scholarly article | Q13442814 |
P356 | DOI | 10.1038/NRI.2017.78 |
P698 | PubMed publication ID | 28787398 |
P50 | author | Angus Buckling | Q68686810 |
Edze R Westra | Q83369943 | ||
Mariann Landsberger | Q88718445 | ||
P2093 | author name string | David Sünderhauf | |
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HOST IMMUNE STATUS DETERMINES SEXUALITY IN A PARASITIC NEMATODE | Q88200902 | ||
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Mutation rates differ among regions of the mammalian genome | Q24498019 | ||
Animal virus replication and RNAi-mediated antiviral silencing in Caenorhabditis elegans | Q24542489 | ||
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Running with the Red Queen: host-parasite coevolution selects for biparental sex | Q24630269 | ||
Antiviral immunity directed by small RNAs | Q24656063 | ||
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Functional bias and spatial organization of genes in mutational hot and cold regions in the human genome | Q24796018 | ||
Genetic diversity and disease control in rice | Q26722326 | ||
Evolutionary Ecology of Prokaryotic Immune Mechanisms | Q26740457 | ||
How Does the VSG Coat of Bloodstream Form African Trypanosomes Interact with External Proteins? | Q26771466 | ||
Structures of a CRISPR-Cas9 R-loop complex primed for DNA cleavage | Q27703932 | ||
A species of small antisense RNA in posttranscriptional gene silencing in plants | Q28146107 | ||
Unexpected consequences of polyandry for parasitism and fitness in the bumblebee, Bombus terrestris | Q28189610 | ||
The RNA silencing endonuclease Argonaute 2 mediates specific antiviral immunity in Drosophila melanogaster | Q28271770 | ||
Heritable true fitness and bright birds: a role for parasites? | Q28278977 | ||
Aberrant innate immune response in lethal infection of macaques with the 1918 influenza virus | Q28283850 | ||
Small CRISPR RNAs guide antiviral defense in prokaryotes | Q28290898 | ||
The CRISPR/Cas bacterial immune system cleaves bacteriophage and plasmid DNA | Q28297640 | ||
Targeted diversity generation by intraterrestrial archaea and archaeal viruses | Q28651699 | ||
The large diverse gene family var encodes proteins involved in cytoadherence and antigenic variation of plasmodium falciparum-infected erythrocytes | Q29393314 | ||
Phage response to CRISPR-encoded resistance in Streptococcus thermophilus | Q29617060 | ||
Induction and suppression of RNA silencing by an animal virus | Q29618494 | ||
CRISPR-Cas systems exploit viral DNA injection to establish and maintain adaptive immunity | Q40268797 | ||
RNA interference against animal viruses: how morbilliviruses generate extended diversity to escape small interfering RNA control | Q40319585 | ||
Inhibition of CRISPR-Cas9 with Bacteriophage Proteins | Q40389062 | ||
Host diversity limits the evolution of parasite local adaptation. | Q40468504 | ||
Bacterial Autoimmunity Due to a Restriction-Modification System | Q40820300 | ||
Sexual selection protects against extinction | Q40928256 | ||
Sex speeds adaptation by altering the dynamics of molecular evolution. | Q40947611 | ||
Co-transcriptional DNA and RNA Cleavage during Type III CRISPR-Cas Immunity | Q40955079 | ||
RAG mutations in human B cell-negative SCID. | Q41159572 | ||
Parasite Exposure Drives Selective Evolution of Constitutive versus Inducible Defense | Q41430570 | ||
Two distinct RNase activities of CRISPR-C2c2 enable guide-RNA processing and RNA detection | Q41558629 | ||
Rapid development of broadly influenza neutralizing antibodies through redundant mutations | Q41710834 | ||
Conditional tolerance of temperate phages via transcription-dependent CRISPR-Cas targeting | Q41760159 | ||
Mating patterns in seminatural populations of mice influenced by MHC genotype | Q41780565 | ||
Priming in the Type I-F CRISPR-Cas system triggers strand-independent spacer acquisition, bi-directionally from the primed protospacer. | Q42092486 | ||
Clonal selection in the germinal centre by regulated proliferation and hypermutation | Q42185336 | ||
Plant virus-derived small interfering RNAs originate predominantly from highly structured single-stranded viral RNAs. | Q42847004 | ||
Female sticklebacks count alleles in a strategy of sexual selection explaining MHC polymorphism | Q44394983 | ||
Ultradeep sequencing analysis of population dynamics of virus escape mutants in RNAi-mediated resistant plants | Q45357579 | ||
RNA-mediated resistance with nonstructural genes from the tobacco etch virus genome | Q45770150 | ||
Genetic basis for species vulnerability in the cheetah | Q46223373 | ||
Inactivation of CRISPR-Cas systems by anti-CRISPR proteins in diverse bacterial species. | Q46495756 | ||
Inbreeding: Disease susceptibility in California sea lions. | Q46613638 | ||
Imaging of germinal center selection events during affinity maturation | Q46722429 | ||
Infection dynamics in coexisting sexual and asexual host populations: support for the Red Queen hypothesis | Q47215136 | ||
High mutation frequencies among Escherichia coli and Salmonella pathogens | Q48057867 | ||
An immunoglobulin heavy chain variable region gene is generated from three segments of DNA: VH, D and JH. | Q48413837 | ||
Diversity and the maintenance of sex by parasites. | Q50451839 | ||
A matching-allele model explains host resistance to parasites. | Q50490602 | ||
Impact of bacterial mutation rate on coevolutionary dynamics between bacteria and phages. | Q50576961 | ||
Costs of CRISPR-Cas-mediated resistance in Streptococcus thermophilus. | Q50987327 | ||
Immigration of susceptible hosts triggers the evolution of alternative parasite defence strategies. | Q51271198 | ||
Cloning of the unculturable parasite Pasteuria ramosa and its Daphnia host reveals extreme genotype-genotype interactions. | Q51614217 | ||
Fitness correlates of heritable variation in antibody responsiveness in a wild mammal. | Q51616195 | ||
The effect of migration on local adaptation in a coevolving host-parasite system. | Q53614683 | ||
PHAGE-MEDIATED SELECTION AND THE EVOLUTION AND MAINTENANCE OF RESTRICTION-MODIFICATION. | Q54242757 | ||
Role of mutator alleles in adaptive evolution. | Q54564129 | ||
Costs and Benefits of High Mutation Rates: Adaptive Evolution of Bacteria in the Mouse Gut | Q56944626 | ||
Highly Variable Mutation Rates in Commensal and Pathogenic Escherichia coli | Q56944671 | ||
Genetic diversity ofDaphnia magnapopulations enhances resistance to parasites | Q57011576 | ||
Evolutionary Causes and Consequences of Immunopathology | Q57077746 | ||
Red Queen hypothesis supported by parasitism in sexual and clonal fish | Q59082735 | ||
Experimental variation in polyandry affects parasite loads and fitness in a bumble-bee | Q59087947 | ||
Evidence from a New Zealand snail for the maintenance of sex by parasitism | Q59094985 | ||
Geographic variation in sterilizing parasite species and the Red Queen | Q63976325 | ||
Diversity achieved by diverse mechanisms: gene conversion in developing B cells of the chicken | Q39592772 | ||
Interaction of the ocr gene 0.3 protein of bacteriophage T7 with EcoKI restriction/modification enzyme | Q39687086 | ||
Bacteria-phage antagonistic coevolution in soil | Q39765326 | ||
Germinal center dynamics revealed by multiphoton microscopy with a photoactivatable fluorescent reporter | Q30498133 | ||
Crystal structure of the V(D)J recombinase RAG1-RAG2 | Q30622421 | ||
BLOC-1 Brings Together the Actin and Microtubule Cytoskeletons to Generate Recycling Endosomes | Q30698610 | ||
Tropism switching in Bordetella bacteriophage defines a family of diversity-generating retroelements | Q30961710 | ||
Host-parasite 'Red Queen' dynamics archived in pond sediment | Q33305626 | ||
High-throughput sequencing of the zebrafish antibody repertoire | Q33441145 | ||
Rate, molecular spectrum, and consequences of human mutation | Q33667179 | ||
Effect of gene induction on the rate of mutagenesis by ICR-191 in Escherichia coli | Q33775896 | ||
The ecology of sexual reproduction | Q33831372 | ||
Parasite adaptation to locally common host genotypes | Q33906650 | ||
Bacteriophage genes that inactivate the CRISPR/Cas bacterial immune system. | Q34034778 | ||
CRISPR-Cas systems: beyond adaptive immunity | Q34040445 | ||
Multiple mechanisms for CRISPR-Cas inhibition by anti-CRISPR proteins | Q34045038 | ||
The diversity-generating benefits of a prokaryotic adaptive immune system | Q34046660 | ||
Mutation load and rapid adaptation favour outcrossing over self-fertilization. | Q34279988 | ||
The role of evolution in the emergence of infectious diseases | Q34282868 | ||
A random six-phase switch regulates pneumococcal virulence via global epigenetic changes | Q34310334 | ||
Somatic diversification of variable lymphocyte receptors in the agnathan sea lamprey | Q34331961 | ||
A CRISPR/Cas system mediates bacterial innate immune evasion and virulence | Q34339102 | ||
MHC class I peptides as chemosensory signals in the vomeronasal organ. | Q34365436 | ||
RNA interference functions as an antiviral immunity mechanism in mammals | Q34376950 | ||
Antiviral RNA interference in mammalian cells | Q34376958 | ||
RNA silencing suppression by plant pathogens: defence, counter-defence and counter-counter-defence | Q34377957 | ||
Evolution of high mutation rates in experimental populations of E. coli | Q34429727 | ||
Natural selection drives extremely rapid evolution in antiviral RNAi genes. | Q34503197 | ||
High frequency of hypermutable Pseudomonas aeruginosa in cystic fibrosis lung infection. | Q34508854 | ||
C2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effector | Q34529451 | ||
CD4+CD25+ regulatory T cells control Leishmania major persistence and immunity | Q34529549 | ||
Self-targeting by CRISPR: gene regulation or autoimmunity? | Q34621188 | ||
The population and evolutionary dynamics of phage and bacteria with CRISPR-mediated immunity | Q34629204 | ||
Coevolution with viruses drives the evolution of bacterial mutation rates. | Q34722064 | ||
Determinism and stochasticity during maturation of the zebrafish antibody repertoire | Q34750049 | ||
Chronic bacterial infections: living with unwanted guests | Q34983834 | ||
The geographic mosaic of sex and the Red Queen. | Q34994005 | ||
Covariation in frequencies of substitution, deletion, transposition, and recombination during eutherian evolution | Q35024015 | ||
Selective packaging of the influenza A genome and consequences for genetic reassortment | Q35163445 | ||
The evolutionary journey of Argonaute proteins | Q35239869 | ||
Mammalian recombination hot spots: properties, control and evolution. | Q35311047 | ||
Tempo and mode of plant RNA virus escape from RNA interference-mediated resistance | Q35383202 | ||
Coevolution drives the emergence of complex traits and promotes evolvability | Q35524588 | ||
The V(D)J recombination activating gene, RAG-1. | Q35633860 | ||
Restriction modification systems as engines of diversity | Q35672969 | ||
T-cell receptor gene homologs are present in the most primitive jawed vertebrates | Q35775029 | ||
The effects of chromatin organization on variation in mutation rates in the genome | Q35845235 | ||
Inflammatory exposure and historical changes in human life-spans | Q35890933 | ||
RAG Represents a Widespread Threat to the Lymphocyte Genome | Q35958144 | ||
Orientation-specific joining of AID-initiated DNA breaks promotes antibody class switching. | Q36116985 | ||
Rate and molecular spectrum of spontaneous mutations in the bacterium Escherichia coli as determined by whole-genome sequencing. | Q36339832 | ||
VLR-based adaptive immunity | Q36478330 | ||
Adaptation to Parasites and Costs of Parasite Resistance in Mutator and Nonmutator Bacteria | Q36596823 | ||
Complex Antigens Drive Permissive Clonal Selection in Germinal Centers | Q36693170 | ||
The evolution of sex: empirical insights into the roles of epistasis and drift | Q36710753 | ||
A family of phase-variable restriction enzymes with differing specificities generated by high-frequency gene rearrangements | Q36812335 | ||
Stress-induced mutagenesis in bacteria. | Q36961683 | ||
Visualizing antibody affinity maturation in germinal centers | Q37078589 | ||
Maternal transfer of antibodies: raising immuno-ecology issues. | Q37122477 | ||
Lineage tracing of human B cells reveals the in vivo landscape of human antibody class switching | Q37146773 | ||
A review of Red Queen models for the persistence of obligate sexual reproduction | Q37737471 | ||
The many faces of RNAi | Q37840757 | ||
Innate and adaptive immunity in bacteria: mechanisms of programmed genetic variation to fight bacteriophages | Q37955485 | ||
A quantitative review of MHC-based mating preference: the role of diversity and dissimilarity. | Q38253845 | ||
Naturally Occurring Off-Switches for CRISPR-Cas9. | Q38725824 | ||
Mosaicism in health and disease - clones picking up speed | Q38784278 | ||
Genetic drift, selection and the evolution of the mutation rate | Q38980350 | ||
Reciprocal inhibition between intracellular antiviral signaling and the RNAi machinery in mammalian cells | Q39090397 | ||
Endogenous DNA Damage as a Source of Genomic Instability in Cancer | Q39130435 | ||
Frequency-dependent selection in bacterial populations | Q39471728 | ||
HUMORAL IMMUNITY. T cell help controls the speed of the cell cycle in germinal center B cells. | Q39553791 | ||
P433 | issue | 11 | |
P304 | page(s) | 719-728 | |
P577 | publication date | 2017-08-07 | |
P1433 | published in | Nature Reviews Immunology | Q43355 |
P1476 | title | Mechanisms and consequences of diversity-generating immune strategies | |
P478 | volume | 17 |
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