Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
---|
HSP70 Heat-Shock Proteins | 33 | 2023 | 78 | 9.960 |
Why?
|
Protein Folding | 55 | 2025 | 260 | 9.190 |
Why?
|
Biochemistry | 18 | 2021 | 50 | 8.690 |
Why?
|
Escherichia coli Proteins | 36 | 2023 | 264 | 6.540 |
Why?
|
Escherichia coli | 56 | 2023 | 695 | 6.310 |
Why?
|
Molecular Chaperones | 19 | 2023 | 99 | 4.970 |
Why?
|
Receptors, Retinoic Acid | 25 | 2018 | 55 | 4.710 |
Why?
|
Periodicals as Topic | 13 | 2021 | 166 | 4.460 |
Why?
|
Proteins | 22 | 2021 | 730 | 4.040 |
Why?
|
Models, Molecular | 60 | 2022 | 1128 | 3.700 |
Why?
|
Protein Conformation | 81 | 2021 | 763 | 3.390 |
Why?
|
Protein Sorting Signals | 33 | 2012 | 55 | 2.960 |
Why?
|
Peptides | 27 | 2013 | 548 | 2.860 |
Why?
|
Heat-Shock Proteins | 12 | 2023 | 65 | 2.500 |
Why?
|
Protein Structure, Secondary | 37 | 2018 | 253 | 2.380 |
Why?
|
Awards and Prizes | 4 | 2019 | 32 | 2.380 |
Why?
|
Molecular Biology | 6 | 2021 | 66 | 2.170 |
Why?
|
Protein Binding | 37 | 2024 | 1552 | 2.070 |
Why?
|
Allosteric Regulation | 12 | 2023 | 68 | 1.940 |
Why?
|
Editorial Policies | 5 | 2021 | 52 | 1.920 |
Why?
|
Protein Domains | 7 | 2023 | 140 | 1.920 |
Why?
|
Societies, Scientific | 3 | 2020 | 32 | 1.890 |
Why?
|
Science | 3 | 2020 | 34 | 1.850 |
Why?
|
Bacterial Proteins | 23 | 2012 | 737 | 1.810 |
Why?
|
Publications | 5 | 2020 | 28 | 1.750 |
Why?
|
Adenosine Triphosphatases | 16 | 2014 | 253 | 1.720 |
Why?
|
Amino Acid Sequence | 69 | 2014 | 1553 | 1.710 |
Why?
|
Proteostasis | 2 | 2025 | 11 | 1.700 |
Why?
|
Adenosine Triphosphate | 16 | 2023 | 289 | 1.700 |
Why?
|
HSC70 Heat-Shock Proteins | 2 | 2024 | 7 | 1.560 |
Why?
|
Molecular Sequence Data | 59 | 2014 | 1951 | 1.520 |
Why?
|
Membrane Transport Proteins | 9 | 2012 | 123 | 1.460 |
Why?
|
Databases, Protein | 2 | 2021 | 46 | 1.450 |
Why?
|
Signal Recognition Particle | 9 | 2009 | 38 | 1.410 |
Why?
|
Peer Review, Research | 3 | 2020 | 46 | 1.410 |
Why?
|
Protein Structure, Tertiary | 27 | 2015 | 656 | 1.370 |
Why?
|
Binding Sites | 23 | 2021 | 881 | 1.260 |
Why?
|
Proteome | 3 | 2022 | 141 | 1.240 |
Why?
|
Magnetic Resonance Spectroscopy | 40 | 2007 | 291 | 1.180 |
Why?
|
Computational Biology | 8 | 2021 | 333 | 1.170 |
Why?
|
Protein Aggregates | 4 | 2024 | 18 | 1.100 |
Why?
|
Endoplasmic Reticulum | 6 | 2024 | 168 | 1.090 |
Why?
|
Nuclear Magnetic Resonance, Biomolecular | 12 | 2017 | 111 | 1.080 |
Why?
|
Biophysics | 2 | 2025 | 41 | 1.060 |
Why?
|
Chaperonin 60 | 12 | 2015 | 19 | 1.050 |
Why?
|
Crystallography, X-Ray | 10 | 2023 | 424 | 1.030 |
Why?
|
Ligands | 7 | 2017 | 411 | 0.990 |
Why?
|
HSP40 Heat-Shock Proteins | 1 | 2024 | 5 | 0.940 |
Why?
|
Synaptosomal-Associated Protein 25 | 1 | 2024 | 10 | 0.940 |
Why?
|
Hydrophobic and Hydrophilic Interactions | 8 | 2021 | 256 | 0.940 |
Why?
|
Kinetics | 20 | 2019 | 751 | 0.930 |
Why?
|
Selenoproteins | 1 | 2024 | 8 | 0.930 |
Why?
|
Glucosyltransferases | 1 | 2024 | 13 | 0.920 |
Why?
|
Circular Dichroism | 30 | 2010 | 107 | 0.920 |
Why?
|
Oligopeptides | 11 | 2007 | 128 | 0.890 |
Why?
|
Glycoproteins | 1 | 2025 | 183 | 0.870 |
Why?
|
History, 21st Century | 7 | 2025 | 162 | 0.860 |
Why?
|
Spectrometry, Fluorescence | 14 | 2012 | 90 | 0.850 |
Why?
|
Thermodynamics | 19 | 2019 | 191 | 0.840 |
Why?
|
Receptors, Virus | 11 | 1994 | 67 | 0.820 |
Why?
|
Publishing | 2 | 2020 | 89 | 0.810 |
Why?
|
Proline | 7 | 2007 | 42 | 0.800 |
Why?
|
Humans | 48 | 2025 | 59393 | 0.790 |
Why?
|
Proteolysis | 4 | 2019 | 136 | 0.770 |
Why?
|
Alkaline Phosphatase | 2 | 2021 | 46 | 0.770 |
Why?
|
Universities | 2 | 2013 | 144 | 0.760 |
Why?
|
Animals | 38 | 2025 | 19643 | 0.740 |
Why?
|
Protein Unfolding | 4 | 2015 | 13 | 0.740 |
Why?
|
HSP90 Heat-Shock Proteins | 1 | 2022 | 64 | 0.730 |
Why?
|
Evolution, Molecular | 6 | 2018 | 298 | 0.690 |
Why?
|
Bacterial Outer Membrane Proteins | 17 | 2007 | 121 | 0.680 |
Why?
|
History, 20th Century | 6 | 2025 | 224 | 0.680 |
Why?
|
Cysteine | 3 | 2011 | 107 | 0.670 |
Why?
|
Allosteric Site | 5 | 2019 | 31 | 0.670 |
Why?
|
Protein Stability | 5 | 2015 | 85 | 0.650 |
Why?
|
alpha 1-Antitrypsin | 3 | 2022 | 87 | 0.650 |
Why?
|
Peer Review | 1 | 2019 | 24 | 0.640 |
Why?
|
Eukaryotic Cells | 3 | 2018 | 57 | 0.640 |
Why?
|
Open Access Publishing | 1 | 2019 | 3 | 0.630 |
Why?
|
Fluorescent Dyes | 6 | 2008 | 196 | 0.630 |
Why?
|
Polyamines | 1 | 2019 | 11 | 0.630 |
Why?
|
Peptides, Cyclic | 8 | 1993 | 20 | 0.620 |
Why?
|
Information Dissemination | 1 | 2020 | 111 | 0.620 |
Why?
|
Tryptophan | 8 | 2012 | 54 | 0.610 |
Why?
|
Lipids | 2 | 2019 | 301 | 0.610 |
Why?
|
Research Design | 2 | 2020 | 555 | 0.600 |
Why?
|
Bacteria | 4 | 2014 | 278 | 0.590 |
Why?
|
Chemistry | 2 | 2016 | 31 | 0.540 |
Why?
|
Biological Science Disciplines | 1 | 2016 | 4 | 0.530 |
Why?
|
Cross-Linking Reagents | 4 | 2012 | 117 | 0.520 |
Why?
|
Peptide Fragments | 10 | 2003 | 400 | 0.510 |
Why?
|
Recombinant Proteins | 11 | 2017 | 689 | 0.500 |
Why?
|
Protein Engineering | 5 | 2008 | 77 | 0.490 |
Why?
|
Models, Biological | 8 | 2014 | 1143 | 0.480 |
Why?
|
Lipid Bilayers | 12 | 1996 | 50 | 0.470 |
Why?
|
Amino Acid Substitution | 4 | 2013 | 234 | 0.470 |
Why?
|
Heat-Shock Response | 1 | 2015 | 35 | 0.470 |
Why?
|
Mutation | 16 | 2019 | 2454 | 0.470 |
Why?
|
Recombinant Fusion Proteins | 5 | 2013 | 490 | 0.470 |
Why?
|
Homeostasis | 3 | 2019 | 346 | 0.460 |
Why?
|
Structure-Activity Relationship | 17 | 2013 | 365 | 0.450 |
Why?
|
Adenosine Diphosphate | 4 | 2023 | 40 | 0.450 |
Why?
|
Substrate Specificity | 9 | 2012 | 333 | 0.440 |
Why?
|
Amino Acids, Aromatic | 1 | 2013 | 7 | 0.430 |
Why?
|
Fatty Acid-Binding Proteins | 4 | 2013 | 21 | 0.430 |
Why?
|
Protein Structure, Quaternary | 5 | 2015 | 100 | 0.420 |
Why?
|
Periplasm | 1 | 2013 | 6 | 0.420 |
Why?
|
Microscopy, Fluorescence | 4 | 2008 | 392 | 0.420 |
Why?
|
Protein Transport | 7 | 2019 | 399 | 0.420 |
Why?
|
Benzophenones | 2 | 2012 | 18 | 0.410 |
Why?
|
Hydrogen Bonding | 7 | 2013 | 125 | 0.400 |
Why?
|
Biopolymers | 2 | 2015 | 69 | 0.390 |
Why?
|
Conserved Sequence | 6 | 2013 | 170 | 0.390 |
Why?
|
Rats | 5 | 2025 | 1910 | 0.390 |
Why?
|
SEC Translocation Channels | 9 | 2012 | 37 | 0.390 |
Why?
|
Organometallic Compounds | 3 | 2007 | 63 | 0.380 |
Why?
|
Protein Interaction Maps | 1 | 2011 | 33 | 0.380 |
Why?
|
Models, Chemical | 4 | 2015 | 137 | 0.370 |
Why?
|
Stress, Physiological | 2 | 2011 | 185 | 0.350 |
Why?
|
Protein Denaturation | 8 | 2012 | 67 | 0.340 |
Why?
|
Nerve Tissue Proteins | 3 | 2007 | 418 | 0.340 |
Why?
|
Heat-Shock Proteins, Small | 1 | 2010 | 1 | 0.340 |
Why?
|
Osmotic Pressure | 2 | 2007 | 15 | 0.340 |
Why?
|
Inteins | 1 | 2010 | 3 | 0.340 |
Why?
|
Molecular Dynamics Simulation | 4 | 2021 | 119 | 0.340 |
Why?
|
Immunoglobulin gamma-Chains | 1 | 2009 | 5 | 0.330 |
Why?
|
Immunoglobulin Light Chains | 1 | 2009 | 17 | 0.320 |
Why?
|
Software | 2 | 2012 | 366 | 0.310 |
Why?
|
Mutagenesis | 3 | 2023 | 129 | 0.310 |
Why?
|
Porins | 11 | 1994 | 70 | 0.300 |
Why?
|
Nuclear Proteins | 3 | 2007 | 750 | 0.300 |
Why?
|
Manuscripts as Topic | 2 | 2019 | 2 | 0.300 |
Why?
|
Amino Acid Motifs | 3 | 2018 | 149 | 0.300 |
Why?
|
Antithrombin III | 2 | 2019 | 14 | 0.300 |
Why?
|
Intercellular Signaling Peptides and Proteins | 1 | 2009 | 152 | 0.290 |
Why?
|
Amino Acids | 3 | 2005 | 140 | 0.280 |
Why?
|
Protein Interaction Domains and Motifs | 3 | 2015 | 83 | 0.280 |
Why?
|
Amyloid | 1 | 2007 | 65 | 0.270 |
Why?
|
Chaperonins | 2 | 2005 | 8 | 0.270 |
Why?
|
Membrane Proteins | 6 | 2024 | 850 | 0.270 |
Why?
|
Research Personnel | 1 | 2008 | 92 | 0.270 |
Why?
|
Betaine | 1 | 2007 | 9 | 0.270 |
Why?
|
Chelating Agents | 1 | 2007 | 46 | 0.270 |
Why?
|
Intracellular Signaling Peptides and Proteins | 1 | 2009 | 327 | 0.270 |
Why?
|
Point Mutation | 3 | 2023 | 160 | 0.270 |
Why?
|
Histidine | 1 | 2007 | 34 | 0.270 |
Why?
|
Molecular Structure | 5 | 2011 | 374 | 0.260 |
Why?
|
Reproducibility of Results | 2 | 2023 | 1555 | 0.260 |
Why?
|
Gonadotropin-Releasing Hormone | 6 | 1996 | 86 | 0.260 |
Why?
|
Staining and Labeling | 1 | 2007 | 124 | 0.250 |
Why?
|
Multigene Family | 2 | 2006 | 92 | 0.240 |
Why?
|
Daptomycin | 1 | 2005 | 9 | 0.240 |
Why?
|
Time Factors | 6 | 2020 | 3614 | 0.240 |
Why?
|
Cytosol | 2 | 2018 | 171 | 0.230 |
Why?
|
Sequence Alignment | 4 | 2012 | 288 | 0.230 |
Why?
|
Data Interpretation, Statistical | 1 | 2005 | 191 | 0.230 |
Why?
|
Alkyl and Aryl Transferases | 3 | 1993 | 7 | 0.230 |
Why?
|
Research | 2 | 2019 | 188 | 0.230 |
Why?
|
Transferases | 3 | 1993 | 16 | 0.230 |
Why?
|
Organic Anion Transporters, Sodium-Dependent | 1 | 2004 | 2 | 0.220 |
Why?
|
Phospholipids | 6 | 2002 | 78 | 0.220 |
Why?
|
Symporters | 1 | 2004 | 13 | 0.220 |
Why?
|
Rotation | 1 | 2023 | 20 | 0.220 |
Why?
|
Signal Transduction | 3 | 2011 | 2898 | 0.220 |
Why?
|
Quality Control | 2 | 2023 | 71 | 0.220 |
Why?
|
Neoplasm Proteins | 2 | 2004 | 278 | 0.210 |
Why?
|
Mutagenesis, Site-Directed | 6 | 2007 | 248 | 0.210 |
Why?
|
GTP Phosphohydrolases | 2 | 2001 | 59 | 0.210 |
Why?
|
Georgia | 2 | 2013 | 87 | 0.200 |
Why?
|
RNA, Bacterial | 3 | 2006 | 68 | 0.200 |
Why?
|
cis-trans-Isomerases | 1 | 2002 | 7 | 0.200 |
Why?
|
Membrane Lipids | 5 | 1991 | 27 | 0.200 |
Why?
|
Protein Processing, Post-Translational | 4 | 1993 | 258 | 0.200 |
Why?
|
Macromolecular Substances | 2 | 2021 | 160 | 0.200 |
Why?
|
Biological Products | 1 | 2024 | 90 | 0.200 |
Why?
|
Temperature | 7 | 2010 | 295 | 0.200 |
Why?
|
Urea | 5 | 2010 | 35 | 0.200 |
Why?
|
Philosophy | 1 | 2022 | 12 | 0.200 |
Why?
|
Trehalose | 2 | 2015 | 8 | 0.190 |
Why?
|
Molecular Conformation | 5 | 2010 | 133 | 0.190 |
Why?
|
Huntingtin Protein | 3 | 2007 | 138 | 0.190 |
Why?
|
Protein Biosynthesis | 3 | 2015 | 297 | 0.190 |
Why?
|
Carrier Proteins | 3 | 2004 | 697 | 0.190 |
Why?
|
In Vitro Techniques | 6 | 2007 | 472 | 0.190 |
Why?
|
alpha 1-Antitrypsin Deficiency | 1 | 2022 | 62 | 0.180 |
Why?
|
Cells | 2 | 2014 | 31 | 0.180 |
Why?
|
Deuterium Exchange Measurement | 2 | 2013 | 18 | 0.180 |
Why?
|
RNA, Ribosomal | 1 | 2001 | 53 | 0.180 |
Why?
|
RNA | 2 | 2001 | 401 | 0.170 |
Why?
|
CHO Cells | 4 | 2024 | 189 | 0.170 |
Why?
|
Phenylalanine | 2 | 2013 | 25 | 0.170 |
Why?
|
Costs and Cost Analysis | 1 | 2020 | 98 | 0.170 |
Why?
|
Serpins | 1 | 2019 | 17 | 0.160 |
Why?
|
Policy | 1 | 2020 | 48 | 0.160 |
Why?
|
Sulfhydryl Compounds | 1 | 2019 | 48 | 0.160 |
Why?
|
Cytoplasm | 2 | 2018 | 270 | 0.160 |
Why?
|
Methyl-CpG-Binding Protein 2 | 2 | 2010 | 15 | 0.160 |
Why?
|
Deuterium | 3 | 2015 | 24 | 0.160 |
Why?
|
Electron Spin Resonance Spectroscopy | 4 | 2017 | 25 | 0.160 |
Why?
|
Serine Endopeptidases | 2 | 2004 | 84 | 0.160 |
Why?
|
Anti-Bacterial Agents | 1 | 2005 | 734 | 0.160 |
Why?
|
Fungal Proteins | 2 | 2003 | 144 | 0.150 |
Why?
|
Europe | 1 | 2019 | 182 | 0.150 |
Why?
|
Eukaryota | 1 | 2018 | 29 | 0.150 |
Why?
|
Fluoresceins | 3 | 2006 | 29 | 0.150 |
Why?
|
United States | 4 | 2019 | 7422 | 0.150 |
Why?
|
Protons | 4 | 2005 | 60 | 0.150 |
Why?
|
Water | 8 | 2005 | 300 | 0.150 |
Why?
|
Sequence Homology, Amino Acid | 3 | 2006 | 356 | 0.150 |
Why?
|
Guidelines as Topic | 1 | 2019 | 154 | 0.150 |
Why?
|
Protozoan Proteins | 1 | 1998 | 86 | 0.140 |
Why?
|
Nitrogen Isotopes | 3 | 2015 | 10 | 0.140 |
Why?
|
Bacteriophage lambda | 4 | 1999 | 18 | 0.140 |
Why?
|
1-Deoxynojirimycin | 1 | 2017 | 2 | 0.140 |
Why?
|
Trimethoprim | 1 | 2017 | 7 | 0.140 |
Why?
|
alpha-Galactosidase | 1 | 2017 | 7 | 0.140 |
Why?
|
Solutions | 5 | 2006 | 64 | 0.140 |
Why?
|
Tetrahydrofolate Dehydrogenase | 1 | 2017 | 15 | 0.140 |
Why?
|
Receptors, LDL | 2 | 1998 | 33 | 0.130 |
Why?
|
Dipeptides | 3 | 1995 | 60 | 0.130 |
Why?
|
Mass Spectrometry | 2 | 2017 | 295 | 0.130 |
Why?
|
Alanine | 3 | 2006 | 49 | 0.130 |
Why?
|
Fluorescence Polarization | 6 | 2000 | 32 | 0.130 |
Why?
|
Micelles | 5 | 1993 | 80 | 0.130 |
Why?
|
Mice | 5 | 2013 | 10288 | 0.130 |
Why?
|
Catalytic Domain | 2 | 2017 | 193 | 0.130 |
Why?
|
Solubility | 4 | 2006 | 177 | 0.130 |
Why?
|
Glutamine | 2 | 2006 | 46 | 0.130 |
Why?
|
Enterotoxins | 1 | 1995 | 20 | 0.120 |
Why?
|
Carboxypeptidases | 2 | 1996 | 7 | 0.120 |
Why?
|
Carbon Isotopes | 1 | 2015 | 17 | 0.120 |
Why?
|
Clustered Regularly Interspaced Short Palindromic Repeats | 1 | 2016 | 91 | 0.120 |
Why?
|
Cricetulus | 3 | 2022 | 99 | 0.120 |
Why?
|
Communication | 1 | 2020 | 546 | 0.120 |
Why?
|
Bacterial Toxins | 1 | 1995 | 60 | 0.120 |
Why?
|
Phase Transition | 1 | 2014 | 20 | 0.120 |
Why?
|
HEK293 Cells | 1 | 2017 | 587 | 0.120 |
Why?
|
Electrophoresis, Polyacrylamide Gel | 3 | 2001 | 178 | 0.120 |
Why?
|
Biological Transport | 4 | 2010 | 288 | 0.120 |
Why?
|
Cell Physiological Phenomena | 1 | 2014 | 12 | 0.110 |
Why?
|
Intrinsically Disordered Proteins | 1 | 2014 | 11 | 0.110 |
Why?
|
Cell Communication | 1 | 2014 | 124 | 0.110 |
Why?
|
Hydrogels | 1 | 2014 | 110 | 0.100 |
Why?
|
Static Electricity | 2 | 2005 | 163 | 0.100 |
Why?
|
Hydrolysis | 2 | 2012 | 141 | 0.100 |
Why?
|
Muscle Fibers, Skeletal | 2 | 2024 | 87 | 0.100 |
Why?
|
Cricetinae | 2 | 2024 | 366 | 0.100 |
Why?
|
Models, Theoretical | 3 | 2006 | 256 | 0.100 |
Why?
|
Maleimides | 1 | 2012 | 7 | 0.100 |
Why?
|
Liposomes | 2 | 1989 | 100 | 0.100 |
Why?
|
Bacillus subtilis | 1 | 2012 | 32 | 0.100 |
Why?
|
Drug Stability | 2 | 2007 | 141 | 0.100 |
Why?
|
Thiosulfate Sulfurtransferase | 1 | 1991 | 1 | 0.090 |
Why?
|
Stereoisomerism | 3 | 1999 | 68 | 0.090 |
Why?
|
Hepatocytes | 2 | 2024 | 196 | 0.090 |
Why?
|
Viscosity | 1 | 2011 | 50 | 0.090 |
Why?
|
Diffusion | 1 | 2011 | 82 | 0.090 |
Why?
|
Hydrogen-Ion Concentration | 4 | 2001 | 450 | 0.090 |
Why?
|
Chaperonin 10 | 4 | 1996 | 5 | 0.090 |
Why?
|
Ubiquitin | 1 | 2011 | 97 | 0.090 |
Why?
|
Polymerization | 1 | 2011 | 34 | 0.090 |
Why?
|
Endocytosis | 1 | 1991 | 149 | 0.090 |
Why?
|
Chemical Phenomena | 6 | 1996 | 94 | 0.090 |
Why?
|
Ficoll | 1 | 2010 | 4 | 0.090 |
Why?
|
Bacterial Physiological Phenomena | 1 | 2010 | 19 | 0.090 |
Why?
|
Genetic Fitness | 1 | 2010 | 30 | 0.090 |
Why?
|
Spectrophotometry, Ultraviolet | 2 | 2003 | 47 | 0.090 |
Why?
|
Saccharomyces cerevisiae | 2 | 2010 | 540 | 0.090 |
Why?
|
Isotope Labeling | 1 | 2010 | 68 | 0.080 |
Why?
|
Intracellular Space | 1 | 2009 | 34 | 0.080 |
Why?
|
Myoglobin | 1 | 1989 | 27 | 0.080 |
Why?
|
Multiprotein Complexes | 2 | 2010 | 153 | 0.080 |
Why?
|
Microscopy, Electron, Scanning | 1 | 2009 | 105 | 0.080 |
Why?
|
PDZ Domains | 1 | 2009 | 2 | 0.080 |
Why?
|
Phosphatidylglycerols | 1 | 1989 | 12 | 0.080 |
Why?
|
Phosphatidylethanolamines | 1 | 1989 | 17 | 0.080 |
Why?
|
Phylogeny | 2 | 2010 | 337 | 0.080 |
Why?
|
Exons | 2 | 2008 | 191 | 0.080 |
Why?
|
Motion | 1 | 2009 | 56 | 0.080 |
Why?
|
Models, Statistical | 1 | 2010 | 299 | 0.080 |
Why?
|
Trifluoroethanol | 3 | 1994 | 4 | 0.080 |
Why?
|
Mutation, Missense | 1 | 2010 | 172 | 0.080 |
Why?
|
Viral Proteins | 1 | 1990 | 253 | 0.080 |
Why?
|
Rett Syndrome | 1 | 2008 | 8 | 0.080 |
Why?
|
Internet | 1 | 2012 | 448 | 0.070 |
Why?
|
Chemistry, Physical | 5 | 1996 | 47 | 0.070 |
Why?
|
Protein Multimerization | 1 | 2009 | 169 | 0.070 |
Why?
|
Amides | 2 | 2002 | 52 | 0.070 |
Why?
|
Serotonin Plasma Membrane Transport Proteins | 1 | 2008 | 23 | 0.070 |
Why?
|
Sequence Deletion | 2 | 2005 | 112 | 0.070 |
Why?
|
Chromatography, High Pressure Liquid | 2 | 1999 | 225 | 0.070 |
Why?
|
Bridged Bicyclo Compounds | 1 | 2007 | 2 | 0.070 |
Why?
|
DNA | 2 | 2010 | 805 | 0.070 |
Why?
|
Nitrilotriacetic Acid | 1 | 2007 | 6 | 0.070 |
Why?
|
Arsenicals | 1 | 2007 | 7 | 0.070 |
Why?
|
Fluorescein | 1 | 2007 | 13 | 0.070 |
Why?
|
Protein Precursors | 1 | 2007 | 75 | 0.070 |
Why?
|
Nucleotides | 1 | 2007 | 44 | 0.070 |
Why?
|
Cell Line | 2 | 2008 | 1983 | 0.070 |
Why?
|
Membrane Potentials | 1 | 2007 | 137 | 0.070 |
Why?
|
Microscopy, Electron, Scanning Transmission | 1 | 2006 | 2 | 0.070 |
Why?
|
Amyloidosis | 1 | 2007 | 62 | 0.070 |
Why?
|
Fluorescence | 2 | 1998 | 83 | 0.070 |
Why?
|
Ion Channels | 1 | 2007 | 88 | 0.070 |
Why?
|
Osmolar Concentration | 1 | 2006 | 88 | 0.070 |
Why?
|
Computer Simulation | 3 | 2014 | 458 | 0.070 |
Why?
|
Cell Membrane | 4 | 2007 | 485 | 0.060 |
Why?
|
Arginine | 2 | 2005 | 110 | 0.060 |
Why?
|
Silk | 1 | 2006 | 6 | 0.060 |
Why?
|
Thermus thermophilus | 1 | 2006 | 19 | 0.060 |
Why?
|
Genetic Variation | 2 | 2002 | 357 | 0.060 |
Why?
|
RNA Helicases | 1 | 2006 | 88 | 0.060 |
Why?
|
Complementarity Determining Regions | 1 | 2006 | 36 | 0.060 |
Why?
|
Disulfides | 2 | 2016 | 62 | 0.060 |
Why?
|
Dimerization | 2 | 2002 | 144 | 0.060 |
Why?
|
Arsenic | 1 | 2005 | 10 | 0.060 |
Why?
|
Colloids | 2 | 1982 | 49 | 0.060 |
Why?
|
Cloning, Molecular | 1 | 2005 | 381 | 0.060 |
Why?
|
Chymotrypsin | 2 | 2001 | 23 | 0.060 |
Why?
|
Peptide Biosynthesis | 1 | 1984 | 10 | 0.060 |
Why?
|
T-Lymphocytes | 1 | 1989 | 984 | 0.060 |
Why?
|
Tretinoin | 2 | 1996 | 49 | 0.060 |
Why?
|
Hydrogen | 4 | 1999 | 50 | 0.050 |
Why?
|
Age Factors | 1 | 2008 | 1503 | 0.050 |
Why?
|
Lectins | 1 | 2023 | 40 | 0.050 |
Why?
|
Ribosomes | 2 | 2006 | 154 | 0.050 |
Why?
|
Peptide Mapping | 1 | 2003 | 28 | 0.050 |
Why?
|
Yeasts | 1 | 2003 | 51 | 0.050 |
Why?
|
Ribonuclease T1 | 1 | 2002 | 3 | 0.050 |
Why?
|
Isomerism | 1 | 2002 | 28 | 0.050 |
Why?
|
Polysaccharides | 1 | 2023 | 140 | 0.050 |
Why?
|
Mammals | 1 | 2024 | 209 | 0.050 |
Why?
|
Molecular Motor Proteins | 1 | 2002 | 34 | 0.050 |
Why?
|
Physical Phenomena | 1 | 2021 | 9 | 0.050 |
Why?
|
Trypsin | 2 | 2017 | 39 | 0.050 |
Why?
|
Catalysis | 1 | 2002 | 152 | 0.050 |
Why?
|
Dose-Response Relationship, Drug | 2 | 2001 | 804 | 0.050 |
Why?
|
Calcium | 1 | 2005 | 555 | 0.050 |
Why?
|
Densitometry | 1 | 2001 | 12 | 0.050 |
Why?
|
Endoplasmic Reticulum, Rough | 1 | 2001 | 5 | 0.050 |
Why?
|
Sequence Analysis, Protein | 1 | 2001 | 33 | 0.050 |
Why?
|
Biotin | 1 | 2001 | 51 | 0.040 |
Why?
|
Dimyristoylphosphatidylcholine | 2 | 1994 | 5 | 0.040 |
Why?
|
Transduction, Genetic | 1 | 2022 | 227 | 0.040 |
Why?
|
Neurons | 1 | 2006 | 863 | 0.040 |
Why?
|
Cryoelectron Microscopy | 1 | 2002 | 184 | 0.040 |
Why?
|
Sodium Dodecyl Sulfate | 3 | 1993 | 30 | 0.040 |
Why?
|
Models, Genetic | 1 | 2001 | 255 | 0.040 |
Why?
|
Enzyme Precursors | 2 | 1991 | 11 | 0.040 |
Why?
|
Membrane Fluidity | 2 | 1994 | 14 | 0.040 |
Why?
|
Phosphatidylcholines | 2 | 1994 | 34 | 0.040 |
Why?
|
Calorimetry, Differential Scanning | 1 | 1999 | 31 | 0.040 |
Why?
|
Clathrin | 1 | 1998 | 23 | 0.040 |
Why?
|
ATPases Associated with Diverse Cellular Activities | 1 | 1998 | 25 | 0.040 |
Why?
|
Carbon | 2 | 2015 | 45 | 0.040 |
Why?
|
Mitochondria | 2 | 1991 | 343 | 0.040 |
Why?
|
Endopeptidase Clp | 1 | 1998 | 35 | 0.040 |
Why?
|
Molecular Probes | 1 | 1998 | 29 | 0.040 |
Why?
|
Cell Extracts | 1 | 2017 | 25 | 0.030 |
Why?
|
Chromatography, Ion Exchange | 1 | 2017 | 25 | 0.030 |
Why?
|
Hormone Antagonists | 1 | 1996 | 12 | 0.030 |
Why?
|
Cells, Cultured | 2 | 2019 | 2092 | 0.030 |
Why?
|
Cathepsin A | 1 | 1996 | 4 | 0.030 |
Why?
|
Spectrum Analysis | 1 | 2017 | 51 | 0.030 |
Why?
|
Ovulation | 1 | 1996 | 28 | 0.030 |
Why?
|
Pituitary Gland | 1 | 1996 | 51 | 0.030 |
Why?
|
Xenopus Proteins | 1 | 1996 | 35 | 0.030 |
Why?
|
Titrimetry | 1 | 1996 | 11 | 0.030 |
Why?
|
Antimicrobial Cationic Peptides | 1 | 1996 | 51 | 0.030 |
Why?
|
Male | 1 | 2016 | 27730 | 0.030 |
Why?
|
Dependovirus | 1 | 2022 | 652 | 0.030 |
Why?
|
Osmometry | 1 | 2015 | 1 | 0.030 |
Why?
|
Genetic Therapy | 1 | 2022 | 733 | 0.030 |
Why?
|
Protease La | 1 | 2015 | 13 | 0.030 |
Why?
|
Cattle | 2 | 2010 | 304 | 0.030 |
Why?
|
Nitrogen Radioisotopes | 1 | 1994 | 16 | 0.030 |
Why?
|
Protein Aggregation, Pathological | 1 | 2014 | 18 | 0.030 |
Why?
|
Membranes | 2 | 1987 | 19 | 0.030 |
Why?
|
Mathematics | 1 | 1994 | 32 | 0.030 |
Why?
|
Phosphates | 1 | 2015 | 90 | 0.030 |
Why?
|
Image Enhancement | 1 | 1996 | 188 | 0.030 |
Why?
|
Melanocyte-Stimulating Hormones | 2 | 1992 | 2 | 0.030 |
Why?
|
Receptors, LHRH | 1 | 1993 | 7 | 0.030 |
Why?
|
Base Sequence | 2 | 1993 | 1302 | 0.030 |
Why?
|
Proto-Oncogene Proteins p21(ras) | 1 | 1993 | 55 | 0.030 |
Why?
|
Oxygen | 1 | 2015 | 312 | 0.030 |
Why?
|
Guanosine Triphosphate | 1 | 1993 | 50 | 0.030 |
Why?
|
GTP-Binding Proteins | 1 | 1993 | 81 | 0.030 |
Why?
|
Indicators and Reagents | 2 | 1991 | 51 | 0.030 |
Why?
|
X-Ray Diffraction | 2 | 1990 | 58 | 0.030 |
Why?
|
Gene Expression | 1 | 1996 | 808 | 0.030 |
Why?
|
Brain | 2 | 1991 | 1485 | 0.030 |
Why?
|
DNA Mutational Analysis | 1 | 1993 | 187 | 0.030 |
Why?
|
Citrate (si)-Synthase | 1 | 1992 | 5 | 0.020 |
Why?
|
Tachykinins | 1 | 1992 | 9 | 0.020 |
Why?
|
Coated Pits, Cell-Membrane | 1 | 1991 | 5 | 0.020 |
Why?
|
Asialoglycoprotein Receptor | 1 | 1991 | 3 | 0.020 |
Why?
|
Submitochondrial Particles | 1 | 1991 | 1 | 0.020 |
Why?
|
Proton-Translocating ATPases | 1 | 1991 | 6 | 0.020 |
Why?
|
DNA, Bacterial | 1 | 1993 | 259 | 0.020 |
Why?
|
Autoradiography | 1 | 1991 | 53 | 0.020 |
Why?
|
Chromatography, Thin Layer | 1 | 1991 | 18 | 0.020 |
Why?
|
Intracellular Membranes | 1 | 1991 | 50 | 0.020 |
Why?
|
Membranes, Artificial | 2 | 1982 | 45 | 0.020 |
Why?
|
Oxytocin | 1 | 1992 | 45 | 0.020 |
Why?
|
Carboxypeptidases A | 1 | 1991 | 1 | 0.020 |
Why?
|
Receptors, Immunologic | 1 | 1991 | 176 | 0.020 |
Why?
|
Viral Tail Proteins | 1 | 1990 | 2 | 0.020 |
Why?
|
Enzyme Stability | 1 | 1991 | 46 | 0.020 |
Why?
|
Coliphages | 1 | 1990 | 17 | 0.020 |
Why?
|
Normal Distribution | 1 | 2010 | 17 | 0.020 |
Why?
|
Surface Properties | 2 | 1989 | 271 | 0.020 |
Why?
|
Apoproteins | 2 | 2000 | 18 | 0.020 |
Why?
|
Biological Transport, Active | 1 | 1990 | 37 | 0.020 |
Why?
|
Whales | 1 | 1989 | 1 | 0.020 |
Why?
|
Nucleic Acid Denaturation | 1 | 2008 | 7 | 0.020 |
Why?
|
Sodium Azide | 1 | 2007 | 4 | 0.020 |
Why?
|
Potassium Chloride | 1 | 2007 | 14 | 0.020 |
Why?
|
Xenopus laevis | 1 | 2007 | 67 | 0.020 |
Why?
|
Muramidase | 2 | 1985 | 46 | 0.020 |
Why?
|
Organophosphorus Compounds | 1 | 1987 | 31 | 0.020 |
Why?
|
Microscopy, Energy-Filtering Transmission Electron | 1 | 2006 | 2 | 0.020 |
Why?
|
Lymphocyte Activation | 1 | 1989 | 743 | 0.020 |
Why?
|
Spectrophotometry, Infrared | 1 | 1986 | 26 | 0.020 |
Why?
|
Pulmonary Surfactants | 1 | 1986 | 12 | 0.020 |
Why?
|
Fluorescence Resonance Energy Transfer | 1 | 2006 | 75 | 0.020 |
Why?
|
Cell Survival | 1 | 2008 | 559 | 0.020 |
Why?
|
Protein Subunits | 1 | 2006 | 165 | 0.020 |
Why?
|
Oocytes | 1 | 2007 | 193 | 0.020 |
Why?
|
Chromatin | 1 | 2010 | 599 | 0.020 |
Why?
|
Enzyme Inhibitors | 1 | 2007 | 347 | 0.020 |
Why?
|
Adenylyl Imidodiphosphate | 1 | 2004 | 4 | 0.010 |
Why?
|
ortho-Aminobenzoates | 1 | 2004 | 7 | 0.010 |
Why?
|
Magnesium | 1 | 2004 | 52 | 0.010 |
Why?
|
Micrococcal Nuclease | 1 | 1983 | 13 | 0.010 |
Why?
|
Phospholipases A | 1 | 1983 | 15 | 0.010 |
Why?
|
Computer Graphics | 2 | 1996 | 19 | 0.010 |
Why?
|
Adaptor Protein Complex alpha Subunits | 1 | 1998 | 3 | 0.010 |
Why?
|
Adaptor Protein Complex 2 | 1 | 1998 | 6 | 0.010 |
Why?
|
Adaptor Proteins, Vesicular Transport | 1 | 1998 | 81 | 0.010 |
Why?
|
Torpedo | 1 | 1996 | 1 | 0.010 |
Why?
|
Magainins | 1 | 1996 | 2 | 0.010 |
Why?
|
Anura | 1 | 1996 | 8 | 0.010 |
Why?
|
Crystallography | 1 | 1996 | 26 | 0.010 |
Why?
|
Nitrogen | 1 | 1996 | 24 | 0.010 |
Why?
|
Glycine | 1 | 1996 | 46 | 0.010 |
Why?
|
Spin Labels | 1 | 1994 | 12 | 0.010 |
Why?
|
Receptors, Peptide | 1 | 1993 | 31 | 0.010 |
Why?
|
Receptors, Cytoplasmic and Nuclear | 1 | 1993 | 142 | 0.010 |
Why?
|
Oxaloacetates | 1 | 1992 | 1 | 0.010 |
Why?
|
Myelin P2 Protein | 1 | 1992 | 1 | 0.010 |
Why?
|
Guanidines | 1 | 1992 | 14 | 0.010 |
Why?
|
Myelin Basic Protein | 1 | 1992 | 21 | 0.010 |
Why?
|
Glycerol | 1 | 1992 | 31 | 0.010 |
Why?
|
Guanidine | 1 | 1992 | 22 | 0.010 |
Why?
|
Serum Albumin, Bovine | 1 | 1992 | 34 | 0.010 |
Why?
|
Sequence Homology, Nucleic Acid | 1 | 1992 | 111 | 0.010 |
Why?
|
Surface Tension | 1 | 1991 | 17 | 0.010 |
Why?
|
Restriction Mapping | 1 | 1991 | 51 | 0.010 |
Why?
|
Female | 2 | 2007 | 30711 | 0.010 |
Why?
|
Oxygen Consumption | 1 | 1991 | 206 | 0.010 |
Why?
|
Secretory Rate | 1 | 1990 | 10 | 0.010 |
Why?
|
Hormones | 1 | 1990 | 60 | 0.010 |
Why?
|
Luteinizing Hormone | 1 | 1990 | 98 | 0.010 |
Why?
|
Drug Design | 1 | 1990 | 136 | 0.000 |
Why?
|
Transcription, Genetic | 1 | 1991 | 840 | 0.000 |
Why?
|
Enkephalins | 1 | 1985 | 16 | 0.000 |
Why?
|
Bradykinin | 1 | 1985 | 8 | 0.000 |
Why?
|
Somatostatin | 1 | 1985 | 18 | 0.000 |
Why?
|
Nitrogen Oxides | 1 | 1981 | 7 | 0.000 |
Why?
|
Propylamines | 1 | 1981 | 8 | 0.000 |
Why?
|
Free Radicals | 1 | 1981 | 18 | 0.000 |
Why?
|
Quaternary Ammonium Compounds | 1 | 1981 | 29 | 0.000 |
Why?
|
Surface-Active Agents | 1 | 1981 | 112 | 0.000 |
Why?
|