Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
---|
DNA Replication | 74 | 2016 | 167 | 9.230 |
Why?
|
DNA-Binding Proteins | 68 | 2016 | 700 | 6.740 |
Why?
|
Plasmids | 47 | 2009 | 258 | 4.270 |
Why?
|
DNA Helicases | 33 | 2016 | 64 | 4.160 |
Why?
|
Escherichia coli | 47 | 2009 | 368 | 3.610 |
Why?
|
Bacterial Proteins | 48 | 2014 | 245 | 3.440 |
Why?
|
Saccharomyces cerevisiae Proteins | 9 | 2016 | 123 | 3.000 |
Why?
|
Saccharomyces cerevisiae | 9 | 2016 | 173 | 2.780 |
Why?
|
DNA, Bacterial | 33 | 2014 | 150 | 2.630 |
Why?
|
Escherichia coli Proteins | 15 | 2009 | 65 | 2.380 |
Why?
|
Trans-Activators | 15 | 2009 | 237 | 1.940 |
Why?
|
DNA, Ribosomal | 8 | 2016 | 59 | 1.750 |
Why?
|
Schizosaccharomyces pombe Proteins | 7 | 2016 | 31 | 1.680 |
Why?
|
Schizosaccharomyces | 8 | 2016 | 31 | 1.680 |
Why?
|
Bacillus subtilis | 15 | 2009 | 49 | 1.590 |
Why?
|
Replication Origin | 6 | 2009 | 8 | 1.360 |
Why?
|
Base Sequence | 46 | 2014 | 1015 | 1.150 |
Why?
|
DNA, Fungal | 5 | 2016 | 20 | 1.120 |
Why?
|
Nucleic Acid Conformation | 20 | 2008 | 92 | 1.090 |
Why?
|
Recombination, Genetic | 4 | 2016 | 62 | 1.040 |
Why?
|
Transcription Factors | 6 | 2016 | 753 | 0.930 |
Why?
|
DNA | 14 | 2008 | 597 | 0.910 |
Why?
|
Cell Cycle Proteins | 6 | 2016 | 230 | 0.880 |
Why?
|
Molecular Sequence Data | 33 | 2015 | 1447 | 0.880 |
Why?
|
DnaB Helicases | 13 | 2009 | 14 | 0.850 |
Why?
|
Transcription, Genetic | 15 | 2010 | 562 | 0.750 |
Why?
|
Chromosomes, Fungal | 3 | 2016 | 14 | 0.740 |
Why?
|
Terminator Regions, Genetic | 8 | 2016 | 8 | 0.670 |
Why?
|
Protein Binding | 20 | 2016 | 1027 | 0.650 |
Why?
|
Binding Sites | 18 | 2008 | 631 | 0.590 |
Why?
|
Enhancer Elements, Genetic | 7 | 2003 | 63 | 0.590 |
Why?
|
Mutation | 18 | 2016 | 1213 | 0.550 |
Why?
|
Chromatids | 1 | 2016 | 8 | 0.550 |
Why?
|
Chromosomes, Bacterial | 3 | 2000 | 7 | 0.500 |
Why?
|
Protein Conformation | 9 | 2008 | 362 | 0.490 |
Why?
|
Repressor Proteins | 2 | 2005 | 183 | 0.450 |
Why?
|
Gene Silencing | 2 | 2014 | 137 | 0.450 |
Why?
|
Nucleic Acid Denaturation | 5 | 2009 | 16 | 0.450 |
Why?
|
Replicon | 9 | 1994 | 13 | 0.440 |
Why?
|
Models, Molecular | 10 | 2014 | 546 | 0.430 |
Why?
|
Genomic Instability | 2 | 2010 | 41 | 0.420 |
Why?
|
Genome, Fungal | 1 | 2010 | 6 | 0.380 |
Why?
|
F-Box Proteins | 1 | 2010 | 14 | 0.370 |
Why?
|
Mutagenesis, Site-Directed | 11 | 2003 | 204 | 0.370 |
Why?
|
DNA-Directed RNA Polymerases | 6 | 2001 | 16 | 0.360 |
Why?
|
Electrophoresis, Polyacrylamide Gel | 12 | 2004 | 272 | 0.350 |
Why?
|
Kinetics | 14 | 2004 | 1047 | 0.350 |
Why?
|
Dimerization | 6 | 2008 | 99 | 0.340 |
Why?
|
Cloning, Molecular | 9 | 2003 | 357 | 0.330 |
Why?
|
Amino Acid Sequence | 12 | 2015 | 1083 | 0.320 |
Why?
|
Phosphorylation | 3 | 2016 | 1200 | 0.320 |
Why?
|
Models, Genetic | 7 | 2006 | 161 | 0.310 |
Why?
|
HSP70 Heat-Shock Proteins | 2 | 2005 | 42 | 0.300 |
Why?
|
DNA Primase | 5 | 2009 | 6 | 0.300 |
Why?
|
Protein Structure, Tertiary | 6 | 2016 | 322 | 0.290 |
Why?
|
Transcription Termination, Genetic | 2 | 2016 | 2 | 0.260 |
Why?
|
Integration Host Factors | 6 | 2009 | 6 | 0.260 |
Why?
|
Genes, Regulator | 4 | 1990 | 17 | 0.250 |
Why?
|
Heat-Shock Proteins | 1 | 2004 | 69 | 0.240 |
Why?
|
F Factor | 1 | 2004 | 1 | 0.240 |
Why?
|
Bacteria | 2 | 2014 | 193 | 0.230 |
Why?
|
Autoradiography | 7 | 2006 | 94 | 0.230 |
Why?
|
Viral Proteins | 4 | 2003 | 150 | 0.230 |
Why?
|
Genes, Bacterial | 7 | 1992 | 40 | 0.230 |
Why?
|
Gene Expression Regulation, Bacterial | 2 | 1996 | 50 | 0.230 |
Why?
|
Regulatory Sequences, Nucleic Acid | 3 | 2010 | 43 | 0.230 |
Why?
|
Adenosine Triphosphatases | 3 | 2004 | 83 | 0.230 |
Why?
|
Silent Information Regulator Proteins, Saccharomyces cerevisiae | 2 | 2016 | 7 | 0.230 |
Why?
|
Sirtuin 2 | 2 | 2016 | 7 | 0.230 |
Why?
|
RNA | 4 | 2006 | 171 | 0.230 |
Why?
|
RNA, Bacterial | 2 | 1996 | 30 | 0.210 |
Why?
|
Electrophoresis, Gel, Two-Dimensional | 4 | 2006 | 50 | 0.200 |
Why?
|
Amino Acid Substitution | 2 | 2014 | 137 | 0.190 |
Why?
|
Genetic Complementation Test | 3 | 2009 | 36 | 0.190 |
Why?
|
Crystallography, X-Ray | 7 | 2016 | 190 | 0.180 |
Why?
|
Substrate Specificity | 4 | 2008 | 234 | 0.180 |
Why?
|
Restriction Mapping | 7 | 1994 | 85 | 0.170 |
Why?
|
Nuclear Proteins | 2 | 2016 | 271 | 0.170 |
Why?
|
Point Mutation | 3 | 2008 | 97 | 0.170 |
Why?
|
R Factors | 4 | 1999 | 8 | 0.170 |
Why?
|
Macromolecular Substances | 3 | 2006 | 122 | 0.170 |
Why?
|
DNA, Superhelical | 3 | 1988 | 8 | 0.170 |
Why?
|
Papillomaviridae | 3 | 1990 | 104 | 0.160 |
Why?
|
Multiprotein Complexes | 2 | 2010 | 56 | 0.160 |
Why?
|
S Phase | 2 | 2010 | 38 | 0.160 |
Why?
|
Genes | 4 | 1987 | 86 | 0.160 |
Why?
|
DNA Primers | 3 | 2004 | 302 | 0.160 |
Why?
|
Codon, Terminator | 1 | 1998 | 6 | 0.160 |
Why?
|
Sequence Alignment | 2 | 2008 | 165 | 0.150 |
Why?
|
RNA Nucleotidyltransferases | 1 | 1996 | 2 | 0.140 |
Why?
|
DNA Restriction Enzymes | 10 | 1987 | 49 | 0.140 |
Why?
|
Oryza | 1 | 2016 | 12 | 0.130 |
Why?
|
Dose-Response Relationship, Drug | 3 | 2004 | 1745 | 0.130 |
Why?
|
Telomerase | 2 | 2006 | 85 | 0.130 |
Why?
|
Open Reading Frames | 3 | 2003 | 25 | 0.130 |
Why?
|
Gene Expression Regulation, Fungal | 1 | 2015 | 32 | 0.130 |
Why?
|
Intracellular Signaling Peptides and Proteins | 1 | 2016 | 216 | 0.120 |
Why?
|
Cross-Linking Reagents | 4 | 2001 | 80 | 0.120 |
Why?
|
Genetic Variation | 1 | 2016 | 220 | 0.120 |
Why?
|
Down-Regulation | 1 | 2016 | 447 | 0.120 |
Why?
|
Microscopy, Electron | 6 | 1992 | 351 | 0.120 |
Why?
|
tau Proteins | 1 | 1994 | 61 | 0.120 |
Why?
|
Exodeoxyribonucleases | 2 | 2010 | 8 | 0.110 |
Why?
|
Bacteriocin Plasmids | 3 | 1994 | 3 | 0.110 |
Why?
|
DNA, Recombinant | 4 | 1986 | 25 | 0.110 |
Why?
|
DNA, Circular | 3 | 1988 | 5 | 0.110 |
Why?
|
Enzyme-Linked Immunosorbent Assay | 2 | 2004 | 507 | 0.110 |
Why?
|
Proteins | 2 | 1999 | 474 | 0.110 |
Why?
|
In Vitro Techniques | 2 | 2004 | 765 | 0.100 |
Why?
|
beta-Galactosidase | 4 | 1985 | 88 | 0.100 |
Why?
|
Peptide Initiation Factors | 1 | 1991 | 11 | 0.100 |
Why?
|
Repetitive Sequences, Nucleic Acid | 3 | 1987 | 37 | 0.100 |
Why?
|
Structure-Activity Relationship | 4 | 2006 | 420 | 0.100 |
Why?
|
Antigens, Polyomavirus Transforming | 1 | 1991 | 15 | 0.100 |
Why?
|
Simian virus 40 | 1 | 1991 | 24 | 0.100 |
Why?
|
Retroelements | 1 | 2010 | 4 | 0.090 |
Why?
|
Lipoproteins | 1 | 1992 | 161 | 0.090 |
Why?
|
Bovine papillomavirus 1 | 2 | 1988 | 3 | 0.090 |
Why?
|
Carrier Proteins | 2 | 1992 | 597 | 0.090 |
Why?
|
DNA, Intergenic | 1 | 2010 | 8 | 0.090 |
Why?
|
RNA Polymerase II | 1 | 2010 | 14 | 0.090 |
Why?
|
Oncogene Proteins | 1 | 2010 | 35 | 0.090 |
Why?
|
Oncogene Proteins, Viral | 1 | 1990 | 21 | 0.090 |
Why?
|
Dideoxynucleotides | 2 | 2004 | 3 | 0.080 |
Why?
|
Thymine Nucleotides | 2 | 2004 | 6 | 0.080 |
Why?
|
Protein Multimerization | 1 | 2009 | 71 | 0.080 |
Why?
|
Cytosine | 1 | 2008 | 12 | 0.080 |
Why?
|
Mutant Proteins | 1 | 2008 | 45 | 0.080 |
Why?
|
Tryptophan | 1 | 2008 | 65 | 0.080 |
Why?
|
Deoxyribonuclease I | 4 | 1994 | 16 | 0.080 |
Why?
|
DNA Fingerprinting | 3 | 1992 | 11 | 0.070 |
Why?
|
Protein Transport | 1 | 2008 | 280 | 0.070 |
Why?
|
Protein Folding | 2 | 1998 | 82 | 0.070 |
Why?
|
Protein Structure, Secondary | 2 | 1999 | 136 | 0.070 |
Why?
|
Genes, Viral | 1 | 1987 | 44 | 0.070 |
Why?
|
Oligonucleotide Probes | 3 | 1991 | 35 | 0.070 |
Why?
|
Edetic Acid | 2 | 1996 | 29 | 0.070 |
Why?
|
Oligonucleotides | 2 | 2003 | 34 | 0.070 |
Why?
|
Protein Subunits | 1 | 2006 | 99 | 0.070 |
Why?
|
DNA, Ribosomal Spacer | 1 | 2005 | 1 | 0.070 |
Why?
|
Chromatin Immunoprecipitation | 1 | 2006 | 52 | 0.070 |
Why?
|
Genes, Fungal | 1 | 2005 | 24 | 0.070 |
Why?
|
Oligodeoxyribonucleotides | 3 | 1994 | 35 | 0.070 |
Why?
|
Protein Biosynthesis | 2 | 1996 | 181 | 0.070 |
Why?
|
Protein Interaction Mapping | 1 | 2006 | 62 | 0.070 |
Why?
|
Immunoprecipitation | 1 | 2006 | 132 | 0.070 |
Why?
|
Time Factors | 2 | 2004 | 4655 | 0.060 |
Why?
|
Circular Dichroism | 2 | 2003 | 99 | 0.060 |
Why?
|
Galactosidases | 1 | 1985 | 2 | 0.060 |
Why?
|
Endopeptidase Clp | 1 | 2004 | 4 | 0.060 |
Why?
|
ATPases Associated with Diverse Cellular Activities | 1 | 2004 | 14 | 0.060 |
Why?
|
HSP40 Heat-Shock Proteins | 1 | 2004 | 8 | 0.060 |
Why?
|
Genes, Switch | 1 | 2004 | 1 | 0.060 |
Why?
|
Genetic Engineering | 1 | 1984 | 41 | 0.060 |
Why?
|
Chromatin | 1 | 2004 | 76 | 0.060 |
Why?
|
Animals | 2 | 2014 | 20881 | 0.060 |
Why?
|
Sodium Dodecyl Sulfate | 1 | 2004 | 24 | 0.060 |
Why?
|
Molecular Chaperones | 1 | 2004 | 81 | 0.060 |
Why?
|
Cell Nucleolus | 1 | 2003 | 14 | 0.060 |
Why?
|
Catalysis | 1 | 2004 | 123 | 0.060 |
Why?
|
Methylation | 3 | 1991 | 56 | 0.060 |
Why?
|
Ribonuclease H | 1 | 2003 | 1 | 0.060 |
Why?
|
Origin Recognition Complex | 1 | 2003 | 5 | 0.060 |
Why?
|
Hydroxyurea | 1 | 2004 | 57 | 0.060 |
Why?
|
Gene Deletion | 1 | 2004 | 235 | 0.060 |
Why?
|
Recombinant Proteins | 2 | 1996 | 742 | 0.060 |
Why?
|
Adenosine Triphosphate | 1 | 2004 | 314 | 0.050 |
Why?
|
Genotype | 2 | 2016 | 786 | 0.050 |
Why?
|
DNA, Single-Stranded | 2 | 1998 | 41 | 0.050 |
Why?
|
Electrophoresis, Agar Gel | 2 | 1992 | 32 | 0.050 |
Why?
|
Chromatography, Affinity | 1 | 2001 | 73 | 0.050 |
Why?
|
Collagen | 1 | 1984 | 636 | 0.050 |
Why?
|
Azides | 1 | 2001 | 56 | 0.050 |
Why?
|
Molecular Weight | 2 | 1993 | 358 | 0.050 |
Why?
|
Operon | 3 | 1985 | 7 | 0.050 |
Why?
|
Gene Expression | 2 | 1996 | 770 | 0.050 |
Why?
|
Tyrosine | 1 | 2001 | 196 | 0.050 |
Why?
|
Models, Biological | 1 | 2004 | 981 | 0.040 |
Why?
|
Colicins | 1 | 1979 | 1 | 0.040 |
Why?
|
Alkylation | 2 | 1990 | 26 | 0.040 |
Why?
|
Pyridines | 1 | 2001 | 261 | 0.040 |
Why?
|
Mutagenesis | 1 | 1998 | 60 | 0.040 |
Why?
|
Crystallization | 2 | 2015 | 57 | 0.040 |
Why?
|
Species Specificity | 2 | 1994 | 303 | 0.040 |
Why?
|
Prokaryotic Cells | 1 | 1997 | 2 | 0.040 |
Why?
|
Promoter Regions, Genetic | 2 | 1991 | 615 | 0.040 |
Why?
|
Deoxyribonucleoproteins | 1 | 1996 | 2 | 0.040 |
Why?
|
Deoxyribonuclease HindIII | 2 | 1989 | 4 | 0.030 |
Why?
|
Chromosome Mapping | 2 | 1992 | 188 | 0.030 |
Why?
|
Phenanthrolines | 1 | 1996 | 5 | 0.030 |
Why?
|
Acetophenones | 1 | 1996 | 12 | 0.030 |
Why?
|
Photochemistry | 1 | 1996 | 46 | 0.030 |
Why?
|
Ferrous Compounds | 1 | 1996 | 18 | 0.030 |
Why?
|
Computer Graphics | 1 | 1996 | 37 | 0.030 |
Why?
|
RNA Polymerase I | 1 | 2016 | 5 | 0.030 |
Why?
|
Azo Compounds | 1 | 1996 | 33 | 0.030 |
Why?
|
Random Amplified Polymorphic DNA Technique | 1 | 2016 | 1 | 0.030 |
Why?
|
DNA, Plant | 1 | 2016 | 7 | 0.030 |
Why?
|
Gene Expression Regulation, Plant | 1 | 2016 | 19 | 0.030 |
Why?
|
Breeding | 1 | 2016 | 15 | 0.030 |
Why?
|
Hybridization, Genetic | 1 | 2016 | 9 | 0.030 |
Why?
|
Replication Protein A | 1 | 1995 | 9 | 0.030 |
Why?
|
Coliphages | 1 | 1975 | 6 | 0.030 |
Why?
|
Ultraviolet Rays | 1 | 1996 | 130 | 0.030 |
Why?
|
Genetic Markers | 1 | 2016 | 144 | 0.030 |
Why?
|
Biological Transport | 1 | 1995 | 210 | 0.030 |
Why?
|
Genetic Vectors | 2 | 1987 | 312 | 0.030 |
Why?
|
Glutathione Transferase | 1 | 1996 | 166 | 0.030 |
Why?
|
Nucleic Acid Heteroduplexes | 1 | 1995 | 7 | 0.030 |
Why?
|
Molecular Structure | 1 | 1996 | 397 | 0.030 |
Why?
|
Phylogeny | 1 | 2016 | 197 | 0.030 |
Why?
|
Genomics | 1 | 2016 | 168 | 0.030 |
Why?
|
Stereoisomerism | 1 | 1995 | 169 | 0.030 |
Why?
|
Recombinant Fusion Proteins | 1 | 1996 | 376 | 0.030 |
Why?
|
Consensus Sequence | 1 | 1994 | 20 | 0.030 |
Why?
|
Leucine Zippers | 1 | 1994 | 10 | 0.030 |
Why?
|
Iron | 1 | 1996 | 197 | 0.030 |
Why?
|
Endodeoxyribonucleases | 2 | 1983 | 8 | 0.030 |
Why?
|
Peptide Fragments | 1 | 1996 | 483 | 0.030 |
Why?
|
Staphylococcus aureus | 1 | 1994 | 175 | 0.030 |
Why?
|
Hydroxides | 1 | 1991 | 5 | 0.020 |
Why?
|
Novobiocin | 1 | 1991 | 6 | 0.020 |
Why?
|
DNA Topoisomerases, Type II | 1 | 1991 | 13 | 0.020 |
Why?
|
Hydroxyl Radical | 1 | 1991 | 17 | 0.020 |
Why?
|
Chloroplasts | 1 | 1971 | 3 | 0.020 |
Why?
|
Chlorophyta | 1 | 1971 | 5 | 0.020 |
Why?
|
Rifampin | 1 | 1991 | 45 | 0.020 |
Why?
|
Cytoplasm | 1 | 1991 | 155 | 0.020 |
Why?
|
HeLa Cells | 1 | 1991 | 237 | 0.020 |
Why?
|
Templates, Genetic | 1 | 1990 | 9 | 0.020 |
Why?
|
Humans | 2 | 2014 | 68618 | 0.020 |
Why?
|
Gene Library | 1 | 1989 | 68 | 0.020 |
Why?
|
Deoxyribonuclease EcoRI | 1 | 1989 | 6 | 0.020 |
Why?
|
Deoxyribonucleases, Type II Site-Specific | 1 | 1989 | 8 | 0.020 |
Why?
|
Bromodeoxyuridine | 1 | 1989 | 37 | 0.020 |
Why?
|
DNA Probes | 1 | 1989 | 57 | 0.020 |
Why?
|
DNA Ligases | 1 | 1988 | 6 | 0.020 |
Why?
|
Sulfuric Acid Esters | 1 | 1988 | 7 | 0.020 |
Why?
|
Molecular Conformation | 1 | 1988 | 128 | 0.020 |
Why?
|
Transformation, Bacterial | 1 | 1987 | 2 | 0.020 |
Why?
|
RNA, Antisense | 1 | 1987 | 25 | 0.020 |
Why?
|
Allosteric Regulation | 1 | 1988 | 58 | 0.020 |
Why?
|
Nucleic Acid Hybridization | 1 | 1987 | 95 | 0.020 |
Why?
|
Sequence Homology, Nucleic Acid | 1 | 1987 | 95 | 0.020 |
Why?
|
Phenotype | 1 | 1991 | 947 | 0.020 |
Why?
|
Immunoassay | 1 | 1987 | 64 | 0.020 |
Why?
|
Cyclization | 1 | 1987 | 14 | 0.020 |
Why?
|
RNA, Messenger | 1 | 1991 | 1664 | 0.020 |
Why?
|
Distamycins | 1 | 1985 | 1 | 0.020 |
Why?
|
DNA Topoisomerases, Type I | 1 | 1985 | 13 | 0.020 |
Why?
|
T-Phages | 1 | 1985 | 4 | 0.020 |
Why?
|
Bacteriophage lambda | 1 | 1984 | 7 | 0.020 |
Why?
|
Centrifugation, Density Gradient | 2 | 1975 | 36 | 0.010 |
Why?
|
Homeostasis | 1 | 1985 | 291 | 0.010 |
Why?
|
Purines | 1 | 1983 | 39 | 0.010 |
Why?
|
Base Composition | 1 | 1982 | 22 | 0.010 |
Why?
|
Cell-Free System | 1 | 1981 | 43 | 0.010 |
Why?
|
Bacteriophages | 1 | 1981 | 24 | 0.010 |
Why?
|
Cell Membrane | 1 | 1981 | 525 | 0.010 |
Why?
|
Gene Expression Regulation | 1 | 1985 | 1293 | 0.010 |
Why?
|
Ribonucleotides | 1 | 1978 | 26 | 0.010 |
Why?
|
Ribonuclease T1 | 1 | 1977 | 1 | 0.010 |
Why?
|
Oligoribonucleotides | 1 | 1977 | 2 | 0.010 |
Why?
|
Virus Replication | 1 | 1975 | 104 | 0.010 |
Why?
|
X-Ray Diffraction | 1 | 1992 | 53 | 0.010 |
Why?
|
Nucleic Acid Renaturation | 1 | 1971 | 6 | 0.010 |
Why?
|
Densitometry | 1 | 1971 | 15 | 0.010 |
Why?
|
Spectrophotometry | 1 | 1971 | 54 | 0.010 |
Why?
|
Chromatography | 1 | 1971 | 47 | 0.010 |
Why?
|
Magnetic Resonance Spectroscopy | 1 | 1992 | 346 | 0.010 |
Why?
|
Hot Temperature | 1 | 1971 | 152 | 0.010 |
Why?
|
Temperature | 1 | 1971 | 341 | 0.010 |
Why?
|