield KC, Damouny-Naoum N, Dishop MK, Falik-Zaccai TC, Fares F, Fedida A, Ferrero I, Gallagher RC, Garesse R, Gilberti M, González C, Gowan K, Habib C, Halligan RK, Kalfon L, Knight K, Lefeber D, Mamblona L, Mandel H, Mory A, Ottoson J, Paperna T, Pruijn GJM, Rebelo-Guiomar PF, Saada A, Sainz B, Salvemini H, Schoots MH, Smeitink JA, Szukszto MJ, Ter Horst HJ, van den Brandt F, van Spronsen FJ, Veltman JA, Wartchow E, Wintjes LT, Zohar Y, Fernández-Moreno MA, Baris HN, Donnini C, Minczuk M, Rodenburg RJ, Van Hove JLK. Pathogenic variants in glutamyl-tRNAGln amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder. Nat Commun. 2018 10 03; 9(1):4065.
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Driedonks TAP, van der Grein SG, Ariyurek Y, Buermans HPJ, Jekel H, Chow FWN, Wauben MHM, Buck AH, 't Hoen PAC, Nolte-'t Hoen ENM. Immune stimuli shape the small non-coding transcriptome of extracellular vesicles released by dendritic cells. Cell Mol Life Sci. 2018 Oct; 75(20):3857-3875.
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Schmitt MA, Biddle W, Fisk JD. Mapping the Plasticity of the Escherichia coli Genetic Code with Orthogonal Pair-Directed Sense Codon Reassignment. Biochemistry. 2018 05 15; 57(19):2762-2774.
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Pichard-Kostuch A, Zhang W, Liger D, Daugeron MC, Létoquart J, Li de la Sierra-Gallay I, Forterre P, Collinet B, van Tilbeurgh H, Basta T. Structure-function analysis of Sua5 protein reveals novel functional motifs required for the biosynthesis of the universal t6A tRNA modification. RNA. 2018 07; 24(7):926-938.
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Cherry PD, White LK, York K, Hesselberth JR. Genetic bypass of essential RNA repair enzymes in budding yeast. RNA. 2018 03; 24(3):313-323.
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Vantroys E, Larson A, Friederich M, Knight K, Swanson MA, Powell CA, Smet J, Vergult S, De Paepe B, Seneca S, Roeyers H, Menten B, Minczuk M, Vanlander A, Van Hove J, Van Coster R. New insights into the phenotype of FARS2 deficiency. Mol Genet Metab. 2017 12; 122(4):172-181.
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