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 | 79 | 0.380 |
Why?
|
| Apolipoproteins B | 3 | 1996 | 131 | 0.180 |
Why?
|
| Amino Acid Sequence | 13 | 1996 | 2674 | 0.170 |
Why?
|
| Apolipoproteins | 2 | 1996 | 68 | 0.150 |
Why?
|
| Fluorenes | 1 | 1996 | 8 | 0.140 |
Why?
|
| Trimethylsilyl Compounds | 1 | 1996 | 2 | 0.140 |
Why?
|
| Resins, Plant | 1 | 1996 | 3 | 0.140 |
Why?
|
| Molecular Sequence Data | 12 | 1996 | 3865 | 0.140 |
Why?
|
| Acrylic Resins | 1 | 1996 | 25 | 0.140 |
Why?
|
| Peptides | 5 | 1996 | 798 | 0.140 |
Why?
|
| Oligopeptides | 1 | 1996 | 119 | 0.130 |
Why?
|
| Lipoprotein(a) | 2 | 1996 | 113 | 0.130 |
Why?
|
| Hedgehogs | 1 | 1995 | 2 | 0.130 |
Why?
|
| Apolipoproteins E | 2 | 1994 | 188 | 0.120 |
Why?
|
| Peptide Fragments | 3 | 1996 | 745 | 0.110 |
Why?
|
| Amino Acids | 1 | 1996 | 660 | 0.110 |
Why?
|
| Dimyristoylphosphatidylcholine | 1 | 1992 | 5 | 0.100 |
Why?
|
| Lipids | 1 | 1995 | 512 | 0.100 |
Why?
|
| Lipoproteins, HDL | 3 | 1995 | 96 | 0.070 |
Why?
|
| Chromatography, High Pressure Liquid | 3 | 1996 | 337 | 0.070 |
Why?
|
| Lysine | 2 | 1996 | 201 | 0.060 |
Why?
|
| Circular Dichroism | 2 | 1995 | 81 | 0.060 |
Why?
|
| Species Specificity | 2 | 1995 | 550 | 0.050 |
Why?
|
| Apolipoprotein B-100 | 3 | 1996 | 33 | 0.050 |
Why?
|
| Protein Binding | 2 | 1996 | 1732 | 0.040 |
Why?
|
| Lipoproteins, LDL | 3 | 1995 | 114 | 0.040 |
Why?
|
| Disulfides | 2 | 1996 | 78 | 0.040 |
Why?
|
| Hydrofluoric Acid | 1 | 1996 | 1 | 0.030 |
Why?
|
| Acrylamides | 1 | 1996 | 18 | 0.030 |
Why?
|
| Molecular Weight | 1 | 1996 | 390 | 0.030 |
Why?
|
| Epitopes | 2 | 1988 | 427 | 0.030 |
Why?
|
| Apoprotein(a) | 1 | 1996 | 5 | 0.030 |
Why?
|
| Chromatography | 1 | 1996 | 43 | 0.030 |
Why?
|
| Electrophoresis | 1 | 1996 | 46 | 0.030 |
Why?
|
| Chromatography, Affinity | 1 | 1996 | 70 | 0.030 |
Why?
|
| src Homology Domains | 1 | 1995 | 29 | 0.030 |
Why?
|
| Binding Sites | 2 | 1996 | 1292 | 0.030 |
Why?
|
| Phylogeny | 2 | 1995 | 681 | 0.030 |
Why?
|
| Phosphatidylcholine-Sterol O-Acyltransferase | 1 | 1995 | 2 | 0.030 |
Why?
|
| Immunochemistry | 1 | 1995 | 30 | 0.030 |
Why?
|
| src-Family Kinases | 1 | 1995 | 83 | 0.030 |
Why?
|
| Mass Spectrometry | 1 | 1996 | 323 | 0.030 |
Why?
|
| Biological Transport, Active | 1 | 1995 | 87 | 0.030 |
Why?
|
| Cross Reactions | 2 | 1993 | 192 | 0.030 |
Why?
|
| Rabbits | 2 | 1993 | 716 | 0.030 |
Why?
|
| Dogs | 2 | 1993 | 761 | 0.030 |
Why?
|
| Antibodies | 1 | 1996 | 371 | 0.030 |
Why?
|
| Cattle | 2 | 1993 | 555 | 0.030 |
Why?
|
| Gene Transfer Techniques | 1 | 1996 | 374 | 0.030 |
Why?
|
| Molecular Structure | 1 | 1995 | 286 | 0.030 |
Why?
|
| Receptors, LDL | 1 | 1994 | 90 | 0.030 |
Why?
|
| Ducks | 1 | 1993 | 5 | 0.030 |
Why?
|
| Sequence Homology, Amino Acid | 1 | 1995 | 654 | 0.030 |
Why?
|
| 2-Naphthylamine | 1 | 1993 | 6 | 0.030 |
Why?
|
| Molecular Probes | 1 | 1993 | 30 | 0.030 |
Why?
|
| Structure-Activity Relationship | 2 | 1992 | 570 | 0.030 |
Why?
|
| In Vitro Techniques | 1 | 1995 | 968 | 0.030 |
Why?
|
| Protein Structure, Secondary | 1 | 1993 | 238 | 0.030 |
Why?
|
| Cysteine | 1 | 1993 | 132 | 0.030 |
Why?
|
| Lipoproteins | 1 | 1993 | 178 | 0.030 |
Why?
|
| Genetic Vectors | 1 | 1996 | 969 | 0.030 |
Why?
|
| Immune Sera | 1 | 1992 | 93 | 0.020 |
Why?
|
| Genetic Therapy | 1 | 1996 | 706 | 0.020 |
Why?
|
| Gene Expression | 1 | 1996 | 1579 | 0.020 |
Why?
|
| Biological Transport | 1 | 1992 | 347 | 0.020 |
Why?
|
| Enterotoxins | 1 | 1990 | 83 | 0.020 |
Why?
|
| Leukocytes, Mononuclear | 1 | 1990 | 323 | 0.020 |
Why?
|
| Rats | 2 | 1993 | 3657 | 0.020 |
Why?
|
| Trypsin | 1 | 1988 | 95 | 0.020 |
Why?
|
| DNA-Binding Proteins | 1 | 1996 | 2029 | 0.020 |
Why?
|
| Animals | 5 | 1996 | 33723 | 0.020 |
Why?
|
| Antibodies, Monoclonal | 2 | 1988 | 1022 | 0.020 |
Why?
|
| Humans | 10 | 1996 | 122287 | 0.010 |
Why?
|
| T-Lymphocytes | 1 | 1990 | 1678 | 0.010 |
Why?
|
| Peptide Mapping | 2 | 1993 | 43 | 0.010 |
Why?
|
| Kinetics | 2 | 1993 | 1315 | 0.010 |
Why?
|
| Male | 2 | 1995 | 59515 | 0.010 |
Why?
|
| Protein Conformation | 2 | 1990 | 831 | 0.010 |
Why?
|
| DNA | 2 | 1996 | 1606 | 0.010 |
Why?
|
| Cells, Cultured | 2 | 1994 | 3074 | 0.010 |
Why?
|
| Sequence Homology | 1 | 1995 | 62 | 0.010 |
Why?
|
| Serum Albumin, Bovine | 1 | 1993 | 48 | 0.010 |
Why?
|
| Macaca | 1 | 1993 | 61 | 0.010 |
Why?
|
| Endopeptidases | 1 | 1993 | 115 | 0.010 |
Why?
|
| Chickens | 1 | 1993 | 637 | 0.010 |
Why?
|
| Probability | 1 | 1993 | 319 | 0.010 |
Why?
|
| Artifacts | 1 | 1993 | 103 | 0.010 |
Why?
|
| Fluorescent Dyes | 1 | 1993 | 261 | 0.010 |
Why?
|
| Phosphorylation | 1 | 1995 | 1613 | 0.010 |
Why?
|
| Cyanogen Bromide | 1 | 1990 | 4 | 0.010 |
Why?
|
| Cell Line | 1 | 1996 | 2782 | 0.010 |
Why?
|
| Histocompatibility Antigens Class II | 1 | 1990 | 77 | 0.010 |
Why?
|
| Lipid Bilayers | 1 | 1988 | 45 | 0.000 |
Why?
|
| Phosphatidylcholines | 1 | 1988 | 41 | 0.000 |
Why?
|
| Lymphocyte Activation | 1 | 1990 | 680 | 0.000 |
Why?
|
| Models, Chemical | 1 | 1988 | 86 | 0.000 |
Why?
|
| Thermodynamics | 1 | 1988 | 140 | 0.000 |
Why?
|
| Tumor Necrosis Factor-alpha | 1 | 1990 | 671 | 0.000 |
Why?
|
| Radioimmunoassay | 1 | 1987 | 110 | 0.000 |
Why?
|
| Antigen-Antibody Complex | 1 | 1987 | 65 | 0.000 |
Why?
|
| Apolipoproteins A | 1 | 1987 | 46 | 0.000 |
Why?
|
| Receptors, Antigen, T-Cell | 1 | 1990 | 479 | 0.000 |
Why?
|
| Staphylococcus aureus | 1 | 1990 | 457 | 0.000 |
Why?
|
| Cloning, Molecular | 1 | 1988 | 887 | 0.000 |
Why?
|
| Mice, Inbred BALB C | 1 | 1987 | 980 | 0.000 |
Why?
|
| Signal Transduction | 1 | 1995 | 4510 | 0.000 |
Why?
|
| Mice | 1 | 1987 | 17548 | 0.000 |
Why?
|