scholarly article | Q13442814 |
P356 | DOI | 10.1007/S00239-015-9688-6 |
P698 | PubMed publication ID | 26208881 |
P50 | author | Dirk Schulze-Makuch | Q5280870 |
William Bains | Q89834395 | ||
P2860 | cites work | A large fraction of extragenic RNA pol II transcription sites overlap enhancers | Q21145794 |
Comparative genomics reveals 104 candidate structured RNAs from bacteria, archaea, and their metagenomes | Q21184040 | ||
INTRACELLULAR COMPARTMENTATION IN PLANCTOMYCETES | Q22065385 | ||
DNA topoisomerases: structure, function, and mechanism | Q22065417 | ||
What fraction of the human genome is functional? | Q22065769 | ||
Extreme polyploidy in a large bacterium | Q22066338 | ||
The ctenophore genome and the evolutionary origins of neural systems | Q22122130 | ||
Origin of life: The RNA world | Q22122409 | ||
Hallmarks of Cancer: The Next Generation | Q22252312 | ||
Complex archaea that bridge the gap between prokaryotes and eukaryotes | Q22809057 | ||
An AUTS2-Polycomb complex activates gene expression in the CNS. | Q24310429 | ||
Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1 | Q24316558 | ||
Ancestral paralogs and pseudoparalogs and their role in the emergence of the eukaryotic cell | Q24535562 | ||
Regulatory RNAs in bacteria | Q24595082 | ||
Mediation of CTCF transcriptional insulation by DEAD-box RNA-binding protein p68 and steroid receptor RNA activator SRA | Q24611482 | ||
Nucleosome remodeling induced by RNA polymerase II: loss of the H2A/H2B dimer during transcription. | Q52545774 | ||
A small reservoir of disabled ORFs in the yeast genome and its implications for the dynamics of proteome evolution. | Q53878162 | ||
Ploidy in cyanobacteria. | Q54338813 | ||
An intron-encoded protein assists RNA splicing of multiple similar introns of different bacterial genes. | Q54479404 | ||
Packaging paternal chromosomes with protamine. | Q55034779 | ||
The origin of eukaryotes: a reappraisal. | Q55043727 | ||
The ambiguous boundary between genes and pseudogenes: the dead rise up, or do they? | Q57635767 | ||
The Major Architects of Chromatin: Architectural Proteins in Bacteria, Archaea and Eukaryotes | Q58286818 | ||
The H3/H4 tetramer blocks transcript elongation by RNA polymerase II in vitro | Q73674745 | ||
Is gene expression in Halobacterium NRC-1 regulated by multiple TBP and TFB transcription factors? | Q73874047 | ||
The origin and evolution of oxygenic photosynthesis | Q74530080 | ||
Basal and regulated transcription in archaea | Q77063246 | ||
Sequence context effects on oligo(dT) termination signal recognition by Saccharomyces cerevisiae RNA polymerase III | Q81569595 | ||
Nature of the nucleosomal barrier to RNA polymerase II | Q81610323 | ||
Polyploidy in haloarchaea: advantages for growth and survival | Q38225116 | ||
Selective silencing of foreign DNA with low GC content by the H-NS protein in Salmonella | Q38312504 | ||
Distinct mechanisms of transcriptional pausing orchestrated by GAGA factor and M1BP, a novel transcription factor | Q38678210 | ||
The mechanism of antigen receptor gene assembly | Q38722451 | ||
R-loops induce repressive chromatin marks over mammalian gene terminators | Q38949719 | ||
Deep sequencing-based identification of small non-coding RNAs in Streptomyces coelicolor. | Q39175035 | ||
Structure and function of bacterial sigma factors | Q39532182 | ||
Improved strains and plasmid vectors for conditional overexpression of His-tagged proteins in Haloferax volcanii | Q39606788 | ||
Histone-like proteins of the dinoflagellate Crypthecodinium cohnii have homologies to bacterial DNA-binding proteins | Q39774526 | ||
Genome-wide analysis of Polycomb targets in Drosophila melanogaster | Q40274308 | ||
Site-specific recombination: developments and applications | Q40535474 | ||
Statistical mechanic prediction of non-Gomperzian ageing in extremely aged populations | Q40776754 | ||
Translational frameshifting in the control of transposition in bacteria | Q40852573 | ||
Sequence and structural links between distant ADP-ribosyltransferase families. | Q41507554 | ||
Transposition and site-specific recombination: adapting DNA cut-and-paste mechanisms to a variety of genetic rearrangements | Q41625243 | ||
The orientation of DNA in an archaeal transcription initiation complex | Q41758705 | ||
Genetic requirements for the function of the archaeal virus SSV1 in Sulfolobus solfataricus: construction and testing of viral shuttle vectors | Q41844190 | ||
Transcription factor and chromatin features predict genes associated with eQTLs | Q42139343 | ||
Overexpression and purification of halophilic proteins in Haloferax volcanii | Q42164787 | ||
RNA in defense: CRISPRs protect prokaryotes against mobile genetic elements | Q42184018 | ||
Transposons in place of telomeric repeats at a Drosophila telomere | Q42610468 | ||
Determining divergence times of the major kingdoms of living organisms with a protein clock | Q42625957 | ||
Characterization of an efficient coronavirus ribosomal frameshifting signal: requirement for an RNA pseudoknot | Q42646008 | ||
Sir2 and the acetyltransferase, Pat, regulate the archaeal chromatin protein, Alba | Q42653218 | ||
Transcription regulation by the noncoding RNA SRG1 requires Spt2-dependent chromatin deposition in the wake of RNA polymerase II. | Q42707162 | ||
Production of recombinant and tagged proteins in the hyperthermophilic archaeon Sulfolobus solfataricus. | Q43019254 | ||
Crystal structure of an archaeal actin homolog | Q43019641 | ||
Archaeal histone stability, DNA binding, and transcription inhibition above 90 degrees C. | Q43025441 | ||
Shuttle vectors for hyperthermophilic archaea | Q43025518 | ||
Heterologous expression in the Archaea: transcription from Pyrococcus furiosus gdh and mlrA promoters in Haloferax volcanii. | Q43026278 | ||
Development of a genetic system for hyperthermophilic Archaea: expression of a moderate thermophilic bacterial alcohol dehydrogenase gene in Sulfolobus solfataricus | Q43032452 | ||
An abundance of bacterial ADP-ribosyltransferases--implications for the origin of exotoxins and their human homologues | Q43660256 | ||
RNA silencing genes control de novo DNA methylation | Q44664989 | ||
The excludon: a new concept in bacterial antisense RNA-mediated gene regulation | Q44674694 | ||
Role of the DRM and CMT3 methyltransferases in RNA-directed DNA methylation. | Q44696942 | ||
A ncRNA modulates histone modification and mRNA induction in the yeast GAL gene cluster | Q46210954 | ||
Genome-defence small RNAs exapted for epigenetic mating-type inheritance. | Q46896851 | ||
Ancient colour vision: multiple opsin genes in the ancestral vertebrates | Q47369665 | ||
Comprehensive gene expression profile of a normal human liver | Q47881657 | ||
Classics revisited: Comparative morphogenesis of the fetal membranes and accessory uterine structures | Q49054890 | ||
Birth of the snoRNPs: the evolution of the modification-guide snoRNAs. | Q51093637 | ||
Variation across species in the size of the nuclear genome supports the junk-DNA explanation for the C-value paradox | Q52230315 | ||
The DNA (cytosine-5) methyltransferases | Q24614934 | ||
Deep phylogeny, ancestral groups and the four ages of life | Q24618254 | ||
A ceRNA hypothesis: the Rosetta Stone of a hidden RNA language? | Q24629627 | ||
Genome-wide maps of chromatin state in pluripotent and lineage-committed cells | Q24632506 | ||
A coding-independent function of gene and pseudogene mRNAs regulates tumour biology | Q24632651 | ||
Histonelike proteins of bacteria | Q24634363 | ||
Chromosome organization by a nucleoid-associated protein in live bacteria | Q24634543 | ||
Archaea and the prokaryote-to-eukaryote transition | Q24643523 | ||
Origins and evolution of eukaryotic RNA interference | Q24647077 | ||
Noncoding RNA gas5 is a growth arrest- and starvation-associated repressor of the glucocorticoid receptor | Q24650793 | ||
Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression | Q24654249 | ||
Structured RNAs in the ENCODE selected regions of the human genome | Q24673501 | ||
Identification of 17 Pseudomonas aeruginosa sRNAs and prediction of sRNA-encoding genes in 10 diverse pathogens using the bioinformatic tool sRNAPredict2 | Q24685579 | ||
Comprehensive analysis of pseudogenes in prokaryotes: widespread gene decay and failure of putative horizontally transferred genes | Q24801650 | ||
CpG-island fragments from the HNRPA2B1/CBX3 genomic locus reduce silencing and enhance transgene expression from the hCMV promoter/enhancer in mammalian cells | Q24810875 | ||
Disengaging polymerase: terminating RNA polymerase II transcription in budding yeast | Q26851212 | ||
The noncoding RNA revolution-trashing old rules to forge new ones | Q26851952 | ||
Mechanisms and implications of programmed translational frameshifting | Q26852197 | ||
Alzheimer's disease pathologic cascades: who comes first, what drives what | Q26995896 | ||
The multilayered complexity of ceRNA crosstalk and competition | Q27025671 | ||
Structure of Alba: an archaeal chromatin protein modulated by acetylation | Q27639537 | ||
Structure and function of archaeal box C/D sRNP core proteins | Q27640574 | ||
Structural Determinants for Geometry and Information Decoding of tRNA by T Box Leader RNA | Q27680142 | ||
Genome regulation by long noncoding RNAs. | Q27691812 | ||
Solution structure and DNA-binding properties of a thermostable protein from the archaeon Sulfolobus solfataricus | Q27729809 | ||
The crystal structure of the estrogen receptor DNA-binding domain bound to DNA: how receptors discriminate between their response elements | Q27731441 | ||
The leucine zipper: a hypothetical structure common to a new class of DNA binding proteins | Q27860587 | ||
Mechanisms underlying ubiquitination | Q27860656 | ||
Global analysis of protein expression in yeast | Q27860658 | ||
The role of chromatin during transcription | Q27860995 | ||
ATP-driven exchange of histone H2AZ variant catalyzed by SWR1 chromatin remodeling complex | Q27929959 | ||
The release element of the yeast polymerase I transcription terminator can function independently of Reb1p | Q27930488 | ||
Antisense RNA stabilization induces transcriptional gene silencing via histone deacetylation in S. cerevisiae. | Q27930683 | ||
A chromatin remodelling complex involved in transcription and DNA processing. | Q27932458 | ||
Chromatin remodelling at promoters suppresses antisense transcription | Q27932684 | ||
Pseudouridine profiling reveals regulated mRNA pseudouridylation in yeast and human cells | Q27937615 | ||
The transcriptional program of sporulation in budding yeast | Q27938344 | ||
Yeast vectors for the controlled expression of heterologous proteins in different genetic backgrounds | Q28131643 | ||
The molecular biology of the CCAAT-binding factor NF-Y | Q28138416 | ||
Archaeal homologs of eukaryotic methylation guide small nucleolar RNAs: lessons from the Pyrococcus genomes | Q28139917 | ||
A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly | Q28184095 | ||
Computational identification of noncoding RNAs in E. coli by comparative genomics | Q28216022 | ||
The expanding snoRNA world | Q28216313 | ||
Control of developmental regulators by Polycomb in human embryonic stem cells | Q28235841 | ||
Obesity-associated variants within FTO form long-range functional connections with IRX3 | Q28236283 | ||
Global quantification of mammalian gene expression control | Q28238103 | ||
Why O2 is required by complex life on habitable planets and the concept of planetary "oxygenation time" | Q28255018 | ||
Transcription and RNAi in heterochromatic gene silencing | Q28256342 | ||
Concepts in sumoylation: a decade on | Q28257220 | ||
Regulation of heterochromatin by histone methylation and small RNAs | Q28261891 | ||
The nuclear RNA surveillance machinery: the link between ncRNAs and genome structure in budding yeast? | Q28265591 | ||
Mechanisms of gene silencing by double-stranded RNA | Q28282560 | ||
Regulatory RNA in bacterial pathogens | Q28288142 | ||
Noncoding RNA control of the making and breaking of sugars | Q28299682 | ||
Nascent RNA sequencing reveals widespread pausing and divergent initiation at human promoters | Q28302903 | ||
Identification of an RNA-protein complex involved in chloroplast group II intron trans-splicing in Chlamydomonas reinhardtii | Q28361883 | ||
A large intergenic noncoding RNA induced by p53 mediates global gene repression in the p53 response | Q28592069 | ||
Riboswitches and the RNA world | Q28732021 | ||
The oxygenation of the atmosphere and oceans | Q28767425 | ||
Control of translation and mRNA degradation by miRNAs and siRNAs | Q29614239 | ||
Long noncoding RNAs with enhancer-like function in human cells | Q29614328 | ||
Ab initio reconstruction of cell type-specific transcriptomes in mouse reveals the conserved multi-exonic structure of lincRNAs | Q29614329 | ||
Evolution and functions of long noncoding RNAs | Q29614331 | ||
CRISPR/Cas, the immune system of bacteria and archaea | Q29614423 | ||
Genome-wide mapping of Polycomb target genes unravels their roles in cell fate transitions | Q29614512 | ||
The diverse functions of histone lysine methylation | Q29614523 | ||
Crystal structure of Argonaute and its implications for RISC slicer activity | Q29614980 | ||
RNA polymerase is poised for activation across the genome | Q29615047 | ||
The long-range interaction landscape of gene promoters | Q29615403 | ||
RNA-guided RNA cleavage by a CRISPR RNA-Cas protein complex | Q29615785 | ||
Long noncoding RNAs: functional surprises from the RNA world | Q29615826 | ||
CLARE: Cracking the LAnguage of Regulatory Elements | Q31044057 | ||
Genome-wide discovery of human heart enhancers | Q33523952 | ||
Tau promotes neurodegeneration through global chromatin relaxation | Q33575083 | ||
The extinction dynamics of bacterial pseudogenes. | Q33654048 | ||
Bacterial DNA methylation: a cell cycle regulator? | Q33721124 | ||
The transcriptional regulator Rok binds A+T-rich DNA and is involved in repression of a mobile genetic element in Bacillus subtilis. | Q33750107 | ||
Learning to live together: mutualism between self-splicing introns and their hosts | Q33868343 | ||
The integrase family of site-specific recombinases: regional similarities and global diversity | Q33879427 | ||
Genomic copy number of intracellular bacterial symbionts of aphids varies in response to developmental stage and morph of their host | Q33895609 | ||
Genome-wide identification of conserved regulatory function in diverged sequences | Q33917897 | ||
Posttranslational protein modification in Archaea | Q33940312 | ||
Holding it together: chromatin in the Archaea | Q33962706 | ||
6S RNA: a small RNA regulator of transcription | Q34003153 | ||
A status report on RNAi therapeutics | Q34013891 | ||
Differential gene expression profiling of human bone marrow-derived mesenchymal stem cells during adipogenic development | Q34029401 | ||
Invasive implantation and intimate placental associations in a placentotrophic African lizard, Trachylepis ivensi (scincidae). | Q34034317 | ||
PIWI proteins and PIWI-interacting RNAs in the soma | Q34039572 | ||
About the last common ancestor, the universal life-tree and lateral gene transfer: a reappraisal | Q34078677 | ||
The evolution of controlled multitasked gene networks: the role of introns and other noncoding RNAs in the development of complex organisms | Q34086807 | ||
Non-contiguous finished genome sequence and contextual data of the filamentous soil bacterium Ktedonobacter racemifer type strain (SOSP1-21). | Q34105291 | ||
DNA packaging and organization in mammalian spermatozoa: comparison with somatic cells | Q34113389 | ||
Nuclear actin and actin-related proteins in chromatin remodeling. | Q34131471 | ||
Transcription by an archaeal RNA polymerase is slowed but not blocked by an archaeal nucleosome | Q34148817 | ||
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders | Q34162345 | ||
Construction of a shuttle vector for, and spheroplast transformation of, the hyperthermophilic archaeon Pyrococcus abyssi | Q34165738 | ||
Chromatin remodeling around nucleosome-free regions leads to repression of noncoding RNA transcription | Q34190142 | ||
Chromosome separation and segregation in dinoflagellates and bacteria may depend on liquid crystalline states | Q34201632 | ||
Mechanism and regulation of transcription in archaea | Q34205041 | ||
Conserved function of lincRNAs in vertebrate embryonic development despite rapid sequence evolution | Q34242790 | ||
Genome-wide structure and organization of eukaryotic pre-initiation complexes | Q34248195 | ||
Transposable elements: an abundant and natural source of regulatory sequences for host genes. | Q34294946 | ||
Multiple mutations and cancer | Q34327554 | ||
Comparative genomic structure of prokaryotes | Q34371888 | ||
Small RNAs as guardians of the genome | Q29617221 | ||
Multivalent engagement of chromatin modifications by linked binding modules | Q29617236 | ||
Molecular mechanisms of long noncoding RNAs | Q29618027 | ||
Vertebrate pseudogenes | Q29618328 | ||
Processed pseudogenes: characteristics and evolution | Q29618329 | ||
ATP requirements and small interfering RNA structure in the RNA interference pathway | Q29618384 | ||
Introns and the origin of nucleus-cytosol compartmentalization | Q29618633 | ||
Prokaryotic homologs of Argonaute proteins are predicted to function as key components of a novel system of defense against mobile genetic elements | Q30490196 | ||
Three new Jurassic euharamiyidan species reinforce early divergence of mammals | Q30850502 | ||
Monitoring expression profiles of rice genes under cold, drought, and high-salinity stresses and abscisic acid application using cDNA microarray and RNA gel-blot analyses | Q31029661 | ||
A high-resolution map of the three-dimensional chromatin interactome in human cells | Q34378943 | ||
Macromolecular crowding and the mandatory condensation of DNA in bacteria | Q34389116 | ||
An archaeal origin of eukaryotes supports only two primary domains of life | Q34391778 | ||
Organization of the genome and gene expression in a nuclear environment lacking histones and nucleosomes: the amazing dinoflagellates | Q34409901 | ||
Archaeal catabolite repression: a gene regulatory paradigm | Q34418436 | ||
A single female-specific piRNA is the primary determiner of sex in the silkworm | Q34419984 | ||
Pol II waiting in the starting gates: Regulating the transition from transcription initiation into productive elongation. | Q34494012 | ||
The evolution of spliceosomal introns: patterns, puzzles and progress | Q34495531 | ||
Archaeal chromatin and transcription | Q34532838 | ||
Repression of the human dihydrofolate reductase gene by a non-coding interfering transcript | Q34604327 | ||
Protein S-glutathionylation: a regulatory device from bacteria to humans. | Q34918945 | ||
The bacterial replication initiator DnaA. DnaA and oriC, the bacterial mode to initiate DNA replication | Q34987457 | ||
Readers of histone modifications | Q35092783 | ||
A superfamily of protein tags: ubiquitin, SUMO and related modifiers | Q35162583 | ||
Ribosomal frameshifting in the CCR5 mRNA is regulated by miRNAs and the NMD pathway | Q35205095 | ||
Rapid and sequential movement of individual chromosomal loci to specific subcellular locations during bacterial DNA replication | Q35316481 | ||
Polyploidy in archaea and bacteria: about desiccation resistance, giant cell size, long-term survival, enforcement by a eukaryotic host and additional aspects | Q35570351 | ||
Comparative genomics of Drosophila and human core promoters | Q35606015 | ||
Development of a simvastatin selection marker for a hyperthermophilic acidophile, Sulfolobus islandicus | Q35665533 | ||
New Neurons in Aging Brains: Molecular Control by Small Non-Coding RNAs | Q35761683 | ||
Structure, molecular mechanisms, and evolutionary relationships in DNA topoisomerases | Q35771555 | ||
Escherichia coli protein analogs StpA and H-NS: regulatory loops, similar and disparate effects on nucleic acid dynamics | Q35846232 | ||
The intricate world of riboswitches | Q35847087 | ||
Revealing the world of RNA interference | Q35889563 | ||
Mobile group II introns | Q35965810 | ||
Integration of adeno-associated virus (AAV) and recombinant AAV vectors | Q35965997 | ||
Paradoxes of non-trivial gene networks: how cancer-causing mutations can appear to be cancer-protective | Q35978627 | ||
Recoding in archaea | Q36013846 | ||
A synthetic arabinose-inducible promoter confers high levels of recombinant protein expression in hyperthermophilic archaeon Sulfolobus islandicus. | Q36120266 | ||
Archaeal transcription and its regulators | Q36139379 | ||
Pax genes in eye development and evolution | Q36160011 | ||
Global analysis of short RNAs reveals widespread promoter-proximal stalling and arrest of Pol II in Drosophila | Q36214878 | ||
Archaeal chromatin proteins: different structures but common function? | Q36300282 | ||
N6-methyl-adenine: an epigenetic signal for DNA-protein interactions | Q36401376 | ||
LincRNA-p21 suppresses target mRNA translation | Q36431717 | ||
Polycomb response elements and targeting of Polycomb group proteins in Drosophila. | Q36567949 | ||
New insights into transcriptional regulation by H-NS | Q36672112 | ||
Shuttle vector expression in Thermococcus kodakaraensis: contributions of cis elements to protein synthesis in a hyperthermophilic archaeon | Q36672660 | ||
Promoter elements associated with RNA Pol II stalling in the Drosophila embryo | Q36676820 | ||
A DNA-tethered cleavage probe reveals the path for promoter DNA in the yeast preinitiation complex | Q36791309 | ||
Ubiquitin and proteasomes in transcription | Q36799954 | ||
Stalled spliceosomes are a signal for RNAi-mediated genome defense. | Q36819861 | ||
Roles of adaptor proteins in regulation of bacterial proteolysis | Q36823924 | ||
Silencing of xenogeneic DNA by H-NS-facilitation of lateral gene transfer in bacteria by a defense system that recognizes foreign DNA. | Q36851768 | ||
RNA in unexpected places: long non-coding RNA functions in diverse cellular contexts | Q36855920 | ||
The diverse biological roles of mammalian PARPS, a small but powerful family of poly-ADP-ribose polymerases. | Q36992615 | ||
JBP1 and JBP2 are two distinct thymidine hydroxylases involved in J biosynthesis in genomic DNA of African trypanosomes | Q37128117 | ||
Telomere maintenance in Drosophila: rapid transposon evolution at chromosome ends | Q37219447 | ||
Trans-acting antisense RNAs mediate transcriptional gene cosuppression in S. cerevisiae | Q37247112 | ||
Protein-priming of DNA replication | Q37285250 | ||
Enhancer turnover and conserved regulatory function in vertebrate evolution. | Q37304879 | ||
Massive programmed translational jumping in mitochondria. | Q37725356 | ||
DNA condensation in bacteria: Interplay between macromolecular crowding and nucleoid proteins | Q37771079 | ||
Ancestral roles of small RNAs: an Ago-centric perspective | Q37784602 | ||
Protein Acetylation in Archaea, Bacteria, and Eukaryotes | Q37795592 | ||
No-nonsense functions for long noncoding RNAs | Q37865710 | ||
DNA elimination in ciliates: transposon domestication and genome surveillance | Q37930673 | ||
Nonalcoholic fatty liver disease: multimodal treatment options for a pathogenetically multiple-hit disease | Q37991104 | ||
Crosstalk among Epigenetic Pathways Regulates Neurogenesis | Q38010167 | ||
Genetic analysis of mammalian cell differentiation | Q38023540 | ||
Form and function of eukaryotic unstable non-coding RNAs | Q38027970 | ||
RNA polymerase II transcription: structure and mechanism | Q38045685 | ||
Structure and function of long noncoding RNAs in epigenetic regulation | Q38086776 | ||
Why did eukaryotes evolve only once? Genetic and energetic aspects of conflict and conflict mediation | Q38113552 | ||
The RNA polymerase factory and archaeal transcription | Q38131551 | ||
Noncanonical functions of telomerase: implications in telomerase-targeted cancer therapies | Q38193675 | ||
The different shades of fat. | Q38217767 | ||
P433 | issue | 1-2 | |
P921 | main subject | prokaryotes | Q19081 |
evolutionary novelty | Q21074940 | ||
P304 | page(s) | 34-53 | |
P577 | publication date | 2015-07-25 | |
P1433 | published in | Journal of Molecular Evolution | Q6295595 |
P1476 | title | Mechanisms of Evolutionary Innovation Point to Genetic Control Logic as the Key Difference Between Prokaryotes and Eukaryotes. | |
P478 | volume | 81 |
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