| 1 | COG database update 2024 | 15.7 | 81 | Citations (PDF) |
| 2 | Tail-tape-fused virion and non-virion RNA polymerases of a thermophilic virus with an extremely long tail | 13.9 | 8 | Citations (PDF) |
| 3 | Computational analysis of genes with lethal knockout phenotype and prediction of essential genes in archaea | 4.4 | 3 | Citations (PDF) |
| 4 | Diversity, origin, and evolution of the ESCRT systems | 4.4 | 20 | Citations (PDF) |
| 5 | Widespread photosynthesis reaction centre barrel proteins are necessary for haloarchaeal cell division | 16.5 | 13 | Citations (PDF) |
| 6 | tRNA anticodon cleavage by target-activated CRISPR-Cas13a effector | 11.0 | 25 | Citations (PDF) |
| 7 | Regulatory sequence-based discovery of anti-defense genes in archaeal viruses | 13.9 | 6 | Citations (PDF) |
| 8 | Long range segmentation of prokaryotic genomes by gene age and functionality | 15.7 | 5 | Citations (PDF) |
| 9 | Cellular differentiation into hyphae and spores in halophilic archaea | 13.9 | 12 | Citations (PDF) |
| 10 | Compensatory relationship between low-complexity regions and gene paralogy in the evolution of prokaryotes | 7.6 | 12 | Citations (PDF) |
| 11 | Search for Origins of Anti-CRISPR Proteins by Structure Comparison | 3.5 | 10 | Citations (PDF) |
| 12 | Widespread CRISPR-derived RNA regulatory elements in CRISPR-Cas systems | 15.7 | 23 | Citations (PDF) |
| 13 | Uncovering the functional diversity of rare CRISPR-Cas systems with deep terascale clustering | 36.4 | 121 | Citations (PDF) |
| 14 | Diversity, evolution, and classification of the RNA-guided nucleases TnpB and Cas12 | 7.6 | 59 | Citations (PDF) |
| 15 | Cellular homologs of the double jelly-roll major capsid proteins clarify the origins of an ancient virus kingdom | 7.6 | 46 | Citations (PDF) |
| 16 | Small-Molecule Mn Antioxidants in Caenorhabditis elegans and Deinococcus radiodurans Supplant MnSOD Enzymes during Aging and Irradiation | 4.4 | 22 | Citations (PDF) |
| 17 | Phylogenomic analysis of the diversity of graspetides and proteins involved in their biosynthesis | 4.5 | 12 | Citations (PDF) |
| 18 | The tRNA discriminator base defines the mutual orthogonality of two distinct pyrrolysyl-tRNA synthetase/tRNAPyl pairs in the same organism | 15.7 | 11 | Citations (PDF) |
| 19 | Prokaryotic innate immunity through pattern recognition of conserved viral proteins | 36.4 | 221 | Citations (PDF) |
| 20 | Structure of the OMEGA nickase IsrB in complex with ωRNA and target DNA | 38.7 | 32 | Citations (PDF) |
| 21 | RNA-triggered protein cleavage and cell growth arrest by the type III-E CRISPR nuclease-protease | 36.4 | 53 | Citations (PDF) |
| 22 | Structure of the IscB–ωRNA ribonucleoprotein complex, the likely ancestor of CRISPR-Cas9 | 13.9 | 40 | Citations (PDF) |
| 23 | COG database update: focus on microbial diversity, model organisms, and widespread pathogens | 15.7 | 825 | Citations (PDF) |
| 24 | CRISPRidentify: identification of CRISPR arrays using machine learning approach | 15.7 | 79 | Citations (PDF) |
| 25 | Expanded diversity of Asgard archaea and their relationships with eukaryotes | 38.7 | 273 | Citations (PDF) |
| 26 | Exposure to 1-Butanol Exemplifies the Response of the Thermoacidophilic Archaeon Sulfolobus acidocaldarius to Solvent Stress | 3.5 | 15 | Citations (PDF) |
| 27 | Structural Basis for a Dual Function ATP Grasp Ligase That Installs Single and Bicyclic ω-Ester Macrocycles in a New Multicore RiPP Natural Product | 15.0 | 31 | Citations (PDF) |
| 28 | A Unique Gene Module in Thermococcales Archaea Centered on a Hypervariable Protein Containing Immunoglobulin Domains | 3.9 | 2 | Citations (PDF) |
| 29 | CRISPRclassify: Repeat-Based Classification of CRISPR Loci | 3.5 | 27 | Citations (PDF) |
| 30 | Compact RNA editors with small Cas13 proteins | 32.2 | 149 | Citations (PDF) |
| 31 | Evolution of Type IV CRISPR-Cas Systems: Insights from CRISPR Loci in Integrative Conjugative Elements of <i>Acidithiobacillia</i> | 3.5 | 38 | Citations (PDF) |
| 32 | Programmable RNA targeting with the single-protein CRISPR effector Cas7-11 | 38.7 | 239 | Citations (PDF) |
| 33 | The widespread IS200/IS605 transposon family encodes diverse programmable RNA-guided endonucleases | 36.4 | 348 | Citations (PDF) |
| 34 | The bone-degrading enzyme machinery: From multi-component understanding to the treatment of residues from the meat industry | 4.0 | 3 | Citations (PDF) |
| 35 | Machine-learning approach expands the repertoire of anti-CRISPR protein families | 13.9 | 84 | Citations (PDF) |
| 36 | Evolutionary and functional classification of the CARF domain superfamily, key sensors in prokaryotic antivirus defense | 15.7 | 108 | Citations (PDF) |
| 37 | Diverse enzymatic activities mediate antiviral immunity in prokaryotes | 36.4 | 585 | Citations (PDF) |
| 38 | Unprecedented Diversity of Unique CRISPR-Cas-Related Systems and Cas1 Homologs in Asgard Archaea | 3.5 | 22 | Citations (PDF) |
| 39 | Structure and function of virion RNA polymerase of a crAss-like phage | 38.7 | 36 | Citations (PDF) |
| 40 | CRISPR Arrays Away from <i>cas</i> Genes | 3.5 | 32 | Citations (PDF) |
| 41 | Comparative genomics and evolution of trans-activating RNAs in Class 2 CRISPR-Cas systems | 3.4 | 58 | Citations (PDF) |
| 42 | Identification of Dephospho-Coenzyme A (Dephospho-CoA) Kinase in Thermococcus kodakarensis and Elucidation of the Entire CoA Biosynthesis Pathway in Archaea | 4.4 | 18 | Citations (PDF) |
| 43 | Engineering of CRISPR-Cas12b for human genome editing | 13.9 | 325 | Citations (PDF) |
| 44 | RNA-guided DNA insertion with CRISPR-associated transposases | 36.4 | 635 | Citations (PDF) |
| 45 | CRISPR–Cas in mobile genetic elements: counter-defence and beyond | 85.9 | 273 | Citations (PDF) |
| 46 | Antimicrobial Peptides, Polymorphic Toxins, and Self-Nonself Recognition Systems in Archaea: an Untapped Armory for Intermicrobial Conflicts | 4.4 | 56 | Citations (PDF) |
| 47 | Predicted highly derived class 1 CRISPR-Cas system in Haloarchaea containing diverged Cas5 and Cas7 homologs but no CRISPR array | 1.9 | 16 | Citations (PDF) |
| 48 | Unexpected connections between type VI-B CRISPR-Cas systems, bacterial natural competence, ubiquitin signaling network and DNA modification through a distinct family of membrane proteins | 1.9 | 19 | Citations (PDF) |
| 49 | Origins and evolution of CRISPR-Cas systems | 3.8 | 424 | Citations (PDF) |
| 50 | Towards functional characterization of archaeal genomic dark matter | 4.1 | 49 | Citations (PDF) |
| 51 | Integrated mobile genetic elements in Thaumarchaeota | 3.8 | 50 | Citations (PDF) |
| 52 | CRISPR–Cas: Complex Functional Networks and Multiple Roles beyond Adaptive Immunity | 4.2 | 94 | Citations (PDF) |
| 53 | Microbial genome analysis: the COG approach | 6.7 | 278 | Citations (PDF) |
| 54 | Evolutionary classification of CRISPR–Cas systems: a burst of class 2 and derived variants | 85.9 | 2,180 | Citations (PDF) |
| 55 | Anti-CRISPR proteins encoded by archaeal lytic viruses inhibit subtype I-D immunity | 16.5 | 132 | Citations (PDF) |
| 56 | Evolution of Genome Architecture in Archaea: Spontaneous Generation of a New Chromosome in Haloferax volcanii | 4.7 | 30 | Citations (PDF) |
| 57 | Phyletic Distribution and Lineage-Specific Domain Architectures of Archaeal Two-Component Signal Transduction Systems | 2.9 | 55 | Citations (PDF) |
| 58 | Cas13d Is a Compact RNA-Targeting Type VI CRISPR Effector Positively Modulated by a WYL-Domain-Containing Accessory Protein | 13.4 | 443 | Citations (PDF) |
| 59 | DNA silencing by prokaryotic Argonaute proteins adds a new layer of defense against invading nucleic acids | 10.9 | 64 | Citations (PDF) |
| 60 | A Reverse Transcriptase-Cas1 Fusion Protein Contains a Cas6 Domain Required for Both CRISPR RNA Biogenesis and RNA Spacer Acquisition | 13.4 | 27 | Citations (PDF) |
| 61 | Classification and Nomenclature of CRISPR-Cas Systems: Where from Here? | 3.5 | 272 | Citations (PDF) |
| 62 | Systematic prediction of genes functionally linked to CRISPR-Cas systems by gene neighborhood analysis | 7.6 | 165 | Citations (PDF) |
| 63 | Escherichia coli ItaT is a type II toxin that inhibits translation by acetylating isoleucyl-tRNAIle | 15.7 | 39 | Citations (PDF) |
| 64 | Proteomic Analysis of Methanonatronarchaeum thermophilum AMET1, a Representative of a Putative New Class of Euryarchaeota, “Methanonatronarchaeia” | 2.6 | 12 | Citations (PDF) |
| 65 | Myosin-driven transport network in plants | 7.6 | 73 | Citations (PDF) |
| 66 | Diversity and evolution of class 2 CRISPR–Cas systems | 85.9 | 983 | Citations (PDF) |
| 67 | SnapShot: Class 2 CRISPR-Cas SystemsCell, 2017, 168, 328-328.e1 | 34.1 | 164 | Citations (PDF) |
| 68 | SnapShot: Class 1 CRISPR-Cas SystemsCell, 2017, 168, 946-946.e1 | 34.1 | 148 | Citations (PDF) |
| 69 | Early vertebrate origin and diversification of small transmembrane regulators of cellular ion transport | 3.4 | 11 | Citations (PDF) |
| 70 | Discovery of extremely halophilic, methyl-reducing euryarchaea provides insights into the evolutionary origin of methanogenesis | 16.5 | 252 | Citations (PDF) |
| 71 | Diversity, classification and evolution of CRISPR-Cas systems | 7.0 | 1,357 | Citations (PDF) |
| 72 | Reconstruction of the evolution of microbial defense systems | 3.1 | 64 | Citations (PDF) |
| 73 | Cas13b Is a Type VI-B CRISPR-Associated RNA-Guided RNase Differentially Regulated by Accessory Proteins Csx27 and Csx28 | 13.4 | 549 | Citations (PDF) |
| 74 | Mobile Genetic Elements and Evolution of CRISPR-Cas Systems: All the Way There and Back | 2.4 | 166 | Citations (PDF) |
| 75 | The CRISPR Spacer Space Is Dominated by Sequences from Species-Specific Mobilomes | 4.4 | 209 | Citations (PDF) |
| 76 | Recruitment of CRISPR-Cas systems by Tn7-like transposons | 7.6 | 281 | Citations (PDF) |
| 77 | On the Origin of Reverse Transcriptase-Using CRISPR-Cas Systems and Their Hyperdiverse, Enigmatic Spacer Repertoires | 4.4 | 63 | Citations (PDF) |
| 78 | ‘ARMAN’ archaea depend on association with euryarchaeal host in culture and in situ | 13.9 | 136 | Citations (PDF) |
| 79 | Evolutionary Genomics of Defense Systems in Archaea and Bacteria | 9.2 | 338 | Citations (PDF) |
| 80 | Proposed Role for KaiC-Like ATPases as Major Signal Transduction Hubs in Archaea | 4.4 | 16 | Citations (PDF) |
| 81 | Extreme Deviations from Expected Evolutionary Rates in Archaeal Protein Families | 2.4 | 11 | Citations (PDF) |
| 82 | Phylogenomics of Cas4 family nucleases | 3.1 | 76 | Citations (PDF) |
| 83 | Diversity and Evolution of Type IV pili Systems in Archaea | 3.9 | 120 | Citations (PDF) |
| 84 | The genome of AR9, a giant transducing Bacillus phage encoding two multisubunit RNA polymerases | 2.3 | 95 | Citations (PDF) |
| 85 | Crystal Structure of Cpf1 in Complex with Guide RNA and Target DNA | 34.1 | 731 | Citations (PDF) |
| 86 | Diverse evolutionary roots and mechanistic variations of the CRISPR-Cas systems | 36.4 | 619 | Citations (PDF) |
| 87 | C2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effector | 36.4 | 2,154 | Citations (PDF) |
| 88 | Recent Mobility of Casposons, Self-Synthesizing Transposons at the Origin of the CRISPR-Cas Immunity | 2.4 | 36 | Citations (PDF) |
| 89 | ISC, a Novel Group of Bacterial and Archaeal DNA Transposons That Encode Cas9 Homologs | 2.9 | 107 | Citations (PDF) |
| 90 | Evolution of plant δ1-pyrroline-5-carboxylate reductases from phylogenetic and structural perspectives | 4.1 | 22 | Citations (PDF) |
| 91 | Archaeal Clusters of Orthologous Genes (arCOGs): An Update and Application for Analysis of Shared Features between Thermococcales, Methanococcales, and Methanobacteriales | 2.8 | 260 | Citations (PDF) |
| 92 | A non-canonical multisubunit RNA polymerase encoded by a giant bacteriophage | 15.7 | 53 | Citations (PDF) |
| 93 | Expanded microbial genome coverage and improved protein family annotation in the COG database | 15.7 | 1,638 | Citations (PDF) |
| 94 | Comparative genomic analysis of evolutionarily conserved but functionally uncharacterized membrane proteins in archaea: Prediction of novel components of secretion, membrane remodeling and glycosylation systems | 2.9 | 15 | Citations (PDF) |
| 95 | A primase subunit essential for efficient primer synthesis by an archaeal eukaryotic-type primase | 13.9 | 23 | Citations (PDF) |
| 96 | Functional Diversity of Haloacid Dehalogenase Superfamily Phosphatases from Saccharomyces cerevisiae | 2.2 | 100 | Citations (PDF) |
| 97 | Babela massiliensis, a representative of a widespread bacterial phylum with unusual adaptations to parasitism in amoebae | 4.5 | 77 | Citations (PDF) |
| 98 | In vivo genome editing using Staphylococcus aureus Cas9 | 38.7 | 2,577 | Citations (PDF) |
| 99 | An updated evolutionary classification of CRISPR–Cas systems | 85.9 | 2,476 | Citations (PDF) |
| 100 | Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System | 34.1 | 4,498 | Citations (PDF) |
| 101 | Discovery and Functional Characterization of Diverse Class 2 CRISPR-Cas Systems | 13.4 | 1,181 | Citations (PDF) |
| 102 | CARF and WYL domains: ligand-binding regulators of prokaryotic defense systems | 2.4 | 188 | Citations (PDF) |
| 103 | Evolution of replicative DNA polymerases in archaea and their contributions to the eukaryotic replication machinery | 3.9 | 76 | Citations (PDF) |
| 104 | Enzymatic Synthesis of Bioinformatically Predicted Microcin C-Like Compounds Encoded by Diverse Bacteria | 4.4 | 35 | Citations (PDF) |
| 105 | Classification and evolution of type II CRISPR-Cas systems | 15.7 | 487 | Citations (PDF) |
| 106 | Phylogeny of Cas9 determines functional exchangeability of dual-RNA and Cas9 among orthologous type II CRISPR-Cas systems | 15.7 | 344 | Citations (PDF) |
| 107 | Dark matter in archaeal genomes: a rich source of novel mobile elements, defense systems and secretory complexes | 2.2 | 50 | Citations (PDF) |
| 108 | The evolutionary journey of Argonaute proteins | 8.7 | 527 | Citations (PDF) |
| 109 | Casposons: a new superfamily of self-synthesizing DNA transposons at the origin of prokaryotic CRISPR-Cas immunity | 4.0 | 178 | Citations (PDF) |
| 110 | Comprehensive analysis of the HEPN superfamily: identification of novel roles in intra-genomic conflicts, defense, pathogenesis and RNA processing | 4.5 | 260 | Citations (PDF) |
| 111 | Insights into archaeal evolution and symbiosis from the genomes of a nanoarchaeon and its inferred crenarchaeal host from Obsidian Pool, Yellowstone National Park | 4.5 | 109 | Citations (PDF) |
| 112 | Archaeology of Eukaryotic DNA Replication | 7.3 | 78 | Citations (PDF) |
| 113 | Comparative genomics of defense systems in archaea and bacteria | 15.7 | 431 | Citations (PDF) |
| 114 | CRISPR-Cas | 3.4 | 185 | Citations (PDF) |
| 115 | Displacement of the canonical single-stranded DNA-binding protein in the Thermoproteales | 7.6 | 34 | Citations (PDF) |
| 116 | Nature and Intensity of Selection Pressure on CRISPR-Associated Genes | 2.9 | 96 | Citations (PDF) |
| 117 | Live virus-free or die: coupling of antivirus immunity and programmed suicide or dormancy in prokaryotes | 4.5 | 136 | Citations (PDF) |
| 118 | Updated clusters of orthologous genes for Archaea: a complex ancestor of the Archaea and the byways of horizontal gene transfer | 4.5 | 153 | Citations (PDF) |
| 119 | The CMG (CDC45/RecJ, MCM, GINS) complex is a conserved component of the DNA replication system in all archaea and eukaryotes | 4.5 | 84 | Citations (PDF) |
| 120 | Evolution and classification of the CRISPR–Cas systems | 85.9 | 2,373 | Citations (PDF) |
| 121 | The Complete Genome Sequence of Thermoproteus tenax: A Physiologically Versatile Member of the Crenarchaeota | 2.4 | 55 | Citations (PDF) |
| 122 | Unification of Cas protein families and a simple scenario for the origin and evolution of CRISPR-Cas systems | 4.5 | 411 | Citations (PDF) |
| 123 | Defense Islands in Bacterial and Archaeal Genomes and Prediction of Novel Defense Systems | 2.9 | 511 | Citations (PDF) |
| 124 | Evolution of diverse cell division and vesicle formation systems in Archaea | 85.9 | 224 | Citations (PDF) |
| 125 | Archaeal Ubiquitin-Like Proteins: Functional Versatility and Putative Ancestral Involvement in tRNA Modification Revealed by Comparative Genomic Analysis | 1.0 | 29 | Citations (PDF) |
| 126 | Abundance of type I toxin–antitoxin systems in bacteria: searches for new candidates and discovery of novel families | 15.7 | 257 | Citations (PDF) |
| 127 | Comprehensive comparative-genomic analysis of Type 2 toxin-antitoxin systems and related mobile stress response systems in prokaryotes | 4.5 | 419 | Citations (PDF) |
| 128 | Prokaryotic homologs of Argonaute proteins are predicted to function as key components of a novel system of defense against mobile genetic elements | 4.5 | 287 | Citations (PDF) |
| 129 | CRISPR-Cas: an adaptive immunity system in prokaryotes | 2.5 | 107 | Citations (PDF) |
| 130 | Evolutionary primacy of sodium bioenergetics | 4.5 | 155 | Citations (PDF) |
| 131 | Complete genome sequence of the extremely acidophilic methanotroph isolate V4, Methylacidiphilum infernorum, a representative of the bacterial phylum Verrucomicrobia | 4.5 | 236 | Citations (PDF) |
| 132 | A genomic analysis of the archaeal system Ignicoccus hospitalis-Nanoarchaeum equitans | 8.2 | 106 | Citations (PDF) |
| 133 | Encapsulated in silica: genome, proteome and physiology of the thermophilic bacterium Anoxybacillus flavithermus WK1 | 12.8 | 72 | Citations (PDF) |
| 134 | A Novel Family of Sequence-specific Endoribonucleases Associated with the Clustered Regularly Interspaced Short Palindromic Repeats | 2.2 | 187 | Citations (PDF) |
| 135 | Role of Hypermutability in the Evolution of the Genus<i>Oenococcus</i> | 2.9 | 77 | Citations (PDF) |
| 136 | A korarchaeal genome reveals insights into the evolution of the Archaea | 7.6 | 277 | Citations (PDF) |
| 137 | The Deep Archaeal Roots of Eukaryotes | 4.7 | 160 | Citations (PDF) |
| 138 | Evolutionary Genomics of Lactic Acid Bacteria | 2.9 | 263 | Citations (PDF) |
| 139 | Clusters of orthologous genes for 41 archaeal genomes and implications for evolutionary genomics of archaea | 4.5 | 174 | Citations (PDF) |
| 140 | Deinococcus geothermalis: The Pool of Extreme Radiation Resistance Genes Shrinks | 2.4 | 231 | Citations (PDF) |
| 141 | The cyanobacterial genome core and the origin of photosynthesis | 7.6 | 297 | Citations (PDF) |
| 142 | GINS, a central nexus in the archaeal DNA replication fork | 5.2 | 125 | Citations (PDF) |
| 143 | Title is missing! | 4.5 | 1,048 | Citations (PDF) |
| 144 | Cyanobacterial response regulator PatA contains a conserved N-terminal domain (PATAN) with an alpha-helical insertion | 4.8 | 41 | Citations (PDF) |
| 145 | The HicAB cassette, a putative novel, RNA-targeting toxin-antitoxin system in archaea and bacteria | 4.8 | 112 | Citations (PDF) |
| 146 | Kinase Activity of Overexpressed HipA Is Required for Growth Arrest and Multidrug Tolerance in
<i>Escherichia coli</i> | 2.9 | 191 | Citations (PDF) |
| 147 | Genomic analysis of<i>Oenococcus oeni</i>PSU-1 and its relevance to winemaking | 10.9 | 17 | Citations (PDF) |
| 148 | Title is missing! | 3.1 | 164 | Citations (PDF) |
| 149 | Ancestral paralogs and pseudoparalogs and their role in the emergence of the eukaryotic cell | 15.7 | 182 | Citations (PDF) |
| 150 | Evolutionary and functional genomics of the Archaea | 7.0 | 42 | Citations (PDF) |
| 151 | Identification and Functional Verification of Archaeal-Type Phosphoenolpyruvate Carboxylase, a Missing Link in Archaeal Central Carbohydrate Metabolism | 2.9 | 35 | Citations (PDF) |
| 152 | Comparative genomics of the FtsK-HerA superfamily of pumping ATPases: implications for the origins of chromosome segregation, cell division and viral capsid packaging | 15.7 | 306 | Citations (PDF) |
| 153 | Potential genomic determinants of hyperthermophily | 9.9 | 74 | Citations (PDF) |
| 154 | Filling a gap in the central metabolism of archaea: prediction of a novel aconitase by comparative-genomic analysis | 1.9 | 37 | Citations (PDF) |
| 155 | Transcriptome dynamics of Deinococcus radiodurans recovering from ionizing radiation | 7.6 | 363 | Citations (PDF) |
| 156 | A DNA repair system specific for thermophilic Archaea and bacteria predicted by genomic context analysis | 15.7 | 365 | Citations (PDF) |
| 157 | The complete genome of hyperthermophile
<i>Methanopyrus kandleri AV19</i>
and monophyly of archaeal methanogens | 7.6 | 290 | Citations (PDF) |
| 158 | SWIM, a novel Zn-chelating domain present in bacteria, archaea and eukaryotes | 6.7 | 77 | Citations (PDF) |
| 159 | Connected gene neighborhoods in prokaryotic genomes | 15.7 | 178 | Citations (PDF) |
| 160 | Genome Sequence and Comparative Analysis of the Solvent-Producing Bacterium<i>Clostridium acetobutylicum</i> | 2.9 | 745 | Citations (PDF) |
| 161 | Genome of the Extremely Radiation-Resistant Bacterium
<i>Deinococcus radiodurans</i>
Viewed from the Perspective of Comparative Genomics | 7.2 | 677 | Citations (PDF) |
| 162 | The Structure and Evolution of Penelope in the virilis Species Group of Drosophila: An Ancient Lineage of Retroelements | 1.7 | 47 | Citations (PDF) |
| 163 | Horizontal Gene Transfer in Prokaryotes: Quantification and Classification | 9.2 | 1,072 | Citations (PDF) |
| 164 | Lineage-Specific Gene Expansions in Bacterial and Archaeal Genomes | 4.6 | 116 | Citations (PDF) |
| 165 | Title is missing! | 1.1 | 40 | Citations (PDF) |
| 166 | Physiologic Determinants of Radiation Resistance in
Deinococcus radiodurans | 3.5 | 139 | Citations (PDF) |
| 167 | A superfamily of archaeal, bacterial, and eukaryotic proteins homologous to animal transglutaminases | 6.0 | 167 | Citations (PDF) |
| 168 | Short repeats and IS elements in the extremely radiation-resistant bacterium Deinococcus radiodurans and comparison to other bacterial species | 3.1 | 23 | Citations (PDF) |
| 169 | Thermolysin and mitochondrial processing peptidase: How far structure—functional convergence goes | 6.0 | 19 | Citations (PDF) |