Concepts (166)
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 | 18 | 2013 | 38 | 1.360 |
Why?
|
| Apolipoprotein E4 | 9 | 2014 | 19 | 0.730 |
Why?
|
| Apolipoproteins E | 11 | 2014 | 44 | 0.680 |
Why?
|
| Lipoproteins, HDL | 10 | 2013 | 41 | 0.670 |
Why?
|
| Apolipoprotein E3 | 8 | 2014 | 12 | 0.630 |
Why?
|
| Cholesterol | 9 | 2013 | 182 | 0.550 |
Why?
|
| Protein Structure, Tertiary | 23 | 2014 | 283 | 0.440 |
Why?
|
| Lipids | 8 | 2014 | 195 | 0.320 |
Why?
|
| Phosphatidylcholines | 8 | 2014 | 41 | 0.320 |
Why?
|
| Protein Structure, Secondary | 16 | 2013 | 130 | 0.310 |
Why?
|
| Lipid Metabolism | 8 | 2010 | 118 | 0.280 |
Why?
|
| Protein Binding | 17 | 2014 | 632 | 0.280 |
Why?
|
| ATP-Binding Cassette Transporters | 7 | 2011 | 35 | 0.270 |
Why?
|
| Lipoproteins, VLDL | 5 | 2014 | 6 | 0.260 |
Why?
|
| ATP Binding Cassette Transporter 1 | 7 | 2013 | 11 | 0.230 |
Why?
|
| GTP-Binding Protein alpha Subunit, Gi2 | 1 | 2021 | 8 | 0.190 |
Why?
|
| Mutation | 10 | 2012 | 817 | 0.190 |
Why?
|
| Circular Dichroism | 10 | 2012 | 43 | 0.180 |
Why?
|
| Surface Plasmon Resonance | 3 | 2009 | 37 | 0.180 |
Why?
|
| Gene Expression Regulation, Neoplastic | 1 | 2021 | 444 | 0.150 |
Why?
|
| Protein Conformation | 6 | 2010 | 250 | 0.150 |
Why?
|
| Kinetics | 9 | 2014 | 538 | 0.150 |
Why?
|
| Humans | 32 | 2021 | 26828 | 0.150 |
Why?
|
| Protein Denaturation | 7 | 2014 | 28 | 0.150 |
Why?
|
| Protein Stability | 6 | 2014 | 42 | 0.150 |
Why?
|
| Thermodynamics | 6 | 2012 | 86 | 0.140 |
Why?
|
| Amino Acid Substitution | 4 | 2013 | 102 | 0.140 |
Why?
|
| Liposomes | 3 | 2008 | 142 | 0.140 |
Why?
|
| Animals | 16 | 2014 | 9961 | 0.130 |
Why?
|
| Ovarian Neoplasms | 1 | 2021 | 563 | 0.120 |
Why?
|
| Protein Isoforms | 6 | 2014 | 117 | 0.120 |
Why?
|
| Point Mutation | 3 | 2012 | 60 | 0.120 |
Why?
|
| Mice | 11 | 2014 | 4407 | 0.110 |
Why?
|
| Lipoproteins | 3 | 2010 | 95 | 0.110 |
Why?
|
| Phospholipids | 2 | 2004 | 73 | 0.110 |
Why?
|
| Heparin | 2 | 2004 | 110 | 0.110 |
Why?
|
| Hyperlipoproteinemia Type III | 1 | 2013 | 1 | 0.110 |
Why?
|
| Cholesterol, VLDL | 1 | 2013 | 2 | 0.110 |
Why?
|
| Amyloid | 1 | 2012 | 1 | 0.110 |
Why?
|
| Amyloidosis, Familial | 1 | 2012 | 1 | 0.110 |
Why?
|
| Cholesterol, HDL | 1 | 2013 | 58 | 0.110 |
Why?
|
| Lipoproteins, HDL3 | 1 | 2012 | 1 | 0.100 |
Why?
|
| Amino Acid Sequence | 5 | 2013 | 674 | 0.100 |
Why?
|
| Amino Acids, Aromatic | 1 | 2011 | 2 | 0.100 |
Why?
|
| Time Factors | 6 | 2014 | 1562 | 0.090 |
Why?
|
| Macrophages | 4 | 2010 | 273 | 0.090 |
Why?
|
| Chromatography, Gel | 5 | 2012 | 36 | 0.090 |
Why?
|
| Hydrophobic and Hydrophilic Interactions | 4 | 2011 | 43 | 0.090 |
Why?
|
| Intestinal Absorption | 1 | 2009 | 5 | 0.080 |
Why?
|
| Scavenger Receptors, Class B | 1 | 2009 | 5 | 0.080 |
Why?
|
| Microvilli | 1 | 2009 | 7 | 0.080 |
Why?
|
| Dimyristoylphosphatidylcholine | 2 | 2014 | 2 | 0.080 |
Why?
|
| Models, Biological | 3 | 2008 | 446 | 0.080 |
Why?
|
| Models, Molecular | 3 | 2009 | 441 | 0.080 |
Why?
|
| Dermatan Sulfate | 1 | 2008 | 3 | 0.080 |
Why?
|
| Lysine | 3 | 2008 | 71 | 0.080 |
Why?
|
| Unilamellar Liposomes | 3 | 2014 | 4 | 0.080 |
Why?
|
| Heparitin Sulfate | 1 | 2008 | 14 | 0.080 |
Why?
|
| Lipid Bilayers | 2 | 2005 | 15 | 0.080 |
Why?
|
| Cricetinae | 3 | 2013 | 129 | 0.070 |
Why?
|
| Adenosine Triphosphate | 1 | 2007 | 115 | 0.070 |
Why?
|
| Mutagenesis, Site-Directed | 4 | 2011 | 129 | 0.070 |
Why?
|
| Spectrometry, Fluorescence | 4 | 2008 | 63 | 0.070 |
Why?
|
| Polymorphism, Genetic | 2 | 2003 | 163 | 0.060 |
Why?
|
| Binding Sites | 4 | 2008 | 338 | 0.060 |
Why?
|
| Heparan Sulfate Proteoglycans | 1 | 2004 | 9 | 0.060 |
Why?
|
| Sepharose | 1 | 2004 | 14 | 0.060 |
Why?
|
| Cholesterol Esters | 1 | 2004 | 1 | 0.060 |
Why?
|
| Cell Line, Tumor | 2 | 2021 | 1259 | 0.060 |
Why?
|
| 2-Naphthylamine | 2 | 2014 | 2 | 0.060 |
Why?
|
| Pyrenes | 2 | 2014 | 5 | 0.060 |
Why?
|
| Fluorescence Resonance Energy Transfer | 2 | 2014 | 18 | 0.060 |
Why?
|
| Sequence Deletion | 3 | 2013 | 65 | 0.060 |
Why?
|
| Calorimetry | 4 | 2005 | 12 | 0.050 |
Why?
|
| Cell Line | 3 | 2010 | 672 | 0.050 |
Why?
|
| Guanidine | 2 | 2014 | 3 | 0.050 |
Why?
|
| Tryptophan | 2 | 2014 | 39 | 0.050 |
Why?
|
| Triolein | 2 | 2014 | 2 | 0.050 |
Why?
|
| Transcriptome | 1 | 2021 | 198 | 0.040 |
Why?
|
| Immobilized Proteins | 2 | 2009 | 9 | 0.040 |
Why?
|
| Cell Membrane | 3 | 2007 | 235 | 0.040 |
Why?
|
| Mice, Knockout | 2 | 2013 | 783 | 0.040 |
Why?
|
| Fluorescent Dyes | 2 | 2012 | 88 | 0.040 |
Why?
|
| Gene Expression | 2 | 2010 | 406 | 0.040 |
Why?
|
| Particle Size | 2 | 2010 | 96 | 0.040 |
Why?
|
| Structure-Activity Relationship | 2 | 2009 | 200 | 0.040 |
Why?
|
| Prostaglandin-Endoperoxide Synthases | 1 | 1996 | 22 | 0.030 |
Why?
|
| Pregnancy in Diabetics | 1 | 1996 | 21 | 0.030 |
Why?
|
| Central Nervous System | 1 | 1996 | 36 | 0.030 |
Why?
|
| Dinoprostone | 1 | 1996 | 41 | 0.030 |
Why?
|
| Mice, Inbred C57BL | 2 | 2013 | 1476 | 0.030 |
Why?
|
| Spectrophotometry, Ultraviolet | 2 | 2008 | 54 | 0.030 |
Why?
|
| Peptide Fragments | 2 | 2009 | 197 | 0.030 |
Why?
|
| Emulsions | 2 | 2006 | 23 | 0.030 |
Why?
|
| Temperature | 2 | 2009 | 207 | 0.030 |
Why?
|
| Diabetes Mellitus, Experimental | 1 | 1996 | 96 | 0.030 |
Why?
|
| Cells, Cultured | 2 | 2011 | 970 | 0.030 |
Why?
|
| Anilino Naphthalenesulfonates | 2 | 2006 | 2 | 0.030 |
Why?
|
| Chickens | 1 | 2014 | 59 | 0.030 |
Why?
|
| Dose-Response Relationship, Drug | 2 | 2007 | 586 | 0.030 |
Why?
|
| Biological Transport, Active | 1 | 2013 | 17 | 0.030 |
Why?
|
| Protein Structure, Quaternary | 1 | 2013 | 26 | 0.030 |
Why?
|
| Lipolysis | 1 | 2013 | 5 | 0.030 |
Why?
|
| Dependovirus | 1 | 2013 | 9 | 0.030 |
Why?
|
| Microscopy, Atomic Force | 1 | 2012 | 19 | 0.030 |
Why?
|
| Spectroscopy, Fourier Transform Infrared | 1 | 2012 | 35 | 0.030 |
Why?
|
| Deuterium Exchange Measurement | 1 | 2012 | 17 | 0.030 |
Why?
|
| Triglycerides | 1 | 2013 | 117 | 0.030 |
Why?
|
| Guanidines | 1 | 2012 | 6 | 0.030 |
Why?
|
| Genetic Vectors | 1 | 2013 | 107 | 0.030 |
Why?
|
| Hydrogen | 1 | 2012 | 56 | 0.030 |
Why?
|
| Fluorescence | 1 | 2012 | 48 | 0.030 |
Why?
|
| Hydrogen-Ion Concentration | 1 | 2012 | 261 | 0.030 |
Why?
|
| HEK293 Cells | 1 | 2012 | 172 | 0.020 |
Why?
|
| Nuclear Magnetic Resonance, Biomolecular | 2 | 2003 | 55 | 0.020 |
Why?
|
| Transition Temperature | 1 | 2011 | 6 | 0.020 |
Why?
|
| Mass Spectrometry | 1 | 2012 | 186 | 0.020 |
Why?
|
| Mice, Transgenic | 1 | 2013 | 486 | 0.020 |
Why?
|
| Mutation, Missense | 1 | 2010 | 67 | 0.020 |
Why?
|
| Liver | 1 | 2013 | 415 | 0.020 |
Why?
|
| Mutant Proteins | 1 | 2009 | 25 | 0.020 |
Why?
|
| CD36 Antigens | 1 | 2009 | 6 | 0.020 |
Why?
|
| Carbon Radioisotopes | 1 | 2009 | 19 | 0.020 |
Why?
|
| Enterocytes | 1 | 2009 | 14 | 0.020 |
Why?
|
| Hot Temperature | 1 | 2009 | 84 | 0.020 |
Why?
|
| Biological Transport | 1 | 2009 | 111 | 0.020 |
Why?
|
| Intestine, Small | 1 | 2009 | 66 | 0.020 |
Why?
|
| Membrane Transport Proteins | 1 | 2009 | 65 | 0.020 |
Why?
|
| Reverse Transcriptase Polymerase Chain Reaction | 1 | 2009 | 324 | 0.020 |
Why?
|
| Static Electricity | 1 | 2008 | 34 | 0.020 |
Why?
|
| Disulfides | 1 | 2008 | 33 | 0.020 |
Why?
|
| Protein Multimerization | 1 | 2008 | 53 | 0.020 |
Why?
|
| Escherichia coli | 1 | 2010 | 329 | 0.020 |
Why?
|
| Disease Models, Animal | 1 | 2013 | 1393 | 0.020 |
Why?
|
| Swine | 1 | 2008 | 220 | 0.020 |
Why?
|
| Microscopy, Electron | 1 | 2007 | 94 | 0.020 |
Why?
|
| Female | 2 | 2021 | 14463 | 0.020 |
Why?
|
| Molecular Sequence Data | 1 | 2008 | 1036 | 0.020 |
Why?
|
| Protein Folding | 1 | 2006 | 47 | 0.020 |
Why?
|
| Immunohistochemistry | 1 | 2007 | 453 | 0.020 |
Why?
|
| Carbon Isotopes | 1 | 2005 | 43 | 0.020 |
Why?
|
| Surface Properties | 1 | 2005 | 132 | 0.020 |
Why?
|
| Electron Spin Resonance Spectroscopy | 1 | 2004 | 35 | 0.020 |
Why?
|
| Gels | 1 | 2004 | 26 | 0.020 |
Why?
|
| Magnetic Resonance Spectroscopy | 1 | 2005 | 176 | 0.010 |
Why?
|
| Protein Transport | 1 | 2004 | 152 | 0.010 |
Why?
|
| Trifluoroethanol | 1 | 2004 | 2 | 0.010 |
Why?
|
| COS Cells | 1 | 2004 | 48 | 0.010 |
Why?
|
| DNA, Complementary | 1 | 2004 | 76 | 0.010 |
Why?
|
| Sphingomyelins | 1 | 2003 | 11 | 0.010 |
Why?
|
| Thrombin | 1 | 2004 | 68 | 0.010 |
Why?
|
| Fibroblasts | 1 | 2004 | 152 | 0.010 |
Why?
|
| Base Sequence | 1 | 2004 | 573 | 0.010 |
Why?
|
| Amino Acids, Basic | 1 | 2003 | 2 | 0.010 |
Why?
|
| Cyclic AMP | 1 | 2003 | 80 | 0.010 |
Why?
|
| Electrophoresis, Polyacrylamide Gel | 1 | 2004 | 165 | 0.010 |
Why?
|
| Nephelometry and Turbidimetry | 1 | 2002 | 3 | 0.010 |
Why?
|
| Solubility | 1 | 2002 | 73 | 0.010 |
Why?
|
| Up-Regulation | 1 | 2003 | 240 | 0.010 |
Why?
|
| Embryonic and Fetal Development | 1 | 1996 | 9 | 0.010 |
Why?
|
| Maternal-Fetal Exchange | 1 | 1996 | 10 | 0.010 |
Why?
|
| Mice, Inbred ICR | 1 | 1996 | 26 | 0.010 |
Why?
|
| Linear Models | 1 | 1996 | 201 | 0.010 |
Why?
|
| Proteins | 1 | 1996 | 244 | 0.010 |
Why?
|
| Pregnancy | 1 | 1996 | 1131 | 0.010 |
Why?
|
| Male | 1 | 1996 | 12870 | 0.000 |
Why?
|