| Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
|---|
| DNA-Directed RNA Polymerases | 35 | 2015 | 102 | 4.340 |
Why?
|
| Bacteriophage N4 | 15 | 2015 | 24 | 3.800 |
Why?
|
| Escherichia coli | 36 | 2013 | 597 | 3.040 |
Why?
|
| Virion | 14 | 2011 | 59 | 1.860 |
Why?
|
| Coliphages | 27 | 1997 | 59 | 1.780 |
Why?
|
| Transcription, Genetic | 29 | 2011 | 1135 | 1.630 |
Why?
|
| Promoter Regions, Genetic | 19 | 2008 | 937 | 1.320 |
Why?
|
| DNA, Viral | 18 | 2011 | 265 | 1.220 |
Why?
|
| Viral Proteins | 13 | 2015 | 300 | 1.160 |
Why?
|
| DNA-Binding Proteins | 11 | 2003 | 1208 | 1.080 |
Why?
|
| Podoviridae | 7 | 1998 | 7 | 0.900 |
Why?
|
| Sigma Factor | 4 | 2013 | 23 | 0.890 |
Why?
|
| Escherichia coli Proteins | 4 | 2011 | 179 | 0.870 |
Why?
|
| RNA Polymerase II | 6 | 2003 | 55 | 0.740 |
Why?
|
| Nucleic Acid Conformation | 6 | 2008 | 332 | 0.700 |
Why?
|
| Molecular Sequence Data | 20 | 2015 | 3030 | 0.670 |
Why?
|
| Base Sequence | 21 | 2008 | 2330 | 0.550 |
Why?
|
| DNA, Single-Stranded | 6 | 2003 | 92 | 0.540 |
Why?
|
| Viral Structural Proteins | 2 | 2011 | 19 | 0.530 |
Why?
|
| DNA Replication | 5 | 2011 | 164 | 0.530 |
Why?
|
| Amino Acid Sequence | 11 | 2015 | 2062 | 0.500 |
Why?
|
| DNA | 9 | 2008 | 1294 | 0.480 |
Why?
|
| Bacterial Outer Membrane Proteins | 3 | 2008 | 53 | 0.470 |
Why?
|
| Models, Molecular | 4 | 2013 | 1286 | 0.440 |
Why?
|
| Bacteriophages | 2 | 2008 | 47 | 0.430 |
Why?
|
| Genes, Viral | 6 | 1995 | 116 | 0.420 |
Why?
|
| Protein Binding | 8 | 2015 | 1456 | 0.420 |
Why?
|
| Protein Conformation | 2 | 2013 | 881 | 0.410 |
Why?
|
| DNA, Superhelical | 5 | 1998 | 16 | 0.400 |
Why?
|
| DNA Polymerase III | 1 | 2011 | 9 | 0.400 |
Why?
|
| Templates, Genetic | 13 | 2007 | 34 | 0.380 |
Why?
|
| Repressor Proteins | 1 | 2013 | 403 | 0.380 |
Why?
|
| Receptors, Virus | 1 | 2008 | 74 | 0.330 |
Why?
|
| Nucleic Acids | 1 | 2008 | 30 | 0.330 |
Why?
|
| Viral Envelope Proteins | 1 | 2008 | 94 | 0.330 |
Why?
|
| RNA, Viral | 8 | 1995 | 327 | 0.310 |
Why?
|
| Catalytic Domain | 5 | 2015 | 156 | 0.310 |
Why?
|
| Glycoproteins | 1 | 2008 | 234 | 0.300 |
Why?
|
| Gene Expression Regulation | 4 | 2008 | 1920 | 0.300 |
Why?
|
| N-Acetylmuramoyl-L-alanine Amidase | 1 | 2006 | 11 | 0.300 |
Why?
|
| Glycoside Hydrolases | 1 | 2006 | 17 | 0.290 |
Why?
|
| Transcriptional Activation | 3 | 2015 | 280 | 0.290 |
Why?
|
| Genes, Bacterial | 3 | 1993 | 198 | 0.280 |
Why?
|
| Gene Expression Regulation, Enzymologic | 1 | 2006 | 214 | 0.270 |
Why?
|
| Bacteria | 2 | 2008 | 447 | 0.260 |
Why?
|
| Saccharomyces cerevisiae | 2 | 2008 | 434 | 0.260 |
Why?
|
| Cloning, Molecular | 7 | 2006 | 646 | 0.250 |
Why?
|
| Bacterial Proteins | 5 | 2008 | 864 | 0.230 |
Why?
|
| Sequence Homology, Amino Acid | 4 | 2006 | 416 | 0.230 |
Why?
|
| Biochemistry | 1 | 2003 | 27 | 0.220 |
Why?
|
| Virus Replication | 4 | 1995 | 319 | 0.210 |
Why?
|
| Trans-Activators | 2 | 1996 | 429 | 0.200 |
Why?
|
| Mutation | 12 | 2008 | 3967 | 0.190 |
Why?
|
| Recombinant Proteins | 5 | 2003 | 1014 | 0.180 |
Why?
|
| Repetitive Sequences, Nucleic Acid | 6 | 1998 | 135 | 0.170 |
Why?
|
| Nucleotides | 2 | 2011 | 95 | 0.170 |
Why?
|
| Protein Structure, Tertiary | 3 | 2008 | 736 | 0.170 |
Why?
|
| Restriction Mapping | 6 | 1995 | 157 | 0.160 |
Why?
|
| Mutagenesis, Site-Directed | 4 | 2002 | 279 | 0.150 |
Why?
|
| Molecular Weight | 8 | 1993 | 332 | 0.150 |
Why?
|
| RNA | 4 | 2008 | 560 | 0.130 |
Why?
|
| Genetic Complementation Test | 6 | 1995 | 97 | 0.130 |
Why?
|
| Amino Acid Motifs | 2 | 2006 | 116 | 0.130 |
Why?
|
| Electrophoresis, Polyacrylamide Gel | 5 | 2003 | 268 | 0.120 |
Why?
|
| Carbohydrate Epimerases | 1 | 1993 | 4 | 0.120 |
Why?
|
| Kinetics | 12 | 1989 | 1513 | 0.120 |
Why?
|
| DNA-Directed DNA Polymerase | 2 | 1995 | 25 | 0.120 |
Why?
|
| Crystallography, X-Ray | 3 | 2011 | 485 | 0.110 |
Why?
|
| Substrate Specificity | 6 | 2011 | 347 | 0.110 |
Why?
|
| Plasmids | 5 | 2001 | 287 | 0.110 |
Why?
|
| Gene Expression Regulation, Viral | 3 | 1997 | 90 | 0.100 |
Why?
|
| Recombinant Fusion Proteins | 2 | 2003 | 557 | 0.100 |
Why?
|
| Cross-Linking Reagents | 2 | 2003 | 86 | 0.090 |
Why?
|
| Membrane Proteins | 2 | 1993 | 1196 | 0.090 |
Why?
|
| Genes, Reporter | 2 | 2008 | 268 | 0.090 |
Why?
|
| Nucleic Acid Hybridization | 7 | 1990 | 245 | 0.090 |
Why?
|
| Down-Regulation | 1 | 2011 | 504 | 0.090 |
Why?
|
| DNA Primers | 2 | 2002 | 543 | 0.090 |
Why?
|
| Genes | 3 | 1983 | 305 | 0.080 |
Why?
|
| Edetic Acid | 3 | 2006 | 43 | 0.080 |
Why?
|
| Protein Structure, Quaternary | 1 | 2008 | 99 | 0.080 |
Why?
|
| Salts | 1 | 2007 | 16 | 0.080 |
Why?
|
| Transcription Factors | 1 | 1995 | 1565 | 0.070 |
Why?
|
| Salmonella typhi | 1 | 2006 | 7 | 0.070 |
Why?
|
| Hydrogen Bonding | 1 | 2007 | 144 | 0.070 |
Why?
|
| Tryptophan | 1 | 2007 | 90 | 0.070 |
Why?
|
| Exodeoxyribonucleases | 1 | 1986 | 14 | 0.070 |
Why?
|
| Genes, Regulator | 1 | 1986 | 65 | 0.070 |
Why?
|
| alpha-Fetoproteins | 1 | 1986 | 45 | 0.070 |
Why?
|
| Intracellular Membranes | 1 | 2006 | 117 | 0.070 |
Why?
|
| Open Reading Frames | 1 | 2006 | 117 | 0.070 |
Why?
|
| Enzyme Activation | 2 | 2008 | 692 | 0.070 |
Why?
|
| Oligodeoxyribonucleotides | 2 | 1997 | 126 | 0.070 |
Why?
|
| Guanine | 1 | 2007 | 208 | 0.070 |
Why?
|
| Glutamic Acid | 1 | 2006 | 152 | 0.070 |
Why?
|
| Phosphorylation | 1 | 2008 | 1106 | 0.070 |
Why?
|
| Protein Biosynthesis | 2 | 1981 | 378 | 0.070 |
Why?
|
| Microbiology | 1 | 2005 | 2 | 0.070 |
Why?
|
| Saccharomyces cerevisiae Proteins | 1 | 2008 | 276 | 0.070 |
Why?
|
| Bioterrorism | 1 | 2005 | 18 | 0.070 |
Why?
|
| Peptides | 1 | 2008 | 639 | 0.060 |
Why?
|
| Research Support as Topic | 1 | 2005 | 80 | 0.060 |
Why?
|
| Enhancer Elements, Genetic | 1 | 1986 | 266 | 0.060 |
Why?
|
| National Institutes of Health (U.S.) | 1 | 2005 | 122 | 0.060 |
Why?
|
| Sequence Deletion | 2 | 1995 | 205 | 0.060 |
Why?
|
| Adsorption | 2 | 1993 | 54 | 0.060 |
Why?
|
| Chromatography | 1 | 2003 | 28 | 0.060 |
Why?
|
| Chromatography, Affinity | 2 | 1996 | 81 | 0.060 |
Why?
|
| Glucosyltransferases | 3 | 1973 | 25 | 0.060 |
Why?
|
| Binding Sites | 3 | 2011 | 1098 | 0.060 |
Why?
|
| Dimerization | 1 | 2002 | 143 | 0.050 |
Why?
|
| Artificial Gene Fusion | 1 | 2001 | 4 | 0.050 |
Why?
|
| Gene Expression | 2 | 1985 | 1284 | 0.050 |
Why?
|
| Cyclic AMP | 4 | 1975 | 273 | 0.050 |
Why?
|
| Biomedical Research | 1 | 2005 | 375 | 0.050 |
Why?
|
| Protein Structure, Secondary | 2 | 2008 | 330 | 0.050 |
Why?
|
| Genome, Bacterial | 1 | 2001 | 139 | 0.050 |
Why?
|
| Mitochondria | 1 | 2003 | 535 | 0.040 |
Why?
|
| Galactosidases | 3 | 1975 | 14 | 0.040 |
Why?
|
| Magnesium | 3 | 1997 | 177 | 0.040 |
Why?
|
| Dose-Response Relationship, Drug | 1 | 2003 | 1961 | 0.040 |
Why?
|
| RNA, Messenger | 3 | 2011 | 1981 | 0.040 |
Why?
|
| Sequence Analysis, DNA | 1 | 2002 | 853 | 0.040 |
Why?
|
| DNA, Bacterial | 2 | 1996 | 236 | 0.040 |
Why?
|
| Genotype | 3 | 1993 | 1850 | 0.040 |
Why?
|
| Rifampin | 4 | 1981 | 22 | 0.040 |
Why?
|
| Potassium Permanganate | 1 | 1998 | 2 | 0.040 |
Why?
|
| Single-Strand Specific DNA and RNA Endonucleases | 1 | 1998 | 6 | 0.040 |
Why?
|
| Acetaldehyde | 1 | 1998 | 7 | 0.040 |
Why?
|
| Nucleic Acid Denaturation | 2 | 1989 | 34 | 0.040 |
Why?
|
| Base Composition | 1 | 1997 | 35 | 0.040 |
Why?
|
| Phylogeny | 1 | 2002 | 1137 | 0.040 |
Why?
|
| Conserved Sequence | 1 | 1998 | 210 | 0.040 |
Why?
|
| Molecular Biology | 3 | 1973 | 89 | 0.040 |
Why?
|
| Stress, Mechanical | 1 | 1998 | 248 | 0.040 |
Why?
|
| Glycogen | 3 | 1973 | 59 | 0.040 |
Why?
|
| Operon | 2 | 1973 | 48 | 0.040 |
Why?
|
| Uridine Triphosphate | 1 | 1996 | 5 | 0.040 |
Why?
|
| Radioisotope Dilution Technique | 1 | 1996 | 6 | 0.040 |
Why?
|
| Phosphorus Radioisotopes | 1 | 1996 | 19 | 0.040 |
Why?
|
| DNA Footprinting | 1 | 1996 | 18 | 0.030 |
Why?
|
| Deoxyribonuclease I | 1 | 1996 | 28 | 0.030 |
Why?
|
| Time Factors | 2 | 2003 | 5209 | 0.030 |
Why?
|
| Recombination, Genetic | 2 | 1995 | 439 | 0.030 |
Why?
|
| Affinity Labels | 2 | 1992 | 10 | 0.030 |
Why?
|
| Structure-Activity Relationship | 1 | 1995 | 408 | 0.030 |
Why?
|
| Hexosephosphates | 2 | 1971 | 3 | 0.030 |
Why?
|
| Gene Expression Regulation, Bacterial | 1 | 1996 | 204 | 0.030 |
Why?
|
| Saccharomyces | 2 | 1971 | 21 | 0.030 |
Why?
|
| Galactose | 1 | 1973 | 32 | 0.030 |
Why?
|
| Polymerase Chain Reaction | 1 | 1996 | 927 | 0.030 |
Why?
|
| Mutagenesis | 1 | 1993 | 199 | 0.030 |
Why?
|
| Amino Acids | 2 | 2011 | 252 | 0.030 |
Why?
|
| Chloramphenicol | 3 | 1979 | 18 | 0.030 |
Why?
|
| Enzyme Induction | 2 | 1988 | 88 | 0.030 |
Why?
|
| Models, Genetic | 1 | 1998 | 926 | 0.030 |
Why?
|
| RNA, Bacterial | 1 | 1972 | 108 | 0.030 |
Why?
|
| Electrophoresis, Agar Gel | 2 | 1981 | 49 | 0.030 |
Why?
|
| Guanosine Diphosphate | 1 | 2011 | 19 | 0.020 |
Why?
|
| DNA Restriction Enzymes | 2 | 1981 | 98 | 0.020 |
Why?
|
| Histidine | 1 | 1971 | 55 | 0.020 |
Why?
|
| Guanosine Triphosphate | 1 | 2011 | 38 | 0.020 |
Why?
|
| Salmonella typhimurium | 1 | 1971 | 32 | 0.020 |
Why?
|
| Species Specificity | 3 | 1988 | 678 | 0.020 |
Why?
|
| Biocatalysis | 1 | 2011 | 51 | 0.020 |
Why?
|
| Metals | 1 | 2011 | 90 | 0.020 |
Why?
|
| Defective Viruses | 1 | 1989 | 12 | 0.020 |
Why?
|
| Polydeoxyribonucleotides | 1 | 1989 | 5 | 0.020 |
Why?
|
| Chromatography, Ion Exchange | 1 | 1989 | 34 | 0.020 |
Why?
|
| Apoenzymes | 1 | 2008 | 7 | 0.020 |
Why?
|
| Transcription Initiation Site | 1 | 2008 | 45 | 0.020 |
Why?
|
| Base Pairing | 1 | 2008 | 55 | 0.020 |
Why?
|
| DNA Ligases | 1 | 1988 | 13 | 0.020 |
Why?
|
| Terminator Regions, Genetic | 1 | 1988 | 14 | 0.020 |
Why?
|
| Chromosome Mapping | 2 | 1988 | 1074 | 0.020 |
Why?
|
| Arginine | 1 | 2008 | 136 | 0.020 |
Why?
|
| Aminoglycosides | 2 | 1979 | 32 | 0.020 |
Why?
|
| Phosphotransferases | 3 | 1973 | 65 | 0.020 |
Why?
|
| Genetics, Microbial | 3 | 1973 | 15 | 0.020 |
Why?
|
| Cell Membrane | 3 | 1979 | 666 | 0.020 |
Why?
|
| Cryoelectron Microscopy | 1 | 2008 | 91 | 0.020 |
Why?
|
| Chromosome Deletion | 1 | 1988 | 229 | 0.020 |
Why?
|
| Regulatory Sequences, Nucleic Acid | 1 | 1988 | 148 | 0.020 |
Why?
|
| Temperature | 1 | 1988 | 396 | 0.020 |
Why?
|
| Exodeoxyribonuclease V | 1 | 1986 | 4 | 0.020 |
Why?
|
| DNA Polymerase I | 1 | 1986 | 9 | 0.020 |
Why?
|
| Protein Transport | 1 | 2008 | 411 | 0.020 |
Why?
|
| DNA Topoisomerases, Type II | 1 | 1986 | 20 | 0.020 |
Why?
|
| DNA Mutational Analysis | 1 | 1988 | 526 | 0.020 |
Why?
|
| Albumins | 1 | 1986 | 133 | 0.020 |
Why?
|
| Cell-Free System | 2 | 1979 | 51 | 0.020 |
Why?
|
| Alleles | 1 | 1989 | 1127 | 0.020 |
Why?
|
| Biological Warfare | 1 | 2005 | 6 | 0.020 |
Why?
|
| Financing, Government | 1 | 2005 | 23 | 0.020 |
Why?
|
| Peer Review, Research | 1 | 2005 | 36 | 0.020 |
Why?
|
| Glycerol | 3 | 1975 | 32 | 0.020 |
Why?
|
| Tritium | 2 | 1974 | 133 | 0.010 |
Why?
|
| Public Health | 1 | 2005 | 129 | 0.010 |
Why?
|
| Uridine | 2 | 1974 | 56 | 0.010 |
Why?
|
| Macromolecular Substances | 1 | 1983 | 177 | 0.010 |
Why?
|
| Anti-Bacterial Agents | 2 | 1979 | 746 | 0.010 |
Why?
|
| Humans | 3 | 2003 | 86601 | 0.010 |
Why?
|
| Nucleic Acid Heteroduplexes | 1 | 1981 | 11 | 0.010 |
Why?
|
| Photorhabdus | 1 | 2001 | 1 | 0.010 |
Why?
|
| Exonucleases | 1 | 1980 | 8 | 0.010 |
Why?
|
| Bacteriophage lambda | 1 | 1980 | 24 | 0.010 |
Why?
|
| Deoxyribonucleases | 1 | 1980 | 27 | 0.010 |
Why?
|
| Capsid | 1 | 1980 | 34 | 0.010 |
Why?
|
| Antimetabolites | 1 | 1980 | 24 | 0.010 |
Why?
|
| Binding, Competitive | 2 | 1977 | 145 | 0.010 |
Why?
|
| Transfection | 1 | 1981 | 896 | 0.010 |
Why?
|
| Deoxycholic Acid | 1 | 1979 | 10 | 0.010 |
Why?
|
| Adenosine Triphosphate | 2 | 1971 | 314 | 0.010 |
Why?
|
| Oligonucleotide Array Sequence Analysis | 1 | 2001 | 689 | 0.010 |
Why?
|
| Animals | 1 | 1998 | 26581 | 0.010 |
Why?
|
| Receptors, Drug | 1 | 1975 | 54 | 0.010 |
Why?
|
| Methods | 2 | 1975 | 152 | 0.010 |
Why?
|
| Blood Proteins | 1 | 1975 | 144 | 0.010 |
Why?
|
| Haploidy | 2 | 1973 | 31 | 0.010 |
Why?
|
| Autoradiography | 1 | 1974 | 69 | 0.010 |
Why?
|
| DNA Viruses | 1 | 1974 | 16 | 0.010 |
Why?
|
| Erythrocytes | 1 | 1975 | 255 | 0.010 |
Why?
|
| Carbon Isotopes | 1 | 1973 | 76 | 0.010 |
Why?
|
| Peptide Chain Termination, Translational | 1 | 1973 | 6 | 0.010 |
Why?
|
| Peptide Biosynthesis | 1 | 1973 | 17 | 0.010 |
Why?
|
| Peptide Chain Elongation, Translational | 1 | 1973 | 10 | 0.010 |
Why?
|
| Peptide Chain Initiation, Translational | 1 | 1973 | 18 | 0.010 |
Why?
|
| Lysogeny | 1 | 1972 | 11 | 0.010 |
Why?
|
| Peptide Initiation Factors | 1 | 1973 | 27 | 0.010 |
Why?
|
| Peptide Elongation Factors | 1 | 1973 | 28 | 0.010 |
Why?
|
| Glucosephosphate Dehydrogenase | 1 | 1972 | 18 | 0.010 |
Why?
|
| Ribosomes | 1 | 1973 | 111 | 0.010 |
Why?
|
| United States | 1 | 2005 | 6665 | 0.010 |
Why?
|
| Glucose | 2 | 1975 | 638 | 0.010 |
Why?
|
| Phosphoproteins | 1 | 1973 | 254 | 0.010 |
Why?
|
| Uracil Nucleotides | 1 | 1971 | 4 | 0.010 |
Why?
|
| Nucleoside Diphosphate Sugars | 1 | 1971 | 4 | 0.010 |
Why?
|
| Enzyme Repression | 1 | 1971 | 2 | 0.010 |
Why?
|
| Protoplasts | 1 | 1971 | 4 | 0.010 |
Why?
|
| Paper | 1 | 1971 | 10 | 0.010 |
Why?
|
| Mercaptoethanol | 1 | 1971 | 8 | 0.010 |
Why?
|
| Fluorides | 1 | 1971 | 13 | 0.010 |
Why?
|
| Spectrophotometry | 1 | 1971 | 106 | 0.010 |
Why?
|
| Drug Resistance, Microbial | 1 | 1971 | 72 | 0.010 |
Why?
|
| Aspartic Acid | 1 | 1971 | 64 | 0.010 |
Why?
|
| RNA, Transfer | 1 | 1973 | 151 | 0.010 |
Why?
|
| Culture Media | 1 | 1971 | 147 | 0.010 |
Why?
|
| Transduction, Genetic | 1 | 1971 | 153 | 0.010 |
Why?
|
| Microbial Sensitivity Tests | 1 | 1971 | 143 | 0.010 |
Why?
|
| Triazoles | 1 | 1971 | 96 | 0.010 |
Why?
|
| Hydrogen-Ion Concentration | 1 | 1971 | 493 | 0.010 |
Why?
|
| Catalysis | 1 | 1988 | 203 | 0.010 |
Why?
|
| Models, Theoretical | 1 | 1971 | 482 | 0.010 |
Why?
|
| Glucosephosphates | 2 | 1975 | 3 | 0.000 |
Why?
|
| Uridine Diphosphate Sugars | 1 | 1973 | 3 | 0.000 |
Why?
|
| Chromatography, DEAE-Cellulose | 1 | 1973 | 20 | 0.000 |
Why?
|
| Thiourea | 1 | 1973 | 8 | 0.000 |
Why?
|
| Dialysis | 1 | 1973 | 24 | 0.000 |
Why?
|
| Glycogen Synthase | 1 | 1973 | 22 | 0.000 |
Why?
|
| Quaternary Ammonium Compounds | 1 | 1973 | 79 | 0.000 |
Why?
|
| Allosteric Regulation | 1 | 1973 | 68 | 0.000 |
Why?
|
| Models, Chemical | 1 | 1973 | 178 | 0.000 |
Why?
|