Joseph Falke
Concepts (376)
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?
|
---|
Chemotaxis | 43 | 2018 | 130 | 6.980 |
Why?
| Membrane Proteins | 45 | 2018 | 1019 | 5.580 |
Why?
| Bacterial Proteins | 40 | 2015 | 736 | 4.650 |
Why?
| Receptors, Amino Acid | 23 | 2009 | 25 | 3.840 |
Why?
| Signal Transduction | 41 | 2023 | 4513 | 3.480 |
Why?
| Protein Kinase C-alpha | 11 | 2023 | 41 | 3.260 |
Why?
| Protein Kinases | 18 | 2014 | 307 | 3.060 |
Why?
| Lipid Bilayers | 15 | 2023 | 99 | 2.920 |
Why?
| Cell Membrane | 24 | 2021 | 680 | 2.850 |
Why?
| Disulfides | 21 | 2014 | 90 | 2.740 |
Why?
| ras Proteins | 4 | 2022 | 138 | 2.730 |
Why?
| Escherichia coli Proteins | 23 | 2015 | 162 | 2.590 |
Why?
| Calcium | 25 | 2018 | 1108 | 2.580 |
Why?
| Phosphatidylinositol 3-Kinases | 5 | 2022 | 329 | 2.280 |
Why?
| Protein Structure, Tertiary | 32 | 2015 | 796 | 1.920 |
Why?
| Escherichia coli | 33 | 2015 | 720 | 1.840 |
Why?
| Salmonella typhimurium | 20 | 2014 | 164 | 1.790 |
Why?
| Phosphatidylinositol Phosphates | 6 | 2017 | 38 | 1.750 |
Why?
| Mutagenesis, Site-Directed | 27 | 2014 | 345 | 1.720 |
Why?
| Models, Molecular | 43 | 2017 | 1369 | 1.720 |
Why?
| Cysteine | 20 | 2009 | 171 | 1.710 |
Why?
| Aspartic Acid | 16 | 2009 | 77 | 1.660 |
Why?
| Protein Conformation | 35 | 2016 | 805 | 1.660 |
Why?
| Receptors, Cytoplasmic and Nuclear | 8 | 2013 | 192 | 1.610 |
Why?
| Calcium-Binding Proteins | 16 | 2003 | 206 | 1.530 |
Why?
| Phospholipases A | 11 | 2007 | 101 | 1.470 |
Why?
| Methyl-Accepting Chemotaxis Proteins | 24 | 2015 | 25 | 1.430 |
Why?
| Phosphatidylinositol 4,5-Diphosphate | 7 | 2016 | 24 | 1.290 |
Why?
| Protein Binding | 26 | 2023 | 1890 | 1.240 |
Why?
| Histidine Kinase | 19 | 2015 | 33 | 1.230 |
Why?
| Protein Kinase C | 6 | 2018 | 273 | 1.160 |
Why?
| Monosaccharide Transport Proteins | 10 | 1997 | 45 | 1.160 |
Why?
| Periplasmic Binding Proteins | 9 | 1997 | 14 | 1.160 |
Why?
| Kinetics | 34 | 2014 | 1551 | 1.130 |
Why?
| Guanosine Triphosphate | 3 | 2022 | 85 | 1.120 |
Why?
| Protein Structure, Secondary | 16 | 2013 | 325 | 1.070 |
Why?
| Binding Sites | 28 | 2013 | 1168 | 1.050 |
Why?
| Macrophages | 5 | 2020 | 1263 | 1.040 |
Why?
| Guanosine Diphosphate | 2 | 2021 | 19 | 0.930 |
Why?
| Multiprotein Complexes | 3 | 2014 | 140 | 0.920 |
Why?
| Electron Spin Resonance Spectroscopy | 8 | 2012 | 86 | 0.920 |
Why?
| Receptors, Cell Surface | 13 | 2007 | 355 | 0.920 |
Why?
| Intracellular Signaling Peptides and Proteins | 2 | 2016 | 386 | 0.890 |
Why?
| Calmodulin | 4 | 2016 | 71 | 0.890 |
Why?
| Myristoylated Alanine-Rich C Kinase Substrate | 3 | 2018 | 5 | 0.890 |
Why?
| Protein Interaction Mapping | 4 | 2010 | 101 | 0.870 |
Why?
| Calcium Signaling | 4 | 2014 | 217 | 0.870 |
Why?
| Phosphatidylinositols | 3 | 2022 | 54 | 0.830 |
Why?
| Chemoreceptor Cells | 7 | 2007 | 55 | 0.820 |
Why?
| Recombinant Proteins | 13 | 2021 | 1230 | 0.780 |
Why?
| Models, Chemical | 10 | 2013 | 248 | 0.770 |
Why?
| Guanine Nucleotides | 1 | 2021 | 15 | 0.770 |
Why?
| Cytosol | 7 | 2007 | 208 | 0.750 |
Why?
| Protein Engineering | 19 | 2013 | 98 | 0.740 |
Why?
| Class III Phosphatidylinositol 3-Kinases | 1 | 2020 | 1 | 0.730 |
Why?
| rab5 GTP-Binding Proteins | 1 | 2020 | 6 | 0.730 |
Why?
| Pseudopodia | 1 | 2020 | 20 | 0.690 |
Why?
| Phosphatidylserines | 6 | 2014 | 87 | 0.680 |
Why?
| Chromatography, High Pressure Liquid | 1 | 2021 | 470 | 0.670 |
Why?
| Endosomes | 1 | 2020 | 124 | 0.670 |
Why?
| Spin Labels | 5 | 2008 | 44 | 0.650 |
Why?
| Amino Acid Substitution | 11 | 2014 | 262 | 0.610 |
Why?
| Proto-Oncogene Proteins c-akt | 2 | 2011 | 398 | 0.600 |
Why?
| Receptors, Platelet-Derived Growth Factor | 1 | 2017 | 13 | 0.590 |
Why?
| Conserved Sequence | 3 | 2007 | 218 | 0.570 |
Why?
| Cytoplasm | 6 | 2005 | 255 | 0.570 |
Why?
| Enzyme Activation | 9 | 2017 | 785 | 0.570 |
Why?
| Carrier Proteins | 9 | 1997 | 695 | 0.550 |
Why?
| Phosphatidylinositol 3-Kinase | 1 | 2016 | 26 | 0.550 |
Why?
| Adaptor Proteins, Signal Transducing | 3 | 2014 | 367 | 0.540 |
Why?
| Biochemistry | 2 | 2007 | 40 | 0.540 |
Why?
| Dimerization | 8 | 2013 | 176 | 0.530 |
Why?
| Fluorescence Resonance Energy Transfer | 4 | 2013 | 170 | 0.520 |
Why?
| Mutation | 11 | 2021 | 3346 | 0.520 |
Why?
| Protein Interaction Domains and Motifs | 3 | 2014 | 129 | 0.520 |
Why?
| Protein Stability | 2 | 2014 | 157 | 0.510 |
Why?
| Anion Exchange Protein 1, Erythrocyte | 8 | 1986 | 22 | 0.510 |
Why?
| Magnetic Resonance Spectroscopy | 18 | 1996 | 473 | 0.480 |
Why?
| Microscopy, Fluorescence | 6 | 2017 | 396 | 0.480 |
Why?
| Cystine | 1 | 2014 | 14 | 0.470 |
Why?
| Cell Movement | 3 | 2020 | 869 | 0.460 |
Why?
| Eukaryotic Cells | 1 | 2014 | 33 | 0.450 |
Why?
| Chlorides | 9 | 1986 | 127 | 0.450 |
Why?
| 3-Phosphoinositide-Dependent Protein Kinases | 1 | 2013 | 1 | 0.440 |
Why?
| Amino Acid Sequence | 12 | 2016 | 1982 | 0.440 |
Why?
| Spectrometry, Fluorescence | 8 | 2010 | 157 | 0.420 |
Why?
| Lipid Metabolism | 2 | 2007 | 444 | 0.420 |
Why?
| Galactose | 8 | 1997 | 20 | 0.420 |
Why?
| Adaptation, Physiological | 4 | 2020 | 483 | 0.400 |
Why?
| Thermotoga maritima | 2 | 2013 | 10 | 0.390 |
Why?
| Endosomal Sorting Complexes Required for Transport | 1 | 2012 | 34 | 0.390 |
Why?
| Diffusion | 3 | 2023 | 119 | 0.390 |
Why?
| Membrane Lipids | 2 | 2010 | 87 | 0.390 |
Why?
| Point Mutation | 3 | 2009 | 216 | 0.370 |
Why?
| Vesicular Transport Proteins | 1 | 2012 | 83 | 0.370 |
Why?
| Phosphorylation | 7 | 2021 | 1569 | 0.370 |
Why?
| Amino Acid Motifs | 2 | 2009 | 197 | 0.360 |
Why?
| Models, Theoretical | 3 | 2005 | 515 | 0.360 |
Why?
| Protein Structure, Quaternary | 2 | 2013 | 115 | 0.350 |
Why?
| RAW 264.7 Cells | 2 | 2020 | 41 | 0.330 |
Why?
| Bacterial Physiological Phenomena | 3 | 2007 | 57 | 0.320 |
Why?
| Peptide Fragments | 5 | 2016 | 666 | 0.310 |
Why?
| Bacteria | 3 | 2014 | 725 | 0.310 |
Why?
| Isoenzymes | 3 | 2008 | 283 | 0.310 |
Why?
| Oncogenes | 1 | 2008 | 103 | 0.300 |
Why?
| Tryptophan | 5 | 2014 | 136 | 0.300 |
Why?
| Static Electricity | 6 | 2013 | 114 | 0.290 |
Why?
| Biophysics | 3 | 2005 | 69 | 0.280 |
Why?
| Humans | 35 | 2021 | 114689 | 0.280 |
Why?
| Membrane Microdomains | 2 | 2003 | 32 | 0.270 |
Why?
| Glycine | 2 | 2005 | 152 | 0.270 |
Why?
| Animals | 17 | 2020 | 31706 | 0.270 |
Why?
| Protein Domains | 2 | 2017 | 207 | 0.260 |
Why?
| Cell Line | 5 | 2018 | 2637 | 0.260 |
Why?
| Edetic Acid | 2 | 2003 | 47 | 0.240 |
Why?
| Hot Temperature | 4 | 2021 | 302 | 0.230 |
Why?
| Cell Polarity | 2 | 2020 | 131 | 0.230 |
Why?
| Mice | 8 | 2020 | 14869 | 0.220 |
Why?
| Water | 3 | 2004 | 396 | 0.220 |
Why?
| Protein Kinase C beta | 3 | 2014 | 24 | 0.220 |
Why?
| Cations, Divalent | 4 | 2010 | 51 | 0.220 |
Why?
| Spin Trapping | 1 | 2003 | 3 | 0.210 |
Why?
| Peptides | 2 | 2000 | 848 | 0.210 |
Why?
| Recombinant Fusion Proteins | 4 | 2010 | 616 | 0.210 |
Why?
| Surface Properties | 5 | 2004 | 387 | 0.210 |
Why?
| Plasmids | 5 | 2007 | 343 | 0.210 |
Why?
| Molecular Dynamics Simulation | 4 | 2014 | 201 | 0.210 |
Why?
| Electrophoresis, Polyacrylamide Gel | 4 | 2009 | 318 | 0.200 |
Why?
| Phosphatidylcholines | 5 | 2007 | 133 | 0.200 |
Why?
| Cyclophilin A | 1 | 2002 | 24 | 0.200 |
Why?
| Receptors, G-Protein-Coupled | 1 | 2004 | 194 | 0.200 |
Why?
| Phosphotransferases | 1 | 2001 | 25 | 0.200 |
Why?
| Reproducibility of Results | 3 | 2021 | 2765 | 0.190 |
Why?
| Chemotactic Factors | 2 | 2007 | 50 | 0.190 |
Why?
| Hydrolysis | 1 | 2021 | 173 | 0.190 |
Why?
| Metals | 3 | 1997 | 106 | 0.180 |
Why?
| Spectrophotometry, Ultraviolet | 1 | 2021 | 73 | 0.180 |
Why?
| Aspartate Kinase | 1 | 2000 | 1 | 0.180 |
Why?
| Glutamic Acid | 3 | 2011 | 211 | 0.180 |
Why?
| Intracellular Membranes | 1 | 2020 | 73 | 0.180 |
Why?
| Molecular Sequence Data | 6 | 2005 | 2785 | 0.180 |
Why?
| Diclofenac | 1 | 2020 | 14 | 0.180 |
Why?
| Time-Lapse Imaging | 1 | 2020 | 19 | 0.170 |
Why?
| Chelating Agents | 2 | 1997 | 65 | 0.170 |
Why?
| Endocytosis | 1 | 2020 | 148 | 0.170 |
Why?
| Lymphocyte Antigen 96 | 2 | 2010 | 24 | 0.170 |
Why?
| Ibuprofen | 1 | 2020 | 75 | 0.170 |
Why?
| Alanine | 2 | 2013 | 104 | 0.170 |
Why?
| Oxidation-Reduction | 3 | 2010 | 923 | 0.160 |
Why?
| Troponin C | 1 | 1998 | 5 | 0.160 |
Why?
| Ultraviolet Rays | 1 | 2021 | 363 | 0.160 |
Why?
| Membranes, Artificial | 1 | 1998 | 65 | 0.150 |
Why?
| Thermodynamics | 6 | 2002 | 382 | 0.150 |
Why?
| Crystallography, X-Ray | 3 | 2013 | 402 | 0.150 |
Why?
| Phospholipases A2 | 5 | 2006 | 76 | 0.150 |
Why?
| Phosphopeptides | 1 | 2017 | 15 | 0.150 |
Why?
| Synaptotagmins | 2 | 2012 | 20 | 0.150 |
Why?
| Aspirin | 1 | 2020 | 324 | 0.140 |
Why?
| Solvents | 4 | 1999 | 104 | 0.140 |
Why?
| Terbium | 2 | 1996 | 4 | 0.140 |
Why?
| Acetaminophen | 1 | 2020 | 241 | 0.140 |
Why?
| Fluorescent Dyes | 3 | 2007 | 301 | 0.140 |
Why?
| Biophysical Phenomena | 3 | 2010 | 63 | 0.140 |
Why?
| Sf9 Cells | 1 | 2016 | 9 | 0.140 |
Why?
| Spodoptera | 1 | 2016 | 36 | 0.140 |
Why?
| Magnesium | 3 | 1998 | 145 | 0.140 |
Why?
| Leukocytes | 1 | 2018 | 276 | 0.140 |
Why?
| Ligands | 5 | 2010 | 562 | 0.130 |
Why?
| Structure-Activity Relationship | 6 | 2013 | 502 | 0.130 |
Why?
| Fluorine Radioisotopes | 1 | 1996 | 10 | 0.130 |
Why?
| Cloning, Molecular | 5 | 1997 | 522 | 0.130 |
Why?
| Cattle | 2 | 2008 | 920 | 0.130 |
Why?
| Erythrocyte Membrane | 8 | 1986 | 50 | 0.130 |
Why?
| Group IV Phospholipases A2 | 3 | 2006 | 45 | 0.130 |
Why?
| Fluorine | 5 | 1993 | 15 | 0.130 |
Why?
| Macromolecular Substances | 3 | 2010 | 200 | 0.120 |
Why?
| Osmolar Concentration | 3 | 2009 | 173 | 0.120 |
Why?
| Neoplasms | 1 | 2008 | 2097 | 0.120 |
Why?
| Protein Isoforms | 2 | 2013 | 338 | 0.120 |
Why?
| Glutathione Transferase | 2 | 2007 | 93 | 0.120 |
Why?
| Protein Transport | 2 | 2007 | 395 | 0.120 |
Why?
| Substrate Specificity | 3 | 2008 | 352 | 0.120 |
Why?
| Hydrophobic and Hydrophilic Interactions | 2 | 2012 | 176 | 0.120 |
Why?
| Immunity, Innate | 1 | 2020 | 720 | 0.120 |
Why?
| Microarray Analysis | 1 | 2014 | 118 | 0.120 |
Why?
| Bacteriorhodopsins | 2 | 2005 | 10 | 0.120 |
Why?
| Phospholipids | 2 | 2013 | 197 | 0.120 |
Why?
| Hydrogen-Ion Concentration | 4 | 2009 | 511 | 0.120 |
Why?
| Models, Biological | 6 | 2007 | 1621 | 0.120 |
Why?
| Protein Folding | 3 | 2002 | 239 | 0.110 |
Why?
| Biological Transport, Active | 7 | 1986 | 71 | 0.110 |
Why?
| Proteolysis | 1 | 2014 | 142 | 0.110 |
Why?
| Histidine | 2 | 2007 | 57 | 0.110 |
Why?
| Protein Denaturation | 3 | 2002 | 68 | 0.110 |
Why?
| Myocardium | 1 | 1998 | 913 | 0.110 |
Why?
| Fibroblasts | 1 | 2018 | 838 | 0.110 |
Why?
| Nuclear Magnetic Resonance, Biomolecular | 2 | 2007 | 238 | 0.110 |
Why?
| Phospholipases A2, Cytosolic | 1 | 2013 | 6 | 0.110 |
Why?
| Protein Multimerization | 1 | 2014 | 157 | 0.110 |
Why?
| Mutagenesis | 1 | 2013 | 168 | 0.110 |
Why?
| Molecular Docking Simulation | 1 | 2013 | 101 | 0.100 |
Why?
| Trypsin | 1 | 2012 | 66 | 0.100 |
Why?
| Synaptotagmin I | 1 | 2012 | 13 | 0.100 |
Why?
| Multienzyme Complexes | 1 | 2012 | 64 | 0.100 |
Why?
| Computer Simulation | 5 | 2013 | 873 | 0.100 |
Why?
| Molecular Structure | 4 | 1996 | 434 | 0.100 |
Why?
| Bacterial Outer Membrane Proteins | 1 | 2012 | 58 | 0.100 |
Why?
| Transfection | 2 | 2011 | 866 | 0.100 |
Why?
| Myosin-Light-Chain Kinase | 1 | 2012 | 19 | 0.100 |
Why?
| Time Factors | 2 | 2016 | 6116 | 0.100 |
Why?
| NIH 3T3 Cells | 1 | 2011 | 137 | 0.090 |
Why?
| Fluoresceins | 2 | 2003 | 46 | 0.090 |
Why?
| Carbohydrate Metabolism | 1 | 1991 | 48 | 0.090 |
Why?
| Facilitated Diffusion | 1 | 2010 | 3 | 0.090 |
Why?
| Hydrodynamics | 1 | 2010 | 37 | 0.090 |
Why?
| Niflumic Acid | 2 | 1986 | 3 | 0.090 |
Why?
| Toll-Like Receptor 4 | 2 | 2010 | 287 | 0.090 |
Why?
| Sequence Homology, Amino Acid | 2 | 2004 | 353 | 0.090 |
Why?
| Heterocyclic Compounds, 3-Ring | 1 | 2010 | 28 | 0.090 |
Why?
| Single-Cell Analysis | 1 | 2011 | 188 | 0.080 |
Why?
| Toll-Like Receptors | 1 | 2010 | 167 | 0.080 |
Why?
| Methyltransferases | 1 | 2009 | 61 | 0.080 |
Why?
| Crystallization | 2 | 2013 | 136 | 0.080 |
Why?
| Photobleaching | 1 | 2009 | 20 | 0.080 |
Why?
| Least-Squares Analysis | 1 | 2009 | 70 | 0.080 |
Why?
| 3T3 Cells | 1 | 2008 | 140 | 0.080 |
Why?
| Cations | 2 | 2002 | 78 | 0.080 |
Why?
| Hydrogen Bonding | 2 | 2014 | 143 | 0.080 |
Why?
| Blood Proteins | 2 | 2013 | 231 | 0.080 |
Why?
| Phosphoproteins | 2 | 2013 | 298 | 0.070 |
Why?
| Sensory Receptor Cells | 1 | 1988 | 77 | 0.070 |
Why?
| Ethylmaleimide | 2 | 2003 | 18 | 0.070 |
Why?
| Receptors, Neurotransmitter | 1 | 1987 | 15 | 0.070 |
Why?
| Archaeal Proteins | 1 | 2007 | 45 | 0.070 |
Why?
| Cell Survival | 2 | 2008 | 1021 | 0.070 |
Why?
| Nicotinic Acids | 1 | 1986 | 6 | 0.070 |
Why?
| Oligonucleotide Probes | 1 | 2007 | 54 | 0.070 |
Why?
| Feedback | 1 | 2007 | 144 | 0.070 |
Why?
| Benzenesulfonates | 1 | 1986 | 20 | 0.070 |
Why?
| Oxadiazoles | 1 | 1986 | 32 | 0.070 |
Why?
| Lysine | 1 | 2008 | 242 | 0.070 |
Why?
| Taurine | 1 | 1986 | 41 | 0.070 |
Why?
| Calcium Channel Blockers | 1 | 1986 | 114 | 0.070 |
Why?
| Methylation | 2 | 1997 | 208 | 0.070 |
Why?
| 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid | 1 | 1985 | 12 | 0.060 |
Why?
| Swine | 1 | 2008 | 700 | 0.060 |
Why?
| Structural Homology, Protein | 1 | 2005 | 23 | 0.060 |
Why?
| Analgesics, Opioid | 2 | 2010 | 771 | 0.060 |
Why?
| Drug Delivery Systems | 1 | 2008 | 296 | 0.060 |
Why?
| Actins | 1 | 2007 | 381 | 0.060 |
Why?
| Organometallic Compounds | 2 | 2000 | 98 | 0.060 |
Why?
| Motion | 2 | 1996 | 91 | 0.060 |
Why?
| Sequence Homology | 1 | 2004 | 39 | 0.060 |
Why?
| Dogs | 1 | 2005 | 334 | 0.060 |
Why?
| Mathematics | 4 | 1985 | 101 | 0.060 |
Why?
| Membrane Potentials | 1 | 2005 | 248 | 0.060 |
Why?
| Halobacterium | 1 | 1984 | 3 | 0.060 |
Why?
| Periplasm | 1 | 2004 | 10 | 0.060 |
Why?
| Lipopolysaccharides | 1 | 2007 | 823 | 0.060 |
Why?
| Liposomes | 2 | 2012 | 146 | 0.060 |
Why?
| Rhodopsin | 1 | 2004 | 9 | 0.060 |
Why?
| Carotenoids | 1 | 1984 | 35 | 0.060 |
Why?
| Computer Graphics | 2 | 1996 | 41 | 0.060 |
Why?
| Rhodamines | 1 | 2003 | 17 | 0.050 |
Why?
| Cyclic N-Oxides | 1 | 2003 | 30 | 0.050 |
Why?
| Data Interpretation, Statistical | 1 | 2004 | 321 | 0.050 |
Why?
| Fluorescein | 1 | 2003 | 25 | 0.050 |
Why?
| Peptide Library | 1 | 2003 | 81 | 0.050 |
Why?
| Glucose | 3 | 1992 | 897 | 0.050 |
Why?
| Urea | 1 | 2002 | 67 | 0.050 |
Why?
| Sulfhydryl Compounds | 2 | 1998 | 177 | 0.050 |
Why?
| Peptide Hydrolases | 1 | 2003 | 104 | 0.050 |
Why?
| In Vitro Techniques | 2 | 2003 | 1016 | 0.050 |
Why?
| Lipids | 1 | 2005 | 580 | 0.050 |
Why?
| Catalysis | 1 | 2002 | 289 | 0.050 |
Why?
| Nitrogen | 1 | 2002 | 143 | 0.050 |
Why?
| Proteins | 1 | 2007 | 908 | 0.050 |
Why?
| Energy Transfer | 1 | 2001 | 47 | 0.050 |
Why?
| Arginine | 1 | 2002 | 238 | 0.040 |
Why?
| Stilbenes | 3 | 1985 | 36 | 0.040 |
Why?
| Chlorine | 3 | 1985 | 62 | 0.040 |
Why?
| Nitrilotriacetic Acid | 1 | 2000 | 1 | 0.040 |
Why?
| Benzoxazoles | 1 | 1980 | 16 | 0.040 |
Why?
| Chromatography, Affinity | 1 | 2000 | 80 | 0.040 |
Why?
| Indicators and Reagents | 1 | 2000 | 99 | 0.040 |
Why?
| Nickel | 1 | 2000 | 50 | 0.040 |
Why?
| Sequence Alignment | 2 | 1998 | 323 | 0.040 |
Why?
| Staining and Labeling | 1 | 1980 | 134 | 0.040 |
Why?
| Pyrimidinones | 1 | 1980 | 88 | 0.040 |
Why?
| Iodides | 1 | 1998 | 6 | 0.040 |
Why?
| Fluorescence Polarization | 1 | 1998 | 35 | 0.040 |
Why?
| Naphthalenesulfonates | 1 | 1998 | 7 | 0.040 |
Why?
| Isotopes | 2 | 1991 | 27 | 0.040 |
Why?
| Membrane Glycoproteins | 1 | 2001 | 430 | 0.040 |
Why?
| Muscles | 1 | 1980 | 320 | 0.040 |
Why?
| Chickens | 1 | 1998 | 177 | 0.040 |
Why?
| Pain Measurement | 2 | 2010 | 444 | 0.040 |
Why?
| Nerve Tissue Proteins | 1 | 2001 | 529 | 0.040 |
Why?
| Sequence Analysis | 1 | 1996 | 35 | 0.030 |
Why?
| Solubility | 1 | 1997 | 223 | 0.030 |
Why?
| Strontium | 2 | 1998 | 14 | 0.030 |
Why?
| Tetrahydrofolate Dehydrogenase | 1 | 1996 | 14 | 0.030 |
Why?
| Chemistry, Physical | 1 | 1996 | 37 | 0.030 |
Why?
| Chemical Phenomena | 1 | 1996 | 80 | 0.030 |
Why?
| Models, Structural | 1 | 1995 | 37 | 0.030 |
Why?
| L-Lactate Dehydrogenase | 1 | 1996 | 107 | 0.030 |
Why?
| Genetic Engineering | 1 | 1996 | 80 | 0.030 |
Why?
| Flagella | 1 | 1995 | 18 | 0.030 |
Why?
| Anions | 2 | 1985 | 30 | 0.030 |
Why?
| Genes, Bacterial | 1 | 1995 | 157 | 0.030 |
Why?
| p-Fluorophenylalanine | 1 | 1994 | 2 | 0.030 |
Why?
| Glutamates | 1 | 1994 | 57 | 0.030 |
Why?
| Electrons | 1 | 2014 | 71 | 0.030 |
Why?
| Cations, Monovalent | 1 | 1993 | 5 | 0.030 |
Why?
| Cryoelectron Microscopy | 1 | 2014 | 143 | 0.030 |
Why?
| Carboxylic Acids | 1 | 1993 | 26 | 0.030 |
Why?
| Movement | 1 | 1995 | 244 | 0.030 |
Why?
| Iodoacetamide | 1 | 1992 | 5 | 0.030 |
Why?
| Organophosphates | 1 | 1993 | 90 | 0.030 |
Why?
| Trehalose | 1 | 2012 | 30 | 0.030 |
Why?
| Rats | 2 | 2010 | 4958 | 0.020 |
Why?
| Gadolinium | 1 | 1991 | 73 | 0.020 |
Why?
| Molecular Conformation | 1 | 1991 | 135 | 0.020 |
Why?
| Lac Operon | 1 | 1990 | 44 | 0.020 |
Why?
| Infusion Pumps | 1 | 2009 | 31 | 0.020 |
Why?
| Myeloid Differentiation Factor 88 | 1 | 2010 | 90 | 0.020 |
Why?
| Toll-Like Receptor 2 | 1 | 2010 | 110 | 0.020 |
Why?
| Injections, Spinal | 1 | 2009 | 101 | 0.020 |
Why?
| Receptors, Opioid, mu | 1 | 2009 | 52 | 0.020 |
Why?
| Morphine | 1 | 2010 | 121 | 0.020 |
Why?
| Gene Expression Regulation, Bacterial | 1 | 1991 | 285 | 0.020 |
Why?
| Naloxone | 1 | 2009 | 97 | 0.020 |
Why?
| Hyperalgesia | 1 | 2009 | 107 | 0.020 |
Why?
| Analgesia | 1 | 2009 | 82 | 0.020 |
Why?
| Microglia | 1 | 2010 | 202 | 0.020 |
Why?
| Narcotic Antagonists | 1 | 2009 | 136 | 0.020 |
Why?
| Reaction Time | 1 | 2009 | 376 | 0.020 |
Why?
| Allosteric Regulation | 1 | 1987 | 81 | 0.020 |
Why?
| Mice, Inbred BALB C | 1 | 2010 | 1144 | 0.020 |
Why?
| Species Specificity | 1 | 1988 | 542 | 0.020 |
Why?
| Substance Withdrawal Syndrome | 1 | 2009 | 159 | 0.020 |
Why?
| Dinitrofluorobenzene | 1 | 1986 | 7 | 0.020 |
Why?
| Cyclohexanones | 1 | 1986 | 8 | 0.020 |
Why?
| Dipyridamole | 1 | 1986 | 25 | 0.020 |
Why?
| Cell Fractionation | 1 | 1986 | 51 | 0.020 |
Why?
| Phenylglyoxal | 1 | 1985 | 1 | 0.020 |
Why?
| Papain | 1 | 1985 | 3 | 0.020 |
Why?
| 4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic Acid | 1 | 1985 | 8 | 0.020 |
Why?
| Chymotrypsin | 1 | 1985 | 16 | 0.020 |
Why?
| Bromine | 1 | 1985 | 5 | 0.020 |
Why?
| Sonication | 1 | 1985 | 10 | 0.020 |
Why?
| Promoter Regions, Genetic | 1 | 1990 | 1131 | 0.020 |
Why?
| Interleukin-1 | 1 | 2010 | 966 | 0.020 |
Why?
| Bicarbonates | 1 | 1985 | 41 | 0.020 |
Why?
| Muscle, Skeletal | 1 | 1994 | 1473 | 0.020 |
Why?
| Tumor Necrosis Factor-alpha | 1 | 2010 | 1140 | 0.020 |
Why?
| Cold Temperature | 1 | 1985 | 126 | 0.010 |
Why?
| Biological Transport | 1 | 1985 | 373 | 0.010 |
Why?
| Cytoskeleton | 1 | 1985 | 176 | 0.010 |
Why?
| Rats, Sprague-Dawley | 1 | 2009 | 2218 | 0.010 |
Why?
| Halorhodopsins | 1 | 1984 | 1 | 0.010 |
Why?
| Bromides | 1 | 1984 | 5 | 0.010 |
Why?
| Radioisotopes | 1 | 1984 | 28 | 0.010 |
Why?
| Binding, Competitive | 1 | 1984 | 193 | 0.010 |
Why?
| Mice, Knockout | 1 | 2010 | 2570 | 0.010 |
Why?
| Cells, Cultured | 1 | 2010 | 3886 | 0.010 |
Why?
| Phosphatidylethanolamines | 1 | 2002 | 66 | 0.010 |
Why?
| Chick Embryo | 1 | 1980 | 122 | 0.010 |
Why?
| Cell Membrane Permeability | 1 | 1980 | 83 | 0.010 |
Why?
| Barium | 1 | 1998 | 25 | 0.010 |
Why?
| CHO Cells | 1 | 1998 | 138 | 0.010 |
Why?
| Cricetinae | 1 | 1998 | 253 | 0.010 |
Why?
| COS Cells | 1 | 1998 | 175 | 0.010 |
Why?
| Blood Glucose | 1 | 1986 | 1828 | 0.010 |
Why?
| Male | 2 | 2010 | 55599 | 0.010 |
Why?
| Cytochalasin B | 1 | 1986 | 17 | 0.000 |
Why?
|
|
Falke's Networks
Click the "See All" links for more information and interactive visualizations!
Concepts  Derived automatically from this person's publications. _
Co-Authors  People in Profiles who have published with this person. _
Similar People  People who share similar concepts with this person. _
Same Department
People who are also in this person's primary department.
Physical Neighbors  People whose addresses are nearby this person. _
|