| Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
|---|
| Peroxiredoxins | 20 | 2019 | 116 | 3.000 |
Why?
|
| Bacterial Proteins | 15 | 2016 | 79 | 1.440 |
Why?
|
| Oxidation-Reduction | 34 | 2019 | 268 | 1.420 |
Why?
|
| Cysteine | 17 | 2019 | 138 | 1.370 |
Why?
|
| Salmonella typhimurium | 8 | 2018 | 33 | 1.270 |
Why?
|
| Thioredoxins | 5 | 2016 | 21 | 1.100 |
Why?
|
| Thioredoxin-Disulfide Reductase | 4 | 2016 | 11 | 1.030 |
Why?
|
| Peroxidases | 12 | 2017 | 35 | 0.940 |
Why?
|
| Hydrogen Peroxide | 10 | 2018 | 83 | 0.860 |
Why?
|
| Sulfenic Acids | 8 | 2017 | 54 | 0.830 |
Why?
|
| Models, Molecular | 17 | 2018 | 193 | 0.750 |
Why?
|
| Amino Acid Sequence | 24 | 2018 | 283 | 0.730 |
Why?
|
| Escherichia coli | 15 | 2016 | 85 | 0.700 |
Why?
|
| Bacillus anthracis | 4 | 2018 | 9 | 0.700 |
Why?
|
| Entamoeba histolytica | 2 | 2016 | 4 | 0.650 |
Why?
|
| Catalysis | 17 | 2017 | 65 | 0.600 |
Why?
|
| Auranofin | 2 | 2016 | 4 | 0.570 |
Why?
|
| Glycerolphosphate Dehydrogenase | 6 | 2015 | 6 | 0.550 |
Why?
|
| Peroxides | 7 | 2019 | 32 | 0.540 |
Why?
|
| Antiprotozoal Agents | 1 | 2016 | 3 | 0.540 |
Why?
|
| Substrate Specificity | 10 | 2016 | 86 | 0.540 |
Why?
|
| Protozoan Proteins | 1 | 2016 | 9 | 0.540 |
Why?
|
| Kinetics | 18 | 2018 | 209 | 0.520 |
Why?
|
| Molecular Sequence Data | 21 | 2015 | 355 | 0.520 |
Why?
|
| Crystallography, X-Ray | 14 | 2018 | 90 | 0.510 |
Why?
|
| Catalytic Domain | 11 | 2019 | 65 | 0.430 |
Why?
|
| Sequence Alignment | 8 | 2016 | 60 | 0.430 |
Why?
|
| Enzyme Assays | 2 | 2013 | 5 | 0.420 |
Why?
|
| Disulfides | 7 | 2019 | 36 | 0.420 |
Why?
|
| Protein Engineering | 1 | 2010 | 19 | 0.360 |
Why?
|
| Treponema pallidum | 1 | 2010 | 7 | 0.360 |
Why?
|
| Fluorescent Dyes | 1 | 2010 | 48 | 0.360 |
Why?
|
| Bacteria | 1 | 2010 | 46 | 0.350 |
Why?
|
| Mutation | 12 | 2019 | 487 | 0.350 |
Why?
|
| Antioxidants | 1 | 2010 | 114 | 0.340 |
Why?
|
| NADH, NADPH Oxidoreductases | 6 | 2015 | 10 | 0.330 |
Why?
|
| Enterococcus | 6 | 1998 | 9 | 0.330 |
Why?
|
| Flavins | 3 | 2015 | 5 | 0.330 |
Why?
|
| Recombinant Proteins | 8 | 2016 | 247 | 0.310 |
Why?
|
| Protein Processing, Post-Translational | 2 | 2019 | 78 | 0.310 |
Why?
|
| Xanthomonas campestris | 2 | 2016 | 7 | 0.270 |
Why?
|
| Sequence Homology, Amino Acid | 8 | 2015 | 70 | 0.270 |
Why?
|
| Sulfhydryl Compounds | 3 | 2016 | 33 | 0.260 |
Why?
|
| Mycoplasma pneumoniae | 2 | 2015 | 4 | 0.250 |
Why?
|
| Enterococcus faecalis | 6 | 2015 | 10 | 0.250 |
Why?
|
| Phosphotransferases (Alcohol Group Acceptor) | 2 | 2018 | 16 | 0.240 |
Why?
|
| Binding Sites | 10 | 2010 | 130 | 0.230 |
Why?
|
| Flavin-Adenine Dinucleotide | 4 | 2015 | 6 | 0.230 |
Why?
|
| Multienzyme Complexes | 4 | 2015 | 16 | 0.220 |
Why?
|
| Cloning, Molecular | 6 | 2016 | 75 | 0.210 |
Why?
|
| Kininogen, High-Molecular-Weight | 2 | 2014 | 6 | 0.200 |
Why?
|
| Escherichia coli Proteins | 4 | 2013 | 33 | 0.200 |
Why?
|
| Protein Folding | 2 | 2013 | 29 | 0.200 |
Why?
|
| Ferritins | 2 | 2014 | 46 | 0.200 |
Why?
|
| Proton-Translocating ATPases | 7 | 1990 | 16 | 0.190 |
Why?
|
| Glucosamine | 2 | 2010 | 7 | 0.180 |
Why?
|
| Protein Conformation | 7 | 2015 | 84 | 0.180 |
Why?
|
| Streptococcus pyogenes | 2 | 2015 | 16 | 0.180 |
Why?
|
| Enzymes | 1 | 1999 | 5 | 0.180 |
Why?
|
| Animals | 8 | 2017 | 7450 | 0.180 |
Why?
|
| Tyrosine | 1 | 2019 | 23 | 0.170 |
Why?
|
| Coenzyme A | 2 | 2009 | 4 | 0.160 |
Why?
|
| Protein Kinase Inhibitors | 1 | 2018 | 85 | 0.160 |
Why?
|
| Extracellular Signal-Regulated MAP Kinases | 1 | 2017 | 35 | 0.150 |
Why?
|
| Biosensing Techniques | 1 | 2017 | 25 | 0.150 |
Why?
|
| Protein Binding | 3 | 2015 | 201 | 0.150 |
Why?
|
| Protein Structure, Secondary | 2 | 2016 | 47 | 0.140 |
Why?
|
| DNA Damage | 1 | 2017 | 98 | 0.140 |
Why?
|
| Cell Membrane | 3 | 2012 | 96 | 0.140 |
Why?
|
| Fibroblasts | 1 | 2017 | 112 | 0.140 |
Why?
|
| Mutagenesis, Site-Directed | 5 | 2005 | 62 | 0.140 |
Why?
|
| Sulfinic Acids | 1 | 2016 | 13 | 0.140 |
Why?
|
| Epithelial Cells | 1 | 2017 | 142 | 0.140 |
Why?
|
| Structure-Activity Relationship | 7 | 2018 | 80 | 0.140 |
Why?
|
| Oxidoreductases | 2 | 2015 | 26 | 0.130 |
Why?
|
| Anti-Bacterial Agents | 1 | 2018 | 300 | 0.130 |
Why?
|
| DNA | 1 | 2017 | 227 | 0.130 |
Why?
|
| Antirheumatic Agents | 1 | 2016 | 30 | 0.130 |
Why?
|
| Oxidative Stress | 2 | 2015 | 229 | 0.130 |
Why?
|
| Nuclear Magnetic Resonance, Biomolecular | 1 | 2015 | 20 | 0.130 |
Why?
|
| Bacillus subtilis | 2 | 2010 | 3 | 0.130 |
Why?
|
| Organogold Compounds | 1 | 2015 | 4 | 0.130 |
Why?
|
| Signal Transduction | 2 | 2019 | 687 | 0.130 |
Why?
|
| Protein Structure, Tertiary | 6 | 2015 | 99 | 0.130 |
Why?
|
| Hydrogen-Ion Concentration | 7 | 2018 | 65 | 0.130 |
Why?
|
| Proline Oxidase | 1 | 2015 | 4 | 0.130 |
Why?
|
| Flavoproteins | 1 | 2015 | 6 | 0.130 |
Why?
|
| Ubiquinone | 1 | 2015 | 7 | 0.130 |
Why?
|
| CD4-Positive T-Lymphocytes | 1 | 2015 | 57 | 0.130 |
Why?
|
| Transcription, Genetic | 2 | 2010 | 137 | 0.130 |
Why?
|
| Hyperoxaluria, Primary | 1 | 2015 | 7 | 0.130 |
Why?
|
| Hydroxyproline | 1 | 2015 | 9 | 0.130 |
Why?
|
| Humans | 15 | 2019 | 31836 | 0.120 |
Why?
|
| Streptococcus | 2 | 2007 | 8 | 0.120 |
Why?
|
| Gene Expression | 1 | 2016 | 334 | 0.120 |
Why?
|
| CD8-Positive T-Lymphocytes | 1 | 2015 | 91 | 0.120 |
Why?
|
| Genes, Bacterial | 4 | 2015 | 8 | 0.120 |
Why?
|
| Metals, Heavy | 1 | 2014 | 7 | 0.120 |
Why?
|
| Glycosyltransferases | 2 | 2010 | 3 | 0.120 |
Why?
|
| Molecular Weight | 2 | 2010 | 41 | 0.120 |
Why?
|
| Genome, Bacterial | 2 | 2010 | 6 | 0.110 |
Why?
|
| Molecular Structure | 3 | 2018 | 59 | 0.110 |
Why?
|
| Thermodynamics | 7 | 2015 | 46 | 0.110 |
Why?
|
| Base Sequence | 4 | 2000 | 251 | 0.110 |
Why?
|
| Crystallization | 3 | 2009 | 17 | 0.110 |
Why?
|
| Chlamydia | 1 | 2012 | 2 | 0.100 |
Why?
|
| Periplasm | 1 | 2012 | 2 | 0.100 |
Why?
|
| High-Throughput Screening Assays | 1 | 2012 | 12 | 0.100 |
Why?
|
| Electron Transport Chain Complex Proteins | 1 | 2012 | 8 | 0.100 |
Why?
|
| Drug Evaluation, Preclinical | 1 | 2012 | 62 | 0.100 |
Why?
|
| Electron Transport | 2 | 2010 | 16 | 0.100 |
Why?
|
| Spectrophotometry | 3 | 2015 | 22 | 0.100 |
Why?
|
| Borohydrides | 1 | 2010 | 1 | 0.090 |
Why?
|
| Uridine Diphosphate | 1 | 2010 | 1 | 0.090 |
Why?
|
| Intramolecular Lyases | 1 | 2010 | 1 | 0.090 |
Why?
|
| Glycopeptides | 1 | 2010 | 4 | 0.090 |
Why?
|
| Inositol | 1 | 2010 | 5 | 0.090 |
Why?
|
| Eukaryota | 1 | 2010 | 3 | 0.090 |
Why?
|
| Neoplasms | 1 | 2017 | 692 | 0.090 |
Why?
|
| Adenosine Diphosphate | 3 | 1990 | 5 | 0.090 |
Why?
|
| Thiosulfate Sulfurtransferase | 1 | 2009 | 2 | 0.090 |
Why?
|
| Sulfur | 1 | 2009 | 4 | 0.090 |
Why?
|
| Rabbits | 1 | 2010 | 196 | 0.090 |
Why?
|
| Evolution, Molecular | 1 | 2009 | 34 | 0.080 |
Why?
|
| Neovascularization, Pathologic | 1 | 2009 | 82 | 0.080 |
Why?
|
| Lysine | 1 | 1988 | 23 | 0.080 |
Why?
|
| NAD | 3 | 1999 | 27 | 0.070 |
Why?
|
| Serine | 3 | 2013 | 10 | 0.070 |
Why?
|
| Dithionite | 3 | 2007 | 4 | 0.070 |
Why?
|
| Mitochondria | 1 | 2007 | 186 | 0.070 |
Why?
|
| Threonine | 1 | 2005 | 9 | 0.070 |
Why?
|
| Dimerization | 1 | 2005 | 23 | 0.070 |
Why?
|
| Dose-Response Relationship, Drug | 2 | 2018 | 629 | 0.060 |
Why?
|
| Enzyme Activation | 1 | 2005 | 135 | 0.060 |
Why?
|
| Ligands | 2 | 2015 | 80 | 0.060 |
Why?
|
| Models, Chemical | 2 | 2007 | 34 | 0.060 |
Why?
|
| Oligodeoxyribonucleotides | 2 | 1995 | 17 | 0.060 |
Why?
|
| Oxygen | 2 | 2015 | 140 | 0.050 |
Why?
|
| Gene Expression Regulation, Bacterial | 2 | 2000 | 8 | 0.050 |
Why?
|
| Phylogeny | 2 | 2012 | 54 | 0.050 |
Why?
|
| Glycerol Kinase | 2 | 1997 | 2 | 0.050 |
Why?
|
| Protein Tyrosine Phosphatases | 1 | 1999 | 17 | 0.040 |
Why?
|
| Trans-Activators | 1 | 2000 | 46 | 0.040 |
Why?
|
| Streptococcus agalactiae | 1 | 1999 | 5 | 0.040 |
Why?
|
| Monosaccharide Transport Proteins | 1 | 1999 | 8 | 0.040 |
Why?
|
| Histidine | 2 | 1997 | 5 | 0.040 |
Why?
|
| Symporters | 1 | 1999 | 12 | 0.040 |
Why?
|
| Peroxynitrous Acid | 1 | 2019 | 7 | 0.040 |
Why?
|
| Alkaline Phosphatase | 1 | 1999 | 38 | 0.040 |
Why?
|
| Species Specificity | 3 | 2015 | 87 | 0.040 |
Why?
|
| Membrane Transport Proteins | 1 | 1999 | 34 | 0.040 |
Why?
|
| Gene Expression Regulation, Enzymologic | 2 | 1997 | 80 | 0.040 |
Why?
|
| Hydrogen Bonding | 2 | 2010 | 22 | 0.040 |
Why?
|
| Peroxidase | 1 | 2019 | 31 | 0.040 |
Why?
|
| Nitrates | 1 | 2019 | 27 | 0.040 |
Why?
|
| Protein Denaturation | 2 | 2009 | 11 | 0.040 |
Why?
|
| Spectrometry, Fluorescence | 2 | 1999 | 27 | 0.040 |
Why?
|
| Macromolecular Substances | 5 | 1990 | 17 | 0.040 |
Why?
|
| Mice | 2 | 2017 | 2476 | 0.040 |
Why?
|
| Conserved Sequence | 1 | 1998 | 20 | 0.040 |
Why?
|
| Microbial Sensitivity Tests | 1 | 2018 | 63 | 0.040 |
Why?
|
| Amino Acid Motifs | 1 | 2018 | 24 | 0.040 |
Why?
|
| Pseudomonas aeruginosa | 1 | 1998 | 30 | 0.040 |
Why?
|
| Fluorescence | 1 | 2018 | 20 | 0.040 |
Why?
|
| Azides | 2 | 2015 | 2 | 0.040 |
Why?
|
| Polymerase Chain Reaction | 1 | 1998 | 186 | 0.040 |
Why?
|
| Uracil | 1 | 2017 | 6 | 0.040 |
Why?
|
| Guanine | 1 | 2017 | 15 | 0.040 |
Why?
|
| Base Pair Mismatch | 1 | 2017 | 6 | 0.040 |
Why?
|
| NADP | 2 | 2013 | 9 | 0.040 |
Why?
|
| Nanotechnology | 1 | 2017 | 16 | 0.040 |
Why?
|
| Adenine | 1 | 2017 | 15 | 0.040 |
Why?
|
| NIH 3T3 Cells | 1 | 2017 | 43 | 0.040 |
Why?
|
| Plasmids | 3 | 1993 | 48 | 0.040 |
Why?
|
| MAP Kinase Signaling System | 1 | 2017 | 61 | 0.040 |
Why?
|
| DNA Repair | 1 | 2017 | 64 | 0.040 |
Why?
|
| Epigenesis, Genetic | 1 | 2017 | 104 | 0.040 |
Why?
|
| Cell Line | 1 | 2017 | 434 | 0.030 |
Why?
|
| Molecular Dynamics Simulation | 1 | 2015 | 14 | 0.030 |
Why?
|
| Mathematics | 2 | 1993 | 10 | 0.030 |
Why?
|
| Lymphocytic Choriomeningitis | 1 | 2015 | 19 | 0.030 |
Why?
|
| Acridines | 1 | 2015 | 19 | 0.030 |
Why?
|
| Urea | 1 | 2015 | 37 | 0.030 |
Why?
|
| Platinum | 1 | 2015 | 21 | 0.030 |
Why?
|
| Lymphocytic choriomeningitis virus | 1 | 2015 | 22 | 0.030 |
Why?
|
| Arginine | 1 | 1995 | 17 | 0.030 |
Why?
|
| Alanine | 1 | 1995 | 27 | 0.030 |
Why?
|
| Dihydroxyacetone Phosphate | 1 | 2015 | 1 | 0.030 |
Why?
|
| Glyceraldehyde 3-Phosphate | 1 | 2015 | 1 | 0.030 |
Why?
|
| Recombinant Fusion Proteins | 1 | 2015 | 103 | 0.030 |
Why?
|
| Static Electricity | 1 | 2015 | 11 | 0.030 |
Why?
|
| Bordetella pertussis | 1 | 2015 | 7 | 0.030 |
Why?
|
| Furans | 1 | 2015 | 3 | 0.030 |
Why?
|
| Proline | 1 | 2015 | 12 | 0.030 |
Why?
|
| Viral Load | 1 | 2015 | 70 | 0.030 |
Why?
|
| Mutant Proteins | 1 | 2015 | 14 | 0.030 |
Why?
|
| Biocatalysis | 1 | 2015 | 20 | 0.030 |
Why?
|
| Aquaporins | 1 | 1995 | 5 | 0.030 |
Why?
|
| Cell Line, Tumor | 1 | 2017 | 725 | 0.030 |
Why?
|
| Flow Cytometry | 1 | 2015 | 184 | 0.030 |
Why?
|
| Lymphocyte Activation | 1 | 2015 | 88 | 0.030 |
Why?
|
| Terminology as Topic | 1 | 2015 | 64 | 0.030 |
Why?
|
| Adenosine Triphosphate | 3 | 1990 | 53 | 0.030 |
Why?
|
| Sequence Deletion | 2 | 2007 | 40 | 0.030 |
Why?
|
| Enzyme Inhibitors | 1 | 2015 | 164 | 0.030 |
Why?
|
| Amino Acid Substitution | 1 | 2013 | 39 | 0.030 |
Why?
|
| Cytokines | 1 | 2015 | 259 | 0.030 |
Why?
|
| Calcium | 1 | 2015 | 304 | 0.030 |
Why?
|
| Spectrum Analysis | 2 | 2007 | 6 | 0.030 |
Why?
|
| Chromatography, Ion Exchange | 1 | 1993 | 4 | 0.030 |
Why?
|
| Restriction Mapping | 1 | 1993 | 13 | 0.030 |
Why?
|
| Benzene Derivatives | 1 | 2013 | 3 | 0.030 |
Why?
|
| Cells, Cultured | 1 | 2015 | 833 | 0.030 |
Why?
|
| Chromatography, High Pressure Liquid | 1 | 1993 | 94 | 0.030 |
Why?
|
| Magnetic Resonance Spectroscopy | 1 | 1993 | 82 | 0.030 |
Why?
|
| Mice, Inbred C57BL | 1 | 2015 | 766 | 0.030 |
Why?
|
| Ribonucleases | 1 | 1992 | 4 | 0.030 |
Why?
|
| Mice, Inbred C3H | 1 | 2012 | 25 | 0.030 |
Why?
|
| Genetic Vectors | 1 | 1993 | 120 | 0.030 |
Why?
|
| Cricetinae | 1 | 2012 | 39 | 0.030 |
Why?
|
| Glutathione Reductase | 1 | 1992 | 9 | 0.030 |
Why?
|
| Caulobacter crescentus | 1 | 2012 | 2 | 0.030 |
Why?
|
| Data Interpretation, Statistical | 1 | 2013 | 109 | 0.030 |
Why?
|
| Peptide Fragments | 1 | 2015 | 398 | 0.030 |
Why?
|
| Cluster Analysis | 1 | 2012 | 128 | 0.030 |
Why?
|
| Ultracentrifugation | 1 | 2011 | 5 | 0.030 |
Why?
|
| Mutagenesis | 1 | 2011 | 33 | 0.020 |
Why?
|
| Dithiothreitol | 1 | 2010 | 8 | 0.020 |
Why?
|
| Fosfomycin | 1 | 2010 | 1 | 0.020 |
Why?
|
| Nucleotides | 1 | 1990 | 16 | 0.020 |
Why?
|
| Drug Resistance, Bacterial | 1 | 2010 | 40 | 0.020 |
Why?
|
| Multigene Family | 1 | 2010 | 51 | 0.020 |
Why?
|
| Biological Transport, Active | 1 | 2009 | 8 | 0.020 |
Why?
|
| Stress, Physiological | 1 | 2010 | 55 | 0.020 |
Why?
|
| Models, Biological | 1 | 2012 | 391 | 0.020 |
Why?
|
| Isoenzymes | 1 | 2009 | 61 | 0.020 |
Why?
|
| Protein Interaction Mapping | 1 | 2009 | 8 | 0.020 |
Why?
|
| Aspartic Acid | 1 | 1988 | 12 | 0.020 |
Why?
|
| Incubators | 1 | 2008 | 3 | 0.020 |
Why?
|
| Horseradish Peroxidase | 1 | 2008 | 5 | 0.020 |
Why?
|
| Alkylation | 1 | 2008 | 5 | 0.020 |
Why?
|
| Buffers | 1 | 2008 | 9 | 0.020 |
Why?
|
| Absorption | 1 | 2008 | 15 | 0.020 |
Why?
|
| Iodoacetamide | 1 | 2008 | 8 | 0.020 |
Why?
|
| Binding, Competitive | 1 | 2008 | 33 | 0.020 |
Why?
|
| Protein Stability | 1 | 2008 | 25 | 0.020 |
Why?
|
| Glutamine | 1 | 1988 | 9 | 0.020 |
Why?
|
| Sulfites | 1 | 2007 | 2 | 0.020 |
Why?
|
| Glycerophosphates | 1 | 2007 | 4 | 0.020 |
Why?
|
| Protein Structure, Quaternary | 1 | 2007 | 18 | 0.020 |
Why?
|
| Cell Movement | 1 | 2009 | 170 | 0.020 |
Why?
|
| Coenzymes | 2 | 1999 | 3 | 0.020 |
Why?
|
| Endothelial Cells | 1 | 2009 | 189 | 0.020 |
Why?
|
| Pantothenic Acid | 1 | 2007 | 1 | 0.020 |
Why?
|
| Enzyme Stability | 2 | 1999 | 6 | 0.020 |
Why?
|
| Prostatic Neoplasms | 1 | 2009 | 470 | 0.010 |
Why?
|
| Time Factors | 1 | 2008 | 2146 | 0.010 |
Why?
|
| Male | 2 | 2012 | 19091 | 0.010 |
Why?
|
| Trypsin | 1 | 2000 | 11 | 0.010 |
Why?
|
| Adhesins, Bacterial | 1 | 2000 | 2 | 0.010 |
Why?
|
| Hydrolysis | 2 | 1990 | 35 | 0.010 |
Why?
|
| Genes, Reporter | 1 | 2000 | 40 | 0.010 |
Why?
|
| Gene Deletion | 1 | 2000 | 66 | 0.010 |
Why?
|
| Membrane Fusion | 1 | 1999 | 1 | 0.010 |
Why?
|
| Transformation, Bacterial | 1 | 1999 | 1 | 0.010 |
Why?
|
| Protein Sorting Signals | 1 | 1999 | 6 | 0.010 |
Why?
|
| Promoter Regions, Genetic | 1 | 2000 | 208 | 0.010 |
Why?
|
| Alleles | 2 | 1989 | 248 | 0.010 |
Why?
|
| Sequence Analysis | 1 | 1997 | 5 | 0.010 |
Why?
|
| Phosphoenolpyruvate | 1 | 1997 | 4 | 0.010 |
Why?
|
| Phosphotransferases | 1 | 1997 | 4 | 0.010 |
Why?
|
| Phenotype | 1 | 1999 | 635 | 0.010 |
Why?
|
| Female | 1 | 2015 | 19859 | 0.010 |
Why?
|
| Phosphorylation | 1 | 1997 | 230 | 0.010 |
Why?
|
| Deuterium | 1 | 1995 | 9 | 0.010 |
Why?
|
| Electrons | 1 | 1995 | 12 | 0.010 |
Why?
|
| Bacterial Outer Membrane Proteins | 1 | 1995 | 7 | 0.010 |
Why?
|
| Glycerol | 1 | 1995 | 5 | 0.010 |
Why?
|
| Energy Metabolism | 1 | 1995 | 148 | 0.010 |
Why?
|
| Bacillus | 1 | 1992 | 1 | 0.010 |
Why?
|
| Transcription Factors | 1 | 1993 | 180 | 0.010 |
Why?
|
| Oligonucleotides | 1 | 1992 | 30 | 0.010 |
Why?
|
| Guanosine Diphosphate | 1 | 1990 | 2 | 0.010 |
Why?
|
| Aurovertins | 1 | 1990 | 2 | 0.010 |
Why?
|
| Guanosine Triphosphate | 1 | 1990 | 8 | 0.010 |
Why?
|
| Edetic Acid | 1 | 1990 | 8 | 0.010 |
Why?
|
| Mitochondria, Heart | 1 | 1990 | 17 | 0.010 |
Why?
|
| Phosphates | 1 | 1990 | 25 | 0.010 |
Why?
|
| Magnesium | 1 | 1990 | 30 | 0.010 |
Why?
|
| Temperature | 1 | 1990 | 53 | 0.010 |
Why?
|
| Antibodies | 1 | 1990 | 52 | 0.010 |
Why?
|
| Hydroxylamines | 1 | 1989 | 1 | 0.010 |
Why?
|
| Methylnitronitrosoguanidine | 1 | 1989 | 1 | 0.010 |
Why?
|
| Sequence Homology, Nucleic Acid | 1 | 1988 | 18 | 0.010 |
Why?
|
| Models, Theoretical | 1 | 1989 | 136 | 0.000 |
Why?
|
| DNA, Single-Stranded | 1 | 1988 | 13 | 0.000 |
Why?
|
| Genotype | 1 | 1988 | 727 | 0.000 |
Why?
|