Robert Kuchta
Concepts (345)
Concepts are derived automatically from a person's publications.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
---|
DNA Primase | 32 | 2017 | 43 | 5.480 |
Why?
| Viral Proteins | 15 | 2017 | 286 | 4.440 |
Why?
| DNA Polymerase I | 17 | 2011 | 26 | 3.540 |
Why?
| DNA-Directed DNA Polymerase | 14 | 2017 | 44 | 3.240 |
Why?
| Herpesvirus 1, Human | 11 | 2016 | 78 | 3.060 |
Why?
| Exodeoxyribonucleases | 7 | 2017 | 24 | 2.640 |
Why?
| DNA Helicases | 8 | 2017 | 133 | 2.390 |
Why?
| DNA Replication | 19 | 2017 | 203 | 2.320 |
Why?
| DNA | 20 | 2017 | 1356 | 1.920 |
Why?
| Nucleotides | 11 | 2010 | 113 | 1.700 |
Why?
| Deoxyribonucleotides | 9 | 2009 | 17 | 1.440 |
Why?
| Purine Nucleotides | 5 | 2009 | 11 | 1.350 |
Why?
| Virus Replication | 5 | 2013 | 396 | 1.140 |
Why?
| Oxazines | 3 | 2011 | 25 | 1.060 |
Why?
| DNA Primers | 12 | 2010 | 514 | 1.050 |
Why?
| RNA Nucleotidyltransferases | 11 | 1997 | 24 | 1.010 |
Why?
| Ribonucleotides | 4 | 2016 | 25 | 0.880 |
Why?
| Oligonucleotide Array Sequence Analysis | 11 | 2010 | 746 | 0.870 |
Why?
| DNA Polymerase II | 10 | 1997 | 37 | 0.860 |
Why?
| Base Pairing | 10 | 2013 | 59 | 0.820 |
Why?
| Kinetics | 25 | 2016 | 1569 | 0.770 |
Why?
| Geobacillus stearothermophilus | 3 | 2009 | 12 | 0.760 |
Why?
| Substrate Specificity | 14 | 2016 | 357 | 0.750 |
Why?
| Phenothiazines | 2 | 2011 | 7 | 0.730 |
Why?
| Biocatalysis | 2 | 2011 | 64 | 0.710 |
Why?
| Antiviral Agents | 3 | 2016 | 649 | 0.710 |
Why?
| Fluorescent Dyes | 3 | 2013 | 304 | 0.700 |
Why?
| Base Sequence | 26 | 2009 | 2114 | 0.690 |
Why?
| Nucleic Acid Synthesis Inhibitors | 3 | 2016 | 18 | 0.680 |
Why?
| Molecular Sequence Data | 24 | 2010 | 2790 | 0.660 |
Why?
| Polymerase Chain Reaction | 3 | 2011 | 1001 | 0.660 |
Why?
| Purines | 2 | 2011 | 159 | 0.650 |
Why?
| Templates, Genetic | 14 | 2010 | 59 | 0.590 |
Why?
| DNA, Viral | 7 | 2013 | 351 | 0.560 |
Why?
| Acyclovir | 2 | 2016 | 100 | 0.540 |
Why?
| Foscarnet | 1 | 2016 | 18 | 0.530 |
Why?
| Cytosine | 3 | 2013 | 44 | 0.530 |
Why?
| Oligodeoxyribonucleotides | 9 | 2017 | 138 | 0.520 |
Why?
| Models, Molecular | 3 | 2016 | 1390 | 0.510 |
Why?
| Zidovudine | 4 | 2000 | 77 | 0.490 |
Why?
| Hydrogen Bonding | 6 | 2011 | 145 | 0.460 |
Why?
| Herpes Simplex | 1 | 2015 | 88 | 0.460 |
Why?
| Orthomyxoviridae | 3 | 2010 | 35 | 0.450 |
Why?
| Protein Subunits | 3 | 2009 | 204 | 0.440 |
Why?
| Pyrimidines | 2 | 2011 | 376 | 0.430 |
Why?
| Molecular Structure | 7 | 2017 | 447 | 0.430 |
Why?
| DNA-Directed RNA Polymerases | 2 | 2010 | 52 | 0.410 |
Why?
| Herpesviridae Infections | 1 | 2013 | 138 | 0.400 |
Why?
| Taq Polymerase | 1 | 2011 | 10 | 0.380 |
Why?
| Catalytic Domain | 4 | 2016 | 202 | 0.380 |
Why?
| Fluorescence | 2 | 2011 | 154 | 0.380 |
Why?
| Transition Elements | 1 | 2011 | 3 | 0.380 |
Why?
| Thermodynamics | 3 | 2013 | 388 | 0.380 |
Why?
| Ixodes | 1 | 2010 | 10 | 0.370 |
Why?
| Borrelia burgdorferi | 1 | 2010 | 12 | 0.370 |
Why?
| DNA, Circular | 1 | 2010 | 13 | 0.370 |
Why?
| RNA Caps | 1 | 2010 | 31 | 0.370 |
Why?
| DNA, Single-Stranded | 5 | 2016 | 110 | 0.360 |
Why?
| Golgi Apparatus | 4 | 2001 | 91 | 0.360 |
Why?
| Sequence Homology, Amino Acid | 4 | 2009 | 352 | 0.350 |
Why?
| Ribose | 2 | 2008 | 17 | 0.350 |
Why?
| Hypoxanthine | 1 | 2009 | 10 | 0.340 |
Why?
| Guanine | 1 | 2009 | 76 | 0.330 |
Why?
| Organophosphates | 1 | 2009 | 90 | 0.320 |
Why?
| Escherichia coli Proteins | 1 | 2009 | 164 | 0.300 |
Why?
| Influenza A virus | 6 | 2007 | 91 | 0.300 |
Why?
| Recombinant Proteins | 6 | 2016 | 1243 | 0.280 |
Why?
| Polyphosphates | 2 | 2004 | 33 | 0.280 |
Why?
| Deoxyadenine Nucleotides | 3 | 2010 | 13 | 0.260 |
Why?
| RNA, Viral | 6 | 2010 | 565 | 0.260 |
Why?
| Evolution, Molecular | 1 | 2009 | 440 | 0.250 |
Why?
| Thymus Gland | 7 | 1995 | 299 | 0.250 |
Why?
| Carrier Proteins | 2 | 2001 | 701 | 0.250 |
Why?
| Arabinonucleosides | 1 | 2004 | 8 | 0.250 |
Why?
| RNA | 6 | 2009 | 820 | 0.240 |
Why?
| Cytarabine | 1 | 2004 | 52 | 0.240 |
Why?
| Base Pair Mismatch | 1 | 2004 | 14 | 0.240 |
Why?
| Transcription, Genetic | 1 | 2010 | 1310 | 0.240 |
Why?
| Guanosine Triphosphate | 5 | 2008 | 85 | 0.240 |
Why?
| Animals | 25 | 2013 | 32104 | 0.240 |
Why?
| Deoxyguanine Nucleotides | 4 | 2009 | 8 | 0.230 |
Why?
| Arabinonucleotides | 2 | 1995 | 2 | 0.230 |
Why?
| Humans | 42 | 2017 | 115741 | 0.230 |
Why?
| Antineoplastic Agents | 2 | 2009 | 1893 | 0.230 |
Why?
| Cytidine Monophosphate N-Acetylneuraminic Acid | 2 | 2001 | 3 | 0.230 |
Why?
| Deoxycytidine | 1 | 2004 | 140 | 0.230 |
Why?
| Protein Binding | 5 | 2010 | 1917 | 0.230 |
Why?
| Amino Acid Sequence | 5 | 2009 | 2000 | 0.220 |
Why?
| Mass Spectrometry | 1 | 2006 | 645 | 0.220 |
Why?
| Cattle | 10 | 1997 | 935 | 0.220 |
Why?
| Influenza B virus | 3 | 2007 | 34 | 0.210 |
Why?
| Membrane Proteins | 2 | 2001 | 1024 | 0.210 |
Why?
| Ubiquitin-Activating Enzymes | 2 | 2012 | 13 | 0.200 |
Why?
| Glycosphingolipids | 2 | 1999 | 10 | 0.200 |
Why?
| Polymers | 4 | 2010 | 463 | 0.200 |
Why?
| Conserved Sequence | 4 | 2006 | 219 | 0.190 |
Why?
| Adenosine Triphosphate | 5 | 2008 | 431 | 0.190 |
Why?
| Alcohol Drinking | 2 | 2017 | 650 | 0.190 |
Why?
| Nucleosides | 2 | 2013 | 25 | 0.180 |
Why?
| Eukaryotic Cells | 1 | 2000 | 33 | 0.180 |
Why?
| Oligosaccharides | 1 | 2000 | 47 | 0.180 |
Why?
| Polysaccharides | 1 | 2000 | 80 | 0.180 |
Why?
| Binding Sites | 5 | 2010 | 1177 | 0.170 |
Why?
| Manganese | 2 | 1999 | 55 | 0.170 |
Why?
| Uridine Diphosphate N-Acetylglucosamine | 2 | 1996 | 4 | 0.170 |
Why?
| Peptide Chain Initiation, Translational | 1 | 1999 | 38 | 0.170 |
Why?
| G(M3) Ganglioside | 1 | 1999 | 1 | 0.170 |
Why?
| Oligonucleotide Probes | 3 | 2006 | 54 | 0.160 |
Why?
| Intracellular Membranes | 2 | 1996 | 73 | 0.160 |
Why?
| Gangliosides | 1 | 1999 | 19 | 0.160 |
Why?
| Cross-Linking Reagents | 1 | 1999 | 182 | 0.160 |
Why?
| Small Molecule Libraries | 2 | 2017 | 81 | 0.160 |
Why?
| Meteorology | 1 | 2017 | 1 | 0.150 |
Why?
| Arginine | 1 | 1999 | 241 | 0.150 |
Why?
| Sequence Alignment | 3 | 2005 | 327 | 0.150 |
Why?
| Molecular Diagnostic Techniques | 3 | 2007 | 91 | 0.150 |
Why?
| Electrophoresis, Polyacrylamide Gel | 4 | 2012 | 312 | 0.150 |
Why?
| Herpesviridae | 2 | 2013 | 21 | 0.140 |
Why?
| Enzyme Activation | 6 | 2012 | 793 | 0.140 |
Why?
| Influenza, Human | 3 | 2007 | 548 | 0.140 |
Why?
| Aphidicolin | 2 | 1993 | 6 | 0.140 |
Why?
| Amides | 1 | 2017 | 88 | 0.140 |
Why?
| Nucleic Acid Hybridization | 4 | 2010 | 189 | 0.140 |
Why?
| Health Status Indicators | 1 | 2017 | 155 | 0.130 |
Why?
| Acrolein | 1 | 1995 | 23 | 0.130 |
Why?
| Hydrolysis | 1 | 2016 | 179 | 0.130 |
Why?
| Neoplasms | 1 | 2009 | 2118 | 0.130 |
Why?
| Genome, Viral | 2 | 2006 | 121 | 0.130 |
Why?
| Hydrophobic and Hydrophilic Interactions | 2 | 2007 | 177 | 0.130 |
Why?
| Vidarabine Phosphate | 2 | 1995 | 2 | 0.130 |
Why?
| Cell Line | 4 | 2012 | 2651 | 0.120 |
Why?
| Guanosine | 1 | 1995 | 39 | 0.120 |
Why?
| Ubiquitination | 2 | 2012 | 86 | 0.120 |
Why?
| In Vitro Techniques | 4 | 2007 | 1044 | 0.120 |
Why?
| Viruses | 1 | 1996 | 94 | 0.120 |
Why?
| Nucleoside Diphosphate Sugars | 1 | 1994 | 1 | 0.120 |
Why?
| Sensitivity and Specificity | 5 | 2011 | 1730 | 0.120 |
Why?
| Glycosylation | 4 | 2001 | 133 | 0.120 |
Why?
| Binding, Competitive | 4 | 1997 | 200 | 0.120 |
Why?
| Influenza A Virus, H1N1 Subtype | 4 | 2008 | 139 | 0.110 |
Why?
| Exonucleases | 1 | 1993 | 8 | 0.110 |
Why?
| Benzimidazoles | 2 | 2005 | 137 | 0.110 |
Why?
| Influenza A Virus, H5N1 Subtype | 3 | 2007 | 5 | 0.110 |
Why?
| Liver | 2 | 2001 | 1690 | 0.110 |
Why?
| Influenza A Virus, H3N2 Subtype | 3 | 2008 | 40 | 0.110 |
Why?
| DNA-Binding Proteins | 1 | 1999 | 1316 | 0.100 |
Why?
| Sequence Homology, Nucleic Acid | 2 | 2009 | 150 | 0.100 |
Why?
| Peptide Chain Elongation, Translational | 2 | 2004 | 18 | 0.100 |
Why?
| Depsipeptides | 1 | 2012 | 13 | 0.100 |
Why?
| Spectrometry, Fluorescence | 2 | 2010 | 158 | 0.100 |
Why?
| Adaptation, Psychological | 1 | 2016 | 551 | 0.100 |
Why?
| Diterpenes | 1 | 1991 | 32 | 0.100 |
Why?
| Disulfides | 1 | 2012 | 91 | 0.100 |
Why?
| Poliovirus | 2 | 2006 | 77 | 0.100 |
Why?
| Thiazoles | 1 | 2012 | 110 | 0.100 |
Why?
| Ions | 1 | 2011 | 61 | 0.090 |
Why?
| DNA Polymerase beta | 2 | 2002 | 5 | 0.090 |
Why?
| Nymph | 1 | 2010 | 4 | 0.090 |
Why?
| Arachnid Vectors | 1 | 2010 | 3 | 0.090 |
Why?
| RNA, Complementary | 1 | 2010 | 2 | 0.090 |
Why?
| Thymidine Monophosphate | 1 | 2010 | 4 | 0.090 |
Why?
| Adenine | 2 | 2012 | 221 | 0.090 |
Why?
| Allosteric Site | 1 | 2010 | 16 | 0.090 |
Why?
| Polymerization | 1 | 2011 | 119 | 0.090 |
Why?
| Phosphoric Diester Hydrolases | 1 | 2010 | 44 | 0.090 |
Why?
| G1 Phase | 1 | 2010 | 68 | 0.090 |
Why?
| Base Composition | 3 | 1995 | 76 | 0.090 |
Why?
| Antigens, Surface | 1 | 2010 | 151 | 0.090 |
Why?
| Structure-Activity Relationship | 5 | 1996 | 511 | 0.090 |
Why?
| Bacterial Vaccines | 1 | 2010 | 61 | 0.090 |
Why?
| RNA-Directed DNA Polymerase | 2 | 2003 | 34 | 0.090 |
Why?
| Bacterial Outer Membrane Proteins | 1 | 2010 | 58 | 0.090 |
Why?
| Nucleic Acid Conformation | 2 | 2013 | 672 | 0.090 |
Why?
| Alcoholism | 1 | 2016 | 717 | 0.090 |
Why?
| Spodoptera | 1 | 2009 | 37 | 0.090 |
Why?
| Spindle Apparatus | 1 | 2010 | 87 | 0.090 |
Why?
| Nucleic Acid Heteroduplexes | 1 | 2009 | 8 | 0.090 |
Why?
| Lipoproteins | 1 | 2010 | 162 | 0.090 |
Why?
| DNA Topoisomerases | 1 | 2009 | 1 | 0.090 |
Why?
| Topoisomerase Inhibitors | 1 | 2009 | 4 | 0.080 |
Why?
| Protein Multimerization | 1 | 2010 | 160 | 0.080 |
Why?
| Mitosis | 1 | 2010 | 164 | 0.080 |
Why?
| Antimetabolites | 1 | 2009 | 21 | 0.080 |
Why?
| Catalysis | 3 | 2010 | 299 | 0.080 |
Why?
| Tumor Cells, Cultured | 3 | 2000 | 850 | 0.080 |
Why?
| Photochemical Processes | 1 | 2010 | 97 | 0.080 |
Why?
| 2-Aminopurine | 1 | 2009 | 10 | 0.080 |
Why?
| Biopolymers | 1 | 2009 | 26 | 0.080 |
Why?
| Enzyme Inhibitors | 1 | 2012 | 757 | 0.080 |
Why?
| Biological Transport | 2 | 2001 | 375 | 0.080 |
Why?
| Viral Matrix Proteins | 1 | 2008 | 24 | 0.080 |
Why?
| Insecta | 1 | 2008 | 65 | 0.080 |
Why?
| Nitrogen | 1 | 2009 | 148 | 0.080 |
Why?
| Adamantane | 1 | 2008 | 16 | 0.080 |
Why?
| Transfection | 2 | 2012 | 866 | 0.080 |
Why?
| Angiogenesis Inhibitors | 1 | 2009 | 216 | 0.070 |
Why?
| Drug Resistance, Viral | 1 | 2008 | 99 | 0.070 |
Why?
| Escherichia coli | 2 | 1988 | 730 | 0.070 |
Why?
| Virus Cultivation | 1 | 2007 | 25 | 0.070 |
Why?
| Hydro-Lyases | 1 | 1986 | 4 | 0.070 |
Why?
| Metalloproteins | 1 | 1986 | 5 | 0.070 |
Why?
| Poland | 2 | 2017 | 28 | 0.070 |
Why?
| Phosphates | 2 | 1999 | 160 | 0.070 |
Why?
| DNA Damage | 1 | 2009 | 357 | 0.070 |
Why?
| Blotting, Western | 1 | 2009 | 1153 | 0.070 |
Why?
| Iron-Sulfur Proteins | 1 | 1986 | 24 | 0.070 |
Why?
| Cell Cycle Proteins | 1 | 2010 | 553 | 0.070 |
Why?
| Multienzyme Complexes | 1 | 1986 | 64 | 0.070 |
Why?
| Uridine | 1 | 2006 | 29 | 0.070 |
Why?
| Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | 1 | 2007 | 139 | 0.070 |
Why?
| Bacterial Proteins | 1 | 2010 | 739 | 0.060 |
Why?
| Software | 2 | 2006 | 541 | 0.060 |
Why?
| Fluorine | 1 | 2004 | 15 | 0.060 |
Why?
| Chromatography, Liquid | 1 | 2006 | 347 | 0.060 |
Why?
| Inhibitory Concentration 50 | 1 | 2004 | 77 | 0.060 |
Why?
| Magnetic Resonance Spectroscopy | 1 | 2007 | 483 | 0.060 |
Why?
| Protein Processing, Post-Translational | 2 | 1999 | 401 | 0.060 |
Why?
| Pyrimidine Nucleotides | 1 | 2004 | 2 | 0.060 |
Why?
| Transcription Initiation Site | 1 | 2004 | 40 | 0.060 |
Why?
| Chlorides | 1 | 2004 | 130 | 0.060 |
Why?
| HIV | 2 | 1996 | 209 | 0.060 |
Why?
| Deoxyribonuclease I | 2 | 1995 | 34 | 0.060 |
Why?
| RNA, Messenger | 1 | 2010 | 2574 | 0.050 |
Why?
| Models, Biological | 1 | 2009 | 1646 | 0.050 |
Why?
| Phosphorus Radioisotopes | 2 | 2006 | 28 | 0.050 |
Why?
| Cytidine Monophosphate | 1 | 2001 | 1 | 0.050 |
Why?
| Nucleotides, Cyclic | 1 | 2001 | 15 | 0.050 |
Why?
| Uridine Monophosphate | 1 | 2001 | 15 | 0.050 |
Why?
| Cyclin-Dependent Kinase Inhibitor p27 | 2 | 2012 | 69 | 0.050 |
Why?
| Sequence Deletion | 1 | 2002 | 167 | 0.050 |
Why?
| Uridine Triphosphate | 2 | 2000 | 11 | 0.050 |
Why?
| Cytosol | 1 | 2001 | 209 | 0.050 |
Why?
| Indoles | 1 | 2003 | 309 | 0.050 |
Why?
| Mannose | 1 | 2000 | 21 | 0.050 |
Why?
| Cells, Cultured | 1 | 2008 | 3914 | 0.050 |
Why?
| Models, Chemical | 1 | 2001 | 257 | 0.040 |
Why?
| Anions | 1 | 1999 | 31 | 0.040 |
Why?
| Dinucleoside Phosphates | 1 | 1999 | 24 | 0.040 |
Why?
| Radioisotope Dilution Technique | 2 | 1996 | 13 | 0.040 |
Why?
| Tritium | 2 | 1996 | 69 | 0.040 |
Why?
| Thymine Nucleotides | 2 | 2000 | 15 | 0.040 |
Why?
| Photochemistry | 1 | 1999 | 125 | 0.040 |
Why?
| DNA Repair | 1 | 2000 | 190 | 0.040 |
Why?
| Magnesium | 1 | 1999 | 145 | 0.040 |
Why?
| Multigene Family | 1 | 1999 | 193 | 0.040 |
Why?
| Mutagenesis, Site-Directed | 1 | 1999 | 346 | 0.040 |
Why?
| Cytidine Triphosphate | 1 | 1997 | 14 | 0.040 |
Why?
| Phospholipids | 1 | 1999 | 202 | 0.040 |
Why?
| Cell Division | 1 | 1999 | 759 | 0.040 |
Why?
| HeLa Cells | 2 | 2010 | 567 | 0.040 |
Why?
| Nucleic Acid Amplification Techniques | 2 | 2007 | 34 | 0.040 |
Why?
| Uridine Diphosphate Sugars | 1 | 1996 | 2 | 0.030 |
Why?
| Demography | 1 | 2017 | 261 | 0.030 |
Why?
| Iodoacetamide | 1 | 1995 | 5 | 0.030 |
Why?
| Dithiothreitol | 1 | 1995 | 17 | 0.030 |
Why?
| Indicators and Reagents | 1 | 1996 | 100 | 0.030 |
Why?
| DNA Polymerase III | 1 | 1995 | 12 | 0.030 |
Why?
| Reverse Transcriptase Inhibitors | 1 | 1995 | 82 | 0.030 |
Why?
| Reproducibility of Results | 3 | 2007 | 2824 | 0.030 |
Why?
| Ganciclovir | 1 | 1995 | 49 | 0.030 |
Why?
| Rabbits | 1 | 1996 | 752 | 0.030 |
Why?
| Uridine Diphosphate Galactose | 1 | 1994 | 1 | 0.030 |
Why?
| Dideoxynucleotides | 1 | 1994 | 14 | 0.030 |
Why?
| CHO Cells | 1 | 1994 | 140 | 0.030 |
Why?
| DNA, B-Form | 1 | 2013 | 1 | 0.030 |
Why?
| Molecular Weight | 1 | 1994 | 329 | 0.030 |
Why?
| Gene Expression | 1 | 1999 | 1436 | 0.030 |
Why?
| Cricetinae | 1 | 1994 | 260 | 0.030 |
Why?
| Poly dA-dT | 1 | 1993 | 2 | 0.030 |
Why?
| Poly T | 1 | 1993 | 1 | 0.030 |
Why?
| Rats | 1 | 2001 | 5033 | 0.030 |
Why?
| Solvents | 1 | 2013 | 108 | 0.030 |
Why?
| Socioeconomic Factors | 1 | 2017 | 1086 | 0.030 |
Why?
| Middle Aged | 3 | 2017 | 27069 | 0.030 |
Why?
| Arabinofuranosylcytosine Triphosphate | 1 | 1992 | 1 | 0.030 |
Why?
| Telomeric Repeat Binding Protein 1 | 1 | 2012 | 4 | 0.030 |
Why?
| Computational Biology | 2 | 2006 | 537 | 0.030 |
Why?
| Ubiquitin | 1 | 2012 | 64 | 0.020 |
Why?
| Dose-Response Relationship, Drug | 2 | 2012 | 1870 | 0.020 |
Why?
| Proteolysis | 1 | 2012 | 145 | 0.020 |
Why?
| Immunoblotting | 1 | 2012 | 281 | 0.020 |
Why?
| Drug Screening Assays, Antitumor | 1 | 2012 | 180 | 0.020 |
Why?
| Mutation | 3 | 2010 | 3364 | 0.020 |
Why?
| Electrophoretic Mobility Shift Assay | 1 | 2010 | 74 | 0.020 |
Why?
| Surface Plasmon Resonance | 1 | 2010 | 82 | 0.020 |
Why?
| Green Fluorescent Proteins | 1 | 2012 | 377 | 0.020 |
Why?
| HEK293 Cells | 1 | 2012 | 602 | 0.020 |
Why?
| Chemistry | 1 | 1988 | 39 | 0.020 |
Why?
| Aged | 2 | 2017 | 19294 | 0.020 |
Why?
| Chemical Phenomena | 1 | 1988 | 81 | 0.020 |
Why?
| Exodeoxyribonuclease V | 1 | 1988 | 8 | 0.020 |
Why?
| Stress, Psychological | 1 | 2016 | 975 | 0.020 |
Why?
| Macromolecular Substances | 1 | 1988 | 200 | 0.020 |
Why?
| Protein Structure, Tertiary | 1 | 2010 | 804 | 0.020 |
Why?
| Mathematics | 1 | 1987 | 100 | 0.020 |
Why?
| Male | 3 | 2017 | 56050 | 0.020 |
Why?
| Protein-Tyrosine Kinases | 1 | 2010 | 396 | 0.020 |
Why?
| Nigeria | 1 | 2007 | 14 | 0.020 |
Why?
| Kazakhstan | 1 | 2007 | 7 | 0.020 |
Why?
| Indonesia | 1 | 2007 | 18 | 0.020 |
Why?
| DNA, Bacterial | 1 | 1988 | 309 | 0.020 |
Why?
| Vietnam | 1 | 2007 | 21 | 0.020 |
Why?
| Carbocyanines | 1 | 2006 | 30 | 0.020 |
Why?
| Microbial Sensitivity Tests | 1 | 2008 | 299 | 0.020 |
Why?
| Spectrophotometry | 1 | 1986 | 48 | 0.020 |
Why?
| Influenza in Birds | 1 | 2006 | 3 | 0.020 |
Why?
| Female | 3 | 2017 | 60018 | 0.020 |
Why?
| Enzyme Stability | 1 | 1986 | 73 | 0.020 |
Why?
| False Negative Reactions | 1 | 2006 | 50 | 0.020 |
Why?
| Automation | 1 | 2006 | 74 | 0.020 |
Why?
| Databases, Nucleic Acid | 1 | 2006 | 33 | 0.020 |
Why?
| Electron Spin Resonance Spectroscopy | 1 | 1986 | 87 | 0.020 |
Why?
| Electrophoresis, Gel, Two-Dimensional | 1 | 2006 | 101 | 0.020 |
Why?
| False Positive Reactions | 1 | 2006 | 109 | 0.020 |
Why?
| Phosphorylation | 1 | 2010 | 1571 | 0.020 |
Why?
| Orthomyxoviridae Infections | 1 | 2006 | 55 | 0.020 |
Why?
| Neuraminidase | 1 | 2005 | 22 | 0.020 |
Why?
| Birds | 1 | 2006 | 77 | 0.020 |
Why?
| Hemagglutinin Glycoproteins, Influenza Virus | 1 | 2005 | 20 | 0.020 |
Why?
| Respiratory System | 1 | 2007 | 141 | 0.020 |
Why?
| Cell Line, Tumor | 1 | 2012 | 2751 | 0.020 |
Why?
| Microscopy, Fluorescence | 1 | 2006 | 402 | 0.020 |
Why?
| Surveys and Questionnaires | 1 | 2016 | 4669 | 0.020 |
Why?
| Image Interpretation, Computer-Assisted | 1 | 2006 | 243 | 0.010 |
Why?
| Peptide Fragments | 1 | 1988 | 675 | 0.010 |
Why?
| Hot Temperature | 1 | 2005 | 303 | 0.010 |
Why?
| Risk Factors | 1 | 2017 | 8702 | 0.010 |
Why?
| Gene Expression Profiling | 1 | 2010 | 1537 | 0.010 |
Why?
| Phylogeny | 1 | 2006 | 805 | 0.010 |
Why?
| Genotype | 1 | 2006 | 1787 | 0.010 |
Why?
| Retrospective Studies | 1 | 2017 | 12633 | 0.010 |
Why?
| DNA Polymerase gamma | 1 | 2000 | 7 | 0.010 |
Why?
| Deoxycytosine Nucleotides | 1 | 2000 | 11 | 0.010 |
Why?
| HIV Infections | 1 | 1994 | 2474 | 0.010 |
Why?
| Adolescent | 1 | 2017 | 17922 | 0.010 |
Why?
| Algorithms | 1 | 2005 | 1500 | 0.010 |
Why?
| Adult | 1 | 2017 | 30789 | 0.010 |
Why?
| Time Factors | 1 | 2007 | 6171 | 0.010 |
Why?
| Hexosamines | 1 | 1995 | 2 | 0.010 |
Why?
| Leukemia, Erythroblastic, Acute | 1 | 1995 | 8 | 0.010 |
Why?
| Carbohydrate Sequence | 1 | 1995 | 23 | 0.010 |
Why?
| Carbohydrate Conformation | 1 | 1995 | 15 | 0.010 |
Why?
| Galactose | 1 | 1995 | 20 | 0.010 |
Why?
| Mice | 1 | 2012 | 15052 | 0.010 |
Why?
| Mutagenesis | 1 | 1991 | 170 | 0.010 |
Why?
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