 Carlos Catalano
Concepts (195)
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?
|
|---|
| Bacteriophage lambda | 45 | 2020 | 71 | 11.420 |
Why?
| | Virus Assembly | 32 | 2020 | 71 | 8.800 |
Why?
| | DNA, Viral | 33 | 2020 | 419 | 6.030 |
Why?
| | Endodeoxyribonucleases | 30 | 2020 | 61 | 5.510 |
Why?
| | DNA Packaging | 15 | 2019 | 20 | 5.420 |
Why?
| | Genome, Viral | 17 | 2020 | 128 | 4.790 |
Why?
| | Viral Proteins | 21 | 2019 | 330 | 3.370 |
Why?
| | Capsid Proteins | 8 | 2017 | 95 | 3.190 |
Why?
| | Capsid | 12 | 2020 | 98 | 2.860 |
Why?
| | Integration Host Factors | 9 | 2020 | 10 | 1.880 |
Why?
| | Adenosine Triphosphate | 17 | 2020 | 463 | 1.770 |
Why?
| | Glycoproteins | 5 | 2017 | 342 | 1.650 |
Why?
| | Molecular Motor Proteins | 5 | 2011 | 36 | 1.450 |
Why?
| | Adenosine Triphosphatases | 14 | 2019 | 177 | 1.290 |
Why?
| | Hydrolysis | 11 | 2019 | 179 | 0.950 |
Why?
| | Thermodynamics | 6 | 2015 | 420 | 0.900 |
Why?
| | Models, Molecular | 12 | 2017 | 1588 | 0.900 |
Why?
| | Protein Folding | 7 | 2017 | 305 | 0.860 |
Why?
| | Escherichia coli | 9 | 2014 | 780 | 0.700 |
Why?
| | Protein Precursors | 1 | 2017 | 125 | 0.650 |
Why?
| | DNA-Binding Proteins | 10 | 2005 | 1405 | 0.640 |
Why?
| | DNA Helicases | 3 | 2011 | 118 | 0.640 |
Why?
| | Nucleic Acid Conformation | 5 | 2015 | 707 | 0.610 |
Why?
| | Molecular Sequence Data | 13 | 2013 | 3133 | 0.500 |
Why?
| | Escherichia coli Proteins | 2 | 2020 | 159 | 0.480 |
Why?
| | Kinetics | 16 | 2012 | 1777 | 0.470 |
Why?
| | Catalysis | 7 | 2019 | 320 | 0.470 |
Why?
| | DNA Viruses | 2 | 2012 | 13 | 0.450 |
Why?
| | Nanoparticles | 1 | 2014 | 310 | 0.440 |
Why?
| | Protein Multimerization | 3 | 2017 | 170 | 0.440 |
Why?
| | Protein Subunits | 4 | 2006 | 234 | 0.440 |
Why?
| | Protein Structure, Quaternary | 5 | 2019 | 134 | 0.430 |
Why?
| | Peptide Hydrolases | 1 | 2010 | 89 | 0.430 |
Why?
| | Amino Acid Sequence | 9 | 2013 | 2205 | 0.420 |
Why?
| | Ultracentrifugation | 4 | 2017 | 62 | 0.420 |
Why?
| | Protein Conformation | 9 | 2014 | 947 | 0.400 |
Why?
| | Nucleotides | 2 | 2008 | 111 | 0.400 |
Why?
| | Nucleocapsid | 1 | 2008 | 4 | 0.400 |
Why?
| | DNA | 5 | 2015 | 1394 | 0.390 |
Why?
| | Nucleoproteins | 3 | 2019 | 23 | 0.380 |
Why?
| | DNA Replication | 3 | 2006 | 203 | 0.370 |
Why?
| | Promoter Regions, Genetic | 4 | 2017 | 1253 | 0.360 |
Why?
| | Models, Biological | 6 | 2015 | 1853 | 0.330 |
Why?
| | Mutation | 8 | 2019 | 3265 | 0.330 |
Why?
| | Protein Structure, Secondary | 4 | 2017 | 401 | 0.320 |
Why?
| | Biological Assay | 1 | 2006 | 107 | 0.310 |
Why?
| | DNA, Bacterial | 1 | 2006 | 306 | 0.310 |
Why?
| | Holoenzymes | 1 | 2005 | 21 | 0.310 |
Why?
| | Hydrophobic and Hydrophilic Interactions | 2 | 2017 | 178 | 0.280 |
Why?
| | GTP Phosphohydrolases | 2 | 2000 | 66 | 0.260 |
Why?
| | Dimerization | 4 | 2005 | 200 | 0.260 |
Why?
| | Binding Sites | 7 | 2016 | 1320 | 0.250 |
Why?
| | Models, Chemical | 1 | 2004 | 301 | 0.240 |
Why?
| | Protein Stability | 2 | 2013 | 200 | 0.240 |
Why?
| | Adenine Nucleotides | 1 | 2020 | 19 | 0.220 |
Why?
| | Acid Anhydride Hydrolases | 1 | 1999 | 7 | 0.220 |
Why?
| | AAA Domain | 1 | 2019 | 1 | 0.210 |
Why?
| | DNA Polymerase I | 2 | 1990 | 23 | 0.210 |
Why?
| | Cations, Divalent | 2 | 2012 | 53 | 0.210 |
Why?
| | Circular Dichroism | 4 | 2001 | 178 | 0.200 |
Why?
| | Nuclear Magnetic Resonance, Biomolecular | 3 | 2011 | 237 | 0.200 |
Why?
| | Bacterial Proteins | 5 | 2013 | 750 | 0.200 |
Why?
| | Base Sequence | 7 | 2000 | 2351 | 0.200 |
Why?
| | Protein Domains | 2 | 2017 | 209 | 0.190 |
Why?
| | Temperature | 3 | 2011 | 634 | 0.190 |
Why?
| | Sodium Chloride | 2 | 2015 | 172 | 0.190 |
Why?
| | Arginine | 1 | 2019 | 230 | 0.180 |
Why?
| | Phosphates | 1 | 2019 | 175 | 0.180 |
Why?
| | Plasmids | 3 | 2014 | 382 | 0.180 |
Why?
| | Protein Structure, Tertiary | 4 | 2010 | 907 | 0.180 |
Why?
| | Glutamic Acid | 1 | 2019 | 223 | 0.180 |
Why?
| | Substrate Specificity | 4 | 2013 | 409 | 0.180 |
Why?
| | Sequence Deletion | 3 | 2005 | 193 | 0.170 |
Why?
| | Static Electricity | 1 | 2017 | 123 | 0.170 |
Why?
| | Molecular Weight | 3 | 2006 | 353 | 0.170 |
Why?
| | Area Under Curve | 1 | 2017 | 351 | 0.160 |
Why?
| | Molecular Dynamics Simulation | 2 | 2019 | 207 | 0.160 |
Why?
| | Peptide Fragments | 2 | 1999 | 702 | 0.160 |
Why?
| | Magnesium | 2 | 2012 | 152 | 0.160 |
Why?
| | Protein Binding | 5 | 2015 | 2091 | 0.160 |
Why?
| | DNA Polymerase II | 1 | 1995 | 28 | 0.160 |
Why?
| | RNA Nucleotidyltransferases | 1 | 1995 | 29 | 0.160 |
Why?
| | Acrolein | 1 | 1995 | 31 | 0.160 |
Why?
| | Protein Denaturation | 3 | 2001 | 117 | 0.150 |
Why?
| | Bacteriophages | 1 | 2015 | 46 | 0.150 |
Why?
| | Microscopy, Electron | 1 | 2015 | 452 | 0.150 |
Why?
| | Electrophoretic Mobility Shift Assay | 1 | 2014 | 86 | 0.150 |
Why?
| | Enzyme Stability | 3 | 1999 | 101 | 0.150 |
Why?
| | Genes, Bacterial | 1 | 2014 | 164 | 0.140 |
Why?
| | Bacterial Secretion Systems | 1 | 2013 | 5 | 0.140 |
Why?
| | Biomechanical Phenomena | 1 | 2017 | 649 | 0.140 |
Why?
| | Validation Studies as Topic | 1 | 2013 | 21 | 0.140 |
Why?
| | Hydrogen-Ion Concentration | 2 | 2006 | 591 | 0.140 |
Why?
| | Herpesvirus 1, Human | 1 | 2014 | 84 | 0.140 |
Why?
| | Electrophoresis, Polyacrylamide Gel | 2 | 2010 | 379 | 0.140 |
Why?
| | Hemolysin Proteins | 1 | 2013 | 38 | 0.130 |
Why?
| | Cloning, Molecular | 3 | 1999 | 597 | 0.130 |
Why?
| | Ligands | 1 | 2014 | 516 | 0.130 |
Why?
| | Buffers | 2 | 2006 | 79 | 0.130 |
Why?
| | Drug Carriers | 1 | 2013 | 122 | 0.130 |
Why?
| | Sequence Homology, Amino Acid | 2 | 2010 | 413 | 0.130 |
Why?
| | Cross-Linking Reagents | 1 | 2013 | 171 | 0.130 |
Why?
| | Bacillus Phages | 1 | 2011 | 2 | 0.130 |
Why?
| | Gene Expression Regulation, Bacterial | 1 | 2014 | 274 | 0.120 |
Why?
| | Recombinant Proteins | 3 | 2005 | 1460 | 0.120 |
Why?
| | Spectrometry, Fluorescence | 2 | 2005 | 191 | 0.120 |
Why?
| | Urea | 1 | 2012 | 89 | 0.120 |
Why?
| | Lysine | 1 | 2013 | 237 | 0.120 |
Why?
| | Polyamines | 2 | 2006 | 24 | 0.120 |
Why?
| | Binding, Competitive | 2 | 2015 | 211 | 0.110 |
Why?
| | Adenoviridae | 1 | 2011 | 196 | 0.110 |
Why?
| | Pseudomonas aeruginosa | 1 | 2013 | 279 | 0.110 |
Why?
| | Gene Expression | 1 | 2017 | 1575 | 0.110 |
Why?
| | DNA Probes | 1 | 1990 | 69 | 0.110 |
Why?
| | DNA Primers | 3 | 2001 | 606 | 0.110 |
Why?
| | Adenosine Diphosphate | 2 | 2009 | 87 | 0.100 |
Why?
| | Mass Spectrometry | 1 | 2013 | 777 | 0.100 |
Why?
| | Proteins | 1 | 2015 | 969 | 0.100 |
Why?
| | Fluorescent Dyes | 1 | 1990 | 283 | 0.100 |
Why?
| | Virion | 1 | 2008 | 82 | 0.100 |
Why?
| | Spectrophotometry, Ultraviolet | 2 | 2001 | 92 | 0.090 |
Why?
| | Azides | 2 | 2005 | 45 | 0.090 |
Why?
| | Fluorescence | 1 | 2007 | 158 | 0.090 |
Why?
| | Virulence | 1 | 2007 | 241 | 0.080 |
Why?
| | Biophysical Phenomena | 2 | 2007 | 67 | 0.080 |
Why?
| | Acrylamide | 1 | 2005 | 5 | 0.080 |
Why?
| | Photoaffinity Labels | 1 | 2005 | 6 | 0.080 |
Why?
| | Biophysics | 2 | 2007 | 72 | 0.080 |
Why?
| | Macromolecular Substances | 2 | 1998 | 230 | 0.080 |
Why?
| | Energy Metabolism | 1 | 2011 | 924 | 0.080 |
Why?
| | Tryptophan | 1 | 2005 | 131 | 0.070 |
Why?
| | Vanadates | 1 | 2004 | 29 | 0.070 |
Why?
| | Protein Isoforms | 1 | 2005 | 356 | 0.070 |
Why?
| | Helix-Turn-Helix Motifs | 1 | 2002 | 5 | 0.060 |
Why?
| | Adenosine | 1 | 2004 | 249 | 0.060 |
Why?
| | Models, Genetic | 1 | 2005 | 656 | 0.060 |
Why?
| | Structure-Activity Relationship | 1 | 2002 | 555 | 0.060 |
Why?
| | Nitrogen Isotopes | 1 | 2000 | 52 | 0.060 |
Why?
| | Protons | 1 | 2000 | 68 | 0.060 |
Why?
| | Carbon Isotopes | 1 | 2000 | 121 | 0.050 |
Why?
| | Image Processing, Computer-Assisted | 1 | 2005 | 726 | 0.050 |
Why?
| | Nucleoside-Triphosphatase | 1 | 1999 | 5 | 0.050 |
Why?
| | Genes, Viral | 3 | 1997 | 111 | 0.050 |
Why?
| | Magnetic Resonance Spectroscopy | 1 | 2002 | 523 | 0.050 |
Why?
| | Guanosine Triphosphate | 1 | 1999 | 82 | 0.050 |
Why?
| | Allosteric Regulation | 1 | 1999 | 81 | 0.050 |
Why?
| | Endonucleases | 1 | 1999 | 29 | 0.050 |
Why?
| | Histidine | 1 | 1999 | 59 | 0.050 |
Why?
| | Catalytic Domain | 1 | 1999 | 212 | 0.050 |
Why?
| | Sarcosine | 1 | 1998 | 11 | 0.050 |
Why?
| | Gene Expression Regulation, Viral | 1 | 1999 | 103 | 0.050 |
Why?
| | Guanidine | 1 | 1998 | 38 | 0.050 |
Why?
| | Hot Temperature | 1 | 2001 | 377 | 0.050 |
Why?
| | Detergents | 1 | 1998 | 53 | 0.050 |
Why?
| | Solutions | 1 | 1998 | 178 | 0.050 |
Why?
| | Solubility | 1 | 1998 | 271 | 0.050 |
Why?
| | Pseudomonas Phages | 1 | 1997 | 3 | 0.050 |
Why?
| | Terminator Regions, Genetic | 1 | 1997 | 13 | 0.050 |
Why?
| | Suppression, Genetic | 1 | 1997 | 28 | 0.040 |
Why?
| | Imidazoles | 1 | 1998 | 260 | 0.040 |
Why?
| | Iodoacetamide | 1 | 1995 | 5 | 0.040 |
Why?
| | Dithiothreitol | 1 | 1995 | 22 | 0.040 |
Why?
| | DNA Primase | 1 | 1995 | 39 | 0.040 |
Why?
| | Oligodeoxyribonucleotides | 1 | 1995 | 160 | 0.040 |
Why?
| | Point Mutation | 1 | 2016 | 259 | 0.040 |
Why?
| | Vero Cells | 1 | 2014 | 72 | 0.040 |
Why?
| | Receptors, Transferrin | 1 | 2013 | 20 | 0.040 |
Why?
| | Transferrin | 1 | 2013 | 46 | 0.040 |
Why?
| | Virus Internalization | 1 | 2013 | 41 | 0.030 |
Why?
| | Amidohydrolases | 1 | 2013 | 28 | 0.030 |
Why?
| | Restriction Mapping | 1 | 1993 | 92 | 0.030 |
Why?
| | Chromatography, Ion Exchange | 1 | 1993 | 60 | 0.030 |
Why?
| | Muramidase | 1 | 2013 | 77 | 0.030 |
Why?
| | Chromatography, Affinity | 1 | 1993 | 95 | 0.030 |
Why?
| | Viral Plaque Assay | 1 | 2011 | 30 | 0.030 |
Why?
| | Molecular Chaperones | 1 | 2013 | 173 | 0.030 |
Why?
| | HeLa Cells | 1 | 2013 | 637 | 0.030 |
Why?
| | Bacteriophage T4 | 1 | 2010 | 16 | 0.030 |
Why?
| | Tandem Mass Spectrometry | 1 | 2013 | 450 | 0.030 |
Why?
| | Optical Tweezers | 1 | 2010 | 20 | 0.030 |
Why?
| | Computer Graphics | 1 | 1990 | 45 | 0.030 |
Why?
| | Microspheres | 1 | 2010 | 99 | 0.030 |
Why?
| | Amino Acid Motifs | 1 | 2010 | 211 | 0.030 |
Why?
| | Exodeoxyribonuclease V | 1 | 1989 | 8 | 0.030 |
Why?
| | Exodeoxyribonucleases | 1 | 1989 | 23 | 0.030 |
Why?
| | Viral Load | 1 | 2011 | 462 | 0.030 |
Why?
| | Algorithms | 1 | 2015 | 1555 | 0.020 |
Why?
| | Microscopy, Fluorescence | 1 | 2005 | 442 | 0.020 |
Why?
| | DNA, Recombinant | 1 | 2001 | 46 | 0.020 |
Why?
| | Virus Replication | 1 | 2001 | 434 | 0.010 |
Why?
| | Trypsin | 1 | 1997 | 68 | 0.010 |
Why?
| | Affinity Labels | 1 | 1996 | 28 | 0.010 |
Why?
| | Mutagenesis, Site-Directed | 1 | 1996 | 407 | 0.010 |
Why?
| | Animals | 1 | 2014 | 34482 | 0.010 |
Why?
| | Humans | 1 | 2013 | 108073 | 0.000 |
Why?
|
|
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