Carlos Catalano
Concepts (224)
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?
|
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Bacteriophage lambda | 52 | 2025 | 88 | 10.580 |
Why?
| Virus Assembly | 36 | 2025 | 79 | 8.740 |
Why?
| DNA, Viral | 36 | 2025 | 384 | 5.310 |
Why?
| DNA Packaging | 18 | 2025 | 24 | 5.280 |
Why?
| Endodeoxyribonucleases | 32 | 2025 | 67 | 4.550 |
Why?
| Genome, Viral | 17 | 2020 | 132 | 3.800 |
Why?
| Capsid Proteins | 10 | 2022 | 91 | 3.340 |
Why?
| Capsid | 14 | 2022 | 91 | 3.110 |
Why?
| Viral Proteins | 21 | 2019 | 332 | 2.670 |
Why?
| Nanoparticles | 4 | 2022 | 370 | 1.850 |
Why?
| Integration Host Factors | 10 | 2025 | 13 | 1.700 |
Why?
| Adenosine Triphosphate | 17 | 2020 | 483 | 1.400 |
Why?
| Glycoproteins | 5 | 2017 | 340 | 1.330 |
Why?
| Molecular Motor Proteins | 5 | 2011 | 35 | 1.140 |
Why?
| Adenosine Triphosphatases | 14 | 2019 | 166 | 1.030 |
Why?
| Protein Folding | 8 | 2022 | 265 | 0.870 |
Why?
| Escherichia coli | 11 | 2025 | 786 | 0.770 |
Why?
| Models, Molecular | 12 | 2017 | 1486 | 0.750 |
Why?
| Hydrolysis | 11 | 2019 | 191 | 0.740 |
Why?
| Thermodynamics | 6 | 2015 | 408 | 0.720 |
Why?
| Breast Neoplasms | 2 | 2022 | 2139 | 0.650 |
Why?
| Biological Products | 1 | 2022 | 203 | 0.620 |
Why?
| DNA-Binding Proteins | 10 | 2005 | 1433 | 0.530 |
Why?
| Protein Precursors | 1 | 2017 | 126 | 0.520 |
Why?
| HIV Envelope Protein gp160 | 1 | 2015 | 5 | 0.510 |
Why?
| Nucleic Acid Conformation | 5 | 2015 | 706 | 0.490 |
Why?
| AIDS Vaccines | 1 | 2015 | 47 | 0.490 |
Why?
| DNA Helicases | 3 | 2011 | 153 | 0.490 |
Why?
| Molecular Sequence Data | 13 | 2013 | 2854 | 0.430 |
Why?
| Kinetics | 16 | 2012 | 1634 | 0.390 |
Why?
| Escherichia coli Proteins | 2 | 2020 | 181 | 0.380 |
Why?
| Trastuzumab | 2 | 2022 | 100 | 0.370 |
Why?
| Catalysis | 7 | 2019 | 309 | 0.370 |
Why?
| DNA Viruses | 2 | 2012 | 10 | 0.360 |
Why?
| DNA | 6 | 2024 | 1412 | 0.360 |
Why?
| Protein Multimerization | 3 | 2017 | 180 | 0.350 |
Why?
| Protein Subunits | 4 | 2006 | 232 | 0.350 |
Why?
| Amino Acid Sequence | 9 | 2013 | 2060 | 0.350 |
Why?
| Protein Structure, Quaternary | 5 | 2019 | 121 | 0.340 |
Why?
| Ultracentrifugation | 4 | 2017 | 48 | 0.330 |
Why?
| Protein Conformation | 9 | 2014 | 857 | 0.330 |
Why?
| Peptide Hydrolases | 1 | 2010 | 109 | 0.330 |
Why?
| Bacteriophages | 2 | 2024 | 93 | 0.320 |
Why?
| Nucleotides | 2 | 2008 | 118 | 0.320 |
Why?
| Nucleocapsid | 1 | 2008 | 18 | 0.310 |
Why?
| Nucleoproteins | 3 | 2019 | 28 | 0.300 |
Why?
| Promoter Regions, Genetic | 4 | 2017 | 1207 | 0.300 |
Why?
| DNA Replication | 3 | 2006 | 228 | 0.280 |
Why?
| Models, Biological | 6 | 2015 | 1716 | 0.280 |
Why?
| Protein Structure, Secondary | 4 | 2017 | 339 | 0.260 |
Why?
| Mutation | 8 | 2019 | 3723 | 0.260 |
Why?
| Biological Assay | 1 | 2006 | 118 | 0.240 |
Why?
| DNA, Bacterial | 1 | 2006 | 325 | 0.240 |
Why?
| Proteomics | 2 | 2022 | 1008 | 0.240 |
Why?
| Holoenzymes | 1 | 2005 | 21 | 0.240 |
Why?
| Cell Line, Tumor | 2 | 2022 | 3185 | 0.230 |
Why?
| Hydrophobic and Hydrophilic Interactions | 2 | 2017 | 185 | 0.220 |
Why?
| Delayed-Action Preparations | 1 | 2024 | 179 | 0.210 |
Why?
| Binding Sites | 7 | 2016 | 1252 | 0.210 |
Why?
| Ubiquitin-Specific Peptidase 7 | 1 | 2022 | 4 | 0.200 |
Why?
| GTP Phosphohydrolases | 2 | 2000 | 79 | 0.200 |
Why?
| Dimerization | 4 | 2005 | 189 | 0.200 |
Why?
| Temperature | 4 | 2024 | 636 | 0.200 |
Why?
| Models, Chemical | 1 | 2004 | 265 | 0.200 |
Why?
| Protein Stability | 2 | 2013 | 161 | 0.190 |
Why?
| Adenine Nucleotides | 1 | 2020 | 22 | 0.170 |
Why?
| Acid Anhydride Hydrolases | 1 | 1999 | 6 | 0.170 |
Why?
| Base Sequence | 7 | 2000 | 2162 | 0.170 |
Why?
| AAA Domain | 1 | 2019 | 3 | 0.170 |
Why?
| DNA Polymerase I | 2 | 1990 | 29 | 0.160 |
Why?
| Cations, Divalent | 2 | 2012 | 54 | 0.160 |
Why?
| Circular Dichroism | 4 | 2001 | 147 | 0.160 |
Why?
| Bacterial Proteins | 5 | 2013 | 834 | 0.160 |
Why?
| Nuclear Magnetic Resonance, Biomolecular | 3 | 2011 | 251 | 0.160 |
Why?
| Receptor, ErbB-2 | 1 | 2021 | 337 | 0.160 |
Why?
| Protein Domains | 2 | 2017 | 252 | 0.150 |
Why?
| Sodium Chloride | 2 | 2015 | 142 | 0.150 |
Why?
| Protein Structure, Tertiary | 4 | 2010 | 842 | 0.150 |
Why?
| Phosphates | 1 | 2019 | 169 | 0.150 |
Why?
| Plasmids | 3 | 2014 | 358 | 0.140 |
Why?
| Arginine | 1 | 2019 | 264 | 0.140 |
Why?
| Substrate Specificity | 4 | 2013 | 373 | 0.140 |
Why?
| Glutamic Acid | 1 | 2019 | 232 | 0.140 |
Why?
| Sequence Deletion | 3 | 2005 | 181 | 0.140 |
Why?
| Static Electricity | 1 | 2017 | 117 | 0.130 |
Why?
| Vaccines | 1 | 2022 | 404 | 0.130 |
Why?
| Area Under Curve | 1 | 2017 | 292 | 0.130 |
Why?
| Peptide Fragments | 2 | 1999 | 698 | 0.130 |
Why?
| Molecular Weight | 3 | 2006 | 333 | 0.130 |
Why?
| Biomechanical Phenomena | 2 | 2017 | 786 | 0.130 |
Why?
| Protein Binding | 5 | 2015 | 2120 | 0.130 |
Why?
| Molecular Dynamics Simulation | 2 | 2019 | 217 | 0.130 |
Why?
| Magnesium | 2 | 2012 | 151 | 0.130 |
Why?
| RNA Nucleotidyltransferases | 1 | 1995 | 21 | 0.130 |
Why?
| Acrolein | 1 | 1995 | 23 | 0.130 |
Why?
| DNA Polymerase II | 1 | 1995 | 38 | 0.120 |
Why?
| Protein Denaturation | 3 | 2001 | 74 | 0.120 |
Why?
| Microscopy, Electron | 1 | 2015 | 421 | 0.120 |
Why?
| Enzyme Stability | 3 | 1999 | 68 | 0.120 |
Why?
| Electrophoretic Mobility Shift Assay | 1 | 2014 | 83 | 0.110 |
Why?
| Genes, Bacterial | 1 | 2014 | 159 | 0.110 |
Why?
| Biotechnology | 1 | 2014 | 43 | 0.110 |
Why?
| Hydrogen-Ion Concentration | 2 | 2006 | 549 | 0.110 |
Why?
| Bacterial Secretion Systems | 1 | 2013 | 6 | 0.110 |
Why?
| Electrophoresis, Polyacrylamide Gel | 2 | 2010 | 327 | 0.110 |
Why?
| Validation Studies as Topic | 1 | 2013 | 22 | 0.110 |
Why?
| Cloning, Molecular | 3 | 1999 | 536 | 0.110 |
Why?
| Hemolysin Proteins | 1 | 2013 | 34 | 0.110 |
Why?
| Herpesvirus 1, Human | 1 | 2014 | 89 | 0.110 |
Why?
| Antibodies, Neutralizing | 1 | 2015 | 261 | 0.100 |
Why?
| Sequence Homology, Amino Acid | 2 | 2010 | 373 | 0.100 |
Why?
| Drug Carriers | 1 | 2013 | 116 | 0.100 |
Why?
| Recombinant Proteins | 3 | 2005 | 1314 | 0.100 |
Why?
| Buffers | 2 | 2006 | 55 | 0.100 |
Why?
| Ligands | 1 | 2014 | 624 | 0.100 |
Why?
| Cross-Linking Reagents | 1 | 2013 | 205 | 0.100 |
Why?
| Gene Expression Regulation, Bacterial | 1 | 2014 | 324 | 0.100 |
Why?
| Bacillus Phages | 1 | 2011 | 2 | 0.100 |
Why?
| Spectrometry, Fluorescence | 2 | 2005 | 171 | 0.100 |
Why?
| Urea | 1 | 2012 | 76 | 0.100 |
Why?
| Gene Expression | 1 | 2017 | 1487 | 0.090 |
Why?
| Lysine | 1 | 2013 | 278 | 0.090 |
Why?
| Binding, Competitive | 2 | 2015 | 208 | 0.090 |
Why?
| Adenoviridae | 1 | 2011 | 194 | 0.090 |
Why?
| Polyamines | 2 | 2006 | 39 | 0.090 |
Why?
| Pseudomonas aeruginosa | 1 | 2013 | 344 | 0.090 |
Why?
| DNA Primers | 3 | 2001 | 523 | 0.090 |
Why?
| DNA Probes | 1 | 1990 | 61 | 0.090 |
Why?
| Mass Spectrometry | 1 | 2013 | 664 | 0.080 |
Why?
| Adenosine Diphosphate | 2 | 2009 | 79 | 0.080 |
Why?
| Optical Tweezers | 2 | 2025 | 21 | 0.080 |
Why?
| Proteins | 1 | 2015 | 948 | 0.080 |
Why?
| Fluorescent Dyes | 1 | 1990 | 319 | 0.070 |
Why?
| Muramidase | 2 | 2022 | 75 | 0.070 |
Why?
| Virion | 1 | 2008 | 85 | 0.070 |
Why?
| Spectrophotometry, Ultraviolet | 2 | 2001 | 82 | 0.070 |
Why?
| Azides | 2 | 2005 | 46 | 0.070 |
Why?
| Fluorescence | 1 | 2007 | 160 | 0.070 |
Why?
| Virulence | 1 | 2007 | 255 | 0.070 |
Why?
| Humans | 6 | 2022 | 130305 | 0.070 |
Why?
| Energy Metabolism | 1 | 2011 | 841 | 0.060 |
Why?
| Female | 3 | 2022 | 68842 | 0.060 |
Why?
| Biophysical Phenomena | 2 | 2007 | 64 | 0.060 |
Why?
| Acrylamide | 1 | 2005 | 3 | 0.060 |
Why?
| Photoaffinity Labels | 1 | 2005 | 6 | 0.060 |
Why?
| Macromolecular Substances | 2 | 1998 | 212 | 0.060 |
Why?
| Biophysics | 2 | 2007 | 69 | 0.060 |
Why?
| Single Molecule Imaging | 1 | 2025 | 35 | 0.060 |
Why?
| Phage Therapy | 1 | 2024 | 10 | 0.060 |
Why?
| Bone Cements | 1 | 2024 | 44 | 0.060 |
Why?
| Vanadates | 1 | 2004 | 14 | 0.060 |
Why?
| Drug Compounding | 1 | 2024 | 97 | 0.060 |
Why?
| Tryptophan | 1 | 2005 | 169 | 0.060 |
Why?
| Protein Isoforms | 1 | 2005 | 379 | 0.050 |
Why?
| Helix-Turn-Helix Motifs | 1 | 2002 | 5 | 0.050 |
Why?
| Adenosine | 1 | 2004 | 213 | 0.050 |
Why?
| Aluminum Oxide | 1 | 2022 | 12 | 0.050 |
Why?
| Powders | 1 | 2022 | 42 | 0.050 |
Why?
| Models, Genetic | 1 | 2005 | 591 | 0.050 |
Why?
| False Negative Reactions | 1 | 2021 | 52 | 0.050 |
Why?
| Structure-Activity Relationship | 1 | 2002 | 541 | 0.040 |
Why?
| HIV Infections | 1 | 2015 | 2721 | 0.040 |
Why?
| Nitrogen Isotopes | 1 | 2000 | 58 | 0.040 |
Why?
| Image Processing, Computer-Assisted | 1 | 2005 | 745 | 0.040 |
Why?
| Genes, Viral | 3 | 1997 | 94 | 0.040 |
Why?
| Protons | 1 | 2000 | 80 | 0.040 |
Why?
| Carbon Isotopes | 1 | 2000 | 123 | 0.040 |
Why?
| Nucleoside-Triphosphatase | 1 | 1999 | 6 | 0.040 |
Why?
| Magnetic Resonance Spectroscopy | 1 | 2002 | 514 | 0.040 |
Why?
| Guanosine Triphosphate | 1 | 1999 | 92 | 0.040 |
Why?
| Allosteric Regulation | 1 | 1999 | 100 | 0.040 |
Why?
| Endonucleases | 1 | 1999 | 30 | 0.040 |
Why?
| Histidine | 1 | 1999 | 61 | 0.040 |
Why?
| Gene Expression Regulation, Viral | 1 | 1999 | 91 | 0.040 |
Why?
| Sarcosine | 1 | 1998 | 10 | 0.040 |
Why?
| Catalytic Domain | 1 | 1999 | 219 | 0.040 |
Why?
| Guanidine | 1 | 1998 | 22 | 0.040 |
Why?
| Detergents | 1 | 1998 | 45 | 0.040 |
Why?
| Hot Temperature | 1 | 2001 | 366 | 0.040 |
Why?
| Solutions | 1 | 1998 | 148 | 0.040 |
Why?
| Solubility | 1 | 1998 | 235 | 0.040 |
Why?
| Pseudomonas Phages | 1 | 1997 | 3 | 0.040 |
Why?
| Terminator Regions, Genetic | 1 | 1997 | 12 | 0.040 |
Why?
| Suppression, Genetic | 1 | 1997 | 24 | 0.040 |
Why?
| Imidazoles | 1 | 1998 | 231 | 0.030 |
Why?
| Iodoacetamide | 1 | 1995 | 5 | 0.030 |
Why?
| Dithiothreitol | 1 | 1995 | 18 | 0.030 |
Why?
| DNA Primase | 1 | 1995 | 45 | 0.030 |
Why?
| Point Mutation | 1 | 2016 | 227 | 0.030 |
Why?
| Oligodeoxyribonucleotides | 1 | 1995 | 139 | 0.030 |
Why?
| Vero Cells | 1 | 2014 | 70 | 0.030 |
Why?
| Anti-Bacterial Agents | 1 | 2024 | 1712 | 0.030 |
Why?
| Receptors, Transferrin | 1 | 2013 | 23 | 0.030 |
Why?
| Transferrin | 1 | 2013 | 42 | 0.030 |
Why?
| Microscopy, Atomic Force | 1 | 2014 | 115 | 0.030 |
Why?
| Virus Internalization | 1 | 2013 | 46 | 0.030 |
Why?
| Prognosis | 1 | 2022 | 3830 | 0.030 |
Why?
| Amidohydrolases | 1 | 2013 | 30 | 0.030 |
Why?
| Restriction Mapping | 1 | 1993 | 77 | 0.030 |
Why?
| Chromatography, Ion Exchange | 1 | 1993 | 52 | 0.030 |
Why?
| Chromatography, Affinity | 1 | 1993 | 83 | 0.030 |
Why?
| Materials Testing | 1 | 2014 | 346 | 0.030 |
Why?
| Tomography, X-Ray Computed | 1 | 2022 | 2551 | 0.020 |
Why?
| Molecular Chaperones | 1 | 2013 | 174 | 0.020 |
Why?
| Viral Plaque Assay | 1 | 2011 | 29 | 0.020 |
Why?
| HeLa Cells | 1 | 2013 | 607 | 0.020 |
Why?
| Tandem Mass Spectrometry | 1 | 2013 | 453 | 0.020 |
Why?
| Bacteriophage T4 | 1 | 2010 | 15 | 0.020 |
Why?
| Computer Graphics | 1 | 1990 | 42 | 0.020 |
Why?
| Microspheres | 1 | 2010 | 124 | 0.020 |
Why?
| Amino Acid Motifs | 1 | 2010 | 211 | 0.020 |
Why?
| Viral Load | 1 | 2011 | 452 | 0.020 |
Why?
| Exodeoxyribonuclease V | 1 | 1989 | 6 | 0.020 |
Why?
| Exodeoxyribonucleases | 1 | 1989 | 24 | 0.020 |
Why?
| Lung | 1 | 2022 | 3967 | 0.020 |
Why?
| Algorithms | 1 | 2015 | 1638 | 0.020 |
Why?
| Microscopy, Fluorescence | 1 | 2005 | 405 | 0.010 |
Why?
| DNA, Recombinant | 1 | 2001 | 46 | 0.010 |
Why?
| Virus Replication | 1 | 2001 | 450 | 0.010 |
Why?
| Adult | 1 | 2021 | 35711 | 0.010 |
Why?
| Trypsin | 1 | 1997 | 74 | 0.010 |
Why?
| Affinity Labels | 1 | 1996 | 25 | 0.010 |
Why?
| Mutagenesis, Site-Directed | 1 | 1996 | 359 | 0.010 |
Why?
| Animals | 1 | 2014 | 35076 | 0.010 |
Why?
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