Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
---|
DNA-Directed RNA Polymerases | 35 | 2015 | 104 | 3.950 |
Why?
|
Bacteriophage N4 | 15 | 2015 | 24 | 3.450 |
Why?
|
Escherichia coli | 36 | 2013 | 614 | 2.790 |
Why?
|
Virion | 14 | 2011 | 59 | 1.690 |
Why?
|
Coliphages | 27 | 1997 | 59 | 1.610 |
Why?
|
Transcription, Genetic | 29 | 2011 | 1163 | 1.490 |
Why?
|
Promoter Regions, Genetic | 19 | 2008 | 968 | 1.210 |
Why?
|
DNA, Viral | 18 | 2011 | 253 | 1.110 |
Why?
|
Viral Proteins | 13 | 2015 | 286 | 1.070 |
Why?
|
DNA-Binding Proteins | 11 | 2003 | 1247 | 1.000 |
Why?
|
Podoviridae | 7 | 1998 | 7 | 0.820 |
Why?
|
Sigma Factor | 4 | 2013 | 23 | 0.800 |
Why?
|
Escherichia coli Proteins | 4 | 2011 | 184 | 0.790 |
Why?
|
RNA Polymerase II | 6 | 2003 | 57 | 0.670 |
Why?
|
Nucleic Acid Conformation | 6 | 2008 | 346 | 0.630 |
Why?
|
Molecular Sequence Data | 20 | 2015 | 3017 | 0.620 |
Why?
|
Base Sequence | 21 | 2008 | 2317 | 0.510 |
Why?
|
DNA, Single-Stranded | 6 | 2003 | 93 | 0.490 |
Why?
|
Viral Structural Proteins | 2 | 2011 | 17 | 0.480 |
Why?
|
DNA Replication | 5 | 2011 | 173 | 0.480 |
Why?
|
Amino Acid Sequence | 11 | 2015 | 2074 | 0.460 |
Why?
|
DNA | 9 | 2008 | 1308 | 0.440 |
Why?
|
Bacterial Outer Membrane Proteins | 3 | 2008 | 55 | 0.430 |
Why?
|
Models, Molecular | 4 | 2013 | 1336 | 0.400 |
Why?
|
Bacteriophages | 2 | 2008 | 53 | 0.390 |
Why?
|
Genes, Viral | 6 | 1995 | 108 | 0.380 |
Why?
|
Protein Binding | 8 | 2015 | 1513 | 0.380 |
Why?
|
Protein Conformation | 2 | 2013 | 902 | 0.370 |
Why?
|
DNA, Superhelical | 5 | 1998 | 17 | 0.360 |
Why?
|
DNA Polymerase III | 1 | 2011 | 11 | 0.360 |
Why?
|
Templates, Genetic | 13 | 2007 | 33 | 0.340 |
Why?
|
Repressor Proteins | 1 | 2013 | 434 | 0.340 |
Why?
|
Receptors, Virus | 1 | 2008 | 75 | 0.300 |
Why?
|
Nucleic Acids | 1 | 2008 | 32 | 0.300 |
Why?
|
Viral Envelope Proteins | 1 | 2008 | 93 | 0.300 |
Why?
|
RNA, Viral | 8 | 1995 | 301 | 0.280 |
Why?
|
Catalytic Domain | 5 | 2015 | 159 | 0.280 |
Why?
|
Glycoproteins | 1 | 2008 | 234 | 0.280 |
Why?
|
Gene Expression Regulation | 4 | 2008 | 2004 | 0.270 |
Why?
|
N-Acetylmuramoyl-L-alanine Amidase | 1 | 2006 | 11 | 0.270 |
Why?
|
Glycoside Hydrolases | 1 | 2006 | 17 | 0.270 |
Why?
|
Transcriptional Activation | 3 | 2015 | 298 | 0.270 |
Why?
|
Genes, Bacterial | 3 | 1993 | 199 | 0.250 |
Why?
|
Gene Expression Regulation, Enzymologic | 1 | 2006 | 221 | 0.240 |
Why?
|
Saccharomyces cerevisiae | 2 | 2008 | 455 | 0.230 |
Why?
|
Bacteria | 2 | 2008 | 501 | 0.230 |
Why?
|
Cloning, Molecular | 7 | 2006 | 643 | 0.230 |
Why?
|
Sequence Homology, Amino Acid | 4 | 2006 | 420 | 0.210 |
Why?
|
Bacterial Proteins | 5 | 2008 | 907 | 0.210 |
Why?
|
Biochemistry | 1 | 2003 | 29 | 0.200 |
Why?
|
Virus Replication | 4 | 1995 | 323 | 0.190 |
Why?
|
Trans-Activators | 2 | 1996 | 443 | 0.180 |
Why?
|
Mutation | 12 | 2008 | 4204 | 0.170 |
Why?
|
Recombinant Proteins | 5 | 2003 | 1016 | 0.160 |
Why?
|
Repetitive Sequences, Nucleic Acid | 6 | 1998 | 135 | 0.160 |
Why?
|
Protein Structure, Tertiary | 3 | 2008 | 741 | 0.150 |
Why?
|
Nucleotides | 2 | 2011 | 98 | 0.150 |
Why?
|
Restriction Mapping | 6 | 1995 | 152 | 0.140 |
Why?
|
Mutagenesis, Site-Directed | 4 | 2002 | 281 | 0.140 |
Why?
|
Molecular Weight | 8 | 1993 | 332 | 0.130 |
Why?
|
RNA | 4 | 2008 | 589 | 0.120 |
Why?
|
Genetic Complementation Test | 6 | 1995 | 98 | 0.120 |
Why?
|
Amino Acid Motifs | 2 | 2006 | 119 | 0.120 |
Why?
|
Electrophoresis, Polyacrylamide Gel | 5 | 2003 | 268 | 0.110 |
Why?
|
Carbohydrate Epimerases | 1 | 1993 | 4 | 0.110 |
Why?
|
Kinetics | 12 | 1989 | 1550 | 0.110 |
Why?
|
DNA-Directed DNA Polymerase | 2 | 1995 | 24 | 0.110 |
Why?
|
Crystallography, X-Ray | 3 | 2011 | 507 | 0.100 |
Why?
|
Substrate Specificity | 6 | 2011 | 362 | 0.100 |
Why?
|
Plasmids | 5 | 2001 | 288 | 0.100 |
Why?
|
Gene Expression Regulation, Viral | 3 | 1997 | 91 | 0.090 |
Why?
|
Recombinant Fusion Proteins | 2 | 2003 | 559 | 0.090 |
Why?
|
Cross-Linking Reagents | 2 | 2003 | 89 | 0.090 |
Why?
|
Membrane Proteins | 2 | 1993 | 1240 | 0.080 |
Why?
|
Genes, Reporter | 2 | 2008 | 276 | 0.080 |
Why?
|
Nucleic Acid Hybridization | 7 | 1990 | 241 | 0.080 |
Why?
|
DNA Primers | 2 | 2002 | 542 | 0.080 |
Why?
|
Down-Regulation | 1 | 2011 | 523 | 0.080 |
Why?
|
Genes | 3 | 1983 | 307 | 0.080 |
Why?
|
Edetic Acid | 3 | 2006 | 42 | 0.070 |
Why?
|
Protein Structure, Quaternary | 1 | 2008 | 101 | 0.070 |
Why?
|
Salts | 1 | 2007 | 17 | 0.070 |
Why?
|
Salmonella typhi | 1 | 2006 | 7 | 0.070 |
Why?
|
Hydrogen Bonding | 1 | 2007 | 149 | 0.070 |
Why?
|
Transcription Factors | 1 | 1995 | 1684 | 0.070 |
Why?
|
Tryptophan | 1 | 2007 | 103 | 0.070 |
Why?
|
Exodeoxyribonucleases | 1 | 1986 | 17 | 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?
|
Enzyme Activation | 2 | 2008 | 698 | 0.070 |
Why?
|
Open Reading Frames | 1 | 2006 | 120 | 0.070 |
Why?
|
Oligodeoxyribonucleotides | 2 | 1997 | 125 | 0.060 |
Why?
|
Guanine | 1 | 2007 | 207 | 0.060 |
Why?
|
Glutamic Acid | 1 | 2006 | 155 | 0.060 |
Why?
|
Phosphorylation | 1 | 2008 | 1142 | 0.060 |
Why?
|
Protein Biosynthesis | 2 | 1981 | 383 | 0.060 |
Why?
|
Microbiology | 1 | 2005 | 2 | 0.060 |
Why?
|
Bioterrorism | 1 | 2005 | 18 | 0.060 |
Why?
|
Peptides | 1 | 2008 | 656 | 0.060 |
Why?
|
Saccharomyces cerevisiae Proteins | 1 | 2008 | 297 | 0.060 |
Why?
|
Research Support as Topic | 1 | 2005 | 87 | 0.060 |
Why?
|
Enhancer Elements, Genetic | 1 | 1986 | 289 | 0.060 |
Why?
|
National Institutes of Health (U.S.) | 1 | 2005 | 130 | 0.060 |
Why?
|
Sequence Deletion | 2 | 1995 | 211 | 0.050 |
Why?
|
Adsorption | 2 | 1993 | 54 | 0.050 |
Why?
|
Chromatography | 1 | 2003 | 28 | 0.050 |
Why?
|
Chromatography, Affinity | 2 | 1996 | 81 | 0.050 |
Why?
|
Binding Sites | 3 | 2011 | 1130 | 0.050 |
Why?
|
Glucosyltransferases | 3 | 1973 | 26 | 0.050 |
Why?
|
Dimerization | 1 | 2002 | 145 | 0.050 |
Why?
|
Gene Expression | 2 | 1985 | 1312 | 0.050 |
Why?
|
Artificial Gene Fusion | 1 | 2001 | 4 | 0.050 |
Why?
|
Cyclic AMP | 4 | 1975 | 280 | 0.040 |
Why?
|
Biomedical Research | 1 | 2005 | 404 | 0.040 |
Why?
|
Protein Structure, Secondary | 2 | 2008 | 333 | 0.040 |
Why?
|
Genome, Bacterial | 1 | 2001 | 152 | 0.040 |
Why?
|
Galactosidases | 3 | 1975 | 14 | 0.040 |
Why?
|
Magnesium | 3 | 1997 | 177 | 0.040 |
Why?
|
Mitochondria | 1 | 2003 | 599 | 0.040 |
Why?
|
Dose-Response Relationship, Drug | 1 | 2003 | 1939 | 0.040 |
Why?
|
Sequence Analysis, DNA | 1 | 2002 | 874 | 0.040 |
Why?
|
RNA, Messenger | 3 | 2011 | 2037 | 0.040 |
Why?
|
DNA, Bacterial | 2 | 1996 | 247 | 0.040 |
Why?
|
Genotype | 3 | 1993 | 1863 | 0.040 |
Why?
|
Rifampin | 4 | 1981 | 23 | 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 | 37 | 0.030 |
Why?
|
Conserved Sequence | 1 | 1998 | 211 | 0.030 |
Why?
|
Molecular Biology | 3 | 1973 | 90 | 0.030 |
Why?
|
Phylogeny | 1 | 2002 | 1228 | 0.030 |
Why?
|
Stress, Mechanical | 1 | 1998 | 256 | 0.030 |
Why?
|
Glycogen | 3 | 1973 | 60 | 0.030 |
Why?
|
Operon | 2 | 1973 | 50 | 0.030 |
Why?
|
Radioisotope Dilution Technique | 1 | 1996 | 6 | 0.030 |
Why?
|
Uridine Triphosphate | 1 | 1996 | 7 | 0.030 |
Why?
|
Phosphorus Radioisotopes | 1 | 1996 | 21 | 0.030 |
Why?
|
DNA Footprinting | 1 | 1996 | 18 | 0.030 |
Why?
|
Deoxyribonuclease I | 1 | 1996 | 28 | 0.030 |
Why?
|
Time Factors | 2 | 2003 | 5430 | 0.030 |
Why?
|
Recombination, Genetic | 2 | 1995 | 442 | 0.030 |
Why?
|
Affinity Labels | 2 | 1992 | 10 | 0.030 |
Why?
|
Structure-Activity Relationship | 1 | 1995 | 432 | 0.030 |
Why?
|
Hexosephosphates | 2 | 1971 | 3 | 0.030 |
Why?
|
Gene Expression Regulation, Bacterial | 1 | 1996 | 219 | 0.030 |
Why?
|
Saccharomyces | 2 | 1971 | 22 | 0.030 |
Why?
|
Polymerase Chain Reaction | 1 | 1996 | 923 | 0.030 |
Why?
|
Galactose | 1 | 1973 | 33 | 0.030 |
Why?
|
Mutagenesis | 1 | 1993 | 202 | 0.030 |
Why?
|
Amino Acids | 2 | 2011 | 255 | 0.030 |
Why?
|
Chloramphenicol | 3 | 1979 | 18 | 0.030 |
Why?
|
Enzyme Induction | 2 | 1988 | 88 | 0.030 |
Why?
|
Models, Genetic | 1 | 1998 | 967 | 0.020 |
Why?
|
RNA, Bacterial | 1 | 1972 | 111 | 0.020 |
Why?
|
Electrophoresis, Agar Gel | 2 | 1981 | 46 | 0.020 |
Why?
|
Guanosine Diphosphate | 1 | 2011 | 19 | 0.020 |
Why?
|
DNA Restriction Enzymes | 2 | 1981 | 97 | 0.020 |
Why?
|
Guanosine Triphosphate | 1 | 2011 | 38 | 0.020 |
Why?
|
Salmonella typhimurium | 1 | 1971 | 32 | 0.020 |
Why?
|
Species Specificity | 3 | 1988 | 692 | 0.020 |
Why?
|
Biocatalysis | 1 | 2011 | 52 | 0.020 |
Why?
|
Histidine | 1 | 1971 | 75 | 0.020 |
Why?
|
Metals | 1 | 2011 | 100 | 0.020 |
Why?
|
Defective Viruses | 1 | 1989 | 11 | 0.020 |
Why?
|
Polydeoxyribonucleotides | 1 | 1989 | 5 | 0.020 |
Why?
|
Chromatography, Ion Exchange | 1 | 1989 | 33 | 0.020 |
Why?
|
Apoenzymes | 1 | 2008 | 8 | 0.020 |
Why?
|
Transcription Initiation Site | 1 | 2008 | 46 | 0.020 |
Why?
|
Base Pairing | 1 | 2008 | 56 | 0.020 |
Why?
|
DNA Ligases | 1 | 1988 | 13 | 0.020 |
Why?
|
Chromosome Mapping | 2 | 1988 | 1076 | 0.020 |
Why?
|
Terminator Regions, Genetic | 1 | 1988 | 14 | 0.020 |
Why?
|
Arginine | 1 | 2008 | 140 | 0.020 |
Why?
|
Phosphotransferases | 3 | 1973 | 65 | 0.020 |
Why?
|
Aminoglycosides | 2 | 1979 | 33 | 0.020 |
Why?
|
Genetics, Microbial | 3 | 1973 | 15 | 0.020 |
Why?
|
Cell Membrane | 3 | 1979 | 684 | 0.020 |
Why?
|
Chromosome Deletion | 1 | 1988 | 230 | 0.020 |
Why?
|
Temperature | 1 | 1988 | 404 | 0.020 |
Why?
|
Cryoelectron Microscopy | 1 | 2008 | 105 | 0.020 |
Why?
|
Regulatory Sequences, Nucleic Acid | 1 | 1988 | 158 | 0.020 |
Why?
|
Exodeoxyribonuclease V | 1 | 1986 | 4 | 0.020 |
Why?
|
DNA Polymerase I | 1 | 1986 | 9 | 0.020 |
Why?
|
Protein Transport | 1 | 2008 | 430 | 0.020 |
Why?
|
DNA Topoisomerases, Type II | 1 | 1986 | 22 | 0.020 |
Why?
|
DNA Mutational Analysis | 1 | 1988 | 531 | 0.020 |
Why?
|
Albumins | 1 | 1986 | 134 | 0.020 |
Why?
|
Alleles | 1 | 1989 | 1141 | 0.020 |
Why?
|
Cell-Free System | 2 | 1979 | 51 | 0.020 |
Why?
|
Biological Warfare | 1 | 2005 | 6 | 0.020 |
Why?
|
Financing, Government | 1 | 2005 | 24 | 0.010 |
Why?
|
Peer Review, Research | 1 | 2005 | 37 | 0.010 |
Why?
|
Glycerol | 3 | 1975 | 35 | 0.010 |
Why?
|
Tritium | 2 | 1974 | 133 | 0.010 |
Why?
|
Public Health | 1 | 2005 | 145 | 0.010 |
Why?
|
Uridine | 2 | 1974 | 58 | 0.010 |
Why?
|
Macromolecular Substances | 1 | 1983 | 176 | 0.010 |
Why?
|
Anti-Bacterial Agents | 2 | 1979 | 810 | 0.010 |
Why?
|
Nucleic Acid Heteroduplexes | 1 | 1981 | 11 | 0.010 |
Why?
|
Humans | 3 | 2003 | 92337 | 0.010 |
Why?
|
Photorhabdus | 1 | 2001 | 1 | 0.010 |
Why?
|
Exonucleases | 1 | 1980 | 9 | 0.010 |
Why?
|
Bacteriophage lambda | 1 | 1980 | 23 | 0.010 |
Why?
|
Deoxyribonucleases | 1 | 1980 | 30 | 0.010 |
Why?
|
Capsid | 1 | 1980 | 25 | 0.010 |
Why?
|
Antimetabolites | 1 | 1980 | 24 | 0.010 |
Why?
|
Binding, Competitive | 2 | 1977 | 146 | 0.010 |
Why?
|
Transfection | 1 | 1981 | 901 | 0.010 |
Why?
|
Adenosine Triphosphate | 2 | 1971 | 319 | 0.010 |
Why?
|
Deoxycholic Acid | 1 | 1979 | 10 | 0.010 |
Why?
|
Oligonucleotide Array Sequence Analysis | 1 | 2001 | 698 | 0.010 |
Why?
|
Animals | 1 | 1998 | 28003 | 0.010 |
Why?
|
Receptors, Drug | 1 | 1975 | 54 | 0.010 |
Why?
|
Methods | 2 | 1975 | 149 | 0.010 |
Why?
|
Blood Proteins | 1 | 1975 | 149 | 0.010 |
Why?
|
Haploidy | 2 | 1973 | 32 | 0.010 |
Why?
|
Autoradiography | 1 | 1974 | 69 | 0.010 |
Why?
|
Erythrocytes | 1 | 1975 | 251 | 0.010 |
Why?
|
DNA Viruses | 1 | 1974 | 15 | 0.010 |
Why?
|
Carbon Isotopes | 1 | 1973 | 75 | 0.010 |
Why?
|
Peptide Chain Termination, Translational | 1 | 1973 | 6 | 0.010 |
Why?
|
Peptide Biosynthesis | 1 | 1973 | 18 | 0.010 |
Why?
|
Peptide Chain Elongation, Translational | 1 | 1973 | 10 | 0.010 |
Why?
|
Peptide Chain Initiation, Translational | 1 | 1973 | 17 | 0.010 |
Why?
|
Lysogeny | 1 | 1972 | 11 | 0.010 |
Why?
|
Peptide Elongation Factors | 1 | 1973 | 28 | 0.010 |
Why?
|
Glucosephosphate Dehydrogenase | 1 | 1972 | 18 | 0.010 |
Why?
|
Peptide Initiation Factors | 1 | 1973 | 30 | 0.010 |
Why?
|
Ribosomes | 1 | 1973 | 115 | 0.010 |
Why?
|
Glucose | 2 | 1975 | 684 | 0.010 |
Why?
|
United States | 1 | 2005 | 7348 | 0.010 |
Why?
|
Phosphoproteins | 1 | 1973 | 266 | 0.010 |
Why?
|
Enzyme Repression | 1 | 1971 | 2 | 0.010 |
Why?
|
Nucleoside Diphosphate Sugars | 1 | 1971 | 4 | 0.010 |
Why?
|
Uracil Nucleotides | 1 | 1971 | 5 | 0.010 |
Why?
|
Protoplasts | 1 | 1971 | 4 | 0.010 |
Why?
|
Mercaptoethanol | 1 | 1971 | 7 | 0.010 |
Why?
|
Paper | 1 | 1971 | 12 | 0.010 |
Why?
|
Fluorides | 1 | 1971 | 13 | 0.010 |
Why?
|
Spectrophotometry | 1 | 1971 | 108 | 0.010 |
Why?
|
Drug Resistance, Microbial | 1 | 1971 | 75 | 0.010 |
Why?
|
Aspartic Acid | 1 | 1971 | 64 | 0.010 |
Why?
|
Culture Media | 1 | 1971 | 149 | 0.010 |
Why?
|
RNA, Transfer | 1 | 1973 | 167 | 0.010 |
Why?
|
Transduction, Genetic | 1 | 1971 | 161 | 0.010 |
Why?
|
Microbial Sensitivity Tests | 1 | 1971 | 150 | 0.010 |
Why?
|
Triazoles | 1 | 1971 | 108 | 0.010 |
Why?
|
Hydrogen-Ion Concentration | 1 | 1971 | 501 | 0.010 |
Why?
|
Models, Theoretical | 1 | 1971 | 497 | 0.000 |
Why?
|
Catalysis | 1 | 1988 | 210 | 0.000 |
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?
|
Dialysis | 1 | 1973 | 24 | 0.000 |
Why?
|
Thiourea | 1 | 1973 | 10 | 0.000 |
Why?
|
Glycogen Synthase | 1 | 1973 | 22 | 0.000 |
Why?
|
Quaternary Ammonium Compounds | 1 | 1973 | 81 | 0.000 |
Why?
|
Allosteric Regulation | 1 | 1973 | 68 | 0.000 |
Why?
|
Models, Chemical | 1 | 1973 | 181 | 0.000 |
Why?
|