"Ribosomes" 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.
Multicomponent ribonucleoprotein structures found in the CYTOPLASM of all cells, and in MITOCHONDRIA, and PLASTIDS. They function in PROTEIN BIOSYNTHESIS via GENETIC TRANSLATION.
Descriptor ID |
D012270
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MeSH Number(s) |
A11.284.430.214.190.875.811
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Ribosomes".
Below are MeSH descriptors whose meaning is more specific than "Ribosomes".
This graph shows the total number of publications written about "Ribosomes" by people in this website by year, and whether "Ribosomes" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2006 | 0 | 1 | 1 |
2009 | 1 | 1 | 2 |
2011 | 0 | 1 | 1 |
2012 | 1 | 0 | 1 |
2013 | 0 | 1 | 1 |
2014 | 0 | 1 | 1 |
2015 | 1 | 0 | 1 |
2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Ribosomes" by people in Profiles.
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Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration. Brain. 2020 01 01; 143(1):94-111.
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Acrofacial Dysostosis, Cincinnati Type, a Mandibulofacial Dysostosis Syndrome with Limb Anomalies, Is Caused by POLR1A Dysfunction. Am J Hum Genet. 2015 May 07; 96(5):765-74.
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The interaction of cytoplasmic poly(A)-binding protein with eukaryotic initiation factor 4G suppresses nonsense-mediated mRNA decay. RNA. 2014 Oct; 20(10):1579-92.
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Automatic post-picking using MAPPOS improves particle image detection from cryo-EM micrographs. J Struct Biol. 2013 May; 182(2):59-66.
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Genome-wide search for novel human uORFs and N-terminal protein extensions using ribosomal footprinting. Genome Res. 2012 Nov; 22(11):2208-18.
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Assembly, disassembly and recycling: the dynamics of exon junction complexes. RNA Biol. 2011 Jan-Feb; 8(1):24-9.
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Disassembly of exon junction complexes by PYM. Cell. 2009 May 01; 137(3):536-48.
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IGHMBP2 is a ribosome-associated helicase inactive in the neuromuscular disorder distal SMA type 1 (DSMA1). Hum Mol Genet. 2009 Apr 01; 18(7):1288-300.
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Internal ribosome entry sequence-mediated translation initiation triggers nonsense-mediated decay. EMBO Rep. 2006 Jul; 7(7):722-6.