Concepts (107)
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?
|
|---|
| Apolipoprotein A-I | 4 | 1996 | 80 | 0.350 |
Why?
|
| Apolipoproteins B | 3 | 1996 | 144 | 0.160 |
Why?
|
| Amino Acid Sequence | 13 | 1996 | 2409 | 0.160 |
Why?
|
| Apolipoproteins | 2 | 1996 | 69 | 0.140 |
Why?
|
| Molecular Sequence Data | 12 | 1996 | 3507 | 0.130 |
Why?
|
| Acrylic Resins | 1 | 1996 | 7 | 0.130 |
Why?
|
| Fluorenes | 1 | 1996 | 7 | 0.130 |
Why?
|
| Trimethylsilyl Compounds | 1 | 1996 | 2 | 0.130 |
Why?
|
| Resins, Plant | 1 | 1996 | 3 | 0.130 |
Why?
|
| Peptides | 5 | 1996 | 708 | 0.120 |
Why?
|
| Oligopeptides | 1 | 1996 | 105 | 0.120 |
Why?
|
| Hedgehogs | 1 | 1995 | 2 | 0.110 |
Why?
|
| Lipoprotein(a) | 2 | 1996 | 140 | 0.110 |
Why?
|
| Apolipoproteins E | 2 | 1994 | 187 | 0.110 |
Why?
|
| Peptide Fragments | 3 | 1996 | 687 | 0.100 |
Why?
|
| Amino Acids | 1 | 1996 | 562 | 0.100 |
Why?
|
| Dimyristoylphosphatidylcholine | 1 | 1992 | 5 | 0.090 |
Why?
|
| Lipids | 1 | 1995 | 563 | 0.090 |
Why?
|
| Lipoproteins, HDL | 3 | 1995 | 97 | 0.070 |
Why?
|
| Chromatography, High Pressure Liquid | 3 | 1996 | 325 | 0.060 |
Why?
|
| Lysine | 2 | 1996 | 166 | 0.050 |
Why?
|
| Circular Dichroism | 2 | 1995 | 62 | 0.050 |
Why?
|
| Species Specificity | 2 | 1995 | 486 | 0.050 |
Why?
|
| Apolipoprotein B-100 | 3 | 1996 | 36 | 0.040 |
Why?
|
| Protein Binding | 2 | 1996 | 1666 | 0.040 |
Why?
|
| Lipoproteins, LDL | 3 | 1995 | 118 | 0.040 |
Why?
|
| Disulfides | 2 | 1996 | 60 | 0.030 |
Why?
|
| Hydrofluoric Acid | 1 | 1996 | 1 | 0.030 |
Why?
|
| Acrylamides | 1 | 1996 | 27 | 0.030 |
Why?
|
| Molecular Weight | 1 | 1996 | 280 | 0.030 |
Why?
|
| Epitopes | 2 | 1988 | 322 | 0.030 |
Why?
|
| Apoprotein(a) | 1 | 1996 | 6 | 0.030 |
Why?
|
| Chromatography | 1 | 1996 | 29 | 0.030 |
Why?
|
| Electrophoresis | 1 | 1996 | 32 | 0.030 |
Why?
|
| Chromatography, Affinity | 1 | 1996 | 53 | 0.030 |
Why?
|
| Binding Sites | 2 | 1996 | 1150 | 0.030 |
Why?
|
| src Homology Domains | 1 | 1995 | 35 | 0.030 |
Why?
|
| Phylogeny | 2 | 1995 | 706 | 0.030 |
Why?
|
| Phosphatidylcholine-Sterol O-Acyltransferase | 1 | 1995 | 2 | 0.030 |
Why?
|
| Immunochemistry | 1 | 1995 | 8 | 0.030 |
Why?
|
| Biological Transport, Active | 1 | 1995 | 71 | 0.030 |
Why?
|
| src-Family Kinases | 1 | 1995 | 92 | 0.030 |
Why?
|
| Cross Reactions | 2 | 1993 | 158 | 0.030 |
Why?
|
| Mass Spectrometry | 1 | 1996 | 362 | 0.030 |
Why?
|
| Rabbits | 2 | 1993 | 574 | 0.030 |
Why?
|
| Antibodies | 1 | 1996 | 320 | 0.030 |
Why?
|
| Gene Transfer Techniques | 1 | 1996 | 343 | 0.030 |
Why?
|
| Dogs | 2 | 1993 | 614 | 0.030 |
Why?
|
| Cattle | 2 | 1993 | 501 | 0.030 |
Why?
|
| Molecular Structure | 1 | 1995 | 312 | 0.030 |
Why?
|
| Sequence Homology, Amino Acid | 1 | 1995 | 623 | 0.030 |
Why?
|
| Receptors, LDL | 1 | 1994 | 106 | 0.030 |
Why?
|
| Ducks | 1 | 1993 | 3 | 0.030 |
Why?
|
| 2-Naphthylamine | 1 | 1993 | 4 | 0.030 |
Why?
|
| In Vitro Techniques | 1 | 1995 | 809 | 0.030 |
Why?
|
| Molecular Probes | 1 | 1993 | 26 | 0.030 |
Why?
|
| Structure-Activity Relationship | 2 | 1992 | 549 | 0.020 |
Why?
|
| Protein Structure, Secondary | 1 | 1993 | 237 | 0.020 |
Why?
|
| Cysteine | 1 | 1993 | 137 | 0.020 |
Why?
|
| Genetic Vectors | 1 | 1996 | 902 | 0.020 |
Why?
|
| Lipoproteins | 1 | 1993 | 182 | 0.020 |
Why?
|
| Immune Sera | 1 | 1992 | 55 | 0.020 |
Why?
|
| Gene Expression | 1 | 1996 | 1494 | 0.020 |
Why?
|
| Biological Transport | 1 | 1992 | 332 | 0.020 |
Why?
|
| Genetic Therapy | 1 | 1996 | 718 | 0.020 |
Why?
|
| Enterotoxins | 1 | 1990 | 75 | 0.020 |
Why?
|
| Rats | 2 | 1993 | 3400 | 0.020 |
Why?
|
| Leukocytes, Mononuclear | 1 | 1990 | 355 | 0.020 |
Why?
|
| Trypsin | 1 | 1988 | 68 | 0.020 |
Why?
|
| DNA-Binding Proteins | 1 | 1996 | 1976 | 0.020 |
Why?
|
| Animals | 5 | 1996 | 33909 | 0.020 |
Why?
|
| Antibodies, Monoclonal | 2 | 1988 | 982 | 0.010 |
Why?
|
| Humans | 10 | 1996 | 130444 | 0.010 |
Why?
|
| T-Lymphocytes | 1 | 1990 | 1712 | 0.010 |
Why?
|
| Peptide Mapping | 2 | 1993 | 33 | 0.010 |
Why?
|
| Kinetics | 2 | 1993 | 1087 | 0.010 |
Why?
|
| Protein Conformation | 2 | 1990 | 729 | 0.010 |
Why?
|
| Male | 2 | 1995 | 64506 | 0.010 |
Why?
|
| DNA | 2 | 1996 | 1419 | 0.010 |
Why?
|
| Cells, Cultured | 2 | 1994 | 2905 | 0.010 |
Why?
|
| Sequence Homology | 1 | 1995 | 59 | 0.010 |
Why?
|
| Serum Albumin, Bovine | 1 | 1993 | 37 | 0.010 |
Why?
|
| Macaca | 1 | 1993 | 59 | 0.010 |
Why?
|
| Chickens | 1 | 1993 | 269 | 0.010 |
Why?
|
| Endopeptidases | 1 | 1993 | 108 | 0.010 |
Why?
|
| Probability | 1 | 1993 | 306 | 0.010 |
Why?
|
| Artifacts | 1 | 1993 | 104 | 0.010 |
Why?
|
| Fluorescent Dyes | 1 | 1993 | 248 | 0.010 |
Why?
|
| Phosphorylation | 1 | 1995 | 1577 | 0.010 |
Why?
|
| Cell Line | 1 | 1996 | 2577 | 0.010 |
Why?
|
| Cyanogen Bromide | 1 | 1990 | 2 | 0.010 |
Why?
|
| Histocompatibility Antigens Class II | 1 | 1990 | 70 | 0.010 |
Why?
|
| Lipid Bilayers | 1 | 1988 | 43 | 0.000 |
Why?
|
| Phosphatidylcholines | 1 | 1988 | 33 | 0.000 |
Why?
|
| Models, Chemical | 1 | 1988 | 78 | 0.000 |
Why?
|
| Lymphocyte Activation | 1 | 1990 | 630 | 0.000 |
Why?
|
| Thermodynamics | 1 | 1988 | 145 | 0.000 |
Why?
|
| Tumor Necrosis Factor-alpha | 1 | 1990 | 641 | 0.000 |
Why?
|
| Radioimmunoassay | 1 | 1987 | 83 | 0.000 |
Why?
|
| Antigen-Antibody Complex | 1 | 1987 | 52 | 0.000 |
Why?
|
| Apolipoproteins A | 1 | 1987 | 52 | 0.000 |
Why?
|
| Cloning, Molecular | 1 | 1988 | 782 | 0.000 |
Why?
|
| Staphylococcus aureus | 1 | 1990 | 479 | 0.000 |
Why?
|
| Receptors, Antigen, T-Cell | 1 | 1990 | 499 | 0.000 |
Why?
|
| Mice, Inbred BALB C | 1 | 1987 | 973 | 0.000 |
Why?
|
| Signal Transduction | 1 | 1995 | 4672 | 0.000 |
Why?
|
| Mice | 1 | 1987 | 18203 | 0.000 |
Why?
|