Concepts (125)
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?
|
|---|
| Ligases | 11 | 2003 | 45 | 1.370 |
Why?
|
| Ubiquitin-Protein Ligase Complexes | 7 | 2006 | 17 | 0.990 |
Why?
|
| Saccharomyces cerevisiae Proteins | 10 | 2006 | 276 | 0.890 |
Why?
|
| Saccharomyces cerevisiae | 14 | 2006 | 434 | 0.830 |
Why?
|
| Ubiquitins | 8 | 2006 | 38 | 0.610 |
Why?
|
| Ubiquitin-Conjugating Enzymes | 11 | 2006 | 30 | 0.590 |
Why?
|
| Fungal Proteins | 11 | 2001 | 141 | 0.580 |
Why?
|
| Genes, Fungal | 4 | 1996 | 58 | 0.280 |
Why?
|
| Ubiquitin | 2 | 2003 | 93 | 0.270 |
Why?
|
| Cell Cycle | 4 | 1996 | 502 | 0.260 |
Why?
|
| Anaphase-Promoting Complex-Cyclosome | 7 | 2006 | 16 | 0.250 |
Why?
|
| Molecular Sequence Data | 12 | 2002 | 3030 | 0.240 |
Why?
|
| Amino Acid Sequence | 10 | 2002 | 2062 | 0.210 |
Why?
|
| Adenosine Triphosphatases | 1 | 2001 | 153 | 0.190 |
Why?
|
| Models, Molecular | 6 | 2003 | 1286 | 0.190 |
Why?
|
| Trans-Activators | 2 | 2002 | 429 | 0.180 |
Why?
|
| Ubiquitin-Protein Ligases | 6 | 2006 | 165 | 0.170 |
Why?
|
| Structure-Activity Relationship | 4 | 2001 | 408 | 0.140 |
Why?
|
| Genes, Regulator | 1 | 1996 | 65 | 0.140 |
Why?
|
| DNA Repair | 2 | 2002 | 356 | 0.140 |
Why?
|
| Plasmids | 6 | 2003 | 287 | 0.130 |
Why?
|
| Biopolymers | 1 | 1994 | 26 | 0.130 |
Why?
|
| Binding Sites | 4 | 2006 | 1098 | 0.110 |
Why?
|
| Base Sequence | 6 | 1997 | 2330 | 0.110 |
Why?
|
| Mutagenesis, Site-Directed | 2 | 1991 | 279 | 0.110 |
Why?
|
| Protein Binding | 4 | 2003 | 1456 | 0.100 |
Why?
|
| Temperature | 3 | 2003 | 396 | 0.100 |
Why?
|
| Protein Structure, Tertiary | 3 | 2001 | 736 | 0.100 |
Why?
|
| Protein Kinases | 2 | 2006 | 209 | 0.100 |
Why?
|
| DNA-Binding Proteins | 1 | 1996 | 1208 | 0.090 |
Why?
|
| DNA, Superhelical | 2 | 1986 | 16 | 0.090 |
Why?
|
| Lysine | 2 | 2002 | 147 | 0.080 |
Why?
|
| Protein Processing, Post-Translational | 4 | 2006 | 371 | 0.080 |
Why?
|
| Nucleic Acid Conformation | 2 | 1986 | 332 | 0.080 |
Why?
|
| Protein Structure, Secondary | 2 | 2001 | 330 | 0.080 |
Why?
|
| SKP Cullin F-Box Protein Ligases | 1 | 2006 | 3 | 0.070 |
Why?
|
| Cell Wall | 1 | 2006 | 66 | 0.070 |
Why?
|
| Cell Division | 2 | 2001 | 696 | 0.070 |
Why?
|
| Catalytic Domain | 2 | 2003 | 156 | 0.070 |
Why?
|
| Biological Evolution | 1 | 1992 | 919 | 0.060 |
Why?
|
| Sequence Alignment | 2 | 2002 | 351 | 0.060 |
Why?
|
| Cell Cycle Proteins | 1 | 2006 | 388 | 0.060 |
Why?
|
| Precipitin Tests | 1 | 2003 | 108 | 0.060 |
Why?
|
| Esters | 1 | 2003 | 29 | 0.060 |
Why?
|
| Cross-Linking Reagents | 1 | 2003 | 86 | 0.060 |
Why?
|
| Immunoblotting | 1 | 2003 | 268 | 0.060 |
Why?
|
| Recombinant Fusion Proteins | 2 | 1997 | 557 | 0.060 |
Why?
|
| Cysteine | 1 | 2003 | 135 | 0.050 |
Why?
|
| Sequence Homology, Nucleic Acid | 2 | 1992 | 173 | 0.050 |
Why?
|
| Genetic Complementation Test | 2 | 2002 | 97 | 0.050 |
Why?
|
| TNF Receptor-Associated Factor 6 | 1 | 2001 | 6 | 0.050 |
Why?
|
| Gene Expression Regulation, Fungal | 2 | 2006 | 61 | 0.050 |
Why?
|
| DNA Mutational Analysis | 1 | 2003 | 526 | 0.050 |
Why?
|
| Models, Biological | 2 | 2003 | 1749 | 0.050 |
Why?
|
| Amino Acid Motifs | 1 | 2001 | 116 | 0.050 |
Why?
|
| DNA Replication | 1 | 2002 | 164 | 0.050 |
Why?
|
| Macromolecular Substances | 1 | 2001 | 177 | 0.050 |
Why?
|
| DNA Helicases | 1 | 2001 | 79 | 0.050 |
Why?
|
| Nuclear Magnetic Resonance, Biomolecular | 1 | 2000 | 60 | 0.050 |
Why?
|
| Substrate Specificity | 1 | 2001 | 347 | 0.050 |
Why?
|
| Amino Acid Substitution | 1 | 2001 | 339 | 0.050 |
Why?
|
| Blotting, Western | 2 | 1992 | 782 | 0.050 |
Why?
|
| Crystallography, X-Ray | 1 | 2001 | 485 | 0.050 |
Why?
|
| Sequence Homology, Amino Acid | 2 | 2002 | 416 | 0.040 |
Why?
|
| NADH Dehydrogenase | 1 | 1997 | 22 | 0.040 |
Why?
|
| Suppression, Genetic | 1 | 1996 | 30 | 0.030 |
Why?
|
| Phylogeny | 1 | 2001 | 1137 | 0.030 |
Why?
|
| Proteins | 1 | 2001 | 777 | 0.030 |
Why?
|
| Polyubiquitin | 1 | 1994 | 8 | 0.030 |
Why?
|
| Genes, myc | 2 | 1991 | 39 | 0.030 |
Why?
|
| Transcription Factors | 1 | 2002 | 1565 | 0.030 |
Why?
|
| Phosphorylation | 2 | 2006 | 1106 | 0.030 |
Why?
|
| Gene Expression | 2 | 2002 | 1284 | 0.030 |
Why?
|
| Protein Conformation | 1 | 1996 | 881 | 0.030 |
Why?
|
| Chimera | 1 | 1992 | 56 | 0.030 |
Why?
|
| Transcription, Genetic | 2 | 2002 | 1135 | 0.030 |
Why?
|
| Hydrolases | 1 | 1992 | 28 | 0.030 |
Why?
|
| Electrophoresis, Polyacrylamide Gel | 1 | 1992 | 268 | 0.030 |
Why?
|
| beta-Galactosidase | 1 | 1991 | 71 | 0.030 |
Why?
|
| Restriction Mapping | 1 | 1991 | 157 | 0.030 |
Why?
|
| Oligodeoxyribonucleotides | 1 | 1991 | 126 | 0.030 |
Why?
|
| Amino Acids | 1 | 1992 | 252 | 0.020 |
Why?
|
| Oligonucleotides | 1 | 1991 | 92 | 0.020 |
Why?
|
| Cloning, Molecular | 1 | 1992 | 646 | 0.020 |
Why?
|
| Epitopes | 1 | 1991 | 255 | 0.020 |
Why?
|
| Proto-Oncogene Proteins c-myc | 1 | 1991 | 120 | 0.020 |
Why?
|
| Ultraviolet Rays | 1 | 1991 | 193 | 0.020 |
Why?
|
| Rabbits | 1 | 1991 | 636 | 0.020 |
Why?
|
| In Vitro Techniques | 1 | 1991 | 989 | 0.020 |
Why?
|
| Stress, Physiological | 1 | 1991 | 227 | 0.020 |
Why?
|
| DNA, Complementary | 2 | 2002 | 393 | 0.020 |
Why?
|
| Alleles | 1 | 1991 | 1128 | 0.020 |
Why?
|
| Thermodynamics | 2 | 1986 | 309 | 0.020 |
Why?
|
| Repressor Proteins | 1 | 1991 | 403 | 0.020 |
Why?
|
| Homeodomain Proteins | 1 | 1991 | 536 | 0.020 |
Why?
|
| Cyclin-Dependent Kinase Inhibitor Proteins | 1 | 2006 | 2 | 0.020 |
Why?
|
| Spores, Fungal | 1 | 2006 | 17 | 0.020 |
Why?
|
| Enzyme Stability | 1 | 2006 | 39 | 0.020 |
Why?
|
| G1 Phase | 1 | 2006 | 63 | 0.020 |
Why?
|
| rho GTP-Binding Proteins | 1 | 2006 | 54 | 0.020 |
Why?
|
| Mitogen-Activated Protein Kinases | 1 | 2006 | 222 | 0.020 |
Why?
|
| Phenotype | 1 | 1992 | 2378 | 0.020 |
Why?
|
| Antibodies, Monoclonal | 1 | 1991 | 1376 | 0.020 |
Why?
|
| Intracellular Signaling Peptides and Proteins | 1 | 2006 | 379 | 0.020 |
Why?
|
| Oligonucleotide Array Sequence Analysis | 1 | 2006 | 689 | 0.020 |
Why?
|
| Kinetics | 2 | 2000 | 1513 | 0.020 |
Why?
|
| RNA, Messenger | 2 | 2002 | 1981 | 0.010 |
Why?
|
| Two-Hybrid System Techniques | 1 | 2002 | 55 | 0.010 |
Why?
|
| Humans | 4 | 2002 | 86643 | 0.010 |
Why?
|
| Yeasts | 1 | 2000 | 49 | 0.010 |
Why?
|
| Gene Expression Profiling | 1 | 2006 | 1384 | 0.010 |
Why?
|
| DNA | 1 | 1986 | 1294 | 0.010 |
Why?
|
| Sequence Analysis, DNA | 1 | 2002 | 853 | 0.010 |
Why?
|
| Animals | 2 | 2002 | 26582 | 0.010 |
Why?
|
| Galactose | 1 | 1997 | 32 | 0.010 |
Why?
|
| Nuclear Proteins | 1 | 2002 | 696 | 0.010 |
Why?
|
| Biological Transport | 1 | 1997 | 396 | 0.010 |
Why?
|
| Evolution, Molecular | 1 | 2002 | 813 | 0.010 |
Why?
|
| Signal Transduction | 1 | 2006 | 3241 | 0.010 |
Why?
|
| Cell Membrane | 1 | 1997 | 666 | 0.010 |
Why?
|
| Mutation | 1 | 2002 | 3968 | 0.010 |
Why?
|
| Mice | 1 | 2002 | 11352 | 0.000 |
Why?
|
| Polydeoxyribonucleotides | 1 | 1986 | 5 | 0.000 |
Why?
|
| Models, Theoretical | 1 | 1986 | 482 | 0.000 |
Why?
|
| Male | 1 | 2002 | 40965 | 0.000 |
Why?
|