RNA Processing, Post-Transcriptional
"RNA Processing, Post-Transcriptional" 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.
Post-transcriptional biological modification of messenger, transfer, or ribosomal RNAs or their precursors. It includes cleavage, methylation, thiolation, isopentenylation, pseudouridine formation, conformational changes, and association with ribosomal protein.
Descriptor ID |
D012323
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MeSH Number(s) |
G02.111.760 G03.839 G05.308.700
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Concept/Terms |
RNA Processing, Post-Transcriptional- RNA Processing, Post-Transcriptional
- Post-Transcriptional RNA Processing
- Post Transcriptional RNA Processing
- RNA Processing, Posttranscriptional
- Posttranscriptional RNA Processing
- Processing, Posttranscriptional RNA
- Post-Transcriptional RNA Modification
- Modification, Post-Transcriptional RNA
- Modifications, Post-Transcriptional RNA
- Post Transcriptional RNA Modification
- Post-Transcriptional RNA Modifications
- RNA Modification, Post-Transcriptional
- RNA Modifications, Post-Transcriptional
- RNA Processing, Post Transcriptional
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Below are MeSH descriptors whose meaning is more general than "RNA Processing, Post-Transcriptional".
Below are MeSH descriptors whose meaning is more specific than "RNA Processing, Post-Transcriptional".
This graph shows the total number of publications written about "RNA Processing, Post-Transcriptional" by people in this website by year, and whether "RNA Processing, Post-Transcriptional" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1994 | 2 | 0 | 2 | 1996 | 0 | 1 | 1 | 1998 | 3 | 0 | 3 | 1999 | 1 | 0 | 1 | 2001 | 1 | 0 | 1 | 2002 | 2 | 0 | 2 | 2003 | 0 | 1 | 1 | 2004 | 1 | 0 | 1 | 2005 | 2 | 0 | 2 | 2006 | 2 | 0 | 2 | 2007 | 1 | 0 | 1 | 2008 | 1 | 1 | 2 | 2009 | 1 | 1 | 2 | 2010 | 2 | 0 | 2 | 2011 | 5 | 0 | 5 | 2012 | 0 | 1 | 1 | 2014 | 0 | 3 | 3 | 2015 | 3 | 1 | 4 | 2017 | 0 | 1 | 1 | 2019 | 3 | 0 | 3 | 2020 | 1 | 1 | 2 | 2021 | 2 | 0 | 2 |
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Below are the most recent publications written about "RNA Processing, Post-Transcriptional" by people in Profiles.
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Shen H, Gonskikh Y, Stoute J, Liu KF. Human DIMT1 generates N26,6A-dimethylation-containing small RNAs. J Biol Chem. 2021 10; 297(4):101146.
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Jaiswal AK, Truong H, Tran TM, Lin TL, Casero D, Alberti MO, Rao DS. Focused CRISPR-Cas9 genetic screening reveals USO1 as a vulnerability in B-cell acute lymphoblastic leukemia. Sci Rep. 2021 06 23; 11(1):13158.
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Saldi T, Riemondy K, Erickson B, Bentley DL. Alternative RNA structures formed during transcription depend on elongation rate and modify RNA processing. Mol Cell. 2021 04 15; 81(8):1789-1801.e5.
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Weskamp K, Olwin BB, Parker R. Post-Transcriptional Regulation in Skeletal Muscle Development, Repair, and Disease. Trends Mol Med. 2021 05; 27(5):469-481.
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Zhang H, Brown RD, Stenmark KR, Hu CJ. RNA-Binding Proteins in Pulmonary Hypertension. Int J Mol Sci. 2020 May 26; 21(11).
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McMahon M, Contreras A, Holm M, Uechi T, Forester CM, Pang X, Jackson C, Calvert ME, Chen B, Quigley DA, Luk JM, Kelley RK, Gordan JD, Gill RM, Blanchard SC, Ruggero D. A single H/ACA small nucleolar RNA mediates tumor suppression downstream of oncogenic RAS. Elife. 2019 09 03; 8.
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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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Fok WC, Shukla S, Vessoni AT, Brenner KA, Parker R, Sturgeon CM, Batista LFZ. Posttranscriptional modulation of TERC by PAPD5 inhibition rescues hematopoietic development in dyskeratosis congenita. Blood. 2019 03 21; 133(12):1308-1312.
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Borland K, Diesend J, Ito-Kureha T, Heissmeyer V, Hammann C, Buck AH, Michalakis S, Kellner S. Production and Application of Stable Isotope-Labeled Internal Standards for RNA Modification Analysis. Genes (Basel). 2019 01 05; 10(1).
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Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, Boyer O, Revy P, Jobst-Schwan T, Schmidt JM, Lawson JA, Schanze D, Ashraf S, Ullmann JFP, Hoogstraten CA, Boddaert N, Collinet B, Martin G, Liger D, Lovric S, Furlano M, Guerrera IC, Sanchez-Ferras O, Hu JF, Boschat AC, Sanquer S, Menten B, Vergult S, De Rocker N, Airik M, Hermle T, Shril S, Widmeier E, Gee HY, Choi WI, Sadowski CE, Pabst WL, Warejko JK, Daga A, Basta T, Matejas V, Scharmann K, Kienast SD, Behnam B, Beeson B, Begtrup A, Bruce M, Ch'ng GS, Lin SP, Chang JH, Chen CH, Cho MT, Gaffney PM, Gipson PE, Hsu CH, Kari JA, Ke YY, Kiraly-Borri C, Lai WM, Lemyre E, Littlejohn RO, Masri A, Moghtaderi M, Nakamura K, Ozaltin F, Praet M, Prasad C, Prytula A, Roeder ER, Rump P, Schnur RE, Shiihara T, Sinha MD, Soliman NA, Soulami K, Sweetser DA, Tsai WH, Tsai JD, Topaloglu R, Vester U, Viskochil DH, Vatanavicharn N, Waxler JL, Wierenga KJ, Wolf MTF, Wong SN, Leidel SA, Truglio G, Dedon PC, Poduri A, Mane S, Lifton RP, Bouchard M, Kannu P, Chitayat D, Magen D, Callewaert B, van Tilbeurgh H, Zenker M, Antignac C, Hildebrandt F. Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. Nat Genet. 2017 Oct; 49(10):1529-1538.
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