"RNA, Messenger" 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.
RNA sequences that serve as templates for protein synthesis. Bacterial mRNAs are generally primary transcripts in that they do not require post-transcriptional processing. Eukaryotic mRNA is synthesized in the nucleus and must be exported to the cytoplasm for translation. Most eukaryotic mRNAs have a sequence of polyadenylic acid at the 3' end, referred to as the poly(A) tail. The function of this tail is not known for certain, but it may play a role in the export of mature mRNA from the nucleus as well as in helping stabilize some mRNA molecules by retarding their degradation in the cytoplasm.
Descriptor ID |
D012333
|
MeSH Number(s) |
D13.444.735.544
|
Concept/Terms |
mRNA, Polyadenylated- mRNA, Polyadenylated
- RNA, Messenger, Polyadenylated
- Messenger RNA, Polyadenylated
- Polyadenylated Messenger RNA
- RNA, Polyadenylated Messenger
- Polyadenylated mRNA
- Poly(A)+ mRNA
|
Below are MeSH descriptors whose meaning is more general than "RNA, Messenger".
Below are MeSH descriptors whose meaning is more specific than "RNA, Messenger".
This graph shows the total number of publications written about "RNA, Messenger" by people in this website by year, and whether "RNA, Messenger" 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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1995 | 3 | 47 | 50 |
1996 | 10 | 35 | 45 |
1997 | 10 | 52 | 62 |
1998 | 4 | 30 | 34 |
1999 | 3 | 37 | 40 |
2000 | 7 | 41 | 48 |
2001 | 5 | 57 | 62 |
2002 | 4 | 57 | 61 |
2003 | 5 | 63 | 68 |
2004 | 5 | 74 | 79 |
2005 | 5 | 46 | 51 |
2006 | 2 | 46 | 48 |
2007 | 8 | 47 | 55 |
2008 | 8 | 62 | 70 |
2009 | 5 | 41 | 46 |
2010 | 7 | 50 | 57 |
2011 | 3 | 43 | 46 |
2012 | 10 | 41 | 51 |
2013 | 11 | 34 | 45 |
2014 | 10 | 32 | 42 |
2015 | 18 | 41 | 59 |
2016 | 11 | 19 | 30 |
2017 | 9 | 28 | 37 |
2018 | 9 | 20 | 29 |
2019 | 15 | 13 | 28 |
2020 | 3 | 18 | 21 |
2021 | 5 | 17 | 22 |
2022 | 4 | 21 | 25 |
2023 | 1 | 18 | 19 |
2024 | 7 | 13 | 20 |
2025 | 1 | 2 | 3 |
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Below are the most recent publications written about "RNA, Messenger" by people in Profiles.
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N6-methyladenosine reader YTHDF2 in cell state transition and antitumor immunity. RNA. 2025 Feb 19; 31(3):395-401.
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Distinct plasmablast developmental intermediates produce graded expression of IgM secretory transcripts. Cell Rep. 2025 Feb 25; 44(2):115283.
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Quantitative RNA pseudouridine maps reveal multilayered translation control through plant rRNA, tRNA and mRNA pseudouridylation. Nat Plants. 2025 02; 11(2):234-247.
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snoRNA-facilitated protein secretion revealed by transcriptome-wide snoRNA target identification. Cell. 2025 Jan 23; 188(2):465-483.e22.
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Repurposing large-format microarrays for scalable spatial transcriptomics. Nat Methods. 2025 Jan; 22(1):145-155.
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Dynamics of RNA localization to nuclear speckles are connected to splicing efficiency. Sci Adv. 2024 Oct 18; 10(42):eadp7727.
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Microbiome-induced reprogramming in post-transcriptional landscape using nanopore direct RNA sequencing. Cell Rep. 2024 10 22; 43(10):114798.
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Rogaratinib Plus Atezolizumab in Cisplatin-Ineligible Patients With FGFR RNA-Overexpressing Urothelial Cancer: The FORT-2 Phase 1b Nonrandomized Clinical Trial. JAMA Oncol. 2024 Nov; 10(11):1565-1570.
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Global impact of unproductive splicing on human gene expression. Nat Genet. 2024 Sep; 56(9):1851-1861.
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IGF2BP3 promotes mRNA degradation through internal m7G modification. Nat Commun. 2024 Aug 28; 15(1):7421.