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Mobile Group II Introns as Ancestral Eukaryotic Elements
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.10394openalex-snapshot
The spliceosome: the most complex macromolecular machine in the cell?
inferredcites →https://doi.org/10.1007/s00018-013-1469-zopenalex-snapshot
If the cap fits, wear it: an overview of telomeric structures over evolution
inferredcites →https://doi.org/10.1007/s00239-013-9579-7openalex-snapshot
Evolution of Plant Mitochondrial Intron-Encoded Maturases: Frequent Lineage-Specific Loss and Recurrent Intracellular Transfer to the Nucleus
inferredcites →https://doi.org/10.1007/s004380050497openalex-snapshot
A tripartite group II intron in mitochondria of an angiosperm plant
inferredcites →https://doi.org/10.1016/j.bbabio.2015.01.009openalex-snapshot
Organellar maturases: A window into the evolution of the spliceosome
inferredcites →https://doi.org/10.1016/j.cell.2009.02.009openalex-snapshot
The Spliceosome: Design Principles of a Dynamic RNP Machine
inferredcites →https://doi.org/10.1016/j.cell.2012.09.033openalex-snapshot
Visualizing Group II Intron Catalysis through the Stages of Splicing
inferredcites →https://doi.org/10.1016/j.gene.2005.08.017openalex-snapshot
Housekeeping recA gene interrupted by group II intron in the thermophilic Geobacillus kaustophilus
inferredcites →https://doi.org/10.1016/j.margen.2013.12.002openalex-snapshot
The chloroplast genome of the diatom Seminavis robusta: New features introduced through multiple mechanisms of horizontal gene transfer
inferredcites →https://doi.org/10.1016/j.mib.2017.04.003openalex-snapshot
Mobile self-splicing introns and inteins as environmental sensors
inferredcites →https://doi.org/10.1016/j.mito.2007.09.005openalex-snapshot
Cis- and trans-splicing of group II introns in plant mitochondria
inferredcites →https://doi.org/10.1016/j.molcel.2009.03.014openalex-snapshot
Global Regulators Orchestrate Group II Intron Retromobility
inferredcites →https://doi.org/10.1016/j.sbi.2015.12.005openalex-snapshot
CryoEM structures of two spliceosomal complexes: starter and dessert at the spliceosome feast
inferredcites →https://doi.org/10.1016/j.tibs.2017.03.007openalex-snapshot
Structural Insights into the Mechanism of Group II Intron Splicing
inferredcites →https://doi.org/10.1016/j.virol.2015.02.039openalex-snapshot
Origins and evolution of viruses of eukaryotes: The ultimate modularity
inferredcites →https://doi.org/10.1017/s1355838202023087openalex-snapshot
Identification of a family of group II introns encoding LAGLIDADG ORFs typical of group I introns
inferredcites →https://doi.org/10.1021/bi027330bopenalex-snapshot
A Group II Intron Inserted into a Bacterial Heat-Shock Operon Shows Autocatalytic Activity and Unusual Thermostability
inferredcites →https://doi.org/10.1038/hdy.2014.32openalex-snapshot
Insights into the history of a bacterial group II intron remnant from the genomes of the nitrogen-fixing symbionts Sinorhizobium meliloti and Sinorhizobium medicae
inferredcites →https://doi.org/10.1038/nature04531openalex-snapshot
Introns and the origin of nucleus–cytosol compartmentalization
inferredcites →https://doi.org/10.1038/nature07283openalex-snapshot
Structure of the Tribolium castaneum telomerase catalytic subunit TERT
inferredcites →https://doi.org/10.1038/nature19316openalex-snapshot
Cryo-EM structure of the spliceosome immediately after branching
inferredcites →https://doi.org/10.1038/nature21079openalex-snapshot
Cryo-EM structure of a human spliceosome activated for step 2 of splicing
inferredcites →https://doi.org/10.1038/nmeth.3478openalex-snapshot
Efficient and quantitative high-throughput tRNA sequencing
inferredcites →https://doi.org/10.1038/nsmb.3220openalex-snapshot
Structure of a group II intron in complex with its reverse transcriptase
inferredcites →https://doi.org/10.1038/nsmb.3224openalex-snapshot
Crystal structures of a group II intron maturase reveal a missing link in spliceosome evolution
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03649.xopenalex-snapshot
A group II intron has invaded the genus Azotobacter and is inserted within the termination codon of the essential groEL gene
inferredcites →https://doi.org/10.1073/pnas.0700561104openalex-snapshot
Insertion of group II intron retroelements after intrinsic transcriptional terminators
inferredcites →https://doi.org/10.1073/pnas.0702741104openalex-snapshot
Telomere-associated endonuclease-deficient Penelope -like retroelements in diverse eukaryotes
inferredcites →https://doi.org/10.1073/pnas.0909400107openalex-snapshot
An organellar maturase associates with multiple group II introns
inferredcites →https://doi.org/10.1073/pnas.1100266108openalex-snapshot
A widespread class of reverse transcriptase-related cellular genes
inferredcites →https://doi.org/10.1073/pnas.1100278108openalex-snapshot
Retrotransposons that maintain chromosome ends
inferredcites →https://doi.org/10.1073/pnas.1404276111openalex-snapshot
RNA–RNA interactions and pre-mRNA mislocalization as drivers of group II intron loss from nuclear genomes
inferredcites →https://doi.org/10.1074/jbc.m116.750570openalex-snapshot
A Ribonucleoprotein Supercomplex Involved in trans-Splicing of Organelle Group II Introns
inferredcites →https://doi.org/10.1080/15476286.2015.1066956openalex-snapshot
Group II intron lariat: Structural insights into the spliceosome
inferredcites →https://doi.org/10.1080/15476286.2016.1244595openalex-snapshot
Forks in the tracks: Group II introns, spliceosomes, telomeres and beyond
inferredcites →https://doi.org/10.1093/gbe/evw011openalex-snapshot
Group II Intron-MediatedTrans-Splicing in the Gene-Rich Mitochondrial Genome of an Enigmatic Eukaryote,Diphylleia rotans
inferredcites →https://doi.org/10.1093/gbe/evw190openalex-snapshot
Mitochondrion-to-Chloroplast DNA Transfers and Intragenomic Proliferation of Chloroplast Group II Introns inGloeotilopsisGreen Algae (Ulotrichales, Ulvophyceae)
inferredcites →https://doi.org/10.1093/jhered/esp062openalex-snapshot
Endogenous Mechanisms for the Origins of Spliceosomal Introns
inferredcites →https://doi.org/10.1093/molbev/msj047openalex-snapshot
Origin and Evolution of the Chloroplast trnK (matK) Intron: A Model for Evolution of Group II Intron RNA Structures
inferredcites →https://doi.org/10.1093/molbev/msj085openalex-snapshot
Periodic Extinctions of Transposable Elements in Bacterial Lineages: Evidence from Intragenomic Variation in Multiple Genomes
inferredcites →https://doi.org/10.1093/molbev/msn039openalex-snapshot
Extremely Intron-Rich Genes in the Alveolate Ancestors Inferred with a Flexible Maximum-Likelihood Approach
inferredcites →https://doi.org/10.1093/molbev/msp193openalex-snapshot
A Broadscale Phylogenetic Analysis of Group II Intron RNAs and Intron-Encoded Reverse Transcriptases
inferredcites →https://doi.org/10.1093/molbev/msq238openalex-snapshot
Remarkable Abundance and Evolution of Mobile Group II Introns in Wolbachia Bacterial Endosymbionts
inferredcites →https://doi.org/10.1093/nar/21.15.3537openalex-snapshot
Complete sequence ofEuglena gracilischloroplast DNA
inferredcites →https://doi.org/10.1093/nar/gkn095openalex-snapshot
Lateral transfer of introns in the cryptophyte plastid genome
inferredcites →https://doi.org/10.1093/nar/gkn867openalex-snapshot
A diversity of uncharacterized reverse transcriptases in bacteria
inferredcites →https://doi.org/10.1093/nar/gkq847openalex-snapshot
Splicing of the Sinorhizobium meliloti RmInt1 group II intron provides evidence of retroelement behavior
inferredcites →https://doi.org/10.1093/nar/gkr1043openalex-snapshot
Database for bacterial group II introns
inferredcites →https://doi.org/10.1093/nar/gkt1051openalex-snapshot
Visualizing the ai5γ group IIB intron
inferredcites →https://doi.org/10.1098/rstb.2015.0442openalex-snapshot
Viruses and mobile elements as drivers of evolutionary transitions
inferredcites →https://doi.org/10.1099/mic.0.2007/016360-0openalex-snapshot
The S.ma.I2 class C group II intron inserts at integron attC sites
inferredcites →https://doi.org/10.1101/cshperspect.a003616openalex-snapshot
Group II Introns: Mobile Ribozymes that Invade DNA
inferredcites →https://doi.org/10.1101/gad.1905010openalex-snapshot
Nuclear expression of a group II intron is consistent with spliceosomal intron ancestry
inferredcites →https://doi.org/10.1105/tpc.16.00398openalex-snapshot
The Reverse Transcriptase/RNA Maturase Protein MatR Is Required for the Splicing of Various Group II Introns in Brassicaceae Mitochondria
inferredcites →https://doi.org/10.1111/j.1574-6976.2007.00068.xopenalex-snapshot
Bacterial group II introns: not just splicing
inferredcites →https://doi.org/10.1126/science.1153803openalex-snapshot
Crystal Structure of a Self-Spliced Group II Intron
inferredcites →https://doi.org/10.1126/science.aac7629openalex-snapshot
Structure of a yeast spliceosome at 3.6-angstrom resolution
inferredcites →https://doi.org/10.1126/science.aaf9258openalex-snapshot
Crystal structures of a group II intron lariat primed for reverse splicing
inferredcites →https://doi.org/10.1128/jb.00674-09openalex-snapshot
Potential Role of Group IIC-attCIntrons in Integron Cassette Formation
inferredcites →https://doi.org/10.1128/jb.186.8.2393-2401.2004openalex-snapshot
Conserved Target for Group II Intron Insertion in Relaxase Genes of Conjugative Elements of Gram-Positive Bacteria
inferredcites →https://doi.org/10.1128/microbiolspec.mdna3-0050-2014openalex-snapshot
Mobile Bacterial Group II Introns at the Crux of Eukaryotic Evolution
inferredcites →https://doi.org/10.1128/microbiolspec.mdna3-0058-2014openalex-snapshot
An Unexplored Diversity of Reverse Transcriptases in Bacteria
inferredcites →https://doi.org/10.1128/mmbr.00056-13openalex-snapshot
Integrons: Past, Present, and Future
inferredcites →https://doi.org/10.1146/annurev.genet.42.110807.091549openalex-snapshot
The Take and Give Between Retrotransposable Elements and their Hosts
inferredcites →https://doi.org/10.1186/1759-8753-4-28openalex-snapshot
A pipeline of programs for collecting and analyzing group II intron retroelement sequences from GenBank
inferredcites →https://doi.org/10.1186/1759-8753-5-2openalex-snapshot
Biotechnological applications of mobile group II introns and their reverse transcriptases: gene targeting, RNA-seq, and non-coding RNA analysis
inferredcites →https://doi.org/10.1186/gb4145openalex-snapshot
The spliceosomal catalytic core arose in the RNA world… or did it?
inferredcites →https://doi.org/10.1186/s12862-015-0560-5openalex-snapshot
Dynamics of bacterial insertion sequences: can transposition bursts help the elements persist?
inferredcites →https://doi.org/10.1186/s12862-016-0789-7openalex-snapshot
Recent horizontal transfer, functional adaptation and dissemination of a bacterial group II intron
inferredcites →https://doi.org/10.1186/s13100-015-0037-5openalex-snapshot
Evolution of group II introns
inferredcites →https://doi.org/10.1261/rna.2126203openalex-snapshot
ORF-less and reverse-transcriptase-encoding group II introns in archaebacteria, with a pattern of homing into related group II intron ORFs
inferredcites →https://doi.org/10.1261/rna.2184010openalex-snapshot
A group II intron encodes a functional LAGLIDADG homing endonuclease and self-splices under moderate temperature and ionic conditions
inferredcites →https://doi.org/10.1261/rna.2396011openalex-snapshot
Prp8, the pivotal protein of the spliceosomal catalytic center, evolved from a retroelement-encoded reverse transcriptase
inferredcites →https://doi.org/10.1371/journal.pcbi.1002150openalex-snapshot
A Detailed History of Intron-rich Eukaryotic Ancestors Inferred from a Global Survey of 100 Complete Genomes
inferredcites →https://doi.org/10.1371/journal.pone.0052268openalex-snapshot
Selection-Driven Extinction Dynamics for Group II Introns in Enterobacteriales
inferredcites →https://doi.org/10.1371/journal.pone.0053433openalex-snapshot
Evidence for Transitional Stages in the Evolution of Euglenid Group II Introns and Twintrons in the Monomorphina aenigmatica Plastid Genome
inferredcites →https://doi.org/10.1371/journal.pone.0055102openalex-snapshot
Comprehensive Phylogenetic Analysis of Bacterial Group II Intron-Encoded ORFs Lacking the DNA Endonuclease Domain Reveals New Varieties
inferredcites →https://doi.org/10.1371/journal.pone.0058263openalex-snapshot
The Brown Algae Pl.LSU/2 Group II Intron-Encoded Protein Has Functional Reverse Transcriptase and Maturase Activities
inferredcites →https://doi.org/10.1371/journal.pone.0114083openalex-snapshot
Comprehensive Phylogenetic Analysis of Bacterial Reverse Transcriptases
inferredcites →https://doi.org/10.1371/journal.pone.0162275openalex-snapshot
Host Factors Influencing the Retrohoming Pathway of Group II Intron RmInt1, Which Has an Intron-Encoded Protein Naturally Devoid of Endonuclease Activity
inferredcites →https://doi.org/10.2741/klein1openalex-snapshot
Bacterial group II introns and their association with mobile genetic elements
inferredcites →https://doi.org/10.3389/fgene.2015.00321openalex-snapshot
A loopy view of telomere evolution
inferredcites →https://doi.org/10.3389/fpls.2014.00035openalex-snapshot
Group II intron splicing factors in plant mitochondria
inferredcites →https://doi.org/10.3732/ajb.89.10.1651openalex-snapshot
Group II introns as phylogenetic tools: structure, function, and evolutionary constraints
inferredcites →https://doi.org/10.4161/rna.32092openalex-snapshot
Insights into the strategies used by related group II introns to adapt successfully for the colonisation of a bacterial genome
inferredcites →https://doi.org/10.7717/peerj.2627openalex-snapshot
Proliferation of group II introns in the chloroplast genome of the green alga Oedocladium carolinianum (Chlorophyceae)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Characterisation and comparative analysis of mitochondrial genomes of false, yellow, black and blushing morels provide insights on their structure and evolution
inferred← citeshttps://doi.org/10.1002/9783527814527.ch5openalex-snapshot
The Lariat Capping Ribozyme
inferred← citeshttps://doi.org/10.1002/9783527814527.ch6openalex-snapshot
Self‐Splicing Group II Introns
inferred← citeshttps://doi.org/10.1002/ece3.8818openalex-snapshot
Comparative analysis of the complete mitochondrial genomes of four cordyceps fungi
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The evolution of posttranscriptional regulation
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Defense and Immune Systems Evolving from Co-opted Selfish Genetic Elements—From the Origin of Life to the Present
inferred← citeshttps://doi.org/10.1007/978-3-662-60909-5_9openalex-snapshot
Instabilität, Flexibilität und Variabilität des Genoms
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Instabilität, Flexibilität und Variabilität des Genoms
inferred← citeshttps://doi.org/10.1007/s00114-025-01966-4openalex-snapshot
Direct repeats found in the vicinity of intron splice sites
inferred← citeshttps://doi.org/10.1007/s00239-022-10059-zopenalex-snapshot
Structural Analysis of Monomeric RNA-Dependent Polymerases Revisited
inferred← citeshttps://doi.org/10.1007/s42161-023-01310-7openalex-snapshot
Transcriptional profile of selected flavescence dorée phytoplasma genes during infection of insect vectors and host plants
inferred← citeshttps://doi.org/10.1007/s44307-024-00009-9openalex-snapshot
Importance of pre-mRNA splicing and its study tools in plants
inferred← citeshttps://doi.org/10.1007/s44307-025-00087-3openalex-snapshot
Pre-mRNA splicing and its regulation in microalgae and cyanobacteria
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2019.04.004openalex-snapshot
A novel role of U1 snRNP: Splice site selection from a distance
inferred← citeshttps://doi.org/10.1016/j.jgg.2024.08.010openalex-snapshot
PPR21 is involved in the splicing of nad2 introns via interacting with PPR-SMR1 and SPR2 and is essential to maize seed development
inferred← citeshttps://doi.org/10.1016/j.jmb.2020.166758openalex-snapshot
A New Type of Circular RNA derived from Nonconventional Introns in Nuclear Genes of Euglenids
inferred← citeshttps://doi.org/10.1016/j.sbi.2025.103053openalex-snapshot
Structural and biochemical studies of mobile retrotransposon proteins in action
inferred← citeshttps://doi.org/10.1016/j.tibs.2024.03.012openalex-snapshot
Understanding the dynamic design of the spliceosome
inferred← citeshttps://doi.org/10.1016/j.xplc.2022.100493openalex-snapshot
A gap-free genome assembly of Chlamydomonas reinhardtii and detection of translocations induced by CRISPR-mediated mutagenesis
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PMGA: A plant mitochondrial genome annotator
inferred← citeshttps://doi.org/10.1038/s41467-018-04145-4openalex-snapshot
Architecture of the U6 snRNP reveals specific recognition of 3′-end processed U6 snRNA
inferred← citeshttps://doi.org/10.1038/s41467-023-39084-2openalex-snapshot
Origin of minicircular mitochondrial genomes in red algae
inferred← citeshttps://doi.org/10.1038/s41576-021-00385-1openalex-snapshot
Transposable elements shape the evolution of mammalian development
inferred← citeshttps://doi.org/10.1038/s41579-019-0205-6openalex-snapshot
Origin of viruses: primordial replicators recruiting capsids from hosts
inferred← citeshttps://doi.org/10.1038/s41598-020-73461-xopenalex-snapshot
The complete mitochondrial genome of medicinal fungus Taiwanofungus camphoratus reveals gene rearrangements and intron dynamics of Polyporales
inferred← citeshttps://doi.org/10.1038/s41598-022-14477-3openalex-snapshot
Unprecedented frequency of mitochondrial introns in colonial bilaterians
inferred← citeshttps://doi.org/10.1073/pnas.1807709115openalex-snapshot
Testing the retroelement invasion hypothesis for the emergence of the ancestral eukaryotic cell
inferred← citeshttps://doi.org/10.1074/jbc.aw119.008145openalex-snapshot
Back to the future: The intimate and evolving connection between telomere-related factors and genotoxic stress
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Multiple information carried by RNAs: total eclipse or a light at the end of the tunnel?
inferred← citeshttps://doi.org/10.1093/evolut/qpad050openalex-snapshot
First unraveling of the hidden and intricate evolutionary history of a bacterial group II intron family
inferred← citeshttps://doi.org/10.1093/femsre/fuab025openalex-snapshot
Prokaryotic reverse transcriptases: from retroelements to specialized defense systems
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The Coevolution of Fungal Mitochondrial Introns and Their Homing Endonucleases (GIY-YIG and LAGLIDADG)
inferred← citeshttps://doi.org/10.1093/gbe/evaf194openalex-snapshot
Episodic and Ongoing Mechanisms Drive Plastid-Derived Nuclear DNA Evolution in Angiosperms
inferred← citeshttps://doi.org/10.1093/gbe/evag114openalex-snapshot
Recurrent Modular Assembly Drives Independent Origins of Group II Introns Encoding LAGLIDADG Homing Endonucleases
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Does the Pachytene Checkpoint, a Feature of Meiosis, Filter Out Mistakes in Double-Strand DNA Break Repair and as a side-Effect Strongly Promote Adaptive Speciation?
inferred← citeshttps://doi.org/10.1093/jxb/ery432openalex-snapshot
The mitochondrial pentatricopeptide repeat protein EMP12 is involved in the splicing of threenad2introns and seed development in maize
inferred← citeshttps://doi.org/10.1093/nar/gkaa313openalex-snapshot
Group II intron as cold sensor for self-preservation and bacterial conjugation
inferred← citeshttps://doi.org/10.1093/nar/gkaa773openalex-snapshot
Exon and protein positioning in a pre-catalytic group II intron RNP primed for splicing
inferred← citeshttps://doi.org/10.1093/nar/gkab066openalex-snapshot
A RanBP2-type zinc finger protein functions in intron splicing in Arabidopsis mitochondria and is involved in the biogenesis of respiratory complex I
inferred← citeshttps://doi.org/10.1093/nar/gkac242openalex-snapshot
A molecular beacon assay for monitoring RNA splicing
inferred← citeshttps://doi.org/10.1093/nar/gkaf781openalex-snapshot
Plant mitochondrial PORR proteins facilitate group II intron splicing by binding to distinct regions within their target introns
inferred← citeshttps://doi.org/10.1093/nar/gky414openalex-snapshot
Group I introns are widespread in archaea
inferred← citeshttps://doi.org/10.1093/nar/gky416openalex-snapshot
Structural accommodations accompanying splicing of a group II intron RNP
inferred← citeshttps://doi.org/10.1093/nar/gkz1194openalex-snapshot
A functional twintron, ‘zombie’ twintrons and a hypermobile group II intron invading itself in plant mitochondria
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ArabidopsisSSB1, a Mitochondrial Single-Stranded DNA-Binding Protein, is Involved in ABA Response and Mitochondrial RNA Splicing
inferred← citeshttps://doi.org/10.1099/mgen.0.001117openalex-snapshot
Spliceosomal introns in the diplomonad parasite Giardia duodenalis revisited
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Distinct Expansion of Group II Introns Depends on the Type of Intron-encoded Protein and Genomic Signatures in Prokaryotes
inferred← citeshttps://doi.org/10.1101/2023.02.21.529479openalex-snapshot
Introns are derived from transposons
inferred← citeshttps://doi.org/10.1101/cshperspect.a032375openalex-snapshot
Group II Intron RNPs and Reverse Transcriptases: From Retroelements to Research Tools
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Origins and Evolution of the Global RNA Virome
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The Role of Transposable Elements in Emergence of Metazoa
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The Role of Reverse Transcriptase in the Origin of Life
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Functional Dualism of Transposon Transcripts in Evolution of Eukaryotic Genomes
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Interconnected roles of fungal nuclear- and intron-encoded maturases: at the crossroads of mitochondrial intron splicing
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Deep Roots and Splendid Boughs of the Global Plant Virome
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Categorizing 161 plant (streptophyte) mitochondrial group II introns into 29 families of related paralogues finds only limited links between intron mobility and intron-borne maturases
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Complete mitochondrial genome of Laetiporus ailaoshanensis (Laetiporaceae, Basidiomycota): features, evolution, and phylogeny
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Plastid DNA is a major source of nuclear genome complexity and of RNA genes in the orphan crop moringa
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Division of labour in a matrix, rather than phagocytosis or endosymbiosis, as a route for the origin of eukaryotic cells
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Using bioinformatic and phylogenetic approaches to classify transposable elements and understand their complex evolutionary histories
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Methylation of rRNA as a host defense against rampant group II intron retrotransposition
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Yeast U6 snRNA made by RNA polymerase II is less stable but functional
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Bacterial group II introns generate genetic diversity by circularization and trans-splicing from a population of intron-invaded mRNAs
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An Allosteric Network for Spliceosome Activation Revealed by High-Throughput Suppressor Analysis in Saccharomyces cerevisiae
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Plastid DNA is a major source of nuclear genome complexity and of RNA genes in the orphan crop moringa
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Involvement of transposons in epigenetic regulation of embryogenesis
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Influence of retroelements on oncogenes and tumor suppressors in carcinogenesis: A review
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A Bioinformatic Method For Identifying Group II Introns In Organella Genomes
inferred← citeshttps://doi.org/10.3389/fmars.2021.668542openalex-snapshot
Chloroplast Genomes of the Green-Tide Forming Alga Ulva compressa: Comparative Chloroplast Genomics in the Genus Ulva (Ulvophyceae, Chlorophyta)
inferred← citeshttps://doi.org/10.3389/fmicb.2018.00627openalex-snapshot
Contribution of Mobile Group II Introns to Sinorhizobium meliloti Genome Evolution
inferred← citeshttps://doi.org/10.3389/fmicb.2022.849080openalex-snapshot
Distinct Expansion of Group II Introns During Evolution of Prokaryotes and Possible Factors Involved in Its Regulation
inferred← citeshttps://doi.org/10.3389/fmolb.2022.834020openalex-snapshot
Identification of Group II Intron RmInt1 Binding Sites in a Bacterial Genome
inferred← citeshttps://doi.org/10.3389/fpls.2020.00732openalex-snapshot
Two Pentatricopeptide Repeat Proteins Are Required for the Splicing of nad5 Introns in Maize
inferred← citeshttps://doi.org/10.3390/biomedinformatics3040055openalex-snapshot
Identification of a New Drug Binding Site in the RNA-Dependent-RNA-Polymerase (RdRp) Domain
inferred← citeshttps://doi.org/10.3390/cells10082001openalex-snapshot
Organellar Introns in Fungi, Algae, and Plants
inferred← citeshttps://doi.org/10.3390/ijms27062613openalex-snapshot
Structural Remodeling and Enzymatic Replacement Shape the Evolution of Organellar Group II Introns in Ulva
inferred← citeshttps://doi.org/10.3410/f.733278059.793550617openalex-snapshot
Faculty Opinions recommendation of Group I introns are widespread in archaea.
inferred← citeshttps://doi.org/10.3410/f.733278059.793552780openalex-snapshot
Faculty Opinions recommendation of Group I introns are widespread in archaea.
inferred← citeshttps://doi.org/10.5772/intechopen.76051openalex-snapshot
Modulation of Gene Expression by Gene Architecture and Promoter Structure
inferred← citeshttps://doi.org/10.6084/m9.figshare.14177103openalex-snapshot
Additional file 1 of Methylation of rRNA as a host defense against rampant group II intron retrotransposition
inferred← citeshttps://doi.org/10.70675/0a108ecazc435z4d3bza24dz983c27de2b63openalex-snapshot
Analyse fonctionnelle de cibles végétales d’effecteurs du parasitisme du nématode Meloidogyne incognita impliquées dans l’ontogénèse des cellules géantes
inferred← citeshttps://doi.org/10.70675/29eb14fdzf43cz4134z93bazdb1fc926cca9openalex-snapshot
Functional diversity within a ribosomal-like protein family in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.70675/c9da71c3zac1cz426fz8f3az8a3c7fcf3c17openalex-snapshot
Annotation computationnelle de génomes : des organismes uniques aux communautés complexes
inferred← citeshttps://doi.org/10.7124/visnyk.utgis.22.1-2.1683openalex-snapshot
Analysis of nucleotide sequences of bacterial retrointrons for the presence of homology to eukaryotic MGE
inferred← citeshttps://doi.org/10.7554/elife.34268openalex-snapshot
Group II intron inhibits conjugative relaxase expression in bacteria by mRNA targeting
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