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 | 44 | 1.160 |
Why?
|
| Ubiquitin-Protein Ligase Complexes | 7 | 2006 | 18 | 0.840 |
Why?
|
| Saccharomyces cerevisiae Proteins | 10 | 2006 | 310 | 0.750 |
Why?
|
| Saccharomyces cerevisiae | 14 | 2006 | 479 | 0.690 |
Why?
|
| Ubiquitins | 8 | 2006 | 36 | 0.520 |
Why?
|
| Ubiquitin-Conjugating Enzymes | 11 | 2006 | 32 | 0.500 |
Why?
|
| Fungal Proteins | 11 | 2001 | 148 | 0.490 |
Why?
|
| Genes, Fungal | 4 | 1996 | 64 | 0.230 |
Why?
|
| Ubiquitin | 2 | 2003 | 95 | 0.230 |
Why?
|
| Cell Cycle | 4 | 1996 | 518 | 0.230 |
Why?
|
| Molecular Sequence Data | 12 | 2002 | 2896 | 0.210 |
Why?
|
| Anaphase-Promoting Complex-Cyclosome | 7 | 2006 | 19 | 0.210 |
Why?
|
| Amino Acid Sequence | 10 | 2002 | 2005 | 0.190 |
Why?
|
| Adenosine Triphosphatases | 1 | 2001 | 141 | 0.160 |
Why?
|
| Models, Molecular | 6 | 2003 | 1391 | 0.160 |
Why?
|
| Trans-Activators | 2 | 2002 | 447 | 0.150 |
Why?
|
| Ubiquitin-Protein Ligases | 6 | 2006 | 188 | 0.150 |
Why?
|
| Structure-Activity Relationship | 4 | 2001 | 425 | 0.120 |
Why?
|
| DNA Repair | 2 | 2002 | 363 | 0.120 |
Why?
|
| Genes, Regulator | 1 | 1996 | 60 | 0.120 |
Why?
|
| Plasmids | 6 | 2003 | 275 | 0.110 |
Why?
|
| Biopolymers | 1 | 1994 | 29 | 0.110 |
Why?
|
| Binding Sites | 4 | 2006 | 1159 | 0.100 |
Why?
|
| Base Sequence | 6 | 1997 | 2222 | 0.100 |
Why?
|
| Mutagenesis, Site-Directed | 2 | 1991 | 273 | 0.090 |
Why?
|
| Protein Structure, Tertiary | 3 | 2001 | 731 | 0.090 |
Why?
|
| Protein Binding | 4 | 2003 | 1554 | 0.090 |
Why?
|
| Protein Kinases | 2 | 2006 | 212 | 0.080 |
Why?
|
| Temperature | 3 | 2003 | 442 | 0.080 |
Why?
|
| DNA-Binding Proteins | 1 | 1996 | 1255 | 0.080 |
Why?
|
| DNA, Superhelical | 2 | 1986 | 15 | 0.070 |
Why?
|
| Nucleic Acid Conformation | 2 | 1986 | 348 | 0.070 |
Why?
|
| Protein Processing, Post-Translational | 4 | 2006 | 412 | 0.070 |
Why?
|
| Lysine | 2 | 2002 | 181 | 0.070 |
Why?
|
| Protein Structure, Secondary | 2 | 2001 | 340 | 0.070 |
Why?
|
| SKP Cullin F-Box Protein Ligases | 1 | 2006 | 4 | 0.060 |
Why?
|
| Cell Division | 2 | 2001 | 689 | 0.060 |
Why?
|
| Cell Wall | 1 | 2006 | 72 | 0.060 |
Why?
|
| Catalytic Domain | 2 | 2003 | 165 | 0.060 |
Why?
|
| Biological Evolution | 1 | 1992 | 1072 | 0.050 |
Why?
|
| Sequence Alignment | 2 | 2002 | 353 | 0.050 |
Why?
|
| Cell Cycle Proteins | 1 | 2006 | 419 | 0.050 |
Why?
|
| Precipitin Tests | 1 | 2003 | 101 | 0.050 |
Why?
|
| Esters | 1 | 2003 | 31 | 0.050 |
Why?
|
| Cross-Linking Reagents | 1 | 2003 | 89 | 0.050 |
Why?
|
| Recombinant Fusion Proteins | 2 | 1997 | 557 | 0.050 |
Why?
|
| Immunoblotting | 1 | 2003 | 274 | 0.050 |
Why?
|
| Cysteine | 1 | 2003 | 149 | 0.050 |
Why?
|
| Sequence Homology, Nucleic Acid | 2 | 1992 | 157 | 0.040 |
Why?
|
| Genetic Complementation Test | 2 | 2002 | 84 | 0.040 |
Why?
|
| DNA Mutational Analysis | 1 | 2003 | 548 | 0.040 |
Why?
|
| TNF Receptor-Associated Factor 6 | 1 | 2001 | 7 | 0.040 |
Why?
|
| Models, Biological | 2 | 2003 | 1807 | 0.040 |
Why?
|
| Gene Expression Regulation, Fungal | 2 | 2006 | 72 | 0.040 |
Why?
|
| Amino Acid Motifs | 1 | 2001 | 118 | 0.040 |
Why?
|
| Macromolecular Substances | 1 | 2001 | 162 | 0.040 |
Why?
|
| DNA Replication | 1 | 2002 | 169 | 0.040 |
Why?
|
| DNA Helicases | 1 | 2001 | 91 | 0.040 |
Why?
|
| Nuclear Magnetic Resonance, Biomolecular | 1 | 2000 | 65 | 0.040 |
Why?
|
| Amino Acid Substitution | 1 | 2001 | 334 | 0.040 |
Why?
|
| Substrate Specificity | 1 | 2001 | 374 | 0.040 |
Why?
|
| Blotting, Western | 2 | 1992 | 780 | 0.040 |
Why?
|
| Sequence Homology, Amino Acid | 2 | 2002 | 403 | 0.040 |
Why?
|
| Crystallography, X-Ray | 1 | 2001 | 530 | 0.040 |
Why?
|
| NADH Dehydrogenase | 1 | 1997 | 22 | 0.030 |
Why?
|
| Suppression, Genetic | 1 | 1996 | 30 | 0.030 |
Why?
|
| Proteins | 1 | 2001 | 804 | 0.030 |
Why?
|
| Phylogeny | 1 | 2001 | 1339 | 0.030 |
Why?
|
| Polyubiquitin | 1 | 1994 | 8 | 0.030 |
Why?
|
| Genes, myc | 2 | 1991 | 38 | 0.030 |
Why?
|
| Phosphorylation | 2 | 2006 | 1145 | 0.030 |
Why?
|
| Gene Expression | 2 | 2002 | 1320 | 0.030 |
Why?
|
| Transcription Factors | 1 | 2002 | 1717 | 0.030 |
Why?
|
| Protein Conformation | 1 | 1996 | 923 | 0.020 |
Why?
|
| Transcription, Genetic | 2 | 2002 | 1133 | 0.020 |
Why?
|
| Chimera | 1 | 1992 | 52 | 0.020 |
Why?
|
| Hydrolases | 1 | 1992 | 30 | 0.020 |
Why?
|
| Electrophoresis, Polyacrylamide Gel | 1 | 1992 | 238 | 0.020 |
Why?
|
| Restriction Mapping | 1 | 1991 | 119 | 0.020 |
Why?
|
| beta-Galactosidase | 1 | 1991 | 65 | 0.020 |
Why?
|
| Oligodeoxyribonucleotides | 1 | 1991 | 126 | 0.020 |
Why?
|
| Cloning, Molecular | 1 | 1992 | 581 | 0.020 |
Why?
|
| Amino Acids | 1 | 1992 | 246 | 0.020 |
Why?
|
| Oligonucleotides | 1 | 1991 | 93 | 0.020 |
Why?
|
| Epitopes | 1 | 1991 | 258 | 0.020 |
Why?
|
| Ultraviolet Rays | 1 | 1991 | 198 | 0.020 |
Why?
|
| Rabbits | 1 | 1991 | 581 | 0.020 |
Why?
|
| Proto-Oncogene Proteins c-myc | 1 | 1991 | 159 | 0.020 |
Why?
|
| In Vitro Techniques | 1 | 1991 | 945 | 0.020 |
Why?
|
| Stress, Physiological | 1 | 1991 | 256 | 0.020 |
Why?
|
| DNA, Complementary | 2 | 2002 | 380 | 0.020 |
Why?
|
| Alleles | 1 | 1991 | 1159 | 0.020 |
Why?
|
| Thermodynamics | 2 | 1986 | 327 | 0.020 |
Why?
|
| Repressor Proteins | 1 | 1991 | 447 | 0.020 |
Why?
|
| Homeodomain Proteins | 1 | 1991 | 566 | 0.020 |
Why?
|
| Cyclin-Dependent Kinase Inhibitor Proteins | 1 | 2006 | 2 | 0.020 |
Why?
|
| Enzyme Stability | 1 | 2006 | 48 | 0.020 |
Why?
|
| Spores, Fungal | 1 | 2006 | 18 | 0.020 |
Why?
|
| G1 Phase | 1 | 2006 | 66 | 0.020 |
Why?
|
| rho GTP-Binding Proteins | 1 | 2006 | 58 | 0.020 |
Why?
|
| Mitogen-Activated Protein Kinases | 1 | 2006 | 218 | 0.010 |
Why?
|
| Antibodies, Monoclonal | 1 | 1991 | 1416 | 0.010 |
Why?
|
| Phenotype | 1 | 1992 | 2638 | 0.010 |
Why?
|
| Oligonucleotide Array Sequence Analysis | 1 | 2006 | 700 | 0.010 |
Why?
|
| Intracellular Signaling Peptides and Proteins | 1 | 2006 | 403 | 0.010 |
Why?
|
| Kinetics | 2 | 2000 | 1476 | 0.010 |
Why?
|
| RNA, Messenger | 2 | 2002 | 2063 | 0.010 |
Why?
|
| Two-Hybrid System Techniques | 1 | 2002 | 55 | 0.010 |
Why?
|
| Humans | 4 | 2002 | 98080 | 0.010 |
Why?
|
| Yeasts | 1 | 2000 | 50 | 0.010 |
Why?
|
| DNA | 1 | 1986 | 1274 | 0.010 |
Why?
|
| Gene Expression Profiling | 1 | 2006 | 1565 | 0.010 |
Why?
|
| Sequence Analysis, DNA | 1 | 2002 | 911 | 0.010 |
Why?
|
| Galactose | 1 | 1997 | 29 | 0.010 |
Why?
|
| Animals | 2 | 2002 | 28894 | 0.010 |
Why?
|
| Nuclear Proteins | 1 | 2002 | 750 | 0.010 |
Why?
|
| Biological Transport | 1 | 1997 | 401 | 0.010 |
Why?
|
| Signal Transduction | 1 | 2006 | 3620 | 0.010 |
Why?
|
| Evolution, Molecular | 1 | 2002 | 902 | 0.010 |
Why?
|
| Cell Membrane | 1 | 1997 | 673 | 0.010 |
Why?
|
| Mutation | 1 | 2002 | 4392 | 0.000 |
Why?
|
| Mice | 1 | 2002 | 12698 | 0.000 |
Why?
|
| Polydeoxyribonucleotides | 1 | 1986 | 5 | 0.000 |
Why?
|
| Models, Theoretical | 1 | 1986 | 508 | 0.000 |
Why?
|
| Male | 1 | 2002 | 47076 | 0.000 |
Why?
|