Concepts (136)
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?
|
|---|
| Borrelia burgdorferi | 11 | 2018 | 17 | 4.090 |
Why?
|
| Bacterial Proteins | 13 | 2018 | 540 | 2.690 |
Why?
|
| Lyme Disease | 6 | 2018 | 16 | 1.320 |
Why?
|
| Gene Expression Regulation, Bacterial | 7 | 2018 | 149 | 1.190 |
Why?
|
| RNA-Binding Proteins | 3 | 2018 | 146 | 0.970 |
Why?
|
| Antigens, Bacterial | 5 | 2010 | 132 | 0.860 |
Why?
|
| Virulence Factors | 2 | 2013 | 113 | 0.770 |
Why?
|
| Host-Pathogen Interactions | 3 | 2013 | 186 | 0.760 |
Why?
|
| Lipoproteins | 2 | 2011 | 64 | 0.750 |
Why?
|
| Electrophoretic Mobility Shift Assay | 2 | 2018 | 53 | 0.730 |
Why?
|
| DNA-Binding Proteins | 1 | 2018 | 539 | 0.480 |
Why?
|
| Host-Parasite Interactions | 1 | 2013 | 42 | 0.450 |
Why?
|
| Sigma Factor | 1 | 2013 | 19 | 0.440 |
Why?
|
| Mevalonic Acid | 1 | 2012 | 9 | 0.420 |
Why?
|
| Acetates | 1 | 2012 | 21 | 0.420 |
Why?
|
| Superoxide Dismutase | 2 | 2013 | 155 | 0.420 |
Why?
|
| Adaptation, Physiological | 1 | 2013 | 109 | 0.410 |
Why?
|
| Amino Acid Sequence | 5 | 2013 | 1180 | 0.360 |
Why?
|
| Molecular Sequence Data | 5 | 2013 | 1568 | 0.350 |
Why?
|
| Mice, Inbred C3H | 4 | 2011 | 84 | 0.340 |
Why?
|
| Carrier Proteins | 1 | 2011 | 305 | 0.330 |
Why?
|
| Chlamydia muridarum | 4 | 2011 | 104 | 0.330 |
Why?
|
| Mice | 13 | 2013 | 5913 | 0.330 |
Why?
|
| Blotting, Western | 4 | 2013 | 859 | 0.320 |
Why?
|
| Chlamydia Infections | 4 | 2011 | 196 | 0.300 |
Why?
|
| Animals | 15 | 2013 | 15081 | 0.280 |
Why?
|
| Genital Diseases, Female | 3 | 2011 | 37 | 0.270 |
Why?
|
| Cloning, Molecular | 2 | 2018 | 325 | 0.240 |
Why?
|
| Bacterial Vaccines | 3 | 2010 | 125 | 0.230 |
Why?
|
| Ticks | 2 | 2013 | 6 | 0.230 |
Why?
|
| Recombinant Proteins | 2 | 2018 | 515 | 0.210 |
Why?
|
| Polymerase Chain Reaction | 2 | 2018 | 448 | 0.210 |
Why?
|
| Genetic Complementation Test | 3 | 2011 | 59 | 0.210 |
Why?
|
| Francisella | 2 | 2012 | 19 | 0.200 |
Why?
|
| Virulence | 3 | 2011 | 223 | 0.190 |
Why?
|
| Base Sequence | 2 | 2013 | 997 | 0.190 |
Why?
|
| Mutation | 3 | 2013 | 1095 | 0.190 |
Why?
|
| Disease Models, Animal | 3 | 2011 | 1371 | 0.170 |
Why?
|
| Mice, Inbred BALB C | 5 | 2012 | 661 | 0.160 |
Why?
|
| Electrophoresis, Polyacrylamide Gel | 2 | 2009 | 201 | 0.160 |
Why?
|
| Reverse Transcriptase Polymerase Chain Reaction | 2 | 2011 | 623 | 0.160 |
Why?
|
| Up-Regulation | 2 | 2013 | 513 | 0.160 |
Why?
|
| Interferon-gamma | 2 | 2011 | 250 | 0.160 |
Why?
|
| Phenotype | 2 | 2013 | 689 | 0.160 |
Why?
|
| Conserved Sequence | 2 | 2013 | 119 | 0.140 |
Why?
|
| RNA | 1 | 2018 | 241 | 0.130 |
Why?
|
| Open Reading Frames | 2 | 2012 | 77 | 0.130 |
Why?
|
| DNA | 1 | 2018 | 574 | 0.120 |
Why?
|
| Tularemia | 2 | 2012 | 114 | 0.120 |
Why?
|
| Enzyme Activation | 2 | 2013 | 444 | 0.120 |
Why?
|
| Xylose | 1 | 2013 | 11 | 0.110 |
Why?
|
| Sequence Homology, Amino Acid | 2 | 2013 | 269 | 0.110 |
Why?
|
| Protein Binding | 2 | 2013 | 972 | 0.110 |
Why?
|
| Genes, Bacterial | 1 | 2013 | 90 | 0.110 |
Why?
|
| Gene Order | 1 | 2012 | 17 | 0.110 |
Why?
|
| Hydroxymethylglutaryl CoA Reductases | 1 | 2012 | 5 | 0.110 |
Why?
|
| Alkaline Phosphatase | 1 | 2012 | 50 | 0.110 |
Why?
|
| Species Specificity | 1 | 2013 | 245 | 0.110 |
Why?
|
| Mutagenesis, Site-Directed | 1 | 2013 | 188 | 0.110 |
Why?
|
| HSP70 Heat-Shock Proteins | 1 | 2012 | 47 | 0.110 |
Why?
|
| Bacteremia | 1 | 2012 | 30 | 0.110 |
Why?
|
| Female | 9 | 2012 | 20969 | 0.110 |
Why?
|
| Antibodies, Bacterial | 2 | 2010 | 109 | 0.100 |
Why?
|
| Metabolic Networks and Pathways | 1 | 2012 | 67 | 0.100 |
Why?
|
| Manganese | 1 | 2013 | 87 | 0.100 |
Why?
|
| Protein Structure, Tertiary | 1 | 2013 | 408 | 0.100 |
Why?
|
| Sequence Alignment | 1 | 2012 | 265 | 0.100 |
Why?
|
| Hydroxymethylglutaryl-CoA Reductase Inhibitors | 1 | 2012 | 77 | 0.100 |
Why?
|
| Fallopian Tubes | 1 | 2011 | 17 | 0.100 |
Why?
|
| Gene Knockout Techniques | 1 | 2011 | 51 | 0.100 |
Why?
|
| Down-Regulation | 1 | 2013 | 435 | 0.100 |
Why?
|
| Bacterial Outer Membrane Proteins | 1 | 2011 | 52 | 0.090 |
Why?
|
| Two-Hybrid System Techniques | 1 | 2010 | 50 | 0.090 |
Why?
|
| Promoter Regions, Genetic | 1 | 2013 | 515 | 0.090 |
Why?
|
| Repressor Proteins | 1 | 2013 | 249 | 0.090 |
Why?
|
| CD8-Positive T-Lymphocytes | 1 | 2011 | 159 | 0.090 |
Why?
|
| Gene Deletion | 1 | 2010 | 166 | 0.090 |
Why?
|
| Phosphorylation | 1 | 2013 | 928 | 0.090 |
Why?
|
| Tumor Necrosis Factor-alpha | 1 | 2011 | 356 | 0.080 |
Why?
|
| Macrophages | 2 | 2011 | 439 | 0.080 |
Why?
|
| Blotting, Southern | 1 | 2008 | 69 | 0.080 |
Why?
|
| Mutagenesis | 1 | 2008 | 89 | 0.080 |
Why?
|
| Vaginal Diseases | 1 | 2008 | 9 | 0.080 |
Why?
|
| Joints | 1 | 2007 | 7 | 0.080 |
Why?
|
| Neutrophils | 1 | 2008 | 131 | 0.080 |
Why?
|
| Arthritis, Infectious | 1 | 2007 | 4 | 0.080 |
Why?
|
| Epitopes, T-Lymphocyte | 1 | 2008 | 57 | 0.080 |
Why?
|
| Gene Expression Profiling | 1 | 2011 | 626 | 0.070 |
Why?
|
| CD4-Positive T-Lymphocytes | 1 | 2008 | 259 | 0.070 |
Why?
|
| Gene Expression | 1 | 2008 | 674 | 0.060 |
Why?
|
| Oxidative Stress | 1 | 2008 | 938 | 0.050 |
Why?
|
| Mice, Inbred C57BL | 3 | 2011 | 1609 | 0.050 |
Why?
|
| Vagina | 2 | 2011 | 81 | 0.050 |
Why?
|
| Vaccines, Synthetic | 2 | 2010 | 72 | 0.040 |
Why?
|
| Recombinant Fusion Proteins | 2 | 2010 | 295 | 0.040 |
Why?
|
| Oligodeoxyribonucleotides | 2 | 2009 | 52 | 0.040 |
Why?
|
| Mice, Knockout | 2 | 2011 | 933 | 0.040 |
Why?
|
| Humans | 2 | 2018 | 37093 | 0.030 |
Why?
|
| Apoenzymes | 1 | 2013 | 5 | 0.030 |
Why?
|
| Chromatography, DEAE-Cellulose | 1 | 2012 | 8 | 0.030 |
Why?
|
| Hydrogen Bonding | 1 | 2013 | 132 | 0.030 |
Why?
|
| Catalytic Domain | 1 | 2013 | 109 | 0.030 |
Why?
|
| Chaperonin 60 | 1 | 2012 | 18 | 0.030 |
Why?
|
| Molecular Weight | 1 | 2012 | 167 | 0.030 |
Why?
|
| HSP90 Heat-Shock Proteins | 1 | 2012 | 47 | 0.030 |
Why?
|
| Hydrogen Peroxide | 1 | 2013 | 190 | 0.030 |
Why?
|
| Protein Transport | 1 | 2013 | 302 | 0.030 |
Why?
|
| Spectrometry, Mass, Electrospray Ionization | 1 | 2012 | 132 | 0.030 |
Why?
|
| Adenosine Triphosphate | 1 | 2012 | 196 | 0.020 |
Why?
|
| Perforin | 1 | 2011 | 10 | 0.020 |
Why?
|
| Polymyxin B | 1 | 2011 | 8 | 0.020 |
Why?
|
| Saccharomyces cerevisiae | 1 | 2013 | 206 | 0.020 |
Why?
|
| Nitrites | 1 | 2011 | 46 | 0.020 |
Why?
|
| Early Growth Response Protein 1 | 1 | 2010 | 10 | 0.020 |
Why?
|
| DNA-Directed RNA Polymerases | 1 | 2010 | 22 | 0.020 |
Why?
|
| Peptide Fragments | 1 | 2012 | 308 | 0.020 |
Why?
|
| Genetic Vectors | 1 | 2010 | 158 | 0.020 |
Why?
|
| Immunization | 1 | 2010 | 92 | 0.020 |
Why?
|
| Cricetinae | 1 | 2010 | 238 | 0.020 |
Why?
|
| Hela Cells | 1 | 2011 | 366 | 0.020 |
Why?
|
| Vibrio cholerae | 1 | 2010 | 98 | 0.020 |
Why?
|
| Plasmids | 1 | 2010 | 246 | 0.020 |
Why?
|
| Francisella tularensis | 1 | 2010 | 115 | 0.020 |
Why?
|
| Models, Molecular | 1 | 2013 | 808 | 0.020 |
Why?
|
| Colony Count, Microbial | 1 | 2009 | 66 | 0.020 |
Why?
|
| Mitochondria | 1 | 2013 | 487 | 0.020 |
Why?
|
| beta 2-Microglobulin | 1 | 2008 | 10 | 0.020 |
Why?
|
| Adjuvants, Immunologic | 1 | 2009 | 107 | 0.020 |
Why?
|
| Adoptive Transfer | 1 | 2008 | 48 | 0.020 |
Why?
|
| Administration, Intranasal | 1 | 2008 | 79 | 0.020 |
Why?
|
| Antigen Presentation | 1 | 2008 | 54 | 0.020 |
Why?
|
| Endopeptidases | 1 | 2008 | 59 | 0.020 |
Why?
|
| Anti-Bacterial Agents | 1 | 2011 | 352 | 0.020 |
Why?
|
| Escherichia coli | 1 | 2010 | 453 | 0.020 |
Why?
|
| Cells, Cultured | 1 | 2011 | 1518 | 0.020 |
Why?
|
| Signal Transduction | 1 | 2008 | 1908 | 0.010 |
Why?
|