Name | Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
---|
Bacteriophage T7 | 112 | 2022 | 174 | 24.140 |
Why?
|
DNA-Directed DNA Polymerase | 93 | 2020 | 486 | 11.880 |
Why?
|
DNA Primase | 67 | 2022 | 109 | 11.100 |
Why?
|
Viral Proteins | 90 | 2022 | 1900 | 8.160 |
Why?
|
DNA Replication | 90 | 2020 | 1399 | 6.900 |
Why?
|
DNA, Viral | 106 | 2020 | 2225 | 6.590 |
Why?
|
DNA Helicases | 50 | 2022 | 859 | 6.110 |
Why?
|
Thioredoxins | 29 | 2020 | 213 | 4.790 |
Why?
|
Escherichia coli | 129 | 2020 | 4217 | 4.050 |
Why?
|
T-Phages | 58 | 1993 | 90 | 4.000 |
Why?
|
DNA, Single-Stranded | 51 | 2017 | 354 | 3.260 |
Why?
|
Thymine Nucleotides | 23 | 2014 | 63 | 2.810 |
Why?
|
RNA Nucleotidyltransferases | 22 | 1997 | 64 | 2.470 |
Why?
|
Escherichia coli Proteins | 16 | 2020 | 1050 | 2.380 |
Why?
|
DNA-Directed RNA Polymerases | 18 | 2015 | 371 | 2.210 |
Why?
|
DNA | 51 | 2022 | 7301 | 2.060 |
Why?
|
DNA-Binding Proteins | 32 | 2018 | 9648 | 1.840 |
Why?
|
Genes, Viral | 39 | 2008 | 718 | 1.770 |
Why?
|
DNA Primers | 25 | 2017 | 2892 | 1.710 |
Why?
|
Multienzyme Complexes | 7 | 2017 | 686 | 1.680 |
Why?
|
Templates, Genetic | 38 | 2012 | 211 | 1.320 |
Why?
|
Models, Molecular | 34 | 2016 | 5456 | 1.300 |
Why?
|
Virus Replication | 21 | 2012 | 2534 | 1.280 |
Why?
|
Kinetics | 62 | 2017 | 6473 | 1.250 |
Why?
|
Bacteriophages | 4 | 2017 | 356 | 1.200 |
Why?
|
Protein Structure, Tertiary | 23 | 2012 | 3846 | 1.170 |
Why?
|
Ribonucleotides | 13 | 2012 | 117 | 1.070 |
Why?
|
Base Sequence | 77 | 2013 | 12797 | 1.060 |
Why?
|
Nucleotides | 25 | 2013 | 464 | 1.050 |
Why?
|
Coliphages | 50 | 1978 | 120 | 1.040 |
Why?
|
Binding Sites | 39 | 2015 | 6114 | 0.970 |
Why?
|
Molecular Sequence Data | 69 | 2012 | 18111 | 0.960 |
Why?
|
Deoxyribonucleotides | 11 | 2015 | 42 | 0.930 |
Why?
|
Zinc | 9 | 2012 | 684 | 0.910 |
Why?
|
Hydrolysis | 26 | 2011 | 682 | 0.900 |
Why?
|
Surface Plasmon Resonance | 10 | 2018 | 274 | 0.830 |
Why?
|
Protein Structure, Secondary | 12 | 2018 | 1246 | 0.810 |
Why?
|
Amino Acid Sequence | 45 | 2022 | 13815 | 0.800 |
Why?
|
Protein Binding | 34 | 2014 | 9386 | 0.780 |
Why?
|
Oligoribonucleotides | 16 | 2012 | 51 | 0.740 |
Why?
|
Protein Conformation | 26 | 2015 | 4011 | 0.710 |
Why?
|
Substrate Specificity | 18 | 2012 | 1801 | 0.650 |
Why?
|
Manganese | 8 | 2015 | 408 | 0.650 |
Why?
|
Exonucleases | 13 | 2004 | 47 | 0.620 |
Why?
|
Crystallography, X-Ray | 15 | 2016 | 2011 | 0.620 |
Why?
|
Amino Acid Substitution | 11 | 2012 | 1791 | 0.610 |
Why?
|
Genetic Complementation Test | 17 | 2012 | 562 | 0.610 |
Why?
|
Nucleic Acid Synthesis Inhibitors | 4 | 2014 | 112 | 0.600 |
Why?
|
Oligodeoxyribonucleotides | 16 | 2004 | 708 | 0.580 |
Why?
|
Biochemistry | 2 | 2015 | 113 | 0.570 |
Why?
|
Dideoxynucleotides | 3 | 2014 | 13 | 0.560 |
Why?
|
Plasmids | 20 | 2012 | 2307 | 0.560 |
Why?
|
RNA | 6 | 2015 | 2749 | 0.520 |
Why?
|
Genes | 26 | 1990 | 1893 | 0.520 |
Why?
|
Phosphoric Monoester Hydrolases | 12 | 1993 | 431 | 0.510 |
Why?
|
Macromolecular Substances | 10 | 2013 | 1454 | 0.490 |
Why?
|
Flap Endonucleases | 1 | 2014 | 19 | 0.480 |
Why?
|
Nucleic Acid Conformation | 16 | 2015 | 913 | 0.470 |
Why?
|
Magnesium | 16 | 2012 | 813 | 0.460 |
Why?
|
HIV Reverse Transcriptase | 3 | 1999 | 213 | 0.460 |
Why?
|
Phenylalanine | 4 | 2009 | 365 | 0.450 |
Why?
|
RNA, Transfer | 3 | 2013 | 316 | 0.450 |
Why?
|
Synechococcus | 1 | 2012 | 28 | 0.450 |
Why?
|
Tryptophan | 2 | 2012 | 478 | 0.440 |
Why?
|
Insect Viruses | 6 | 1992 | 15 | 0.440 |
Why?
|
Recombination, Genetic | 13 | 2000 | 1586 | 0.430 |
Why?
|
Aquatic Organisms | 1 | 2012 | 48 | 0.430 |
Why?
|
Catalysis | 9 | 2013 | 761 | 0.420 |
Why?
|
Protein Subunits | 4 | 2008 | 959 | 0.410 |
Why?
|
Fimbriae Proteins | 1 | 2012 | 134 | 0.410 |
Why?
|
DNA Nucleotidyltransferases | 20 | 1976 | 193 | 0.410 |
Why?
|
Recombinant Proteins | 19 | 2015 | 6622 | 0.400 |
Why?
|
Diphosphates | 2 | 2011 | 88 | 0.400 |
Why?
|
DNA Breaks, Single-Stranded | 1 | 2011 | 23 | 0.400 |
Why?
|
Bacteriophage M13 | 3 | 2007 | 39 | 0.390 |
Why?
|
Deoxyribonucleases | 26 | 1977 | 214 | 0.380 |
Why?
|
Microscopy, Electron | 17 | 2012 | 2645 | 0.370 |
Why?
|
DNA Polymerase I | 3 | 1997 | 38 | 0.370 |
Why?
|
Suppression, Genetic | 3 | 2009 | 196 | 0.360 |
Why?
|
Phosphotransferases (Alcohol Group Acceptor) | 1 | 2012 | 437 | 0.360 |
Why?
|
Mutagenesis, Site-Directed | 11 | 2006 | 1723 | 0.350 |
Why?
|
Gene Expression Regulation, Viral | 6 | 2012 | 442 | 0.350 |
Why?
|
Mutation | 48 | 2022 | 29786 | 0.340 |
Why?
|
RNA, Viral | 15 | 1997 | 2902 | 0.340 |
Why?
|
Structure-Activity Relationship | 13 | 2010 | 3129 | 0.340 |
Why?
|
Protein Multimerization | 3 | 2012 | 970 | 0.330 |
Why?
|
Oligonucleotides | 8 | 2004 | 572 | 0.330 |
Why?
|
Protein Structure, Quaternary | 5 | 2009 | 436 | 0.330 |
Why?
|
Deoxyribonuclease I | 1 | 2009 | 229 | 0.330 |
Why?
|
Molecular Weight | 24 | 2000 | 2255 | 0.320 |
Why?
|
RNA-Directed DNA Polymerase | 3 | 1998 | 248 | 0.320 |
Why?
|
Uridine Kinase | 1 | 2007 | 6 | 0.320 |
Why?
|
Electrophoresis, Polyacrylamide Gel | 11 | 2012 | 1801 | 0.320 |
Why?
|
Cloning, Molecular | 18 | 2008 | 4320 | 0.320 |
Why?
|
Escherichia coli K12 | 1 | 2007 | 34 | 0.310 |
Why?
|
Cytidine Triphosphate | 5 | 2010 | 17 | 0.310 |
Why?
|
Arginine | 3 | 2009 | 944 | 0.300 |
Why?
|
Models, Biological | 9 | 2016 | 9583 | 0.300 |
Why?
|
Acids | 1 | 2008 | 127 | 0.300 |
Why?
|
Transcription, Genetic | 11 | 2015 | 7722 | 0.300 |
Why?
|
Mutagenesis | 7 | 2012 | 1266 | 0.290 |
Why?
|
Adenosine Triphosphate | 19 | 2012 | 2025 | 0.290 |
Why?
|
DNA Damage | 4 | 2000 | 2432 | 0.290 |
Why?
|
DNA, Bacterial | 20 | 2015 | 1465 | 0.280 |
Why?
|
Amino Acid Motifs | 3 | 2008 | 936 | 0.280 |
Why?
|
Catalytic Domain | 6 | 2016 | 698 | 0.270 |
Why?
|
Measles virus | 6 | 1994 | 68 | 0.270 |
Why?
|
Recombinant Fusion Proteins | 11 | 2006 | 3772 | 0.270 |
Why?
|
Amino Acids, Acidic | 1 | 2005 | 3 | 0.270 |
Why?
|
Viral Fusion Proteins | 6 | 1994 | 95 | 0.270 |
Why?
|
Thymidine Kinase | 4 | 2014 | 290 | 0.260 |
Why?
|
Glutamic Acid | 1 | 2011 | 1169 | 0.260 |
Why?
|
Exodeoxyribonucleases | 6 | 2003 | 180 | 0.260 |
Why?
|
Siphoviridae | 1 | 2004 | 7 | 0.260 |
Why?
|
Sequence Deletion | 5 | 2014 | 1526 | 0.250 |
Why?
|
Salmonella Phages | 2 | 2004 | 11 | 0.250 |
Why?
|
Lysine | 3 | 2010 | 1007 | 0.240 |
Why?
|
Hydrophobic and Hydrophilic Interactions | 2 | 2018 | 407 | 0.240 |
Why?
|
Sequence Homology, Amino Acid | 8 | 2010 | 2839 | 0.240 |
Why?
|
DNA Repair | 7 | 2000 | 2046 | 0.230 |
Why?
|
Genome, Bacterial | 2 | 2015 | 760 | 0.220 |
Why?
|
Poxviridae | 3 | 1992 | 37 | 0.220 |
Why?
|
Viral Structural Proteins | 5 | 2002 | 103 | 0.220 |
Why?
|
DNA, Circular | 4 | 1998 | 97 | 0.220 |
Why?
|
Histidine | 4 | 2009 | 313 | 0.220 |
Why?
|
Thymidine | 4 | 2014 | 310 | 0.210 |
Why?
|
Scattering, Small Angle | 2 | 2013 | 59 | 0.200 |
Why?
|
Promoter Regions, Genetic | 10 | 2012 | 5867 | 0.200 |
Why?
|
Enzyme Stability | 2 | 2013 | 210 | 0.200 |
Why?
|
Bacteriophage T4 | 4 | 2009 | 33 | 0.200 |
Why?
|
Ligases | 14 | 1971 | 333 | 0.200 |
Why?
|
Chromatography, Gel | 11 | 2003 | 668 | 0.200 |
Why?
|
Models, Genetic | 9 | 2010 | 3494 | 0.190 |
Why?
|
Chromatography | 15 | 2002 | 206 | 0.190 |
Why?
|
Mutant Proteins | 4 | 2015 | 500 | 0.190 |
Why?
|
Deoxyguanine Nucleotides | 6 | 2010 | 21 | 0.190 |
Why?
|
X-Ray Diffraction | 2 | 2013 | 420 | 0.190 |
Why?
|
Osmolar Concentration | 5 | 2010 | 683 | 0.180 |
Why?
|
Biocatalysis | 2 | 2012 | 167 | 0.180 |
Why?
|
Dimerization | 4 | 2003 | 893 | 0.180 |
Why?
|
Cysteine | 3 | 2009 | 874 | 0.180 |
Why?
|
Molecular Conformation | 3 | 2010 | 563 | 0.180 |
Why?
|
Bacterial Proteins | 12 | 1998 | 3848 | 0.170 |
Why?
|
Transcription Factors, General | 1 | 1999 | 11 | 0.170 |
Why?
|
Cytosine | 4 | 2012 | 216 | 0.170 |
Why?
|
Chromosomes | 2 | 2000 | 596 | 0.170 |
Why?
|
Hot Temperature | 7 | 2001 | 1354 | 0.170 |
Why?
|
Salmonella typhimurium | 2 | 2004 | 351 | 0.170 |
Why?
|
Deoxyribonucleases, Type II Site-Specific | 1 | 1999 | 170 | 0.160 |
Why?
|
Transcriptional Elongation Factors | 1 | 1999 | 166 | 0.160 |
Why?
|
Translocation, Genetic | 2 | 2000 | 1420 | 0.150 |
Why?
|
Pyrimidine Dimers | 1 | 1997 | 18 | 0.150 |
Why?
|
Nucleic Acid Heteroduplexes | 1 | 1997 | 47 | 0.150 |
Why?
|
Podoviridae | 2 | 2015 | 5 | 0.150 |
Why?
|
Phosphorus Isotopes | 19 | 1971 | 126 | 0.140 |
Why?
|
Polynucleotides | 16 | 1975 | 35 | 0.140 |
Why?
|
Bacteriophage lambda | 5 | 2010 | 147 | 0.140 |
Why?
|
Zidovudine | 1 | 1998 | 620 | 0.140 |
Why?
|
Chromatography, Affinity | 5 | 2005 | 549 | 0.140 |
Why?
|
Restriction Mapping | 6 | 1994 | 878 | 0.130 |
Why?
|
Tyrosine-tRNA Ligase | 1 | 2015 | 10 | 0.130 |
Why?
|
Gene Expression Regulation, Bacterial | 2 | 1993 | 1122 | 0.130 |
Why?
|
Fluorescence Polarization | 2 | 2012 | 132 | 0.130 |
Why?
|
Bacteriophage T3 | 1 | 1994 | 2 | 0.130 |
Why?
|
Fluorine | 1 | 2015 | 83 | 0.130 |
Why?
|
Gene Expression Regulation, Enzymologic | 2 | 1998 | 1213 | 0.130 |
Why?
|
Bacillus subtilis | 4 | 2015 | 359 | 0.130 |
Why?
|
Salts | 2 | 2012 | 65 | 0.130 |
Why?
|
Gene Deletion | 3 | 2015 | 2751 | 0.130 |
Why?
|
Dideoxynucleosides | 1 | 1995 | 122 | 0.130 |
Why?
|
Adenosine Triphosphatases | 2 | 2013 | 839 | 0.130 |
Why?
|
Pyrimidine Phosphorylases | 1 | 2014 | 2 | 0.130 |
Why?
|
Centrifugation, Density Gradient | 19 | 1985 | 313 | 0.130 |
Why?
|
Transcription Initiation Site | 1 | 2015 | 196 | 0.120 |
Why?
|
Metalloproteins | 1 | 1994 | 100 | 0.120 |
Why?
|
Ultracentrifugation | 3 | 2012 | 182 | 0.120 |
Why?
|
Hemagglutinins, Viral | 2 | 1991 | 67 | 0.120 |
Why?
|
Cyanobacteria | 1 | 2013 | 49 | 0.120 |
Why?
|
Eukaryotic Initiation Factor-4A | 1 | 2013 | 20 | 0.120 |
Why?
|
Growth Inhibitors | 1 | 2015 | 385 | 0.120 |
Why?
|
Cryoelectron Microscopy | 1 | 2017 | 571 | 0.120 |
Why?
|
Isoenzymes | 3 | 2000 | 1726 | 0.120 |
Why?
|
Nuclear Magnetic Resonance, Biomolecular | 3 | 2016 | 507 | 0.120 |
Why?
|
Proteins | 3 | 2004 | 6103 | 0.120 |
Why?
|
Guanosine Triphosphate | 4 | 2009 | 321 | 0.110 |
Why?
|
Tritium | 18 | 1975 | 745 | 0.110 |
Why?
|
Sequence Alignment | 6 | 2001 | 2256 | 0.110 |
Why?
|
Retirement | 1 | 2015 | 215 | 0.110 |
Why?
|
Genetic Vectors | 5 | 1992 | 3420 | 0.110 |
Why?
|
RNA Stability | 1 | 2015 | 321 | 0.110 |
Why?
|
Endonucleases | 4 | 2012 | 380 | 0.110 |
Why?
|
Hydrogen-Ion Concentration | 8 | 2012 | 2557 | 0.110 |
Why?
|
Static Electricity | 2 | 2010 | 267 | 0.110 |
Why?
|
Coenzymes | 1 | 2012 | 91 | 0.110 |
Why?
|
Genes, Suppressor | 2 | 2007 | 48 | 0.110 |
Why?
|
Binding, Competitive | 3 | 2008 | 1157 | 0.110 |
Why?
|
Chromatography, DEAE-Cellulose | 12 | 1992 | 87 | 0.110 |
Why?
|
Genes, Bacterial | 3 | 1993 | 1079 | 0.110 |
Why?
|
Drug Resistance | 1 | 1998 | 1609 | 0.100 |
Why?
|
Cell Line | 12 | 2000 | 15997 | 0.100 |
Why?
|
Vanadates | 1 | 2011 | 82 | 0.100 |
Why?
|
Polymerase Chain Reaction | 6 | 2000 | 6171 | 0.100 |
Why?
|
X-Rays | 1 | 2012 | 301 | 0.100 |
Why?
|
Crystallization | 2 | 2003 | 524 | 0.100 |
Why?
|
Temperature | 10 | 2012 | 2206 | 0.100 |
Why?
|
Monosaccharide Transport Proteins | 1 | 1993 | 440 | 0.100 |
Why?
|
Gene Knockout Techniques | 1 | 2014 | 809 | 0.100 |
Why?
|
Small Molecule Libraries | 1 | 2016 | 720 | 0.100 |
Why?
|
Diffusion | 1 | 2013 | 833 | 0.100 |
Why?
|
Nucleoside-Phosphate Kinase | 1 | 2010 | 23 | 0.090 |
Why?
|
Scattering, Radiation | 1 | 2012 | 498 | 0.090 |
Why?
|
Chemical Phenomena | 12 | 1997 | 518 | 0.090 |
Why?
|
Allosteric Site | 1 | 2010 | 103 | 0.090 |
Why?
|
Galactosidases | 1 | 1990 | 56 | 0.090 |
Why?
|
Metals | 3 | 2012 | 719 | 0.090 |
Why?
|
Bacterial Outer Membrane Proteins | 1 | 1993 | 404 | 0.090 |
Why?
|
Membrane Fusion | 3 | 1994 | 273 | 0.090 |
Why?
|
Genetics, Microbial | 10 | 1972 | 60 | 0.090 |
Why?
|
Chromatography, Ion Exchange | 9 | 1989 | 305 | 0.090 |
Why?
|
Mammals | 3 | 2000 | 1143 | 0.090 |
Why?
|
Alanine | 1 | 2012 | 572 | 0.090 |
Why?
|
Amino Acids | 2 | 2015 | 1736 | 0.090 |
Why?
|
beta-Galactosidase | 2 | 1991 | 573 | 0.090 |
Why?
|
ATP-Binding Cassette Transporters | 1 | 1993 | 560 | 0.090 |
Why?
|
X-Ray Absorption Spectroscopy | 1 | 2009 | 5 | 0.090 |
Why?
|
Peptide Fragments | 5 | 2008 | 5097 | 0.090 |
Why?
|
History, 20th Century | 2 | 2015 | 2740 | 0.090 |
Why?
|
Time Factors | 12 | 2014 | 40075 | 0.090 |
Why?
|
Phosphates | 3 | 1990 | 786 | 0.080 |
Why?
|
Treponema pallidum | 1 | 1989 | 40 | 0.080 |
Why?
|
Zinc Compounds | 1 | 2009 | 35 | 0.080 |
Why?
|
Operon | 3 | 1985 | 363 | 0.080 |
Why?
|
Sequence Analysis, DNA | 4 | 2015 | 4803 | 0.080 |
Why?
|
Allosteric Regulation | 1 | 2010 | 408 | 0.080 |
Why?
|
Electrophoresis, Agar Gel | 4 | 1997 | 212 | 0.080 |
Why?
|
History, 21st Century | 1 | 2015 | 1534 | 0.080 |
Why?
|
Schools, Medical | 1 | 2015 | 880 | 0.080 |
Why?
|
Nucleotide Mapping | 1 | 1987 | 20 | 0.080 |
Why?
|
Tyrosine | 1 | 2012 | 1461 | 0.080 |
Why?
|
Multiprotein Complexes | 1 | 2014 | 1119 | 0.080 |
Why?
|
Repressor Proteins | 2 | 2009 | 3023 | 0.070 |
Why?
|
RNA, Messenger | 8 | 1993 | 13033 | 0.070 |
Why?
|
Rifampin | 2 | 2007 | 315 | 0.070 |
Why?
|
HIV-1 | 2 | 1998 | 6939 | 0.070 |
Why?
|
Dose-Response Relationship, Drug | 3 | 2004 | 10943 | 0.070 |
Why?
|
Cell Physiological Phenomena | 1 | 2007 | 154 | 0.070 |
Why?
|
Protein Folding | 1 | 2010 | 843 | 0.070 |
Why?
|
Solvents | 1 | 2007 | 302 | 0.070 |
Why?
|
Chlorides | 1 | 2009 | 667 | 0.070 |
Why?
|
Enzyme Inhibitors | 1 | 2016 | 3798 | 0.070 |
Why?
|
Thermodynamics | 2 | 2004 | 596 | 0.070 |
Why?
|
GTP-Binding Proteins | 1 | 1990 | 970 | 0.070 |
Why?
|
Sulfinic Acids | 1 | 2005 | 13 | 0.070 |
Why?
|
Alkaline Phosphatase | 10 | 1975 | 865 | 0.060 |
Why?
|
Phosphorylation | 2 | 2014 | 8436 | 0.060 |
Why?
|
Base Composition | 2 | 2003 | 293 | 0.060 |
Why?
|
2-Acetylaminofluorene | 1 | 2004 | 10 | 0.060 |
Why?
|
Pyrophosphatases | 2 | 1999 | 137 | 0.060 |
Why?
|
Ligands | 2 | 2009 | 3282 | 0.060 |
Why?
|
Zinc Fingers | 2 | 1999 | 585 | 0.060 |
Why?
|
Magnesium Chloride | 2 | 1999 | 32 | 0.060 |
Why?
|
Cross-Linking Reagents | 2 | 1998 | 694 | 0.060 |
Why?
|
Viral Tail Proteins | 1 | 2004 | 4 | 0.060 |
Why?
|
Oligonucleotide Probes | 5 | 1991 | 427 | 0.060 |
Why?
|
Sequence Homology, Nucleic Acid | 3 | 2004 | 1085 | 0.060 |
Why?
|
Fluorenes | 1 | 2004 | 160 | 0.060 |
Why?
|
Drug Resistance, Viral | 1 | 2008 | 820 | 0.060 |
Why?
|
Antigens, Bacterial | 1 | 1989 | 1171 | 0.060 |
Why?
|
Nucleotidyltransferases | 6 | 1969 | 220 | 0.050 |
Why?
|
Virulence | 1 | 2006 | 1333 | 0.050 |
Why?
|
Vaccinia virus | 4 | 1994 | 349 | 0.050 |
Why?
|
Lepidoptera | 2 | 1992 | 23 | 0.050 |
Why?
|
Thiazolidinediones | 1 | 2005 | 476 | 0.050 |
Why?
|
Ribosomes | 3 | 1991 | 500 | 0.050 |
Why?
|
Membrane Proteins | 3 | 1994 | 7880 | 0.050 |
Why?
|
Adenine Nucleotides | 6 | 1971 | 121 | 0.050 |
Why?
|
Mutation, Missense | 1 | 2011 | 2564 | 0.050 |
Why?
|
Gene Expression Regulation | 4 | 2004 | 12072 | 0.050 |
Why?
|
Thymine | 2 | 1999 | 68 | 0.050 |
Why?
|
Toluene | 2 | 1971 | 32 | 0.050 |
Why?
|
HIV | 1 | 1989 | 1604 | 0.050 |
Why?
|
Genes, Essential | 1 | 2002 | 183 | 0.050 |
Why?
|
Chemistry | 10 | 1973 | 352 | 0.050 |
Why?
|
Point Mutation | 3 | 1996 | 1623 | 0.050 |
Why?
|
Exodeoxyribonuclease V | 1 | 2000 | 9 | 0.050 |
Why?
|
Phosphotransferases | 8 | 1972 | 308 | 0.050 |
Why?
|
Hydroxyapatites | 3 | 1989 | 75 | 0.050 |
Why?
|
Disulfides | 1 | 2003 | 457 | 0.050 |
Why?
|
Introns | 1 | 2004 | 991 | 0.050 |
Why?
|
Phosphorus Radioisotopes | 6 | 1975 | 104 | 0.050 |
Why?
|
Kanamycin Kinase | 1 | 2000 | 34 | 0.050 |
Why?
|
Chromosome Mapping | 8 | 1981 | 4740 | 0.050 |
Why?
|
Ribosomal Protein S6 Kinases | 1 | 2000 | 205 | 0.050 |
Why?
|
Protein Transport | 1 | 2006 | 1988 | 0.050 |
Why?
|
DNA Restriction Enzymes | 4 | 1987 | 570 | 0.050 |
Why?
|
Gene Conversion | 1 | 2000 | 71 | 0.050 |
Why?
|
Chemistry, Physical | 2 | 1997 | 156 | 0.040 |
Why?
|
Transduction, Genetic | 4 | 1977 | 913 | 0.040 |
Why?
|
Enzyme Activation | 2 | 2013 | 3701 | 0.040 |
Why?
|
Blotting, Southern | 1 | 2000 | 803 | 0.040 |
Why?
|
Databases, Genetic | 1 | 2006 | 1783 | 0.040 |
Why?
|
Protein Engineering | 1 | 2003 | 540 | 0.040 |
Why?
|
Enzyme Induction | 5 | 1971 | 475 | 0.040 |
Why?
|
Research | 6 | 1964 | 1999 | 0.040 |
Why?
|
Threonine | 1 | 1999 | 279 | 0.040 |
Why?
|
Biopolymers | 1 | 1999 | 189 | 0.040 |
Why?
|
Host-Pathogen Interactions | 1 | 2007 | 1477 | 0.040 |
Why?
|
Genes, Regulator | 5 | 2004 | 378 | 0.040 |
Why?
|
Molecular Structure | 1 | 2003 | 1899 | 0.040 |
Why?
|
Nucleic Acid Denaturation | 7 | 1974 | 111 | 0.040 |
Why?
|
Animals | 19 | 2000 | 168757 | 0.040 |
Why?
|
Metformin | 1 | 2005 | 835 | 0.040 |
Why?
|
DNA Polymerase III | 1 | 1998 | 55 | 0.040 |
Why?
|
Durapatite | 2 | 1989 | 161 | 0.040 |
Why?
|
Sulfhydryl Compounds | 4 | 1992 | 298 | 0.040 |
Why?
|
Exons | 1 | 2004 | 2437 | 0.040 |
Why?
|
Oxidation-Reduction | 3 | 2008 | 2187 | 0.040 |
Why?
|
Cytidine Monophosphate | 1 | 1997 | 19 | 0.040 |
Why?
|
Electrophoresis | 5 | 1971 | 240 | 0.040 |
Why?
|
Models, Structural | 1 | 1997 | 361 | 0.040 |
Why?
|
Stem Cells | 2 | 2000 | 3567 | 0.040 |
Why?
|
Guanosine | 1 | 1997 | 61 | 0.040 |
Why?
|
Giant Cells | 2 | 1994 | 187 | 0.040 |
Why?
|
Glycosylation | 4 | 1994 | 1126 | 0.040 |
Why?
|
Uridine Monophosphate | 1 | 1997 | 70 | 0.040 |
Why?
|
DNA Mutational Analysis | 3 | 1997 | 4186 | 0.040 |
Why?
|
Nucleic Acid Hybridization | 2 | 1989 | 1375 | 0.030 |
Why?
|
Cell Fusion | 3 | 1994 | 297 | 0.030 |
Why?
|
Conserved Sequence | 1 | 1999 | 1202 | 0.030 |
Why?
|
Adenosine Diphosphate | 1 | 1997 | 425 | 0.030 |
Why?
|
Thermus | 1 | 1995 | 11 | 0.030 |
Why?
|
Deoxycytosine Nucleotides | 2 | 1998 | 14 | 0.030 |
Why?
|
Time-Lapse Imaging | 1 | 2016 | 195 | 0.030 |
Why?
|
Protein Processing, Post-Translational | 3 | 1994 | 1990 | 0.030 |
Why?
|
DNA Ligases | 2 | 2010 | 80 | 0.030 |
Why?
|
Papain | 2 | 1990 | 64 | 0.030 |
Why?
|
Cell-Free System | 4 | 1979 | 344 | 0.030 |
Why?
|
Adenosine Monophosphate | 1 | 1997 | 275 | 0.030 |
Why?
|
Species Specificity | 3 | 1992 | 2478 | 0.030 |
Why?
|
Reverse Transcriptase Inhibitors | 1 | 1998 | 615 | 0.030 |
Why?
|
Hemolysis | 3 | 1994 | 420 | 0.030 |
Why?
|
In Situ Hybridization, Fluorescence | 1 | 2000 | 2649 | 0.030 |
Why?
|
Nucleotidases | 2 | 1964 | 31 | 0.030 |
Why?
|
Cations, Divalent | 2 | 1990 | 166 | 0.030 |
Why?
|
Carbon Isotopes | 4 | 1971 | 467 | 0.030 |
Why?
|
Magnetic Resonance Spectroscopy | 2 | 2004 | 3760 | 0.030 |
Why?
|
Proteome | 1 | 2004 | 1799 | 0.030 |
Why?
|
Surface Properties | 1 | 1997 | 1184 | 0.030 |
Why?
|
Circular Dichroism | 1 | 1994 | 354 | 0.030 |
Why?
|
Maltose-Binding Proteins | 1 | 1993 | 62 | 0.030 |
Why?
|
Hypoglycemic Agents | 1 | 2005 | 2872 | 0.030 |
Why?
|
Peptidoglycan | 1 | 2015 | 246 | 0.030 |
Why?
|
Isoelectric Focusing | 1 | 1992 | 181 | 0.030 |
Why?
|
Protein Biosynthesis | 4 | 1990 | 2126 | 0.030 |
Why?
|
Nitroso Compounds | 1 | 1972 | 72 | 0.030 |
Why?
|
Ethylmaleimide | 4 | 1975 | 76 | 0.030 |
Why?
|
Chromosomes, Bacterial | 3 | 1981 | 282 | 0.030 |
Why?
|
Inclusion Bodies, Viral | 1 | 1992 | 45 | 0.030 |
Why?
|
Leucine Zippers | 1 | 1992 | 117 | 0.030 |
Why?
|
Distemper | 1 | 1991 | 4 | 0.030 |
Why?
|
Chemical Precipitation | 1 | 1991 | 179 | 0.030 |
Why?
|
Drug Stability | 4 | 1974 | 291 | 0.030 |
Why?
|
Cell Wall | 1 | 2015 | 422 | 0.030 |
Why?
|
Ultraviolet Rays | 5 | 1977 | 1060 | 0.030 |
Why?
|
Polyethyleneimine | 1 | 1991 | 63 | 0.030 |
Why?
|
Guanidines | 1 | 1972 | 193 | 0.030 |
Why?
|
Fluorescence | 1 | 2014 | 751 | 0.020 |
Why?
|
Software | 2 | 1999 | 4443 | 0.020 |
Why?
|
RNA, Bacterial | 1 | 1993 | 390 | 0.020 |
Why?
|
Codon | 2 | 1990 | 611 | 0.020 |
Why?
|
Solubility | 2 | 1988 | 1085 | 0.020 |
Why?
|
Genome, Viral | 1 | 1994 | 667 | 0.020 |
Why?
|
Phosphatidylinositol 3-Kinases | 1 | 2000 | 2938 | 0.020 |
Why?
|
Deoxyadenine Nucleotides | 1 | 1990 | 12 | 0.020 |
Why?
|
Lysogeny | 3 | 1977 | 67 | 0.020 |
Why?
|
Polynucleotide 5'-Hydroxyl-Kinase | 1 | 2010 | 8 | 0.020 |
Why?
|
Autoanalysis | 1 | 1990 | 72 | 0.020 |
Why?
|
Ribonucleases | 2 | 1975 | 287 | 0.020 |
Why?
|
Digoxigenin | 1 | 2010 | 26 | 0.020 |
Why?
|
Transfection | 1 | 1999 | 5892 | 0.020 |
Why?
|
Insulin | 1 | 2005 | 6580 | 0.020 |
Why?
|
Peptide Termination Factors | 1 | 1990 | 55 | 0.020 |
Why?
|
Facilitated Diffusion | 1 | 2010 | 1 | 0.020 |
Why?
|
Enzyme Precursors | 1 | 1990 | 176 | 0.020 |
Why?
|
DNA Viruses | 3 | 1974 | 36 | 0.020 |
Why?
|
Hemagglutination Tests | 1 | 1990 | 75 | 0.020 |
Why?
|
DNA, Recombinant | 3 | 1987 | 476 | 0.020 |
Why?
|
Solutions | 1 | 2011 | 426 | 0.020 |
Why?
|
Diptera | 1 | 1990 | 53 | 0.020 |
Why?
|
Spectrometry, Fluorescence | 1 | 1992 | 689 | 0.020 |
Why?
|
Proteolipids | 1 | 1990 | 117 | 0.020 |
Why?
|
Streptomycin | 3 | 1975 | 69 | 0.020 |
Why?
|
Viral Core Proteins | 1 | 1990 | 162 | 0.020 |
Why?
|
Peptide Chain Elongation, Translational | 1 | 1989 | 33 | 0.020 |
Why?
|
Pulmonary Surfactants | 1 | 1990 | 162 | 0.020 |
Why?
|
Protein Sorting Signals | 1 | 1990 | 281 | 0.020 |
Why?
|
Humans | 13 | 2018 | 744343 | 0.020 |
Why?
|
Nucleoside-Triphosphatase | 1 | 1988 | 19 | 0.020 |
Why?
|
Saccharomyces cerevisiae Proteins | 1 | 1999 | 1888 | 0.020 |
Why?
|
Biotin | 1 | 2010 | 254 | 0.020 |
Why?
|
Poly A | 1 | 1989 | 185 | 0.020 |
Why?
|
Half-Life | 1 | 1990 | 661 | 0.020 |
Why?
|
Edetic Acid | 2 | 1983 | 276 | 0.020 |
Why?
|
Frameshift Mutation | 1 | 1990 | 399 | 0.020 |
Why?
|
Radiation Effects | 3 | 1972 | 68 | 0.020 |
Why?
|
Adenoviruses, Human | 1 | 1990 | 257 | 0.020 |
Why?
|
Dithiothreitol | 1 | 1987 | 101 | 0.020 |
Why?
|
Carbohydrates | 1 | 1990 | 394 | 0.020 |
Why?
|
Inhibitory Concentration 50 | 1 | 2008 | 459 | 0.020 |
Why?
|
Centrifugation, Zonal | 3 | 1974 | 14 | 0.020 |
Why?
|
Drug Resistance, Bacterial | 1 | 2015 | 1035 | 0.020 |
Why?
|
Paramyxoviridae | 1 | 1986 | 9 | 0.020 |
Why?
|
Free Radicals | 1 | 1987 | 237 | 0.020 |
Why?
|
Peptide Library | 1 | 2008 | 349 | 0.020 |
Why?
|
United States | 1 | 2015 | 69872 | 0.020 |
Why?
|
Peptide Hydrolases | 2 | 1987 | 634 | 0.020 |
Why?
|
Parainfluenza Virus 1, Human | 1 | 1986 | 28 | 0.020 |
Why?
|
Electrons | 2 | 1964 | 268 | 0.020 |
Why?
|
Neurospora | 1 | 1965 | 7 | 0.020 |
Why?
|
Protein Interaction Domains and Motifs | 1 | 2008 | 474 | 0.020 |
Why?
|
Polysaccharides | 1 | 1972 | 1053 | 0.020 |
Why?
|
Protein Precursors | 1 | 1990 | 1154 | 0.020 |
Why?
|
Viral Vaccines | 1 | 1991 | 636 | 0.020 |
Why?
|
Peptide Chain Initiation, Translational | 1 | 1986 | 103 | 0.020 |
Why?
|
Sodium Dodecyl Sulfate | 2 | 1975 | 131 | 0.020 |
Why?
|
Cellulose | 3 | 1972 | 121 | 0.020 |
Why?
|
Blotting, Western | 2 | 1990 | 5179 | 0.020 |
Why?
|
Single-Strand Specific DNA and RNA Endonucleases | 1 | 1983 | 31 | 0.010 |
Why?
|
Sulfonylurea Compounds | 1 | 2005 | 204 | 0.010 |
Why?
|
Computer Simulation | 1 | 1997 | 6196 | 0.010 |
Why?
|
Nucleosides | 1 | 1964 | 138 | 0.010 |
Why?
|
Mice | 2 | 2000 | 81183 | 0.010 |
Why?
|
Gene Expression | 2 | 1994 | 7799 | 0.010 |
Why?
|
Hydrogen Bonding | 1 | 2003 | 293 | 0.010 |
Why?
|
Carrier Proteins | 2 | 1993 | 5021 | 0.010 |
Why?
|
Depression, Chemical | 2 | 1974 | 191 | 0.010 |
Why?
|
Nucleic Acids | 1 | 1965 | 182 | 0.010 |
Why?
|
Drosophila | 1 | 1990 | 1491 | 0.010 |
Why?
|
Metabolism | 1 | 1964 | 196 | 0.010 |
Why?
|
Rabbits | 1 | 1989 | 4894 | 0.010 |
Why?
|
Cytosine Nucleotides | 2 | 1971 | 11 | 0.010 |
Why?
|
Carcinogens | 1 | 2004 | 466 | 0.010 |
Why?
|
Tunicamycin | 2 | 1994 | 112 | 0.010 |
Why?
|
Microscopy | 2 | 1964 | 903 | 0.010 |
Why?
|
Fluorescent Dyes | 1 | 2010 | 1917 | 0.010 |
Why?
|
Hydroxylamines | 2 | 1971 | 40 | 0.010 |
Why?
|
Virion | 1 | 2004 | 433 | 0.010 |
Why?
|
Mutagens | 2 | 1972 | 168 | 0.010 |
Why?
|
Paper | 2 | 1971 | 85 | 0.010 |
Why?
|
Bacteriophage phi X 174 | 1 | 1981 | 20 | 0.010 |
Why?
|
Diabetes Mellitus, Type 2 | 1 | 2005 | 11725 | 0.010 |
Why?
|
Base Pair Mismatch | 1 | 2001 | 97 | 0.010 |
Why?
|
Microscopy, Fluorescence | 1 | 2008 | 2699 | 0.010 |
Why?
|
Trypsin | 2 | 1975 | 511 | 0.010 |
Why?
|
cdc42 GTP-Binding Protein | 1 | 2000 | 194 | 0.010 |
Why?
|
Endoribonucleases | 1 | 1981 | 229 | 0.010 |
Why?
|
Rec A Recombinases | 1 | 1999 | 51 | 0.010 |
Why?
|
Ultrasonics | 2 | 1974 | 212 | 0.010 |
Why?
|
Ribonuclease III | 1 | 1981 | 275 | 0.010 |
Why?
|
Vero Cells | 2 | 1991 | 485 | 0.010 |
Why?
|
Cells, Cultured | 3 | 2003 | 19229 | 0.010 |
Why?
|
Mercaptoethanol | 2 | 1971 | 64 | 0.010 |
Why?
|
Iron | 1 | 1987 | 1774 | 0.010 |
Why?
|
Transcription Factors | 1 | 1999 | 12208 | 0.010 |
Why?
|
Esters | 2 | 1971 | 210 | 0.010 |
Why?
|
Pancreas | 3 | 1971 | 1686 | 0.010 |
Why?
|
Biotinylation | 1 | 1998 | 179 | 0.010 |
Why?
|
Nalidixic Acid | 1 | 1977 | 19 | 0.010 |
Why?
|
Cell Membrane | 1 | 1987 | 3748 | 0.010 |
Why?
|
N-Glycosyl Hydrolases | 2 | 1967 | 68 | 0.010 |
Why?
|
Spheroplasts | 1 | 1976 | 6 | 0.010 |
Why?
|
Tosyllysine Chloromethyl Ketone | 1 | 1975 | 5 | 0.010 |
Why?
|
Antigen-Antibody Reactions | 1 | 1976 | 363 | 0.010 |
Why?
|
Oxygen | 1 | 1987 | 4189 | 0.010 |
Why?
|
Protein Kinase C | 1 | 2000 | 1227 | 0.010 |
Why?
|
Transformation, Genetic | 1 | 1976 | 192 | 0.010 |
Why?
|
5-Methylcytosine | 1 | 1976 | 154 | 0.010 |
Why?
|
Electrophoresis, Disc | 1 | 1975 | 70 | 0.010 |
Why?
|
Spectrophotometry, Ultraviolet | 1 | 1975 | 220 | 0.010 |
Why?
|
Chromosome Deletion | 1 | 1980 | 1401 | 0.010 |
Why?
|
Genome | 1 | 2004 | 1808 | 0.010 |
Why?
|
Micrococcus | 1 | 1974 | 13 | 0.010 |
Why?
|
Sulfhydryl Reagents | 1 | 1974 | 32 | 0.010 |
Why?
|
Hexosaminidases | 1 | 1994 | 54 | 0.010 |
Why?
|
Dactinomycin | 1 | 1974 | 318 | 0.010 |
Why?
|
Glucose | 1 | 1966 | 4397 | 0.010 |
Why?
|
Phosphoric Diester Hydrolases | 1 | 1975 | 197 | 0.010 |
Why?
|
Drug Resistance, Microbial | 1 | 1977 | 862 | 0.010 |
Why?
|
Crosses, Genetic | 1 | 1974 | 791 | 0.010 |
Why?
|
Nitrosoguanidines | 1 | 1972 | 8 | 0.010 |
Why?
|
Maltose | 1 | 1972 | 34 | 0.010 |
Why?
|
Deoxyribonucleosides | 1 | 1971 | 7 | 0.010 |
Why?
|
Cell Fractionation | 1 | 1972 | 252 | 0.010 |
Why?
|
Distemper Virus, Canine | 1 | 1991 | 2 | 0.010 |
Why?
|
Methods | 1 | 1972 | 1129 | 0.010 |
Why?
|
Chromatography, Paper | 1 | 1971 | 77 | 0.010 |
Why?
|
Snakes | 1 | 1971 | 30 | 0.010 |
Why?
|
Bacteriolysis | 1 | 1971 | 51 | 0.010 |
Why?
|
Chromatography, Thin Layer | 1 | 1971 | 223 | 0.010 |
Why?
|
Guanine Nucleotides | 1 | 1971 | 68 | 0.010 |
Why?
|
Muramidase | 1 | 1971 | 174 | 0.010 |
Why?
|
Insulin Resistance | 1 | 2005 | 3864 | 0.010 |
Why?
|
Genetic Code | 1 | 1971 | 154 | 0.010 |
Why?
|
Apatites | 1 | 1970 | 19 | 0.010 |
Why?
|
Specific Pathogen-Free Organisms | 1 | 1991 | 226 | 0.010 |
Why?
|
Double-Blind Method | 1 | 2005 | 12026 | 0.010 |
Why?
|
Venoms | 1 | 1971 | 91 | 0.010 |
Why?
|
Bacteria | 2 | 1974 | 2114 | 0.010 |
Why?
|
Stimulation, Chemical | 1 | 1970 | 326 | 0.010 |
Why?
|
Autoradiography | 1 | 1971 | 745 | 0.010 |
Why?
|
Precipitin Tests | 1 | 1991 | 829 | 0.010 |
Why?
|
Moths | 1 | 1990 | 87 | 0.010 |
Why?
|
Genes, Synthetic | 1 | 1990 | 90 | 0.010 |
Why?
|
Regulatory Sequences, Nucleic Acid | 1 | 1994 | 794 | 0.010 |
Why?
|
Quaternary Ammonium Compounds | 1 | 1970 | 205 | 0.010 |
Why?
|
Mathematics | 1 | 1971 | 728 | 0.010 |
Why?
|
Sulfates | 1 | 1970 | 390 | 0.010 |
Why?
|
Genotype | 2 | 1974 | 12951 | 0.010 |
Why?
|
Cross Reactions | 1 | 1991 | 841 | 0.010 |
Why?
|
Biological Transport | 1 | 1994 | 2118 | 0.010 |
Why?
|
Immunization, Secondary | 1 | 1991 | 340 | 0.010 |
Why?
|
Transferases | 1 | 1969 | 75 | 0.010 |
Why?
|
Glucosyltransferases | 1 | 1969 | 98 | 0.010 |
Why?
|
Genetic Linkage | 1 | 1974 | 2421 | 0.010 |
Why?
|
Vaccines, Synthetic | 1 | 1991 | 634 | 0.010 |
Why?
|
Phosphoric Acids | 1 | 1968 | 24 | 0.000 |
Why?
|
Morpholines | 1 | 1971 | 571 | 0.000 |
Why?
|
Fluorescent Antibody Technique | 1 | 1991 | 2505 | 0.000 |
Why?
|
Dogs | 1 | 1991 | 3912 | 0.000 |
Why?
|
Drug Synergism | 1 | 1970 | 1792 | 0.000 |
Why?
|
Chymotrypsin | 1 | 1964 | 149 | 0.000 |
Why?
|
Centrifugation | 1 | 1964 | 122 | 0.000 |
Why?
|
Viscosity | 1 | 1964 | 328 | 0.000 |
Why?
|
HeLa Cells | 1 | 1990 | 3128 | 0.000 |
Why?
|
Adenine | 1 | 1968 | 936 | 0.000 |
Why?
|
Radiation Dosage | 1 | 1971 | 1928 | 0.000 |
Why?
|
Cattle | 1 | 1968 | 3922 | 0.000 |
Why?
|
Antibodies | 1 | 1970 | 2460 | 0.000 |
Why?
|
Cell Survival | 1 | 1972 | 5882 | 0.000 |
Why?
|
Cricetinae | 1 | 1986 | 2472 | 0.000 |
Why?
|
Antibodies, Viral | 1 | 1991 | 3176 | 0.000 |
Why?
|
Vaccination | 1 | 1991 | 3278 | 0.000 |
Why?
|
Membrane Glycoproteins | 1 | 1990 | 3768 | 0.000 |
Why?
|
Phenotype | 1 | 1976 | 16365 | 0.000 |
Why?
|
Aged | 1 | 2005 | 163280 | 0.000 |
Why?
|
Cobalt | 1 | 1973 | 158 | 0.000 |
Why?
|
Spectrophotometry | 1 | 1973 | 313 | 0.000 |
Why?
|
Hydrogen | 1 | 1973 | 164 | 0.000 |
Why?
|
Electron Transport | 1 | 1973 | 211 | 0.000 |
Why?
|
Middle Aged | 1 | 2005 | 213383 | 0.000 |
Why?
|
Adult | 1 | 2005 | 214055 | 0.000 |
Why?
|
Models, Chemical | 1 | 1973 | 626 | 0.000 |
Why?
|
Copper | 1 | 1973 | 366 | 0.000 |
Why?
|
Male | 1 | 2005 | 350118 | 0.000 |
Why?
|
Sodium | 1 | 1973 | 1623 | 0.000 |
Why?
|
Female | 1 | 2005 | 380194 | 0.000 |
Why?
|