 Thomas Perkins
Concepts (151)
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?
|
|---|
| Microscopy, Atomic Force | 24 | 2021 | 118 | 7.780 |
Why?
| | Bacteriorhodopsins | 7 | 2021 | 12 | 4.360 |
Why?
| | DNA | 20 | 2022 | 1388 | 4.040 |
Why?
| | Optical Tweezers | 8 | 2022 | 20 | 3.300 |
Why?
| | Nucleic Acid Conformation | 13 | 2020 | 670 | 2.460 |
Why?
| | Protein Unfolding | 5 | 2019 | 34 | 2.240 |
Why?
| | Protein Folding | 7 | 2021 | 250 | 2.140 |
Why?
| | Thermodynamics | 8 | 2021 | 392 | 2.130 |
Why?
| | Proteins | 6 | 2021 | 938 | 2.130 |
Why?
| | Gold | 6 | 2017 | 102 | 1.670 |
Why?
| | Nanotechnology | 5 | 2018 | 120 | 1.450 |
Why?
| | Spectrum Analysis | 3 | 2018 | 88 | 1.260 |
Why?
| | Biophysics | 4 | 2016 | 73 | 1.250 |
Why?
| | Single Molecule Imaging | 5 | 2021 | 35 | 1.220 |
Why?
| | Exodeoxyribonuclease V | 3 | 2016 | 8 | 1.190 |
Why?
| | DNA, Single-Stranded | 3 | 2022 | 114 | 1.120 |
Why?
| | Micromanipulation | 4 | 2007 | 12 | 1.090 |
Why?
| | Escherichia coli | 2 | 2022 | 758 | 1.040 |
Why?
| | Optics and Photonics | 2 | 2017 | 44 | 1.010 |
Why?
| | Nanostructures | 3 | 2012 | 100 | 0.970 |
Why?
| | Imaging, Three-Dimensional | 3 | 2020 | 499 | 0.920 |
Why?
| | Models, Chemical | 6 | 2020 | 274 | 0.870 |
Why?
| | Escherichia coli Proteins | 2 | 2016 | 170 | 0.820 |
Why?
| | Lipid Bilayers | 5 | 2021 | 100 | 0.750 |
Why?
| | Mechanical Phenomena | 3 | 2021 | 86 | 0.750 |
Why?
| | Models, Molecular | 4 | 2021 | 1435 | 0.730 |
Why?
| | Retina | 2 | 2019 | 278 | 0.710 |
Why?
| | Polycomb Repressive Complex 2 | 1 | 2020 | 60 | 0.690 |
Why?
| | Lasers | 5 | 2017 | 124 | 0.650 |
Why?
| | Digoxigenin | 1 | 2017 | 2 | 0.640 |
Why?
| | Microscopy | 3 | 2017 | 125 | 0.640 |
Why?
| | Computer-Aided Design | 1 | 2017 | 42 | 0.620 |
Why?
| | HIV | 1 | 2018 | 210 | 0.600 |
Why?
| | Halobacterium salinarum | 2 | 2021 | 3 | 0.590 |
Why?
| | Molecular Motor Proteins | 2 | 2014 | 34 | 0.530 |
Why?
| | Algorithms | 4 | 2018 | 1541 | 0.510 |
Why?
| | RNA, Viral | 1 | 2018 | 572 | 0.510 |
Why?
| | DNA, Bacterial | 1 | 2016 | 314 | 0.510 |
Why?
| | DNA-Binding Proteins | 2 | 2017 | 1346 | 0.450 |
Why?
| | Protein Binding | 5 | 2020 | 1975 | 0.430 |
Why?
| | Intercalating Agents | 1 | 2011 | 5 | 0.420 |
Why?
| | Polymerase Chain Reaction | 2 | 2013 | 1012 | 0.420 |
Why?
| | Elasticity | 3 | 2011 | 193 | 0.420 |
Why?
| | Surface Properties | 4 | 2019 | 397 | 0.410 |
Why?
| | Base Pairing | 2 | 2009 | 59 | 0.400 |
Why?
| | Kinetics | 6 | 2016 | 1624 | 0.390 |
Why?
| | Purple Membrane | 1 | 2010 | 1 | 0.390 |
Why?
| | DNA, Viral | 3 | 1997 | 356 | 0.340 |
Why?
| | Subtraction Technique | 2 | 2007 | 27 | 0.330 |
Why?
| | Binding Sites | 4 | 2017 | 1224 | 0.330 |
Why?
| | Hydrogen-Ion Concentration | 2 | 2021 | 536 | 0.310 |
Why?
| | Image Interpretation, Computer-Assisted | 2 | 2007 | 220 | 0.280 |
Why?
| | Ligands | 2 | 2017 | 567 | 0.260 |
Why?
| | Equipment Design | 3 | 2017 | 519 | 0.260 |
Why?
| | Calibration | 2 | 2016 | 135 | 0.250 |
Why?
| | Hot Temperature | 1 | 2006 | 334 | 0.250 |
Why?
| | Motion | 3 | 2014 | 95 | 0.230 |
Why?
| | Exodeoxyribonucleases | 1 | 2003 | 22 | 0.230 |
Why?
| | Image Enhancement | 1 | 2004 | 181 | 0.230 |
Why?
| | Sensitivity and Specificity | 4 | 2009 | 1795 | 0.210 |
Why?
| | Type III Secretion Systems | 1 | 2021 | 9 | 0.200 |
Why?
| | DNA Helicases | 1 | 2022 | 131 | 0.190 |
Why?
| | Bacterial Physiological Phenomena | 1 | 2021 | 57 | 0.190 |
Why?
| | Amino Acid Substitution | 1 | 2021 | 276 | 0.180 |
Why?
| | Point Mutation | 1 | 2021 | 228 | 0.180 |
Why?
| | Protein Denaturation | 1 | 2019 | 73 | 0.180 |
Why?
| | Base Sequence | 1 | 2003 | 2159 | 0.170 |
Why?
| | Aluminum Silicates | 1 | 2019 | 12 | 0.170 |
Why?
| | Buffers | 1 | 2019 | 56 | 0.170 |
Why?
| | Protein Multimerization | 1 | 2020 | 161 | 0.170 |
Why?
| | Time Factors | 4 | 2013 | 6412 | 0.160 |
Why?
| | Automation | 1 | 2018 | 77 | 0.160 |
Why?
| | Breeding | 1 | 2018 | 56 | 0.160 |
Why?
| | RecQ Helicases | 1 | 2017 | 9 | 0.160 |
Why?
| | Protein Conformation, alpha-Helical | 1 | 2017 | 15 | 0.160 |
Why?
| | Protein Conformation, beta-Strand | 1 | 2017 | 16 | 0.150 |
Why?
| | Bacteriophage lambda | 4 | 2003 | 81 | 0.150 |
Why?
| | Optical Fibers | 1 | 2017 | 18 | 0.150 |
Why?
| | Nucleic Acid Denaturation | 2 | 2009 | 30 | 0.150 |
Why?
| | Stress, Mechanical | 3 | 2013 | 443 | 0.150 |
Why?
| | Image Processing, Computer-Assisted | 3 | 2010 | 709 | 0.150 |
Why?
| | Adenylyl Imidodiphosphate | 1 | 2016 | 5 | 0.140 |
Why?
| | Bayes Theorem | 1 | 2018 | 344 | 0.140 |
Why?
| | Reproducibility of Results | 3 | 2013 | 2874 | 0.140 |
Why?
| | Adenosine Diphosphate | 1 | 2016 | 88 | 0.140 |
Why?
| | Protein Refolding | 1 | 2015 | 1 | 0.140 |
Why?
| | Bacterial Proteins | 1 | 2021 | 759 | 0.130 |
Why?
| | Temperature | 1 | 2017 | 622 | 0.120 |
Why?
| | Adenosine Triphosphate | 1 | 2016 | 439 | 0.120 |
Why?
| | Spectrophotometry, Infrared | 1 | 2013 | 54 | 0.120 |
Why?
| | Torsion, Mechanical | 1 | 2013 | 7 | 0.120 |
Why?
| | Immobilized Proteins | 1 | 2013 | 12 | 0.110 |
Why?
| | Limit of Detection | 1 | 2013 | 55 | 0.110 |
Why?
| | Protein Conformation | 1 | 2016 | 848 | 0.110 |
Why?
| | Signal-To-Noise Ratio | 1 | 2013 | 59 | 0.110 |
Why?
| | Hydrodynamics | 1 | 2013 | 37 | 0.110 |
Why?
| | Genomics | 1 | 2018 | 706 | 0.110 |
Why?
| | Genotype | 1 | 2018 | 1882 | 0.110 |
Why?
| | Silicon Compounds | 1 | 2012 | 2 | 0.110 |
Why?
| | DNA Primers | 1 | 2013 | 533 | 0.110 |
Why?
| | Movement | 1 | 2014 | 248 | 0.100 |
Why?
| | Particle Size | 1 | 2013 | 345 | 0.100 |
Why?
| | Gene Expression | 1 | 2016 | 1489 | 0.100 |
Why?
| | Molecular Structure | 1 | 2011 | 459 | 0.090 |
Why?
| | Staining and Labeling | 1 | 2010 | 146 | 0.090 |
Why?
| | Light | 1 | 2013 | 342 | 0.090 |
Why?
| | Biotin | 1 | 2010 | 24 | 0.090 |
Why?
| | Polymorphism, Single Nucleotide | 1 | 2018 | 2062 | 0.090 |
Why?
| | Optical Devices | 1 | 2009 | 12 | 0.090 |
Why?
| | Vacuum | 1 | 2009 | 14 | 0.090 |
Why?
| | Glass | 1 | 2009 | 44 | 0.090 |
Why?
| | Microscopy, Fluorescence | 3 | 1995 | 412 | 0.080 |
Why?
| | Cold Temperature | 1 | 2009 | 132 | 0.080 |
Why?
| | Transcription Factor TFIIA | 1 | 2007 | 8 | 0.080 |
Why?
| | TATA Box | 1 | 2007 | 24 | 0.080 |
Why?
| | TATA-Box Binding Protein | 1 | 2007 | 22 | 0.080 |
Why?
| | Membrane Proteins | 1 | 2013 | 1055 | 0.080 |
Why?
| | Thermography | 1 | 2006 | 12 | 0.070 |
Why?
| | Energy Transfer | 1 | 2006 | 52 | 0.070 |
Why?
| | Online Systems | 1 | 2004 | 26 | 0.060 |
Why?
| | Equipment Failure Analysis | 1 | 2004 | 139 | 0.060 |
Why?
| | Enzyme Stability | 1 | 2004 | 75 | 0.060 |
Why?
| | Fluorescent Dyes | 2 | 1997 | 316 | 0.060 |
Why?
| | Consensus Sequence | 1 | 2003 | 70 | 0.060 |
Why?
| | Macromolecular Substances | 1 | 2004 | 201 | 0.060 |
Why?
| | Stochastic Processes | 1 | 2003 | 66 | 0.060 |
Why?
| | Hydrogen Bonding | 1 | 2003 | 146 | 0.060 |
Why?
| | Oligodeoxyribonucleotides | 1 | 2003 | 139 | 0.060 |
Why?
| | Electrophoresis, Polyacrylamide Gel | 1 | 2003 | 332 | 0.060 |
Why?
| | Probability | 1 | 2003 | 305 | 0.050 |
Why?
| | Software | 1 | 2007 | 613 | 0.050 |
Why?
| | Enzyme Activation | 1 | 2004 | 828 | 0.050 |
Why?
| | Viral Proteins | 1 | 2003 | 296 | 0.050 |
Why?
| | Gram-Negative Bacteria | 1 | 2021 | 70 | 0.050 |
Why?
| | Salmonella | 1 | 2021 | 54 | 0.050 |
Why?
| | Protein Stability | 1 | 2021 | 164 | 0.050 |
Why?
| | Humans | 3 | 2020 | 118974 | 0.040 |
Why?
| | Chemistry, Physical | 1 | 1997 | 40 | 0.040 |
Why?
| | Chemical Phenomena | 1 | 1997 | 82 | 0.040 |
Why?
| | Entropy | 1 | 1997 | 35 | 0.040 |
Why?
| | Fluorescence | 1 | 1997 | 159 | 0.040 |
Why?
| | Biopolymers | 1 | 1995 | 26 | 0.030 |
Why?
| | Cattle | 1 | 2018 | 978 | 0.030 |
Why?
| | Protein Structure, Secondary | 1 | 2015 | 338 | 0.030 |
Why?
| | Microspheres | 1 | 1994 | 130 | 0.030 |
Why?
| | Solutions | 1 | 1994 | 156 | 0.030 |
Why?
| | Models, Statistical | 1 | 2018 | 636 | 0.030 |
Why?
| | Fluorescence Resonance Energy Transfer | 1 | 2007 | 183 | 0.020 |
Why?
| | Computer Simulation | 1 | 2007 | 922 | 0.010 |
Why?
| | Mutation | 1 | 2007 | 3457 | 0.010 |
Why?
| | Animals | 1 | 2018 | 33381 | 0.010 |
Why?
|
|
Perkins's Networks
Click the "See All" links for more information and interactive visualizations!
Concepts  Derived automatically from this person's publications. _
Co-Authors People in Profiles who have published with this person. _
Similar People People who share similar concepts with this person. _
Same Department
People who are also in this person's primary department.
Physical Neighbors People whose addresses are nearby this person. _
|