Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
---|
Ion Channels | 23 | 2019 | 246 | 3.540 |
Why?
|
Gramicidin | 23 | 2019 | 24 | 3.360 |
Why?
|
Models, Molecular | 41 | 2017 | 1286 | 2.250 |
Why?
|
Molecular Dynamics Simulation | 8 | 2020 | 245 | 2.190 |
Why?
|
Lipid Bilayers | 18 | 2019 | 134 | 2.120 |
Why?
|
RNA, Long Noncoding | 8 | 2019 | 102 | 1.820 |
Why?
|
Potassium Channels | 11 | 2014 | 340 | 1.540 |
Why?
|
Models, Chemical | 14 | 2014 | 178 | 1.490 |
Why?
|
Water | 16 | 2014 | 277 | 1.240 |
Why?
|
Computer Simulation | 27 | 2014 | 1078 | 1.190 |
Why?
|
Protein Conformation | 46 | 2015 | 881 | 1.080 |
Why?
|
Bacterial Proteins | 9 | 2014 | 864 | 1.010 |
Why?
|
Thermodynamics | 26 | 2012 | 309 | 0.960 |
Why?
|
Ion Channel Gating | 6 | 2014 | 324 | 0.900 |
Why?
|
Membrane Potentials | 9 | 2008 | 435 | 0.790 |
Why?
|
Potassium | 8 | 2012 | 281 | 0.720 |
Why?
|
Cell Membrane | 5 | 2007 | 666 | 0.680 |
Why?
|
Biophysics | 16 | 2021 | 152 | 0.680 |
Why?
|
Porins | 4 | 2011 | 21 | 0.670 |
Why?
|
Potassium Channel Blockers | 3 | 2012 | 64 | 0.600 |
Why?
|
Protein Structure, Secondary | 15 | 2020 | 330 | 0.570 |
Why?
|
Oligonucleotides | 1 | 2017 | 92 | 0.570 |
Why?
|
Models, Biological | 13 | 2008 | 1749 | 0.560 |
Why?
|
Gene Knockdown Techniques | 1 | 2017 | 236 | 0.550 |
Why?
|
Lanolin | 1 | 2015 | 1 | 0.550 |
Why?
|
Ointments | 1 | 2015 | 12 | 0.550 |
Why?
|
Chromatography, Gas | 1 | 2015 | 28 | 0.550 |
Why?
|
Cosmetics | 1 | 2015 | 7 | 0.540 |
Why?
|
Ions | 6 | 2013 | 74 | 0.540 |
Why?
|
Maf Transcription Factors | 1 | 2015 | 2 | 0.530 |
Why?
|
Computational Biology | 5 | 2021 | 528 | 0.530 |
Why?
|
Entropy | 2 | 2013 | 38 | 0.520 |
Why?
|
Cholesterol | 2 | 2015 | 356 | 0.510 |
Why?
|
Potassium Channels, Voltage-Gated | 3 | 2017 | 122 | 0.500 |
Why?
|
Tetraethylammonium | 2 | 2006 | 24 | 0.500 |
Why?
|
Proteins | 4 | 2020 | 777 | 0.470 |
Why?
|
Macromolecular Substances | 6 | 2012 | 177 | 0.470 |
Why?
|
Software | 7 | 2020 | 654 | 0.460 |
Why?
|
Muramidase | 1 | 2013 | 34 | 0.460 |
Why?
|
Salts | 1 | 2013 | 16 | 0.450 |
Why?
|
Binding Sites | 16 | 2015 | 1098 | 0.440 |
Why?
|
Membrane Proteins | 12 | 2011 | 1196 | 0.430 |
Why?
|
Protons | 7 | 2001 | 98 | 0.430 |
Why?
|
Statistics as Topic | 1 | 2013 | 238 | 0.420 |
Why?
|
Ion Transport | 5 | 2006 | 81 | 0.410 |
Why?
|
Neisseria meningitidis | 1 | 2011 | 8 | 0.410 |
Why?
|
Metals | 1 | 2012 | 90 | 0.410 |
Why?
|
Potassium Channels, Inwardly Rectifying | 1 | 2012 | 119 | 0.410 |
Why?
|
Cytoplasm | 1 | 2012 | 281 | 0.410 |
Why?
|
Solvents | 5 | 2014 | 96 | 0.400 |
Why?
|
Electrophysiological Phenomena | 1 | 2011 | 49 | 0.400 |
Why?
|
Metals, Alkali | 1 | 2010 | 1 | 0.380 |
Why?
|
Streptomyces | 2 | 2000 | 20 | 0.370 |
Why?
|
Protein Folding | 3 | 2017 | 282 | 0.340 |
Why?
|
Cell Membrane Permeability | 2 | 2006 | 119 | 0.340 |
Why?
|
Enhancer Elements, Genetic | 3 | 2017 | 266 | 0.340 |
Why?
|
Membrane Transport Proteins | 1 | 2010 | 166 | 0.340 |
Why?
|
Amino Acid Sequence | 17 | 2020 | 2062 | 0.330 |
Why?
|
Electric Conductivity | 5 | 2015 | 144 | 0.330 |
Why?
|
T-Lymphocytes | 1 | 2015 | 1195 | 0.330 |
Why?
|
Bacteriorhodopsins | 4 | 1999 | 10 | 0.330 |
Why?
|
Markov Chains | 1 | 2008 | 125 | 0.320 |
Why?
|
Sodium | 3 | 1999 | 341 | 0.320 |
Why?
|
Biophysical Phenomena | 12 | 2002 | 120 | 0.320 |
Why?
|
Static Electricity | 8 | 2010 | 89 | 0.300 |
Why?
|
Dimyristoylphosphatidylcholine | 5 | 2003 | 11 | 0.300 |
Why?
|
Arginine | 1 | 2007 | 136 | 0.300 |
Why?
|
Crystallography, X-Ray | 8 | 2014 | 485 | 0.290 |
Why?
|
Idiopathic Pulmonary Fibrosis | 2 | 2019 | 165 | 0.290 |
Why?
|
Mathematical Computing | 1 | 2006 | 21 | 0.280 |
Why?
|
Quantum Theory | 4 | 2020 | 28 | 0.280 |
Why?
|
Peptides | 6 | 2009 | 639 | 0.270 |
Why?
|
Anti-Bacterial Agents | 2 | 2003 | 746 | 0.270 |
Why?
|
Fibroblasts | 2 | 2019 | 729 | 0.270 |
Why?
|
Monocytes | 3 | 2017 | 214 | 0.270 |
Why?
|
Hydrogen Bonding | 10 | 2000 | 144 | 0.270 |
Why?
|
Ligands | 6 | 2014 | 433 | 0.270 |
Why?
|
Models, Theoretical | 7 | 2013 | 482 | 0.250 |
Why?
|
Systems Theory | 1 | 2004 | 2 | 0.250 |
Why?
|
Aquaporins | 1 | 2004 | 14 | 0.250 |
Why?
|
Magnesium | 3 | 2012 | 177 | 0.240 |
Why?
|
Kinetics | 14 | 2004 | 1513 | 0.230 |
Why?
|
Escherichia coli | 5 | 2002 | 597 | 0.230 |
Why?
|
Carbon-Carbon Lyases | 2 | 1993 | 2 | 0.230 |
Why?
|
4-Aminobenzoic Acid | 2 | 1993 | 6 | 0.230 |
Why?
|
Immunoglobulin Fab Fragments | 1 | 2023 | 81 | 0.220 |
Why?
|
Inflammation | 3 | 2018 | 920 | 0.220 |
Why?
|
Structure-Activity Relationship | 4 | 2010 | 408 | 0.220 |
Why?
|
Dimerization | 4 | 2019 | 143 | 0.210 |
Why?
|
Protein Structure, Tertiary | 4 | 2012 | 736 | 0.210 |
Why?
|
Electrons | 2 | 2013 | 49 | 0.210 |
Why?
|
Molecular Conformation | 6 | 2010 | 96 | 0.200 |
Why?
|
Escherichia coli Proteins | 2 | 1993 | 179 | 0.200 |
Why?
|
Extracellular Space | 1 | 2001 | 90 | 0.200 |
Why?
|
Complementarity Determining Regions | 1 | 2020 | 24 | 0.190 |
Why?
|
Antibody Affinity | 1 | 2020 | 38 | 0.190 |
Why?
|
Alkaline Phosphatase | 4 | 2004 | 132 | 0.190 |
Why?
|
Antibody Specificity | 1 | 2020 | 129 | 0.190 |
Why?
|
Animals | 37 | 2020 | 26582 | 0.190 |
Why?
|
Electron Spin Resonance Spectroscopy | 3 | 2013 | 306 | 0.190 |
Why?
|
Chlorides | 3 | 2012 | 103 | 0.190 |
Why?
|
Cations, Monovalent | 1 | 1999 | 6 | 0.180 |
Why?
|
Cells, Cultured | 4 | 2019 | 2818 | 0.180 |
Why?
|
Membrane Lipids | 2 | 2000 | 40 | 0.170 |
Why?
|
Shaker Superfamily of Potassium Channels | 3 | 2012 | 49 | 0.170 |
Why?
|
Porosity | 2 | 2012 | 60 | 0.170 |
Why?
|
Magnetic Resonance Spectroscopy | 6 | 1999 | 318 | 0.170 |
Why?
|
Antibodies, Monoclonal | 3 | 2023 | 1376 | 0.170 |
Why?
|
S100 Calcium Binding Protein G | 1 | 1998 | 22 | 0.170 |
Why?
|
Oligopeptides | 3 | 2008 | 179 | 0.170 |
Why?
|
Calcium | 2 | 2006 | 1156 | 0.170 |
Why?
|
Interleukin-1beta | 1 | 2018 | 78 | 0.170 |
Why?
|
Phosphatidylethanolamines | 1 | 1998 | 15 | 0.170 |
Why?
|
Gene Expression Regulation | 2 | 2018 | 1920 | 0.160 |
Why?
|
Cell Line | 4 | 2017 | 2468 | 0.160 |
Why?
|
Electricity | 2 | 2008 | 23 | 0.160 |
Why?
|
Myositis, Inclusion Body | 1 | 2017 | 2 | 0.160 |
Why?
|
Phosphoglycerate Kinase | 2 | 1997 | 17 | 0.150 |
Why?
|
Molecular Sequence Data | 12 | 2002 | 3030 | 0.150 |
Why?
|
Chromatin | 8 | 1986 | 380 | 0.150 |
Why?
|
Isoleucine | 1 | 2017 | 17 | 0.150 |
Why?
|
Threonine | 1 | 2017 | 33 | 0.150 |
Why?
|
Cnidarian Venoms | 1 | 2017 | 19 | 0.150 |
Why?
|
Cartilage, Articular | 2 | 2016 | 67 | 0.140 |
Why?
|
Histones | 9 | 1992 | 311 | 0.140 |
Why?
|
Biomedical Research | 1 | 2021 | 376 | 0.140 |
Why?
|
Humans | 23 | 2021 | 86643 | 0.140 |
Why?
|
Transcriptome | 2 | 2019 | 580 | 0.140 |
Why?
|
src-Family Kinases | 2 | 2015 | 74 | 0.140 |
Why?
|
Sodium Channels | 1 | 2017 | 129 | 0.140 |
Why?
|
Osteoarthritis, Hip | 1 | 2016 | 23 | 0.140 |
Why?
|
Lipopolysaccharides | 2 | 2014 | 286 | 0.140 |
Why?
|
Chondrocytes | 1 | 2016 | 60 | 0.140 |
Why?
|
Transaminases | 2 | 1993 | 34 | 0.140 |
Why?
|
Nucleosomes | 7 | 1989 | 54 | 0.140 |
Why?
|
Protein Kinases | 2 | 2015 | 209 | 0.140 |
Why?
|
Spin Labels | 2 | 2013 | 102 | 0.130 |
Why?
|
Osteoarthritis, Knee | 1 | 2016 | 63 | 0.130 |
Why?
|
Permeability | 2 | 2006 | 137 | 0.130 |
Why?
|
Proto-Oncogene Proteins c-abl | 1 | 2015 | 30 | 0.130 |
Why?
|
Fluorescence Resonance Energy Transfer | 2 | 2012 | 94 | 0.130 |
Why?
|
Mesylates | 2 | 2013 | 15 | 0.130 |
Why?
|
Dioxolanes | 1 | 1994 | 8 | 0.130 |
Why?
|
Reference Standards | 1 | 2015 | 159 | 0.130 |
Why?
|
Liposomes | 3 | 2004 | 91 | 0.130 |
Why?
|
Cell Nucleus | 1 | 2017 | 579 | 0.120 |
Why?
|
Numerical Analysis, Computer-Assisted | 1 | 2014 | 33 | 0.120 |
Why?
|
Algorithms | 6 | 2014 | 1830 | 0.120 |
Why?
|
Mutagenesis, Site-Directed | 2 | 2001 | 279 | 0.120 |
Why?
|
In Vitro Techniques | 6 | 2016 | 989 | 0.120 |
Why?
|
Diffusion | 4 | 2001 | 93 | 0.120 |
Why?
|
Bacteriophage T4 | 1 | 2013 | 8 | 0.120 |
Why?
|
Peptides, Cyclic | 1 | 1993 | 43 | 0.120 |
Why?
|
High-Throughput Screening Assays | 1 | 2014 | 55 | 0.120 |
Why?
|
Glycosylphosphatidylinositols | 3 | 2004 | 8 | 0.110 |
Why?
|
Molecular Biology | 1 | 2014 | 89 | 0.110 |
Why?
|
Cyclic N-Oxides | 1 | 2013 | 33 | 0.110 |
Why?
|
Probability | 2 | 2013 | 355 | 0.110 |
Why?
|
Communicable Diseases | 1 | 2014 | 63 | 0.110 |
Why?
|
Solutions | 1 | 2013 | 85 | 0.110 |
Why?
|
Lung | 1 | 2019 | 1170 | 0.110 |
Why?
|
Spermine | 1 | 2012 | 18 | 0.110 |
Why?
|
Stress, Mechanical | 2 | 2006 | 248 | 0.110 |
Why?
|
Molecular Structure | 4 | 2017 | 287 | 0.110 |
Why?
|
Lipids | 4 | 2009 | 269 | 0.100 |
Why?
|
Ouabain | 1 | 2011 | 24 | 0.100 |
Why?
|
Sodium-Potassium-Exchanging ATPase | 1 | 2011 | 78 | 0.100 |
Why?
|
1,2-Dipalmitoylphosphatidylcholine | 2 | 2000 | 9 | 0.100 |
Why?
|
DNA | 8 | 1994 | 1294 | 0.100 |
Why?
|
Glycylglycine | 1 | 2010 | 1 | 0.100 |
Why?
|
Biological Transport | 3 | 2000 | 396 | 0.090 |
Why?
|
Thermotoga maritima | 1 | 2010 | 15 | 0.090 |
Why?
|
Membrane Microdomains | 2 | 2008 | 54 | 0.090 |
Why?
|
RNA | 1 | 2014 | 560 | 0.090 |
Why?
|
Protein Binding | 9 | 2015 | 1456 | 0.090 |
Why?
|
Cation Transport Proteins | 1 | 2010 | 64 | 0.090 |
Why?
|
Protein Multimerization | 1 | 2011 | 173 | 0.090 |
Why?
|
Substrate Specificity | 1 | 2010 | 347 | 0.090 |
Why?
|
Receptors, Glutamate | 1 | 2009 | 24 | 0.090 |
Why?
|
Retinaldehyde | 3 | 1999 | 4 | 0.090 |
Why?
|
Epitopes | 3 | 2023 | 255 | 0.080 |
Why?
|
Protein Transport | 1 | 2010 | 411 | 0.080 |
Why?
|
Receptors, Neuropeptide | 1 | 2008 | 7 | 0.080 |
Why?
|
Light | 2 | 2009 | 289 | 0.080 |
Why?
|
Nanotechnology | 1 | 2009 | 68 | 0.080 |
Why?
|
Oxygen | 2 | 2010 | 726 | 0.080 |
Why?
|
Receptors, Opioid, mu | 1 | 2008 | 45 | 0.080 |
Why?
|
Protein Denaturation | 4 | 1997 | 106 | 0.080 |
Why?
|
Liver | 8 | 1992 | 1230 | 0.080 |
Why?
|
Detergents | 2 | 2008 | 34 | 0.080 |
Why?
|
Babesiosis | 1 | 1987 | 4 | 0.070 |
Why?
|
Birefringence | 8 | 1985 | 9 | 0.070 |
Why?
|
Hydrophobic and Hydrophilic Interactions | 1 | 2007 | 93 | 0.070 |
Why?
|
Erythrocyte Membrane | 1 | 1987 | 60 | 0.070 |
Why?
|
Trypsin | 3 | 1983 | 95 | 0.070 |
Why?
|
Kv1.2 Potassium Channel | 1 | 2006 | 22 | 0.070 |
Why?
|
Chlorine | 1 | 2006 | 8 | 0.070 |
Why?
|
Barium | 1 | 2006 | 31 | 0.070 |
Why?
|
Protein Subunits | 1 | 2006 | 122 | 0.070 |
Why?
|
Energy Transfer | 1 | 2006 | 25 | 0.070 |
Why?
|
Stereoisomerism | 3 | 2017 | 102 | 0.070 |
Why?
|
Nuclear Magnetic Resonance, Biomolecular | 2 | 2003 | 60 | 0.070 |
Why?
|
Temperature | 4 | 2003 | 396 | 0.070 |
Why?
|
Rats | 14 | 2009 | 3990 | 0.070 |
Why?
|
Computer Graphics | 3 | 2000 | 100 | 0.070 |
Why?
|
Scattering, Radiation | 4 | 2011 | 114 | 0.070 |
Why?
|
Tubulin | 3 | 1994 | 58 | 0.070 |
Why?
|
Xenopus laevis | 3 | 2012 | 137 | 0.070 |
Why?
|
Enzyme Stability | 4 | 2004 | 39 | 0.060 |
Why?
|
Intestinal Mucosa | 3 | 2003 | 797 | 0.060 |
Why?
|
Motion | 3 | 1994 | 85 | 0.060 |
Why?
|
Schizosaccharomyces | 3 | 2001 | 54 | 0.060 |
Why?
|
Signal Transduction | 1 | 2014 | 3241 | 0.060 |
Why?
|
Carbon-Nitrogen Ligases | 2 | 1993 | 4 | 0.060 |
Why?
|
Spectrin | 1 | 1982 | 15 | 0.060 |
Why?
|
DNA Polymerase beta | 1 | 2002 | 4 | 0.060 |
Why?
|
Base Pair Mismatch | 1 | 2002 | 27 | 0.050 |
Why?
|
Mathematics | 3 | 1991 | 190 | 0.050 |
Why?
|
Potassium Channels, Calcium-Activated | 1 | 2002 | 19 | 0.050 |
Why?
|
Time Factors | 2 | 2008 | 5210 | 0.050 |
Why?
|
Mutagenesis | 1 | 2002 | 199 | 0.050 |
Why?
|
Gene Expression Profiling | 2 | 2018 | 1384 | 0.050 |
Why?
|
Cysteine | 1 | 2002 | 135 | 0.050 |
Why?
|
DNA Primers | 1 | 2002 | 543 | 0.050 |
Why?
|
Oocytes | 3 | 2011 | 221 | 0.050 |
Why?
|
src Homology Domains | 1 | 2001 | 44 | 0.050 |
Why?
|
NF-kappa B | 2 | 2014 | 444 | 0.050 |
Why?
|
Phospholipids | 1 | 2001 | 111 | 0.050 |
Why?
|
Circular Dichroism | 10 | 1995 | 117 | 0.050 |
Why?
|
Cross Reactions | 1 | 2020 | 106 | 0.050 |
Why?
|
Glutamic Acid | 2 | 2009 | 152 | 0.050 |
Why?
|
Cattle | 5 | 2003 | 376 | 0.050 |
Why?
|
Potassium Chloride | 1 | 2000 | 87 | 0.050 |
Why?
|
Electrochemistry | 3 | 1995 | 61 | 0.050 |
Why?
|
Lipid Metabolism | 1 | 2001 | 196 | 0.050 |
Why?
|
Prostaglandin-Endoperoxide Synthases | 1 | 2000 | 37 | 0.050 |
Why?
|
Wheat Germ Agglutinins | 1 | 1999 | 16 | 0.040 |
Why?
|
Molecular Weight | 3 | 2001 | 332 | 0.040 |
Why?
|
Proteolipids | 1 | 1999 | 8 | 0.040 |
Why?
|
Energy Metabolism | 1 | 2001 | 271 | 0.040 |
Why?
|
Acetylglucosamine | 1 | 1999 | 17 | 0.040 |
Why?
|
Protein-Tyrosine Kinases | 1 | 2001 | 302 | 0.040 |
Why?
|
Halobacterium salinarum | 2 | 1999 | 3 | 0.040 |
Why?
|
Zinc | 1 | 1999 | 91 | 0.040 |
Why?
|
Calbindins | 1 | 1998 | 19 | 0.040 |
Why?
|
Melitten | 1 | 1998 | 9 | 0.040 |
Why?
|
Chemokine CCL2 | 1 | 2018 | 47 | 0.040 |
Why?
|
Interleukin-8 | 1 | 2018 | 86 | 0.040 |
Why?
|
Electrophysiology | 1 | 1999 | 401 | 0.040 |
Why?
|
Membranes | 1 | 1998 | 36 | 0.040 |
Why?
|
Vacuum | 1 | 1997 | 10 | 0.040 |
Why?
|
Collagen | 2 | 1983 | 269 | 0.040 |
Why?
|
Cell Compartmentation | 1 | 1997 | 69 | 0.040 |
Why?
|
Neutrons | 2 | 1997 | 58 | 0.040 |
Why?
|
Protein Structure, Quaternary | 2 | 2012 | 99 | 0.040 |
Why?
|
Interleukin-6 | 1 | 2018 | 256 | 0.040 |
Why?
|
Proto-Oncogene Proteins | 1 | 2001 | 645 | 0.040 |
Why?
|
Antibodies, Antinuclear | 1 | 2017 | 83 | 0.040 |
Why?
|
Proton-Translocating ATPases | 3 | 1992 | 23 | 0.040 |
Why?
|
Models, Structural | 1 | 1997 | 58 | 0.040 |
Why?
|
Calorimetry | 1 | 1996 | 15 | 0.040 |
Why?
|
Surface Tension | 1 | 1996 | 8 | 0.040 |
Why?
|
Models, Genetic | 1 | 2002 | 926 | 0.040 |
Why?
|
Protein Stability | 1 | 2017 | 99 | 0.040 |
Why?
|
Enzymes, Immobilized | 4 | 2004 | 11 | 0.040 |
Why?
|
Femoral Neck Fractures | 1 | 2016 | 11 | 0.030 |
Why?
|
Interleukin-1 | 1 | 2016 | 71 | 0.030 |
Why?
|
Computers | 2 | 2002 | 112 | 0.030 |
Why?
|
Microscopy | 1 | 1996 | 87 | 0.030 |
Why?
|
Amino Acids | 3 | 2011 | 252 | 0.030 |
Why?
|
Schiff Bases | 1 | 1995 | 2 | 0.030 |
Why?
|
Middle Aged | 3 | 2019 | 25028 | 0.030 |
Why?
|
Protein Processing, Post-Translational | 1 | 1997 | 371 | 0.030 |
Why?
|
Epigenesis, Genetic | 1 | 2019 | 479 | 0.030 |
Why?
|
Phosphatidylcholines | 1 | 1994 | 48 | 0.030 |
Why?
|
High Mobility Group Proteins | 1 | 1994 | 26 | 0.030 |
Why?
|
Microscopy, Electron | 2 | 1993 | 503 | 0.030 |
Why?
|
Up-Regulation | 1 | 2017 | 712 | 0.030 |
Why?
|
p38 Mitogen-Activated Protein Kinases | 1 | 2014 | 125 | 0.030 |
Why?
|
Arthroplasty, Replacement, Hip | 1 | 2016 | 102 | 0.030 |
Why?
|
Tryptophan | 2 | 1992 | 90 | 0.030 |
Why?
|
Arthroplasty, Replacement, Knee | 1 | 2016 | 111 | 0.030 |
Why?
|
Chemistry, Physical | 1 | 1994 | 29 | 0.030 |
Why?
|
Cations | 1 | 1994 | 30 | 0.030 |
Why?
|
Chemical Phenomena | 1 | 1994 | 72 | 0.030 |
Why?
|
MAP Kinase Signaling System | 1 | 2014 | 192 | 0.030 |
Why?
|
Spectroscopy, Fourier Transform Infrared | 3 | 1999 | 30 | 0.030 |
Why?
|
Reverse Transcriptase Polymerase Chain Reaction | 1 | 2016 | 879 | 0.030 |
Why?
|
Electric Stimulation | 1 | 2015 | 347 | 0.030 |
Why?
|
Research Design | 1 | 1997 | 594 | 0.030 |
Why?
|
Female | 5 | 2019 | 44532 | 0.030 |
Why?
|
Hepatitis Virus, Duck | 1 | 1993 | 1 | 0.030 |
Why?
|
Histidine | 1 | 1993 | 55 | 0.030 |
Why?
|
Binding, Competitive | 1 | 1993 | 145 | 0.030 |
Why?
|
Glutamates | 1 | 1993 | 89 | 0.030 |
Why?
|
X-Ray Diffraction | 1 | 1993 | 124 | 0.030 |
Why?
|
Terbium | 1 | 2012 | 4 | 0.030 |
Why?
|
Electrophoresis, Polyacrylamide Gel | 3 | 1989 | 268 | 0.030 |
Why?
|
Chorismic Acid | 1 | 1992 | 1 | 0.030 |
Why?
|
Coordination Complexes | 1 | 2012 | 19 | 0.030 |
Why?
|
Solubility | 3 | 2003 | 177 | 0.030 |
Why?
|
Glutaminase | 1 | 1992 | 12 | 0.030 |
Why?
|
Antigens, Viral | 1 | 1993 | 143 | 0.030 |
Why?
|
Viral Envelope Proteins | 1 | 1993 | 94 | 0.030 |
Why?
|
Male | 5 | 2019 | 40965 | 0.030 |
Why?
|
Conserved Sequence | 1 | 1993 | 210 | 0.030 |
Why?
|
Sequence Homology, Amino Acid | 1 | 1993 | 416 | 0.030 |
Why?
|
Nucleic Acid Conformation | 3 | 1985 | 332 | 0.030 |
Why?
|
Cytokines | 1 | 2016 | 776 | 0.030 |
Why?
|
Glutamine | 1 | 1992 | 76 | 0.030 |
Why?
|
Nucleotides | 1 | 1992 | 95 | 0.030 |
Why?
|
Boron Compounds | 1 | 2011 | 20 | 0.030 |
Why?
|
X-Rays | 1 | 2011 | 130 | 0.030 |
Why?
|
Case-Control Studies | 1 | 2016 | 1805 | 0.030 |
Why?
|
Molecular Probe Techniques | 1 | 2011 | 9 | 0.020 |
Why?
|
Kv1.3 Potassium Channel | 1 | 2011 | 14 | 0.020 |
Why?
|
Acetone | 1 | 1990 | 6 | 0.020 |
Why?
|
Viral Proteins | 1 | 1993 | 300 | 0.020 |
Why?
|
Enzyme Activation | 2 | 2004 | 692 | 0.020 |
Why?
|
Dimethyl Sulfoxide | 1 | 1990 | 38 | 0.020 |
Why?
|
Promoter Regions, Genetic | 1 | 2014 | 937 | 0.020 |
Why?
|
Spectrometry, Fluorescence | 3 | 1999 | 85 | 0.020 |
Why?
|
Immunity, Innate | 1 | 2014 | 409 | 0.020 |
Why?
|
Protein Kinase Inhibitors | 1 | 2015 | 589 | 0.020 |
Why?
|
Edetic Acid | 1 | 2010 | 43 | 0.020 |
Why?
|
Nuclear Proteins | 1 | 1994 | 696 | 0.020 |
Why?
|
Protein Engineering | 1 | 2011 | 140 | 0.020 |
Why?
|
Aged | 2 | 2017 | 18415 | 0.020 |
Why?
|
Titrimetry | 1 | 2009 | 15 | 0.020 |
Why?
|
Hydrogen-Ion Concentration | 3 | 1996 | 493 | 0.020 |
Why?
|
Azo Compounds | 1 | 2009 | 13 | 0.020 |
Why?
|
Transcription, Genetic | 1 | 2014 | 1135 | 0.020 |
Why?
|
Carbohydrates | 1 | 2009 | 47 | 0.020 |
Why?
|
Maleimides | 1 | 2009 | 29 | 0.020 |
Why?
|
Mitochondria, Heart | 1 | 1989 | 50 | 0.020 |
Why?
|
Nucleic Acids | 1 | 2009 | 30 | 0.020 |
Why?
|
Base Sequence | 1 | 1993 | 2330 | 0.020 |
Why?
|
Quinoxalines | 1 | 2009 | 50 | 0.020 |
Why?
|
Fluorescence Recovery After Photobleaching | 1 | 2008 | 13 | 0.020 |
Why?
|
Microcomputers | 1 | 1988 | 26 | 0.020 |
Why?
|
Adenosine Triphosphatases | 1 | 1989 | 153 | 0.020 |
Why?
|
Cell Fractionation | 1 | 2008 | 71 | 0.020 |
Why?
|
Polyethylene Glycols | 1 | 2011 | 363 | 0.020 |
Why?
|
DNA-Binding Proteins | 1 | 1994 | 1208 | 0.020 |
Why?
|
Genomics | 1 | 2014 | 720 | 0.020 |
Why?
|
Patch-Clamp Techniques | 1 | 2009 | 396 | 0.020 |
Why?
|
Models, Statistical | 1 | 2011 | 574 | 0.020 |
Why?
|
Mitochondria | 1 | 1991 | 535 | 0.020 |
Why?
|
Blood Protein Electrophoresis | 1 | 1987 | 15 | 0.020 |
Why?
|
Fructose-Bisphosphatase | 1 | 1986 | 2 | 0.020 |
Why?
|
Peptide Fragments | 3 | 1994 | 460 | 0.020 |
Why?
|
Phosphorylation | 3 | 2001 | 1106 | 0.020 |
Why?
|
Dogs | 1 | 1987 | 685 | 0.020 |
Why?
|
Carrier Proteins | 1 | 1989 | 673 | 0.020 |
Why?
|
Chickens | 2 | 2001 | 212 | 0.020 |
Why?
|
Guanidines | 2 | 1997 | 31 | 0.020 |
Why?
|
Guanidine | 2 | 1997 | 17 | 0.020 |
Why?
|
Microtubule-Associated Proteins | 1 | 1985 | 176 | 0.020 |
Why?
|
Antibodies | 1 | 1985 | 350 | 0.010 |
Why?
|
Xenopus | 1 | 2003 | 125 | 0.010 |
Why?
|
Octoxynol | 1 | 2003 | 8 | 0.010 |
Why?
|
Membrane Fluidity | 1 | 2003 | 8 | 0.010 |
Why?
|
Swine | 3 | 1994 | 555 | 0.010 |
Why?
|
Sulfhydryl Reagents | 1 | 2002 | 8 | 0.010 |
Why?
|
Sequence Homology | 1 | 2002 | 28 | 0.010 |
Why?
|
Microscopy, Atomic Force | 1 | 2002 | 52 | 0.010 |
Why?
|
Isoenzymes | 2 | 2000 | 271 | 0.010 |
Why?
|
Proto-Oncogene Proteins c-hck | 1 | 2001 | 1 | 0.010 |
Why?
|
Biological Assay | 1 | 2001 | 78 | 0.010 |
Why?
|
HeLa Cells | 1 | 2002 | 498 | 0.010 |
Why?
|
Tyrosine | 1 | 2001 | 133 | 0.010 |
Why?
|
Serine Endopeptidases | 2 | 1992 | 145 | 0.010 |
Why?
|
Hot Temperature | 2 | 1995 | 206 | 0.010 |
Why?
|
Neurons | 1 | 2009 | 1546 | 0.010 |
Why?
|
Cyclooxygenase 1 | 1 | 2000 | 5 | 0.010 |
Why?
|
Apoenzymes | 1 | 1999 | 7 | 0.010 |
Why?
|
Chromatography, High Pressure Liquid | 2 | 1992 | 315 | 0.010 |
Why?
|
Amino Acid Substitution | 1 | 2001 | 339 | 0.010 |
Why?
|
Monte Carlo Method | 1 | 2000 | 185 | 0.010 |
Why?
|
Spectrophotometry, Infrared | 1 | 1999 | 18 | 0.010 |
Why?
|
Glycolipids | 1 | 1999 | 29 | 0.010 |
Why?
|
Darkness | 1 | 1999 | 49 | 0.010 |
Why?
|
Pepsin A | 1 | 1978 | 5 | 0.010 |
Why?
|
Pronase | 1 | 1978 | 6 | 0.010 |
Why?
|
Adult | 1 | 2017 | 25648 | 0.010 |
Why?
|
Viscosity | 1 | 1978 | 46 | 0.010 |
Why?
|
Acetates | 1 | 1978 | 66 | 0.010 |
Why?
|
Sodium Chloride | 1 | 1978 | 88 | 0.010 |
Why?
|
Malate Dehydrogenase | 1 | 1977 | 8 | 0.010 |
Why?
|
L-Lactate Dehydrogenase | 1 | 1977 | 68 | 0.010 |
Why?
|
Lipoproteins | 1 | 1997 | 135 | 0.010 |
Why?
|
Disease | 1 | 1997 | 90 | 0.010 |
Why?
|
Golgi Apparatus | 1 | 1997 | 117 | 0.010 |
Why?
|
Fourier Analysis | 1 | 1997 | 125 | 0.010 |
Why?
|
Random Allocation | 1 | 1997 | 332 | 0.010 |
Why?
|
Glycoproteins | 1 | 1997 | 234 | 0.010 |
Why?
|
Membrane Glycoproteins | 1 | 1997 | 428 | 0.010 |
Why?
|
Recombinant Proteins | 1 | 1997 | 1014 | 0.010 |
Why?
|
Skin | 1 | 1978 | 554 | 0.010 |
Why?
|
Ducks | 1 | 1993 | 8 | 0.010 |
Why?
|
Neutralization Tests | 1 | 1993 | 77 | 0.010 |
Why?
|
Inosine Triphosphate | 1 | 1992 | 2 | 0.010 |
Why?
|
Guanine Nucleotides | 1 | 1992 | 14 | 0.010 |
Why?
|
Adenine Nucleotides | 1 | 1992 | 63 | 0.010 |
Why?
|
Mutation | 1 | 2003 | 3968 | 0.010 |
Why?
|
Testis | 1 | 1992 | 152 | 0.010 |
Why?
|
Myocardium | 2 | 1989 | 529 | 0.010 |
Why?
|
Acrylamide | 1 | 1991 | 2 | 0.010 |
Why?
|
Iodides | 1 | 1991 | 18 | 0.010 |
Why?
|
Acrylamides | 1 | 1991 | 30 | 0.010 |
Why?
|
Antibodies, Viral | 1 | 1993 | 293 | 0.010 |
Why?
|
Adenosine Diphosphate | 1 | 1991 | 55 | 0.010 |
Why?
|
Adenosine Triphosphate | 1 | 1991 | 314 | 0.010 |
Why?
|
Mitochondrial Proton-Translocating ATPases | 1 | 1989 | 5 | 0.010 |
Why?
|
Oligomycins | 1 | 1989 | 5 | 0.010 |
Why?
|
Precipitin Tests | 1 | 1989 | 108 | 0.010 |
Why?
|
Centrifugation, Density Gradient | 1 | 1986 | 112 | 0.000 |
Why?
|
Spectrophotometry, Ultraviolet | 1 | 1986 | 43 | 0.000 |
Why?
|
Osmolar Concentration | 1 | 1986 | 181 | 0.000 |
Why?
|
Allosteric Regulation | 1 | 1986 | 68 | 0.000 |
Why?
|
Ultracentrifugation | 1 | 1985 | 42 | 0.000 |
Why?
|
Electrophoresis, Agar Gel | 1 | 1985 | 49 | 0.000 |
Why?
|
Filtration | 1 | 1985 | 25 | 0.000 |
Why?
|
Cyclic AMP | 1 | 1986 | 273 | 0.000 |
Why?
|
Phosphoproteins | 1 | 1986 | 254 | 0.000 |
Why?
|
Methylation | 1 | 1985 | 251 | 0.000 |
Why?
|
Erythrocytes | 1 | 1985 | 255 | 0.000 |
Why?
|
Micrococcal Nuclease | 1 | 1984 | 8 | 0.000 |
Why?
|
Rabbits | 1 | 1985 | 636 | 0.000 |
Why?
|
Membranes, Artificial | 1 | 1983 | 40 | 0.000 |
Why?
|
Electrophoresis, Disc | 1 | 1977 | 22 | 0.000 |
Why?
|
Carboxyhemoglobin | 1 | 1977 | 16 | 0.000 |
Why?
|
Chromatography, Affinity | 1 | 1977 | 81 | 0.000 |
Why?
|
Phenols | 1 | 1977 | 40 | 0.000 |
Why?
|
Brain | 1 | 1985 | 2216 | 0.000 |
Why?
|