| Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
|---|
| rab GTP-Binding Proteins | 24 | 2021 | 79 | 5.120 |
Why?
|
| Guanine Nucleotide Exchange Factors | 15 | 2021 | 60 | 3.640 |
Why?
|
| GTPase-Activating Proteins | 17 | 2021 | 63 | 3.440 |
Why?
|
| Guanosine Triphosphate | 14 | 2021 | 50 | 2.840 |
Why?
|
| Receptors, Cytoplasmic and Nuclear | 8 | 2020 | 140 | 2.310 |
Why?
|
| Endosomes | 17 | 2016 | 170 | 2.110 |
Why?
|
| Vesicular Transport Proteins | 14 | 2021 | 103 | 1.900 |
Why?
|
| Models, Molecular | 28 | 2019 | 1115 | 1.600 |
Why?
|
| Cell Membrane | 18 | 2020 | 489 | 1.580 |
Why?
|
| ADP-Ribosylation Factors | 5 | 2020 | 20 | 1.390 |
Why?
|
| GTP Phosphohydrolases | 7 | 2021 | 59 | 1.360 |
Why?
|
| Guanosine Diphosphate | 8 | 2019 | 19 | 1.280 |
Why?
|
| Protein Structure, Tertiary | 24 | 2019 | 663 | 1.260 |
Why?
|
| Phosphatidylinositol Phosphates | 11 | 2020 | 40 | 1.180 |
Why?
|
| High-Throughput Screening Assays | 2 | 2021 | 73 | 1.160 |
Why?
|
| Protein Binding | 25 | 2021 | 1545 | 1.120 |
Why?
|
| Amino Acid Sequence | 29 | 2020 | 1580 | 1.060 |
Why?
|
| rab5 GTP-Binding Proteins | 11 | 2010 | 21 | 1.030 |
Why?
|
| Substrate Specificity | 12 | 2021 | 321 | 1.010 |
Why?
|
| Crystallography, X-Ray | 18 | 2019 | 419 | 0.970 |
Why?
|
| Binding Sites | 17 | 2021 | 874 | 0.890 |
Why?
|
| Protein Conformation | 21 | 2014 | 762 | 0.890 |
Why?
|
| Molecular Sequence Data | 26 | 2013 | 1977 | 0.870 |
Why?
|
| Legionella pneumophila | 5 | 2014 | 10 | 0.820 |
Why?
|
| Protein Transport | 15 | 2016 | 394 | 0.810 |
Why?
|
| COP-Coated Vesicles | 1 | 2021 | 2 | 0.770 |
Why?
|
| Intracellular Signaling Peptides and Proteins | 8 | 2020 | 322 | 0.770 |
Why?
|
| Bacterial Proteins | 5 | 2014 | 743 | 0.770 |
Why?
|
| Membrane Proteins | 8 | 2020 | 843 | 0.710 |
Why?
|
| Kinetics | 16 | 2021 | 733 | 0.700 |
Why?
|
| Phosphatidylinositol 4,5-Diphosphate | 1 | 2019 | 16 | 0.670 |
Why?
|
| Recombinant Fusion Proteins | 6 | 2017 | 502 | 0.670 |
Why?
|
| Endocytosis | 8 | 2014 | 148 | 0.660 |
Why?
|
| Inositol Phosphates | 4 | 2020 | 18 | 0.660 |
Why?
|
| Sequence Homology, Amino Acid | 14 | 2017 | 357 | 0.650 |
Why?
|
| Parkinson Disease | 1 | 2020 | 97 | 0.650 |
Why?
|
| Pleckstrin Homology Domains | 1 | 2017 | 1 | 0.600 |
Why?
|
| Membrane Fusion | 3 | 2016 | 74 | 0.590 |
Why?
|
| Phosphatidylinositols | 4 | 2020 | 48 | 0.580 |
Why?
|
| Animals | 45 | 2020 | 19595 | 0.540 |
Why?
|
| Hydrolysis | 8 | 2016 | 138 | 0.520 |
Why?
|
| Saccharomyces cerevisiae Proteins | 3 | 2021 | 418 | 0.490 |
Why?
|
| Recombinant Proteins | 14 | 2019 | 693 | 0.470 |
Why?
|
| Cell Cycle | 1 | 2016 | 379 | 0.460 |
Why?
|
| Myoglobin | 9 | 1994 | 27 | 0.460 |
Why?
|
| Adaptor Proteins, Signal Transducing | 2 | 2015 | 415 | 0.460 |
Why?
|
| Intracellular Membranes | 3 | 2020 | 50 | 0.430 |
Why?
|
| Glucose Transporter Type 4 | 4 | 2012 | 56 | 0.390 |
Why?
|
| Sequence Alignment | 5 | 2017 | 290 | 0.380 |
Why?
|
| Autoantigens | 2 | 2010 | 125 | 0.370 |
Why?
|
| Allosteric Regulation | 3 | 2021 | 69 | 0.370 |
Why?
|
| Humans | 46 | 2021 | 59280 | 0.360 |
Why?
|
| Blood Proteins | 3 | 2010 | 72 | 0.340 |
Why?
|
| Static Electricity | 5 | 2013 | 164 | 0.330 |
Why?
|
| Mice | 16 | 2020 | 10249 | 0.320 |
Why?
|
| Protein Conformation, beta-Strand | 2 | 2019 | 10 | 0.320 |
Why?
|
| Protein Conformation, alpha-Helical | 2 | 2019 | 21 | 0.320 |
Why?
|
| Enzyme Activation | 6 | 2013 | 351 | 0.310 |
Why?
|
| Structure-Activity Relationship | 8 | 2013 | 374 | 0.310 |
Why?
|
| Mutation | 17 | 2007 | 2425 | 0.310 |
Why?
|
| Phosphoproteins | 3 | 2010 | 216 | 0.310 |
Why?
|
| Surface Plasmon Resonance | 4 | 2013 | 33 | 0.310 |
Why?
|
| Adipocytes | 4 | 2012 | 252 | 0.310 |
Why?
|
| Point Mutation | 3 | 2021 | 162 | 0.310 |
Why?
|
| Signal Transduction | 8 | 2019 | 2885 | 0.300 |
Why?
|
| Cloning, Molecular | 2 | 2019 | 385 | 0.300 |
Why?
|
| Endoplasmic Reticulum | 3 | 2021 | 167 | 0.300 |
Why?
|
| Phosphotyrosine | 2 | 2012 | 23 | 0.290 |
Why?
|
| Amino Acid Motifs | 6 | 2019 | 152 | 0.290 |
Why?
|
| GTP-Binding Proteins | 2 | 1999 | 80 | 0.290 |
Why?
|
| Escherichia coli | 4 | 2019 | 681 | 0.280 |
Why?
|
| Catalytic Domain | 5 | 2021 | 184 | 0.280 |
Why?
|
| Gene Expression | 3 | 2019 | 808 | 0.270 |
Why?
|
| I-kappa B Kinase | 1 | 2006 | 48 | 0.270 |
Why?
|
| Phospholipids | 4 | 2015 | 79 | 0.260 |
Why?
|
| Allosteric Site | 2 | 2017 | 31 | 0.260 |
Why?
|
| Proteins | 2 | 2001 | 742 | 0.250 |
Why?
|
| Biocatalysis | 3 | 2015 | 46 | 0.250 |
Why?
|
| Carrier Proteins | 2 | 2007 | 709 | 0.250 |
Why?
|
| rab1 GTP-Binding Proteins | 4 | 2014 | 6 | 0.250 |
Why?
|
| Mutagenesis, Site-Directed | 8 | 2004 | 254 | 0.240 |
Why?
|
| Protein Multimerization | 2 | 2019 | 163 | 0.240 |
Why?
|
| Inositol 1,4,5-Trisphosphate | 1 | 2004 | 27 | 0.240 |
Why?
|
| Phosphorylation | 4 | 2020 | 861 | 0.220 |
Why?
|
| Alternative Splicing | 1 | 2004 | 120 | 0.220 |
Why?
|
| Membrane Microdomains | 1 | 2003 | 48 | 0.220 |
Why?
|
| Nuclear Proteins | 2 | 2021 | 759 | 0.210 |
Why?
|
| Genetic Vectors | 3 | 2019 | 813 | 0.210 |
Why?
|
| Protein Structure, Quaternary | 2 | 2003 | 99 | 0.200 |
Why?
|
| Lipid Metabolism | 1 | 2003 | 200 | 0.200 |
Why?
|
| Calcium-Binding Proteins | 1 | 2002 | 84 | 0.190 |
Why?
|
| 3T3-L1 Cells | 5 | 2020 | 83 | 0.190 |
Why?
|
| Saccharomyces cerevisiae | 2 | 2021 | 529 | 0.190 |
Why?
|
| Liposomes | 3 | 2019 | 98 | 0.190 |
Why?
|
| Protein Interaction Domains and Motifs | 2 | 2019 | 82 | 0.190 |
Why?
|
| Helix-Turn-Helix Motifs | 1 | 2001 | 2 | 0.190 |
Why?
|
| DNA Mutational Analysis | 3 | 2007 | 195 | 0.190 |
Why?
|
| Monomeric GTP-Binding Proteins | 1 | 2021 | 39 | 0.180 |
Why?
|
| HeLa Cells | 7 | 2014 | 527 | 0.180 |
Why?
|
| Zinc Fingers | 3 | 2010 | 95 | 0.180 |
Why?
|
| Phosphatidylinositol 3-Kinases | 2 | 2003 | 168 | 0.180 |
Why?
|
| Transducin | 3 | 1996 | 7 | 0.180 |
Why?
|
| Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 | 1 | 2020 | 6 | 0.180 |
Why?
|
| Amino Acid Substitution | 3 | 2010 | 253 | 0.170 |
Why?
|
| Phosphates | 1 | 2020 | 88 | 0.170 |
Why?
|
| Models, Biological | 5 | 2012 | 1138 | 0.160 |
Why?
|
| Evolution, Molecular | 3 | 2007 | 291 | 0.160 |
Why?
|
| Insulin | 3 | 2012 | 687 | 0.160 |
Why?
|
| Conserved Sequence | 3 | 2007 | 171 | 0.160 |
Why?
|
| GTP-Binding Protein alpha Subunits, Gs | 1 | 1998 | 11 | 0.150 |
Why?
|
| Adenylyl Cyclases | 1 | 1998 | 21 | 0.150 |
Why?
|
| Protein Structure, Secondary | 4 | 2004 | 249 | 0.150 |
Why?
|
| Tyrosine | 2 | 2013 | 95 | 0.150 |
Why?
|
| Catalysis | 2 | 2016 | 153 | 0.150 |
Why?
|
| Molecular Dynamics Simulation | 1 | 2017 | 114 | 0.140 |
Why?
|
| Carbon Monoxide | 5 | 1994 | 59 | 0.130 |
Why?
|
| COS Cells | 8 | 2012 | 174 | 0.130 |
Why?
|
| trans-Golgi Network | 1 | 2014 | 7 | 0.120 |
Why?
|
| Mitochondrial Proton-Translocating ATPases | 1 | 2014 | 7 | 0.120 |
Why?
|
| Spectrometry, Fluorescence | 1 | 2015 | 90 | 0.120 |
Why?
|
| Legionnaires' Disease | 1 | 2014 | 8 | 0.120 |
Why?
|
| Caenorhabditis elegans Proteins | 2 | 2010 | 396 | 0.110 |
Why?
|
| Autophagy | 1 | 2016 | 205 | 0.110 |
Why?
|
| Green Fluorescent Proteins | 5 | 2007 | 352 | 0.110 |
Why?
|
| Virulence Factors | 1 | 2014 | 84 | 0.110 |
Why?
|
| Seizures | 1 | 2014 | 117 | 0.110 |
Why?
|
| Caenorhabditis elegans | 3 | 2010 | 617 | 0.110 |
Why?
|
| Cysteine | 2 | 1993 | 107 | 0.110 |
Why?
|
| GTP-Binding Protein alpha Subunits | 1 | 2013 | 7 | 0.110 |
Why?
|
| Hypoparathyroidism | 1 | 2013 | 7 | 0.110 |
Why?
|
| Germ-Line Mutation | 1 | 2013 | 47 | 0.110 |
Why?
|
| Phenylalanine | 2 | 2004 | 25 | 0.100 |
Why?
|
| Cell Movement | 2 | 2016 | 422 | 0.100 |
Why?
|
| Proto-Oncogene Proteins c-akt | 2 | 2012 | 185 | 0.100 |
Why?
|
| Escherichia coli Proteins | 1 | 2015 | 258 | 0.100 |
Why?
|
| Fluorescence Resonance Energy Transfer | 2 | 2010 | 72 | 0.100 |
Why?
|
| Clathrin | 1 | 2012 | 23 | 0.100 |
Why?
|
| Receptors, Transferrin | 1 | 2012 | 35 | 0.100 |
Why?
|
| Aluminum Compounds | 2 | 2006 | 10 | 0.100 |
Why?
|
| Fluorides | 2 | 2006 | 21 | 0.100 |
Why?
|
| rab3A GTP-Binding Protein | 2 | 2001 | 4 | 0.100 |
Why?
|
| rab4 GTP-Binding Proteins | 1 | 2010 | 3 | 0.090 |
Why?
|
| Secretory Pathway | 1 | 2010 | 5 | 0.090 |
Why?
|
| In Vitro Techniques | 2 | 2010 | 475 | 0.090 |
Why?
|
| Transferrin | 2 | 2008 | 67 | 0.090 |
Why?
|
| Drosophila melanogaster | 1 | 2014 | 480 | 0.090 |
Why?
|
| Hypoglycemic Agents | 1 | 2012 | 211 | 0.090 |
Why?
|
| Rats | 3 | 2006 | 1907 | 0.090 |
Why?
|
| Integrins | 1 | 2010 | 108 | 0.080 |
Why?
|
| Cattle | 5 | 1996 | 306 | 0.080 |
Why?
|
| Protons | 1 | 1989 | 60 | 0.080 |
Why?
|
| Microfilament Proteins | 1 | 2010 | 116 | 0.080 |
Why?
|
| Multiprotein Complexes | 1 | 2010 | 148 | 0.080 |
Why?
|
| Drosophila Proteins | 1 | 2014 | 681 | 0.080 |
Why?
|
| Lactose Synthase | 2 | 1985 | 3 | 0.080 |
Why?
|
| Nerve Tissue Proteins | 2 | 2002 | 421 | 0.080 |
Why?
|
| Peptide Fragments | 2 | 2004 | 353 | 0.080 |
Why?
|
| Epidermal Growth Factor | 1 | 2008 | 52 | 0.080 |
Why?
|
| Actins | 1 | 2010 | 259 | 0.080 |
Why?
|
| DNA-Binding Proteins | 2 | 2006 | 1128 | 0.080 |
Why?
|
| Phylogeny | 1 | 2009 | 331 | 0.070 |
Why?
|
| Alanine | 2 | 2001 | 46 | 0.070 |
Why?
|
| Fats | 1 | 2007 | 18 | 0.070 |
Why?
|
| Molecular Conformation | 2 | 2006 | 132 | 0.070 |
Why?
|
| Poly Adenosine Diphosphate Ribose | 1 | 2006 | 3 | 0.070 |
Why?
|
| HEK293 Cells | 3 | 2014 | 571 | 0.070 |
Why?
|
| ADP Ribose Transferases | 1 | 2006 | 62 | 0.070 |
Why?
|
| RNA, Viral | 1 | 2007 | 265 | 0.070 |
Why?
|
| Hepacivirus | 1 | 2007 | 140 | 0.070 |
Why?
|
| Virus Replication | 1 | 2007 | 303 | 0.060 |
Why?
|
| Ligands | 4 | 2003 | 421 | 0.060 |
Why?
|
| Ubiquitin | 1 | 2006 | 95 | 0.060 |
Why?
|
| Lysosomes | 1 | 2006 | 162 | 0.060 |
Why?
|
| Hydrogen Bonding | 1 | 2005 | 125 | 0.060 |
Why?
|
| Dimerization | 2 | 2003 | 146 | 0.060 |
Why?
|
| Models, Genetic | 1 | 2006 | 253 | 0.060 |
Why?
|
| Heme | 3 | 1993 | 27 | 0.060 |
Why?
|
| Glycine | 1 | 2004 | 45 | 0.060 |
Why?
|
| Asparagine | 2 | 2001 | 24 | 0.050 |
Why?
|
| Calmodulin | 1 | 2003 | 19 | 0.050 |
Why?
|
| Membrane Glycoproteins | 2 | 2007 | 669 | 0.050 |
Why?
|
| Mitogen-Activated Protein Kinase Kinases | 1 | 2002 | 52 | 0.050 |
Why?
|
| Synaptotagmins | 1 | 2002 | 6 | 0.050 |
Why?
|
| GTP Phosphohydrolase-Linked Elongation Factors | 1 | 2001 | 1 | 0.050 |
Why?
|
| ortho-Aminobenzoates | 1 | 2001 | 7 | 0.050 |
Why?
|
| Calcium | 2 | 2003 | 552 | 0.050 |
Why?
|
| Protein-Tyrosine Kinases | 1 | 2002 | 113 | 0.050 |
Why?
|
| T-Lymphocytes | 1 | 2006 | 963 | 0.050 |
Why?
|
| Exocytosis | 1 | 2001 | 60 | 0.050 |
Why?
|
| Protein Kinase C | 1 | 2002 | 98 | 0.050 |
Why?
|
| Lipids | 1 | 2003 | 305 | 0.050 |
Why?
|
| Mitogen-Activated Protein Kinases | 1 | 2002 | 201 | 0.050 |
Why?
|
| Aspartic Acid | 1 | 2001 | 29 | 0.050 |
Why?
|
| Tryptophan | 1 | 2001 | 54 | 0.050 |
Why?
|
| Serine | 1 | 2001 | 83 | 0.050 |
Why?
|
| MAP Kinase Signaling System | 1 | 2002 | 201 | 0.050 |
Why?
|
| Nuclear Magnetic Resonance, Biomolecular | 1 | 2001 | 110 | 0.050 |
Why?
|
| src Homology Domains | 1 | 2000 | 21 | 0.040 |
Why?
|
| Biological Transport, Active | 2 | 2012 | 39 | 0.040 |
Why?
|
| Epitopes | 1 | 2001 | 298 | 0.040 |
Why?
|
| Guanylyl Imidodiphosphate | 1 | 1999 | 2 | 0.040 |
Why?
|
| rab3 GTP-Binding Proteins | 1 | 1999 | 2 | 0.040 |
Why?
|
| Cell Line | 3 | 2011 | 2014 | 0.040 |
Why?
|
| Eukaryota | 1 | 2019 | 29 | 0.040 |
Why?
|
| Magnesium | 1 | 1999 | 58 | 0.040 |
Why?
|
| Time Factors | 3 | 2012 | 3567 | 0.040 |
Why?
|
| Base Sequence | 1 | 2001 | 1311 | 0.040 |
Why?
|
| Computer Graphics | 2 | 1994 | 23 | 0.040 |
Why?
|
| Vacuoles | 2 | 2007 | 27 | 0.040 |
Why?
|
| Microscopy, Fluorescence | 3 | 2003 | 397 | 0.030 |
Why?
|
| Golgi Apparatus | 2 | 2007 | 64 | 0.030 |
Why?
|
| Thermodynamics | 2 | 1994 | 194 | 0.030 |
Why?
|
| Nitric Oxide | 2 | 1994 | 144 | 0.030 |
Why?
|
| Adenosine Triphosphate | 1 | 1998 | 287 | 0.030 |
Why?
|
| Spectrophotometry | 2 | 1993 | 31 | 0.030 |
Why?
|
| Lactalbumin | 2 | 1985 | 6 | 0.030 |
Why?
|
| Amino Acids | 2 | 2001 | 140 | 0.030 |
Why?
|
| Water | 2 | 1994 | 295 | 0.030 |
Why?
|
| Rod Cell Outer Segment | 1 | 1994 | 7 | 0.030 |
Why?
|
| Sirtuin 3 | 1 | 2014 | 12 | 0.030 |
Why?
|
| Peptide Elongation Factor Tu | 1 | 1994 | 7 | 0.030 |
Why?
|
| Ceramides | 1 | 2014 | 23 | 0.030 |
Why?
|
| Transcription Factors | 1 | 2002 | 1456 | 0.030 |
Why?
|
| Acetylation | 1 | 2014 | 111 | 0.030 |
Why?
|
| Protein Processing, Post-Translational | 1 | 1996 | 255 | 0.030 |
Why?
|
| Spectrum Analysis | 1 | 1994 | 51 | 0.030 |
Why?
|
| Proto-Oncogene Proteins p21(ras) | 1 | 1994 | 56 | 0.030 |
Why?
|
| Metabolic Networks and Pathways | 1 | 2014 | 72 | 0.030 |
Why?
|
| Mathematics | 1 | 1993 | 28 | 0.030 |
Why?
|
| Genes, Dominant | 1 | 2013 | 55 | 0.030 |
Why?
|
| Genetic Linkage | 1 | 2013 | 101 | 0.030 |
Why?
|
| Receptors, Cell Surface | 1 | 1996 | 438 | 0.030 |
Why?
|
| Glycerol | 1 | 1993 | 30 | 0.030 |
Why?
|
| Exome | 1 | 2013 | 73 | 0.030 |
Why?
|
| Pedigree | 1 | 2013 | 190 | 0.030 |
Why?
|
| Membrane Lipids | 1 | 2012 | 26 | 0.030 |
Why?
|
| 14-3-3 Proteins | 1 | 2012 | 19 | 0.030 |
Why?
|
| Luminescent Proteins | 2 | 2003 | 129 | 0.030 |
Why?
|
| Stress, Physiological | 1 | 2014 | 185 | 0.030 |
Why?
|
| Two-Hybrid System Techniques | 1 | 2012 | 65 | 0.030 |
Why?
|
| Vero Cells | 1 | 2012 | 74 | 0.030 |
Why?
|
| Mutant Proteins | 1 | 2012 | 105 | 0.030 |
Why?
|
| NIH 3T3 Cells | 1 | 2012 | 96 | 0.020 |
Why?
|
| Sequence Analysis, DNA | 1 | 2013 | 396 | 0.020 |
Why?
|
| Cytosol | 2 | 2003 | 167 | 0.020 |
Why?
|
| Cell Extracts | 1 | 2011 | 25 | 0.020 |
Why?
|
| Male | 2 | 2013 | 27478 | 0.020 |
Why?
|
| Neuroblastoma | 1 | 2012 | 85 | 0.020 |
Why?
|
| Genome-Wide Association Study | 1 | 2013 | 324 | 0.020 |
Why?
|
| Transfection | 2 | 2003 | 673 | 0.020 |
Why?
|
| Ribosomal Protein S6 Kinases, 70-kDa | 1 | 2010 | 19 | 0.020 |
Why?
|
| Cytochalasin D | 1 | 2010 | 20 | 0.020 |
Why?
|
| Extracellular Signal-Regulated MAP Kinases | 1 | 2010 | 70 | 0.020 |
Why?
|
| Female | 5 | 2014 | 30797 | 0.020 |
Why?
|
| ErbB Receptors | 1 | 2010 | 111 | 0.020 |
Why?
|
| Milk | 2 | 1985 | 50 | 0.020 |
Why?
|
| Magnetic Resonance Spectroscopy | 1 | 1989 | 292 | 0.020 |
Why?
|
| Guanine Nucleotide Dissociation Inhibitors | 1 | 2007 | 1 | 0.020 |
Why?
|
| Gene Silencing | 1 | 2010 | 377 | 0.020 |
Why?
|
| Hydrogen-Ion Concentration | 1 | 1989 | 427 | 0.020 |
Why?
|
| Chemotaxis | 1 | 2007 | 47 | 0.020 |
Why?
|
| Glucose | 1 | 2010 | 444 | 0.020 |
Why?
|
| Adenosine Diphosphate Ribose | 1 | 2006 | 12 | 0.020 |
Why?
|
| Viral Envelope Proteins | 1 | 2007 | 107 | 0.020 |
Why?
|
| Phosphoric Diester Hydrolases | 1 | 2006 | 17 | 0.020 |
Why?
|
| Structural Homology, Protein | 1 | 2006 | 20 | 0.020 |
Why?
|
| Biological Transport | 1 | 2007 | 287 | 0.020 |
Why?
|
| RNA Interference | 1 | 2010 | 589 | 0.020 |
Why?
|
| Viral Nonstructural Proteins | 1 | 2007 | 92 | 0.020 |
Why?
|
| Neurons | 1 | 2012 | 856 | 0.020 |
Why?
|
| Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | 1 | 2006 | 81 | 0.020 |
Why?
|
| Glucosamine | 1 | 1985 | 31 | 0.020 |
Why?
|
| Host-Pathogen Interactions | 1 | 2007 | 238 | 0.020 |
Why?
|
| Child | 1 | 2014 | 4298 | 0.010 |
Why?
|
| Cell Survival | 1 | 2006 | 553 | 0.010 |
Why?
|
| Photolysis | 2 | 1994 | 16 | 0.010 |
Why?
|
| Sensitivity and Specificity | 1 | 2007 | 1093 | 0.010 |
Why?
|
| Chromatography, Gel | 1 | 2003 | 65 | 0.010 |
Why?
|
| Lipid Bilayers | 1 | 2003 | 49 | 0.010 |
Why?
|
| Cell Line, Tumor | 1 | 2007 | 1369 | 0.010 |
Why?
|
| Gene Expression Regulation | 1 | 2010 | 1536 | 0.010 |
Why?
|
| MEF2 Transcription Factors | 1 | 2002 | 10 | 0.010 |
Why?
|
| MAP Kinase Kinase 3 | 1 | 2002 | 10 | 0.010 |
Why?
|
| Myogenic Regulatory Factors | 1 | 2002 | 12 | 0.010 |
Why?
|
| Sulfonamides | 1 | 2003 | 123 | 0.010 |
Why?
|
| Valine | 2 | 1994 | 30 | 0.010 |
Why?
|
| Cells, Cultured | 1 | 2006 | 2102 | 0.010 |
Why?
|
| p38 Mitogen-Activated Protein Kinases | 1 | 2002 | 125 | 0.010 |
Why?
|
| Dose-Response Relationship, Drug | 1 | 2003 | 810 | 0.010 |
Why?
|
| Plasmids | 1 | 2001 | 280 | 0.010 |
Why?
|
| 3T3 Cells | 1 | 2000 | 108 | 0.010 |
Why?
|
| Retinal Rod Photoreceptor Cells | 1 | 1996 | 21 | 0.010 |
Why?
|
| Guanosine 5'-O-(3-Thiotriphosphate) | 1 | 1994 | 7 | 0.010 |
Why?
|
| Mutagenesis | 1 | 1994 | 129 | 0.010 |
Why?
|
| Spectroscopy, Fourier Transform Infrared | 1 | 1994 | 48 | 0.010 |
Why?
|
| Histidine | 1 | 1994 | 31 | 0.010 |
Why?
|
| Lysine | 1 | 1994 | 75 | 0.010 |
Why?
|
| Spectrophotometry, Infrared | 1 | 1993 | 27 | 0.010 |
Why?
|
| Photochemistry | 1 | 1993 | 23 | 0.010 |
Why?
|
| Solutions | 1 | 1993 | 62 | 0.010 |
Why?
|
| Data Interpretation, Statistical | 1 | 1993 | 196 | 0.010 |
Why?
|
| Temperature | 1 | 1993 | 300 | 0.010 |
Why?
|
| X-Ray Diffraction | 1 | 1990 | 56 | 0.010 |
Why?
|
| Cyanides | 1 | 1989 | 3 | 0.010 |
Why?
|
| Codon | 1 | 1989 | 47 | 0.010 |
Why?
|
| Molecular Structure | 1 | 1990 | 375 | 0.010 |
Why?
|
| Galactosyltransferases | 1 | 1985 | 17 | 0.000 |
Why?
|