 Bob Eisenberg
Concepts (231)
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?
|
|---|
| Ion Channels | 36 | 2015 | 239 | 7.240 |
Why?
| | Models, Biological | 44 | 2014 | 416 | 6.050 |
Why?
| | Calcium Channels | 18 | 2014 | 127 | 4.960 |
Why?
| | Calcium | 29 | 2016 | 472 | 3.600 |
Why?
| | Ions | 20 | 2015 | 55 | 3.500 |
Why?
| | Computer Simulation | 24 | 2015 | 214 | 3.100 |
Why?
| | Models, Chemical | 17 | 2012 | 46 | 2.840 |
Why?
| | Models, Molecular | 16 | 2016 | 102 | 2.740 |
Why?
| | Ion Channel Gating | 21 | 2011 | 200 | 2.630 |
Why?
| | Static Electricity | 24 | 2014 | 43 | 2.340 |
Why?
| | Porins | 9 | 2013 | 23 | 2.320 |
Why?
| | Sodium | 14 | 2016 | 68 | 1.950 |
Why?
| | Biophysics | 16 | 2013 | 45 | 1.920 |
Why?
| | Electric Conductivity | 29 | 2013 | 86 | 1.710 |
Why?
| | Action Potentials | 8 | 2018 | 104 | 1.330 |
Why?
| | Electrochemistry | 9 | 2011 | 44 | 1.300 |
Why?
| | Thermodynamics | 13 | 2013 | 50 | 1.260 |
Why?
| | Membrane Potentials | 27 | 2004 | 214 | 1.240 |
Why?
| | Electrophysiology | 26 | 2006 | 153 | 1.230 |
Why?
| | Bacterial Outer Membrane Proteins | 4 | 2013 | 11 | 1.220 |
Why?
| | Escherichia coli Proteins | 3 | 2013 | 12 | 1.180 |
Why?
| | Ion Transport | 12 | 2016 | 39 | 1.120 |
Why?
| | Cell Membrane | 10 | 2009 | 128 | 1.120 |
Why?
| | Models, Theoretical | 8 | 2013 | 92 | 1.080 |
Why?
| | Water | 6 | 2015 | 35 | 1.040 |
Why?
| | Sodium Channels | 4 | 2013 | 15 | 0.970 |
Why?
| | Solutions | 6 | 2013 | 18 | 0.940 |
Why?
| | Physical Phenomena | 2 | 2018 | 3 | 0.890 |
Why?
| | Nanostructures | 3 | 2007 | 12 | 0.890 |
Why?
| | Semiconductors | 3 | 2007 | 4 | 0.870 |
Why?
| | Microfluidics | 2 | 2008 | 7 | 0.860 |
Why?
| | Lipid Bilayers | 4 | 2012 | 83 | 0.840 |
Why?
| | Microelectrodes | 10 | 2007 | 36 | 0.780 |
Why?
| | Calcium Channels, L-Type | 6 | 2011 | 54 | 0.770 |
Why?
| | Sodium-Calcium Exchanger | 1 | 2016 | 21 | 0.770 |
Why?
| | Chlorides | 3 | 2013 | 28 | 0.750 |
Why?
| | Escherichia coli | 3 | 2013 | 66 | 0.750 |
Why?
| | Muscles | 14 | 1987 | 73 | 0.740 |
Why?
| | Protein Conformation | 8 | 2014 | 93 | 0.730 |
Why?
| | Muscle Contraction | 11 | 1992 | 81 | 0.720 |
Why?
| | Enzymes | 2 | 2012 | 7 | 0.720 |
Why?
| | Catalytic Domain | 2 | 2012 | 14 | 0.710 |
Why?
| | Sarcoplasmic Reticulum | 11 | 1997 | 214 | 0.700 |
Why?
| | Cations | 3 | 2013 | 16 | 0.690 |
Why?
| | Animals | 41 | 2013 | 4705 | 0.680 |
Why?
| | Gramicidin | 3 | 2013 | 3 | 0.670 |
Why?
| | Quantum Theory | 2 | 2010 | 6 | 0.660 |
Why?
| | Nanotechnology | 3 | 2009 | 14 | 0.650 |
Why?
| | Mutation | 3 | 2013 | 407 | 0.650 |
Why?
| | Elementary Particle Interactions | 1 | 2013 | 3 | 0.620 |
Why?
| | Algorithms | 6 | 2015 | 374 | 0.620 |
Why?
| | Biophysical Phenomena | 11 | 2007 | 36 | 0.600 |
Why?
| | N-Acetylneuraminic Acid | 1 | 2012 | 4 | 0.580 |
Why?
| | Diffusion | 8 | 2009 | 31 | 0.540 |
Why?
| | Protein Engineering | 2 | 2008 | 7 | 0.540 |
Why?
| | Biosensing Techniques | 2 | 2008 | 12 | 0.530 |
Why?
| | Computational Biology | 2 | 2012 | 26 | 0.500 |
Why?
| | Lens, Crystalline | 8 | 1986 | 32 | 0.450 |
Why?
| | Monte Carlo Method | 9 | 2013 | 54 | 0.440 |
Why?
| | Binding Sites | 8 | 2014 | 86 | 0.440 |
Why?
| | Body Fluids | 1 | 2008 | 20 | 0.440 |
Why?
| | Anesthetics | 1 | 2008 | 11 | 0.440 |
Why?
| | Poisson Distribution | 6 | 2014 | 26 | 0.440 |
Why?
| | Potassium Channels | 5 | 2001 | 41 | 0.430 |
Why?
| | Hydrogen-Ion Concentration | 6 | 2012 | 181 | 0.430 |
Why?
| | Biological Factors | 1 | 2007 | 8 | 0.430 |
Why?
| | Cell Membrane Permeability | 6 | 2009 | 63 | 0.420 |
Why?
| | Physiology | 1 | 2007 | 4 | 0.420 |
Why?
| | Engineering | 1 | 2007 | 2 | 0.420 |
Why?
| | Silicon | 1 | 2007 | 4 | 0.420 |
Why?
| | Kinetics | 10 | 2009 | 282 | 0.420 |
Why?
| | Nerve Endings | 1 | 2007 | 4 | 0.410 |
Why?
| | Mechanotransduction, Cellular | 1 | 2007 | 6 | 0.410 |
Why?
| | Proteins | 2 | 2009 | 86 | 0.410 |
Why?
| | Biological Transport | 4 | 2012 | 47 | 0.400 |
Why?
| | Models, Statistical | 6 | 2005 | 132 | 0.400 |
Why?
| | Synapses | 1 | 2007 | 43 | 0.400 |
Why?
| | Patch-Clamp Techniques | 2 | 2004 | 135 | 0.380 |
Why?
| | Movement | 1 | 2007 | 153 | 0.370 |
Why?
| | Entropy | 2 | 2014 | 7 | 0.340 |
Why?
| | Aquaporins | 1 | 2003 | 9 | 0.330 |
Why?
| | In Vitro Techniques | 13 | 2000 | 252 | 0.330 |
Why?
| | Oligopeptides | 2 | 2009 | 35 | 0.320 |
Why?
| | Permeability | 6 | 2011 | 136 | 0.320 |
Why?
| | Neurons | 1 | 2007 | 363 | 0.310 |
Why?
| | Technology, Pharmaceutical | 1 | 2002 | 2 | 0.300 |
Why?
| | Pharmacogenetics | 1 | 2002 | 7 | 0.300 |
Why?
| | Patents as Topic | 1 | 2002 | 5 | 0.300 |
Why?
| | Mathematics | 16 | 1996 | 34 | 0.300 |
Why?
| | Protons | 1 | 2003 | 99 | 0.300 |
Why?
| | Substrate Specificity | 2 | 2013 | 35 | 0.300 |
Why?
| | Protein Structure, Secondary | 3 | 2006 | 26 | 0.290 |
Why?
| | Protein Binding | 4 | 2014 | 143 | 0.280 |
Why?
| | Reproducibility of Results | 3 | 2013 | 722 | 0.280 |
Why?
| | Perfusion | 2 | 1992 | 22 | 0.270 |
Why?
| | Porosity | 4 | 2009 | 65 | 0.270 |
Why?
| | Glutamic Acid | 2 | 2011 | 36 | 0.260 |
Why?
| | Membrane Proteins | 3 | 2006 | 181 | 0.250 |
Why?
| | Electric Impedance | 3 | 2009 | 18 | 0.230 |
Why?
| | Osmolar Concentration | 3 | 2013 | 37 | 0.220 |
Why?
| | Lasers | 1 | 2018 | 13 | 0.220 |
Why?
| | Gallopamil | 4 | 1987 | 8 | 0.210 |
Why?
| | Muscle Proteins | 1 | 1997 | 25 | 0.210 |
Why?
| | Biological Transport, Active | 3 | 2012 | 19 | 0.210 |
Why?
| | Myocardium | 1 | 1999 | 172 | 0.210 |
Why?
| | Potassium Chloride | 3 | 2012 | 6 | 0.210 |
Why?
| | Nephropidae | 3 | 1994 | 5 | 0.200 |
Why?
| | Heart | 1 | 1997 | 100 | 0.200 |
Why?
| | Equipment Failure Analysis | 2 | 2007 | 118 | 0.200 |
Why?
| | Equipment Design | 2 | 2007 | 179 | 0.200 |
Why?
| | Cell Physiological Phenomena | 4 | 1980 | 6 | 0.190 |
Why?
| | Methanocaldococcus | 1 | 2016 | 1 | 0.190 |
Why?
| | Buffers | 3 | 2012 | 15 | 0.190 |
Why?
| | Dose-Response Relationship, Drug | 3 | 2012 | 496 | 0.180 |
Why?
| | Sensitivity and Specificity | 3 | 2008 | 561 | 0.180 |
Why?
| | Extracellular Space | 2 | 1986 | 12 | 0.170 |
Why?
| | Humans | 11 | 2013 | 24903 | 0.170 |
Why?
| | Verapamil | 2 | 1984 | 36 | 0.160 |
Why?
| | Brevibacillus | 1 | 2013 | 1 | 0.160 |
Why?
| | Calcium-Transporting ATPases | 1 | 1992 | 25 | 0.150 |
Why?
| | Biopolymers | 1 | 2012 | 3 | 0.150 |
Why?
| | Particle Size | 3 | 2012 | 67 | 0.150 |
Why?
| | Ionic Liquids | 1 | 2012 | 1 | 0.150 |
Why?
| | Myofibrils | 4 | 1978 | 6 | 0.140 |
Why?
| | Potassium | 5 | 2007 | 66 | 0.140 |
Why?
| | Rana pipiens | 9 | 1986 | 53 | 0.130 |
Why?
| | Myosins | 1 | 1990 | 7 | 0.130 |
Why?
| | Actins | 1 | 1990 | 59 | 0.120 |
Why?
| | Cations, Divalent | 2 | 2006 | 13 | 0.120 |
Why?
| | Oscillometry | 2 | 2007 | 7 | 0.120 |
Why?
| | Nanotubes | 1 | 2009 | 3 | 0.120 |
Why?
| | Electrolytes | 1 | 2009 | 13 | 0.120 |
Why?
| | HIV Protease | 1 | 2009 | 9 | 0.120 |
Why?
| | HIV Protease Inhibitors | 1 | 2009 | 19 | 0.120 |
Why?
| | Linear Models | 1 | 2009 | 253 | 0.110 |
Why?
| | Anura | 9 | 1981 | 15 | 0.110 |
Why?
| | Gases | 1 | 2008 | 4 | 0.110 |
Why?
| | Ocular Physiological Phenomena | 1 | 1988 | 2 | 0.110 |
Why?
| | Fractional Precipitation | 1 | 2007 | 1 | 0.110 |
Why?
| | Ultrafiltration | 1 | 2007 | 6 | 0.110 |
Why?
| | Sodium Chloride | 3 | 2005 | 43 | 0.110 |
Why?
| | Systems Integration | 1 | 2007 | 5 | 0.100 |
Why?
| | Biomimetics | 1 | 2007 | 7 | 0.100 |
Why?
| | Transistors, Electronic | 1 | 2006 | 1 | 0.100 |
Why?
| | Stress, Mechanical | 1 | 2007 | 174 | 0.100 |
Why?
| | Oxygen | 2 | 2011 | 77 | 0.100 |
Why?
| | Materials Testing | 1 | 2006 | 127 | 0.090 |
Why?
| | Intercellular Junctions | 2 | 1982 | 9 | 0.090 |
Why?
| | Salts | 1 | 2005 | 1 | 0.090 |
Why?
| | Electric Capacitance | 1 | 2004 | 6 | 0.090 |
Why?
| | Rana temporaria | 4 | 1985 | 10 | 0.090 |
Why?
| | Electromagnetic Fields | 1 | 2004 | 12 | 0.090 |
Why?
| | Cations, Monovalent | 2 | 2006 | 11 | 0.080 |
Why?
| | Paralysis | 1 | 1984 | 16 | 0.080 |
Why?
| | Models, Structural | 2 | 1981 | 6 | 0.080 |
Why?
| | Purkinje Fibers | 1 | 1983 | 2 | 0.080 |
Why?
| | Heart Conduction System | 1 | 1983 | 35 | 0.080 |
Why?
| | Magnesium | 2 | 1994 | 45 | 0.080 |
Why?
| | Calcium Channel Blockers | 1 | 1983 | 37 | 0.080 |
Why?
| | Chemistry, Physical | 1 | 2003 | 3 | 0.080 |
Why?
| | Chemical Phenomena | 1 | 2003 | 7 | 0.080 |
Why?
| | Dinitrophenols | 1 | 1982 | 2 | 0.080 |
Why?
| | Uncoupling Agents | 1 | 1982 | 7 | 0.080 |
Why?
| | Cell Communication | 1 | 1982 | 35 | 0.080 |
Why?
| | Temperature | 3 | 1995 | 80 | 0.070 |
Why?
| | Cytoplasm | 2 | 1979 | 43 | 0.070 |
Why?
| | Ryanodine Receptor Calcium Release Channel | 2 | 2007 | 162 | 0.070 |
Why?
| | Chloride Channels | 1 | 2001 | 11 | 0.070 |
Why?
| | Osmosis | 1 | 2000 | 9 | 0.070 |
Why?
| | Rana catesbeiana | 2 | 1992 | 9 | 0.060 |
Why?
| | Nerve Tissue | 1 | 1979 | 2 | 0.060 |
Why?
| | Membranes | 2 | 1993 | 10 | 0.060 |
Why?
| | Lithium | 2 | 2009 | 28 | 0.050 |
Why?
| | Probability | 1 | 1997 | 92 | 0.050 |
Why?
| | Structure-Activity Relationship | 2 | 2009 | 55 | 0.050 |
Why?
| | Epithelium | 2 | 1988 | 34 | 0.050 |
Why?
| | Molecular Structure | 1 | 1996 | 49 | 0.050 |
Why?
| | Fourier Analysis | 2 | 2010 | 10 | 0.050 |
Why?
| | Mutagenesis, Site-Directed | 2 | 2006 | 26 | 0.050 |
Why?
| | Methods | 2 | 2011 | 26 | 0.050 |
Why?
| | Motion | 1 | 1995 | 27 | 0.040 |
Why?
| | Molecular Dynamics Simulation | 1 | 2013 | 10 | 0.040 |
Why?
| | Time Factors | 4 | 1982 | 1600 | 0.040 |
Why?
| | Molecular Conformation | 1 | 1993 | 17 | 0.040 |
Why?
| | Tyrothricin | 1 | 1973 | 1 | 0.040 |
Why?
| | Nystatin | 1 | 1973 | 3 | 0.040 |
Why?
| | Protein Multimerization | 1 | 2013 | 19 | 0.040 |
Why?
| | Amphotericin B | 1 | 1973 | 8 | 0.040 |
Why?
| | Software | 1 | 2013 | 55 | 0.040 |
Why?
| | Caffeine | 2 | 1985 | 61 | 0.040 |
Why?
| | Vanadates | 1 | 1992 | 3 | 0.040 |
Why?
| | Triazines | 1 | 1992 | 8 | 0.040 |
Why?
| | Ruthenium Red | 1 | 1992 | 8 | 0.040 |
Why?
| | Ryanodine | 1 | 1992 | 19 | 0.040 |
Why?
| | Indoles | 1 | 1992 | 66 | 0.040 |
Why?
| | Micromanipulation | 1 | 1992 | 2 | 0.040 |
Why?
| | Aspartic Acid | 1 | 2011 | 17 | 0.030 |
Why?
| | Microscopy, Electron | 2 | 1982 | 93 | 0.030 |
Why?
| | Biological Evolution | 1 | 1990 | 23 | 0.030 |
Why?
| | Parasympathomimetics | 1 | 1989 | 4 | 0.030 |
Why?
| | Protein Structure, Tertiary | 1 | 2009 | 90 | 0.030 |
Why?
| | Barium | 1 | 2009 | 13 | 0.030 |
Why?
| | Polyethylene Terephthalates | 1 | 2009 | 4 | 0.030 |
Why?
| | Binding, Competitive | 1 | 2009 | 31 | 0.030 |
Why?
| | Stochastic Processes | 1 | 1988 | 15 | 0.030 |
Why?
| | Cysteine | 1 | 2006 | 11 | 0.030 |
Why?
| | Cesium | 1 | 2006 | 13 | 0.030 |
Why?
| | Electricity | 1 | 2006 | 10 | 0.030 |
Why?
| | Electric Stimulation | 2 | 1979 | 88 | 0.020 |
Why?
| | Glutathione | 1 | 2006 | 32 | 0.020 |
Why?
| | Sequence Analysis, Protein | 1 | 2006 | 5 | 0.020 |
Why?
| | Lysine | 1 | 2006 | 14 | 0.020 |
Why?
| | Xenopus | 1 | 1986 | 6 | 0.020 |
Why?
| | Pressure | 1 | 1986 | 69 | 0.020 |
Why?
| | Hypertonic Solutions | 2 | 1974 | 3 | 0.020 |
Why?
| | Sheep | 1 | 1983 | 34 | 0.020 |
Why?
| | Recombinant Proteins | 1 | 2004 | 293 | 0.020 |
Why?
| | Cells, Cultured | 1 | 1986 | 750 | 0.020 |
Why?
| | 2,4-Dinitrophenol | 1 | 1982 | 1 | 0.020 |
Why?
| | Xenopus laevis | 1 | 1982 | 11 | 0.020 |
Why?
| | Cells | 1 | 1980 | 3 | 0.020 |
Why?
| | Macromolecular Substances | 1 | 1980 | 24 | 0.020 |
Why?
| | Organoids | 1 | 1980 | 8 | 0.020 |
Why?
| | Microtubules | 1 | 1977 | 29 | 0.010 |
Why?
| | Physics | 1 | 1995 | 3 | 0.010 |
Why?
| | Detergents | 1 | 1974 | 4 | 0.010 |
Why?
| | Potentiometry | 1 | 1974 | 1 | 0.010 |
Why?
| | Glycerol | 1 | 1974 | 3 | 0.010 |
Why?
| | Sucrose | 1 | 1974 | 20 | 0.010 |
Why?
| | Evaluation Studies as Topic | 1 | 1974 | 55 | 0.010 |
Why?
| | Electrodes | 1 | 1973 | 17 | 0.010 |
Why?
|
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