"RNA-Binding Proteins" 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.
Proteins that bind to RNA molecules. Included here are RIBONUCLEOPROTEINS and other proteins whose function is to bind specifically to RNA.
Descriptor ID |
D016601
|
MeSH Number(s) |
D12.776.157.725 D12.776.664.962
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "RNA-Binding Proteins".
Below are MeSH descriptors whose meaning is more specific than "RNA-Binding Proteins".
This graph shows the total number of publications written about "RNA-Binding Proteins" by people in this website by year, and whether "RNA-Binding Proteins" 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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1999 | 1 | 0 | 1 |
2003 | 1 | 0 | 1 |
2004 | 1 | 1 | 2 |
2005 | 1 | 0 | 1 |
2006 | 2 | 0 | 2 |
2007 | 1 | 0 | 1 |
2008 | 0 | 2 | 2 |
2009 | 2 | 2 | 4 |
2010 | 1 | 0 | 1 |
2011 | 5 | 0 | 5 |
2012 | 2 | 0 | 2 |
2013 | 5 | 4 | 9 |
2014 | 3 | 2 | 5 |
2015 | 3 | 6 | 9 |
2016 | 3 | 1 | 4 |
2017 | 1 | 1 | 2 |
2018 | 4 | 2 | 6 |
2019 | 3 | 0 | 3 |
2020 | 2 | 1 | 3 |
2021 | 2 | 0 | 2 |
2022 | 1 | 2 | 3 |
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Below are the most recent publications written about "RNA-Binding Proteins" by people in Profiles.
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A MademoiseLLE domain binding platform links the key RNA transporter to endosomes. PLoS Genet. 2022 06; 18(6):e1010269.
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Exon junction complex-associated multi-adapter RNPS1 nucleates splicing regulatory complexes to maintain transcriptome surveillance. Nucleic Acids Res. 2022 06 10; 50(10):5899-5918.
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Human UPF3A and UPF3B enable fault-tolerant activation of nonsense-mediated mRNA decay. EMBO J. 2022 05 16; 41(10):e109191.
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Targeting the cytoplasmic polyadenylation element-binding protein CPEB4 protects against diet-induced obesity and microbiome dysbiosis. Mol Metab. 2021 12; 54:101388.
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Biallelic variants in YRDC cause a developmental disorder with progeroid features. Hum Genet. 2021 Dec; 140(12):1679-1693.
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A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q. Z Kinder Jugendpsychiatr Psychother. 2020 Nov; 48(6):478-489.
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The STRIPAK signaling complex regulates dephosphorylation of GUL1, an RNA-binding protein that shuttles on endosomes. PLoS Genet. 2020 09; 16(9):e1008819.
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CASC3 promotes transcriptome-wide activation of nonsense-mediated decay by the exon junction complex. Nucleic Acids Res. 2020 09 04; 48(15):8626-8644.
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The genomic and clinical landscape of fetal akinesia. Genet Med. 2020 03; 22(3):511-523.
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Novel EXOSC3 pathogenic variant results in a mild course of neurologic disease with cerebellum involvement. Eur J Med Genet. 2020 Feb; 63(2):103649.