| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | Steven Zimmerly | |
| Alan M Lambowitz | |||
| P2860 | cites work | RNA and protein catalysis in group II intron splicing and mobility reactions using purified components | Q78021333 |
| DNA target site requirements for homing in vivo of a bacterial group II intron encoding a protein lacking the DNA endonuclease domain | Q78862316 | ||
| A DEAD protein that activates intron self-splicing without unwinding RNA | Q79450362 | ||
| The receptor for branch-site docking within a group II intron active site | Q80263521 | ||
| A second divalent metal ion in the group II intron reaction center | Q80512184 | ||
| A mutation in At-nMat1a, which encodes a nuclear gene having high similarity to group II intron maturase, causes impaired splicing of mitochondrial NAD4 transcript and altered carbon metabolism in Arabidopsis thaliana | Q83169600 | ||
| Group II intron protein localization and insertion sites are affected by polyphosphate | Q21145870 | ||
| CRS1 is a novel group II intron splicing factor that was derived from a domain of ancient origin. | Q24540043 | ||
| A general two-metal-ion mechanism for catalytic RNA | Q24562157 | ||
| Evolutionary relationships among group II intron-encoded proteins and identification of a conserved domain that may be related to maturase function | Q24628951 | ||
| A complex twintron is excised as four individual introns | Q24633818 | ||
| Tertiary architecture of the Oceanobacillus iheyensis group II intron | Q24650825 | ||
| Making ends meet: repairing breaks in bacterial DNA by non-homologous end-joining | Q25255347 | ||
| A novel multifunctional factor involved in trans-splicing of chloroplast introns in Chlamydomonas | Q25257126 | ||
| Structural insights into group II intron catalysis and branch-site selection | Q27638009 | ||
| Solution structure of domain 5 of a group II intron ribozyme reveals a new RNA motif | Q27643034 | ||
| Crystal Structure of a Self-Spliced Group II Intron | Q27650229 | ||
| Structural basis for exon recognition by a group II intron | Q27652671 | ||
| The splicing of yeast mitochondrial group I and group II introns requires a DEAD-box protein with RNA chaperone function | Q27932450 | ||
| Involvement of DEAD-box proteins in group I and group II intron splicing. Biochemical characterization of Mss116p, ATP hydrolysis-dependent and -independent mechanisms, and general RNA chaperone activity | Q27933736 | ||
| Reverse transcriptase activity associated with maturase-encoding group II introns in yeast mitochondria | Q27934112 | ||
| Mitochondrial splicing requires a protein from a novel helicase family | Q27938735 | ||
| The DIVa Maturase Binding Site in the Yeast Group II Intron aI2 Is Essential for Intron Homing but Not for In Vivo Splicing | Q27938866 | ||
| Retrotransposition of a yeast group II intron occurs by reverse splicing directly into ectopic DNA sites | Q27939889 | ||
| A novel base-pairing interaction between U2 and U6 snRNAs suggests a mechanism for the catalytic activation of the spliceosome | Q28201291 | ||
| Group II and group III introns of twintrons: potential relationships with nuclear pre-mRNA introns | Q28249708 | ||
| A single active-site region for a group II intron | Q28258438 | ||
| Gene targeting using zinc finger nucleases | Q28265983 | ||
| Comparative and functional anatomy of group II catalytic introns—a review | Q28272931 | ||
| Reverse transcription of R2Bm RNA is primed by a nick at the chromosomal target site: A mechanism for non-LTR retrotransposition | Q28297748 | ||
| Mechanism of maturase-promoted group II intron splicing | Q28366346 | ||
| An organellar maturase associates with multiple group II introns | Q28748480 | ||
| Coevolution of group II intron RNA structures with their intron-encoded reverse transcriptases | Q28768509 | ||
| Origin and evolution of retroelements based upon their reverse transcriptase sequences | Q29614742 | ||
| Introns and the origin of nucleus-cytosol compartmentalization | Q29618633 | ||
| The generality of self-splicing RNA: relationship to nuclear mRNA splicing | Q30457101 | ||
| Stereochemistry of RNA cleavage by the Tetrahymena ribozyme and evidence that the chemical step is not rate-limiting | Q30457783 | ||
| Group II introns as controllable gene targeting vectors for genetic manipulation of bacteria | Q30773032 | ||
| Retroids in archaea: phylogeny and lateral origins | Q30940021 | ||
| A group II intron-encoded maturase functions preferentially in cis and requires both the reverse transcriptase and X domains to promote RNA splicing | Q33203803 | ||
| Group II introns break new boundaries: presence in a bilaterian's genome | Q33316053 | ||
| Group II intron-based gene targeting reactions in eukaryotes | Q33366500 | ||
| EcI5, a group IIB intron with high retrohoming frequency: DNA target site recognition and use in gene targeting | Q33401171 | ||
| Multiple homing pathways used by yeast mitochondrial group II introns | Q33605483 | ||
| RecA-independent ectopic transposition in vivo of a bacterial group II intron | Q33825991 | ||
| The age and evolution of non-LTR retrotransposable elements | Q33864837 | ||
| A tertiary interaction that links active-site domains to the 5' splice site of a group II intron | Q33911726 | ||
| Protein-free small nuclear RNAs catalyze a two-step splicing reaction | Q34018172 | ||
| A catalytically active group II intron domain 5 can function in the U12-dependent spliceosome | Q34131822 | ||
| Phylogenetic relationships among group II intron ORFs | Q34277841 | ||
| Structure and activities of group II introns | Q34296736 | ||
| Evidence for two active sites in the spliceosome provided by stereochemistry of pre-mRNA splicing | Q34357049 | ||
| A DEAD-box protein alone promotes group II intron splicing and reverse splicing by acting as an RNA chaperone | Q34574382 | ||
| Branch-point attack in group II introns is a highly reversible transesterification, providing a potential proofreading mechanism for 5'-splice site selection. | Q34693499 | ||
| The take and give between retrotransposable elements and their hosts | Q34804306 | ||
| Rules for DNA target-site recognition by a lactococcal group II intron enable retargeting of the intron to specific DNA sequences | Q35187802 | ||
| A bacterial group II intron encoding reverse transcriptase, maturase, and DNA endonuclease activities: biochemical demonstration of maturase activity and insertion of new genetic information within the intron | Q35195250 | ||
| Insertion of group II intron retroelements after intrinsic transcriptional terminators | Q35800281 | ||
| Mobile group II introns | Q35965810 | ||
| Bacterial group II introns: not just splicing | Q36765046 | ||
| Group II intron domain 5 facilitates a trans-splicing reaction | Q36790013 | ||
| Cis- and trans-splicing of group II introns in plant mitochondria | Q37002206 | ||
| The recent origins of introns | Q37068347 | ||
| A plant-specific RNA-binding domain revealed through analysis of chloroplast group II intron splicing | Q37132718 | ||
| Linear group II intron RNAs can retrohome in eukaryotes and may use nonhomologous end-joining for cDNA ligation. | Q37416526 | ||
| The ribozyme core of group II introns: a structure in want of partners | Q37418459 | ||
| AtnMat2, a nuclear-encoded maturase required for splicing of group-II introns in Arabidopsis mitochondria. | Q37426601 | ||
| Genome-wide analysis of RNA-protein interactions in plants | Q37545621 | ||
| Trans-splicing of organelle introns--a detour to continuous RNAs | Q37567604 | ||
| Chloroplast RNA metabolism | Q37700597 | ||
| Intron phylogeny: a new hypothesis | Q37778081 | ||
| On the origin of RNA splicing and introns | Q38151500 | ||
| Group II intron ribozymes that cleave DNA and RNA linkages with similar efficiency, and lack contacts with substrate 2'-hydroxyl groups | Q38289601 | ||
| Metal ion coordination by the AGC triad in domain 5 contributes to group II intron catalysis | Q38296517 | ||
| Tight binding of the 5' exon to domain I of a group II self-splicing intron requires completion of the intron active site | Q38328106 | ||
| The two steps of group II intron self-splicing are mechanistically distinguishable. | Q38334466 | ||
| Structural features in the C-terminal region of the Sinorhizobium meliloti RmInt1 group II intron-encoded protein contribute to its maturase and intron DNA-insertion function. | Q38348456 | ||
| Effects of Maturase Binding and Mg2+ Concentration on Group II Intron RNA Folding Investigated by UV Cross-Linking | Q38348690 | ||
| The pathway for DNA recognition and RNA integration by a group II intron retrotransposon | Q38356119 | ||
| Characterization of the C-terminal DNA-binding/DNA endonuclease region of a group II intron-encoded protein | Q38360036 | ||
| A conserved element that stabilizes the group II intron active site | Q38569049 | ||
| Do DEAD-box proteins promote group II intron splicing without unwinding RNA? | Q39694970 | ||
| Putative proteins related to group II intron reverse transcriptase/maturases are encoded by nuclear genes in higher plants | Q39698037 | ||
| Linking the group II intron catalytic domains: tertiary contacts and structural features of domain 3. | Q39705177 | ||
| Comparative analysis of splicing of the complete set of chloroplast group II introns in three higher plant mutants | Q39729170 | ||
| Genetic identification of potential RNA-binding regions in a group II intron-encoded reverse transcriptase | Q39773403 | ||
| Group II intron mobility using nascent strands at DNA replication forks to prime reverse transcription | Q39918422 | ||
| Stereochemical selectivity of group II intron splicing, reverse splicing, and hydrolysis reactions | Q40016920 | ||
| Splicing defective mutants of the COXI gene of yeast mitochondrial DNA: initial definition of the maturase domain of the group II intron aI2 | Q40400021 | ||
| A three-dimensional perspective on exon binding by a group II self-splicing intron | Q40431332 | ||
| Selection of cryptic 5′ splice sites by group II intron RNAsin vitro | Q40554423 | ||
| Group II introns designed to insert into therapeutically relevant DNA target sites in human cells | Q40867534 | ||
| Trans-splicing of pre-mRNA in plants, animals, and protists | Q40870327 | ||
| The RmInt1 group II intron has two different retrohoming pathways for mobility using predominantly the nascent lagging strand at DNA replication forks for priming. | Q40900573 | ||
| Retrohoming: cDNA-mediated mobility of group II introns requires a catalytic RNA. | Q40939387 | ||
| An RNA conformational change between the two chemical steps of group II self-splicing. | Q41075208 | ||
| Restoration of the self-splicing activity of a defective group II intron by a small trans-acting RNA. | Q41172666 | ||
| Self-splicing of a group IIC intron: 5' exon recognition and alternative 5' splicing events implicate the stem-loop motif of a transcriptional terminator | Q41283911 | ||
| Mutations at the lariat acceptor site allow self-splicing of a group II intron without lariat formation | Q41357714 | ||
| The stereochemical course of group II intron self-splicing. | Q41663788 | ||
| Recruitment of host functions suggests a repair pathway for late steps in group II intron retrohoming | Q41854959 | ||
| A conserved 3' extension in unusual group II introns is important for efficient second-step splicing | Q41906230 | ||
| Group II intron endonucleases use both RNA and protein subunits for recognition of specific sequences in double-stranded DNA. | Q41911702 | ||
| The linear form of a group II intron catalyzes efficient autocatalytic reverse splicing, establishing a potential for mobility | Q41938330 | ||
| A factor related to pseudouridine synthases is required for chloroplast group II intron trans-splicing in Chlamydomonas reinhardtii | Q41962191 | ||
| Unwinding by local strand separation is critical for the function of DEAD-box proteins as RNA chaperones | Q42103595 | ||
| Global regulators orchestrate group II intron retromobility | Q42105024 | ||
| A three-dimensional model of a group II intron RNA and its interaction with the intron-encoded reverse transcriptase | Q42157990 | ||
| Domain structure and three-dimensional model of a group II intron-encoded reverse transcriptase | Q42182452 | ||
| Group II introns in eubacteria and archaea: ORF-less introns and new varieties | Q42208247 | ||
| Trans-splicing versatility of the Ll.LtrB group II intron | Q42210927 | ||
| Atomic force microscopy reveals DNA bending during group II intron ribonucleoprotein particle integration into double-stranded DNA | Q42419015 | ||
| Multiple physical forms of excised group II intron RNAs in wheat mitochondria | Q42523713 | ||
| Group IIC intron mobility into attC sites involves a bulged DNA stem-loop motif | Q42566192 | ||
| A reverse transcriptase/maturase promotes splicing by binding at its own coding segment in a group II intron RNA. | Q42610169 | ||
| A small chloroplast RNA may be required for trans-splicing in chlamydomonas reinhardtii | Q42616116 | ||
| A broadscale phylogenetic analysis of group II intron RNAs and intron-encoded reverse transcriptases | Q42632009 | ||
| High-affinity binding site for a group II intron-encoded reverse transcriptase/maturase within a stem-loop structure in the intron RNA. | Q42632069 | ||
| The reverse-transcriptase-like proteins encoded by group II introns in the mitochondrial genome of the brown alga Pylaiella littoralis belong to two different lineages which apparently coevolved with the group II ribosyme lineages | Q42648697 | ||
| A tripartite group II intron in mitochondria of an angiosperm plant | Q42662376 | ||
| Binding of a group II intron-encoded reverse transcriptase/maturase to its high affinity intron RNA binding site involves sequence-specific recognition and autoregulates translation | Q42677867 | ||
| Identification of a family of group II introns encoding LAGLIDADG ORFs typical of group I introns | Q42689247 | ||
| Identification and characterization of bacterial class E group II introns. | Q42689303 | ||
| ORF-less and reverse-transcriptase-encoding group II introns in archaebacteria, with a pattern of homing into related group II intron ORFs | Q42693768 | ||
| A structural analysis of the group II intron active site and implications for the spliceosome | Q42852645 | ||
| Complete genome structure of the thermophilic cyanobacterium Thermosynechococcus elongatus BP-1. | Q43031212 | ||
| Interaction of a group II intron ribonucleoprotein endonuclease with its DNA target site investigated by DNA footprinting and modification interference | Q43616239 | ||
| Excision of group II introns as circles. | Q43711760 | ||
| Integration of group II intron bI1 into a foreign RNA by reversal of the self-splicing reaction in vitro | Q43954197 | ||
| Transposition and exon shuffling by group II intron RNA molecules in pieces | Q44733602 | ||
| Assembly of an active group II intron-maturase complex by protein dimerization | Q47445196 | ||
| Transcription, splicing and editing of plastid RNAs in the nonphotosynthetic plant Epifagus virginiana | Q48069538 | ||
| Many independent origins of trans splicing of a plant mitochondrial group II intron | Q48171849 | ||
| Use of computer-designed group II introns to disrupt Escherichia coli DExH/D-box protein and DNA helicase genes. | Q52003938 | ||
| Retrotransposition of the Ll.LtrB group II intron proceeds predominantly via reverse splicing into DNA targets. | Q52946056 | ||
| Excision of the Sinorhizobium meliloti group II intron RmInt1 as circles in vivo. | Q53607394 | ||
| Group II intron mobility in yeast mitochondria: target DNA-primed reverse transcription activity of aI1 and reverse splicing into DNA transposition sites in vitro. | Q53946266 | ||
| An intron-encoded protein assists RNA splicing of multiple similar introns of different bacterial genes. | Q54479404 | ||
| Retrotransposition strategies of the Lactococcus lactis Ll.LtrB group II intron are dictated by host identity and cellular environment. | Q54488321 | ||
| The DEAD-box protein PMH2 is required for efficient group II intron splicing in mitochondria of Arabidopsis thaliana. | Q54705833 | ||
| Retrohoming of a bacterial group II intron: mobility via complete reverse splicing, independent of homologous DNA recombination | Q56902551 | ||
| Group II intron splicing in vivo by first-step hydrolysis | Q56902748 | ||
| Catalytic site components common to both splicing steps of a group II intron | Q57909426 | ||
| Group II intron mobility occurs by target DNA-primed reverse transcription | Q64389534 | ||
| New reactions catalyzed by a group II intron ribozyme with RNA and DNA substrates | Q67542085 | ||
| "Five easy pieces" | Q68053624 | ||
| Group II intron self-splicing. Alternative reaction conditions yield novel products | Q69819167 | ||
| An mRNA maturase is encoded by the first intron of the mitochondrial gene for the subunit I of cytochrome oxidase in S. cerevisiae | Q70179325 | ||
| Two competing pathways for self-splicing by group II introns: a quantitative analysis of in vitro reaction rates and products | Q71020719 | ||
| Metal ion binding sites in a group II intron core | Q73256925 | ||
| Mobility of yeast mitochondrial group II introns: engineering a new site specificity and retrohoming via full reverse splicing | Q73266484 | ||
| Domains 2 and 3 interact to form critical elements of the group II intron active site | Q73567987 | ||
| The architectural organization and mechanistic function of group II intron structural elements | Q74782086 | ||
| P433 | issue | 8 | |
| P921 | main subject | ribozyme | Q205858 |
| P304 | page(s) | a003616 | |
| P577 | publication date | 2011-08-01 | |
| P1433 | published in | Cold Spring Harbor Perspectives in Biology | Q3927509 |
| P1476 | title | Group II introns: mobile ribozymes that invade DNA. | |
| P478 | volume | 3 |
| Q89138133 | A Highly Proliferative Group IIC Intron from Geobacillus stearothermophilus Reveals New Features of Group II Intron Mobility and Splicing |
| Q42725798 | A Ribonucleoprotein Supercomplex Involved in trans-Splicing of Organelle Group II Introns. |
| Q92283358 | A group II intron-encoded protein interacts with the cellular replicative machinery through the β-sliding clamp |
| Q28652574 | A novel arabinose-inducible genetic operation system developed for Clostridium cellulolyticum |
| Q39310453 | A novel spliceosome-mediated trans-splicing can change our view on genome complexity of the divergent eukaryote Giardia intestinalis. |
| Q35124814 | A pangenomic analysis of the Nannochloropsis organellar genomes reveals novel genetic variations in key metabolic genes |
| Q39815541 | A pipeline of programs for collecting and analyzing group II intron retroelement sequences from GenBank |
| Q91957384 | A predicted Francisella tularensis DXD-motif glycosyltransferase blocks immune activation |
| Q35981916 | A short PPR protein required for the splicing of specific group II introns in angiosperm chloroplasts |
| Q38387036 | A survey of transposable element classification systems--a call for a fundamental update to meet the challenge of their diversity and complexity. |
| Q28679306 | A targetron system for gene targeting in thermophiles and its application in Clostridium thermocellum |
| Q34385600 | A widespread self-cleaving ribozyme class is revealed by bioinformatics. |
| Q38344563 | Activating the branch-forming splicing pathway by reengineering the ribozyme component of a natural group II intron |
| Q41941348 | Alternative splicing of a group II intron in a surface layer protein gene in Clostridium tetani |
| Q91670966 | An Integrated Model of Minor Intron Emergence and Conservation |
| Q33878716 | An intronic open reading frame was released from one of group II introns in the mitochondrial genome of the haptophyte Chrysochromulina sp. NIES-1333. |
| Q47148230 | Analysis of the Roles of the Arabidopsis nMAT2 and PMH2 Proteins Provided with New Insights into the Regulation of Group II Intron Splicing in Land-Plant Mitochondria. |
| Q34539796 | Applications of CRISPR technologies in research and beyond |
| Q38722587 | Bacterial group I introns: mobile RNA catalysts |
| Q90062826 | Bacterial group II intron genomic neighborhoods reflect survival strategies: hiding and hijacking |
| Q59789685 | Bacterial group II introns generate genetic diversity by circularization and trans-splicing from a population of intron-invaded mRNAs |
| Q38017924 | Biomolecular computing systems: principles, progress and potential |
| Q37501759 | Biotechnological applications of mobile group II introns and their reverse transcriptases: gene targeting, RNA-seq, and non-coding RNA analysis |
| Q38602804 | Chloroplast genome expansion by intron multiplication in the basal psychrophilic euglenoid Eutreptiella pomquetensis |
| Q38667655 | Circularization pathway of a bacterial group II intron |
| Q26850610 | Classification and evolution of type II CRISPR-Cas systems |
| Q58754128 | Comparison of the Mitochondrial Genome Sequences of Six Isolates Suggests Short Fragment Insertions as a Potential Factor Leading to Larger Genomic Size |
| Q42097931 | Complete Genome Sequence of the RmInt1 Group II Intronless Sinorhizobium meliloti Strain RMO17. |
| Q91917473 | Comprehensive analysis of chromosomal mobile genetic elements in the gut microbiome reveals phylum-level niche-adaptive gene pools |
| Q90570397 | Comprehensive genomic analyses with 115 plastomes from algae to seed plants: structure, gene contents, GC contents, and introns |
| Q53407367 | Contribution of Mobile Group II Introns to Sinorhizobium meliloti Genome Evolution. |
| Q39305330 | Contribution of base-pairing interactions between group II intron fragments during trans-splicing in vivo |
| Q39523373 | Convergent Evolution of Fern-Specific Mitochondrial Group II Intron atp1i361g2 and Its Ancient Source Paralogue rps3i249g2 and Independent Losses of Intron and RNA Editing among Pteridaceae |
| Q36791493 | Convergent evolution of twintron-like configurations: One is never enough |
| Q27722247 | Cryo-EM structure of the spliceosome immediately after branching |
| Q34339669 | Crystal structure of a eukaryotic group II intron lariat |
| Q52946238 | Crystal structures of a group II intron lariat primed for reverse splicing. |
| Q36984139 | Crystal structures of a group II intron maturase reveal a missing link in spliceosome evolution |
| Q38367245 | Current progress of targetron technology: development, improvement and application in metabolic engineering |
| Q47226763 | Current status and perspectives of genome editing technology for microalgae. |
| Q92825854 | DNA cleavage and reverse splicing of ribonucleoprotein particles reconstituted in vitro with linear RmInt1 RNA |
| Q38535893 | Diversity-generating Retroelements in Phage and Bacterial Genomes |
| Q35915026 | Dynamic Evolution of the Chloroplast Genome in the Green Algal Classes Pedinophyceae and Trebouxiophyceae |
| Q55408150 | Editorial: Genome Invading RNA Networks. |
| Q36902486 | Emancipating Chlamydia: Advances in the Genetic Manipulation of a Recalcitrant Intracellular Pathogen |
| Q41127837 | Emerging views about the molecular structure of the spliceosomal catalytic center |
| Q26795689 | Endosymbiotic theories for eukaryote origin |
| Q37833951 | Engineering of obligate intracellular bacteria: progress, challenges and paradigms |
| Q37218544 | Enhanced group II intron retrohoming in magnesium-deficient Escherichia coli via selection of mutations in the ribozyme core |
| Q30651181 | Enzyme engineering through evolution: thermostable recombinant group II intron reverse transcriptases provide new tools for RNA research and biotechnology |
| Q42961127 | Eukaryotic penelope-like retroelements encode hammerhead ribozyme motifs. |
| Q34541937 | Evidence for transitional stages in the evolution of euglenid group II introns and twintrons in the Monomorphina aenigmatica plastid genome |
| Q34043967 | Evolution of group II introns |
| Q42615568 | Evolution of plant mitochondrial intron-encoded maturases: frequent lineage-specific loss and recurrent intracellular transfer to the nucleus |
| Q38812834 | Forks in the tracks: Group II introns, spliceosomes, telomeres and beyond |
| Q60213473 | Functional annotation and distribution overview of RNA families in 27 Streptococcus agalactiae genomes |
| Q41188072 | Functionality of In vitro Reconstituted Group II Intron RmInt1-Derived Ribonucleoprotein Particles |
| Q28486941 | Genetic and biochemical assays reveal a key role for replication restart proteins in group II intron retrohoming |
| Q55271170 | Group II intron inhibits conjugative relaxase expression in bacteria by mRNA targeting. |
| Q38539839 | Group II intron lariat: Structural insights into the spliceosome |
| Q38193808 | Group II intron splicing factors in plant mitochondria |
| Q42845292 | Group II intron-ribosome association protects intron RNA from degradation |
| Q26766154 | Group II introns: versatile ribozymes and retroelements |
| Q35621488 | Homing endonucleases: from genetic anomalies to programmable genomic clippers |
| Q36121461 | Host Factors Influencing the Retrohoming Pathway of Group II Intron RmInt1, Which Has an Intron-Encoded Protein Naturally Devoid of Endonuclease Activity. |
| Q43097132 | Identification of a chloroplast ribonucleoprotein complex containing trans-splicing factors, intron RNA, and novel components |
| Q43019860 | Improvement of ClosTron for successive gene disruption in Clostridium cellulolyticum using a pyrF-based screening system |
| Q42141811 | In vitro characterization of the splicing efficiency and fidelity of the RmInt1 group II intron as a means of controlling the dispersion of its host mobile element. |
| Q40756396 | Inactivation of group II intron RmInt1 in the Sinorhizobium meliloti genome |
| Q45858948 | Insertion of Group II Intron-Based Ribozyme Switches into Homing Endonuclease Genes |
| Q64110598 | Insights Into Non-coding RNAs as Novel Antimicrobial Drugs |
| Q34271710 | Insights into the history of a bacterial group II intron remnant from the genomes of the nitrogen-fixing symbionts Sinorhizobium meliloti and Sinorhizobium medicae. |
| Q38284531 | Insights into the strategies used by related group II introns to adapt successfully for the colonisation of a bacterial genome |
| Q35490223 | Interaction between conjugative and retrotransposable elements in horizontal gene transfer |
| Q38027121 | Intronic features that determine the selection of the 3' splice site. |
| Q34372484 | Isolation and characterization of functional tripartite group II introns using a Tn5-based genetic screen |
| Q52596119 | Large Diversity of Nonstandard Genes and Dynamic Evolution of Chloroplast Genomes in Siphonous Green Algae (Bryopsidales, Chlorophyta). |
| Q58925949 | Lariat lessons |
| Q38123746 | Lives that introns lead after splicing |
| Q35082768 | Localization of a bacterial group II intron-encoded protein in eukaryotic nuclear splicing-related cell compartments. |
| Q42416972 | Localization of a bacterial group II intron-encoded protein in human cells. |
| Q48049590 | Loss of two introns from the Magnolia tripetala mitochondrial cox2 gene implicates horizontal gene transfer and gene conversion as a novel mechanism of intron loss |
| Q89870636 | Machine learning of reverse transcription signatures of variegated polymerases allows mapping and discrimination of methylated purines in limited transcriptomes |
| Q45935768 | Mechanism for DNA transposons to generate introns on genomic scales. |
| Q92491150 | Metal ions and sugar puckering balance single-molecule kinetic heterogeneity in RNA and DNA tertiary contacts |
| Q33561083 | Mitochondria, the Cell Cycle, and the Origin of Sex via a Syncytial Eukaryote Common Ancestor |
| Q39345212 | Mitochondrial Genome of Prasinophyte Alga Pyramimonas parkeae |
| Q46944792 | Mitochondrial genome sequence of the potato powdery scab pathogen Spongospora subterranea |
| Q38693580 | Mitochondrial genomes of the green macroalga Ulva pertusa (Ulvophyceae, Chlorophyta): novel insights into the evolution of mitogenomes in the Ulvophyceae. |
| Q35865203 | Mitochondrial group I and group II introns in the sponge orders Agelasida and Axinellida |
| Q35387075 | Mobile Bacterial Group II Introns at the Crux of Eukaryotic Evolution |
| Q88799639 | Mobile Group II Introns as Ancestral Eukaryotic Elements |
| Q30541056 | Mobile elements in a single-filament orange Guaymas Basin Beggiatoa ("Candidatus Maribeggiatoa") sp. draft genome: evidence for genetic exchange with cyanobacteria |
| Q39291036 | Mobile self-splicing introns and inteins as environmental sensors |
| Q39323715 | Multiple checkpoints for the expression of the chloroplast-encoded splicing factor MatK. |
| Q33842991 | Multiple introns in a deep-sea Annelid (Decemunciger: Ampharetidae) mitochondrial genome |
| Q27681415 | NMR structure of the 5' splice site in the group IIB intron Sc.ai5 --conformational requirements for exon-intron recognition |
| Q55497184 | On the Origin and Evolutionary Relationships of the Reverse Transcriptases Associated With Type III CRISPR-Cas Systems. |
| Q58612172 | Optimal molecular crowding accelerates group II intron folding and maximizes catalysis |
| Q36592450 | Organellar Genomes of White Spruce (Picea glauca): Assembly and Annotation |
| Q27498824 | Origin and evolution of spliceosomal introns |
| Q33653714 | Origin of spliceosomal introns and alternative splicing |
| Q47605873 | Origins and emergent evolution of life: the colloid microsphere hypothesis revisited |
| Q34467155 | Origins and evolution of viruses of eukaryotes: The ultimate modularity |
| Q93140244 | PPR-SMR1 is required for the splicing of multiple mitochondrial introns, interacts with Zm-mCSF1, and is essential for seed development in maize |
| Q33758169 | Phylogenetic Analysis of Nuclear-Encoded RNA Maturases |
| Q26822420 | Physiology of the read-write genome |
| Q98565963 | Precision design of stable genetic circuits carried in highly-insulated E. coli genomic landing pads |
| Q37122972 | Predicted group II intron lineages E and F comprise catalytically active ribozymes. |
| Q37613647 | Programmable Genome Editing Tools and their Regulation for Efficient Genome Engineering |
| Q37383302 | Proliferation of group II introns in the chloroplast genome of the green alga Oedocladium carolinianum (Chlorophyceae). |
| Q27025517 | RNA helicase proteins as chaperones and remodelers |
| Q38093803 | RNA processing and decay in plastids |
| Q42984641 | RNA sequencing provides evidence for functional variability between naturally co-existing Alteromonas macleodii lineages |
| Q28652686 | RNA sociology: group behavioral motifs of RNA consortia |
| Q33606836 | RNA-RNA interactions and pre-mRNA mislocalization as drivers of group II intron loss from nuclear genomes |
| Q34991792 | Rapid targeted gene disruption in Bacillus anthracis |
| Q36169739 | Recent horizontal transfer, functional adaptation and dissemination of a bacterial group II intron |
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