Concepts (59)
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?
|
---|
Thioredoxins | 16 | 2009 | 42 | 1.780 |
Why?
|
Peptide Fragments | 11 | 2008 | 308 | 1.070 |
Why?
|
Escherichia coli | 13 | 2006 | 453 | 0.850 |
Why?
|
Protein Folding | 8 | 2006 | 127 | 0.790 |
Why?
|
Protein Structure, Secondary | 8 | 2009 | 183 | 0.490 |
Why?
|
Magnetic Resonance Spectroscopy | 7 | 2008 | 289 | 0.310 |
Why?
|
Nuclear Magnetic Resonance, Biomolecular | 7 | 2009 | 84 | 0.260 |
Why?
|
Models, Biological | 1 | 2006 | 677 | 0.210 |
Why?
|
Models, Molecular | 7 | 2006 | 808 | 0.180 |
Why?
|
Circular Dichroism | 5 | 2000 | 62 | 0.160 |
Why?
|
Kinetics | 5 | 2000 | 708 | 0.140 |
Why?
|
Protein Denaturation | 4 | 2006 | 43 | 0.130 |
Why?
|
Temperature | 4 | 2007 | 286 | 0.130 |
Why?
|
Thermodynamics | 3 | 2006 | 216 | 0.120 |
Why?
|
Protein Conformation | 5 | 2007 | 389 | 0.110 |
Why?
|
Protein Structure, Tertiary | 2 | 2006 | 408 | 0.100 |
Why?
|
Escherichia coli Proteins | 3 | 2007 | 126 | 0.090 |
Why?
|
Spectrometry, Fluorescence | 3 | 1999 | 208 | 0.090 |
Why?
|
Repressor Proteins | 1 | 1992 | 249 | 0.080 |
Why?
|
Ultracentrifugation | 2 | 1999 | 16 | 0.080 |
Why?
|
Proline | 2 | 2000 | 43 | 0.080 |
Why?
|
Spin Labels | 1 | 2008 | 9 | 0.080 |
Why?
|
Nitrogen Isotopes | 4 | 2008 | 17 | 0.070 |
Why?
|
Carbon Isotopes | 4 | 2008 | 38 | 0.070 |
Why?
|
Pliability | 1 | 2006 | 5 | 0.070 |
Why?
|
Guanidine | 3 | 2001 | 13 | 0.060 |
Why?
|
Oxidation-Reduction | 3 | 2001 | 431 | 0.060 |
Why?
|
Hot Temperature | 2 | 2001 | 128 | 0.060 |
Why?
|
Computer Simulation | 1 | 2006 | 362 | 0.060 |
Why?
|
Bacterial Proteins | 3 | 2001 | 540 | 0.050 |
Why?
|
Peptides | 1 | 2004 | 320 | 0.050 |
Why?
|
Recombinant Fusion Proteins | 1 | 2001 | 295 | 0.050 |
Why?
|
Amino Acid Sequence | 3 | 2004 | 1180 | 0.040 |
Why?
|
Amino Acid Substitution | 1 | 2000 | 132 | 0.040 |
Why?
|
Hydrolysis | 1 | 1999 | 99 | 0.040 |
Why?
|
Dimerization | 1 | 1999 | 112 | 0.040 |
Why?
|
Stereoisomerism | 1 | 2000 | 167 | 0.040 |
Why?
|
Molecular Sequence Data | 3 | 2004 | 1568 | 0.040 |
Why?
|
Models, Chemical | 1 | 1999 | 207 | 0.040 |
Why?
|
Binding Sites | 1 | 1999 | 651 | 0.040 |
Why?
|
Protein Binding | 1 | 1999 | 972 | 0.030 |
Why?
|
Polyethylene Glycols | 2 | 2005 | 84 | 0.030 |
Why?
|
Gene Expression | 1 | 1997 | 674 | 0.030 |
Why?
|
Models, Structural | 1 | 1992 | 9 | 0.030 |
Why?
|
Macromolecular Substances | 1 | 1992 | 96 | 0.030 |
Why?
|
Diffusion | 1 | 2008 | 50 | 0.020 |
Why?
|
Motion | 1 | 2007 | 27 | 0.020 |
Why?
|
Protons | 1 | 2008 | 84 | 0.020 |
Why?
|
Crystallography, X-Ray | 1 | 2008 | 265 | 0.020 |
Why?
|
Crystallization | 1 | 2005 | 86 | 0.020 |
Why?
|
Data Interpretation, Statistical | 1 | 2004 | 111 | 0.010 |
Why?
|
Buffers | 1 | 2001 | 16 | 0.010 |
Why?
|
Calorimetry, Differential Scanning | 1 | 2001 | 30 | 0.010 |
Why?
|
Half-Life | 1 | 2001 | 54 | 0.010 |
Why?
|
Solutions | 1 | 2001 | 62 | 0.010 |
Why?
|
Models, Theoretical | 1 | 2001 | 217 | 0.010 |
Why?
|
Hydrogen-Ion Concentration | 1 | 2001 | 364 | 0.010 |
Why?
|
Isomerism | 1 | 1998 | 63 | 0.010 |
Why?
|
Humans | 1 | 2001 | 37093 | 0.000 |
Why?
|