Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
---|
Cysteine Synthase | 44 | 2013 | 44 | 6.800 |
Why?
|
Saccharomyces cerevisiae | 31 | 2015 | 172 | 5.810 |
Why?
|
Kinetics | 141 | 2012 | 538 | 4.570 |
Why?
|
Malate Dehydrogenase | 34 | 2008 | 36 | 3.910 |
Why?
|
Saccharopine Dehydrogenases | 14 | 2015 | 28 | 3.750 |
Why?
|
Saccharomyces cerevisiae Proteins | 15 | 2015 | 110 | 3.420 |
Why?
|
Salmonella typhimurium | 28 | 2012 | 68 | 2.990 |
Why?
|
Hydrogen-Ion Concentration | 76 | 2015 | 261 | 2.930 |
Why?
|
Lysine | 22 | 2012 | 71 | 2.840 |
Why?
|
Ascaris suum | 21 | 2008 | 23 | 2.740 |
Why?
|
Phosphogluconate Dehydrogenase | 15 | 2008 | 15 | 2.660 |
Why?
|
NAD | 33 | 2012 | 81 | 2.580 |
Why?
|
Alcohol Oxidoreductases | 14 | 2015 | 34 | 2.430 |
Why?
|
Pyridoxal Phosphate | 22 | 2011 | 24 | 2.430 |
Why?
|
Catalysis | 43 | 2015 | 133 | 2.110 |
Why?
|
Oxo-Acid-Lyases | 8 | 2011 | 16 | 1.990 |
Why?
|
Mutagenesis, Site-Directed | 25 | 2015 | 129 | 1.880 |
Why?
|
Deuterium | 37 | 2012 | 50 | 1.810 |
Why?
|
Models, Molecular | 34 | 2012 | 441 | 1.800 |
Why?
|
Binding Sites | 50 | 2011 | 338 | 1.790 |
Why?
|
Liver | 25 | 2006 | 415 | 1.620 |
Why?
|
Models, Chemical | 22 | 2011 | 88 | 1.610 |
Why?
|
Bacterial Proteins | 11 | 2013 | 474 | 1.590 |
Why?
|
NADP | 17 | 2009 | 38 | 1.580 |
Why?
|
Phosphofructokinase-1 | 17 | 1999 | 17 | 1.290 |
Why?
|
Protein Conformation | 28 | 2015 | 250 | 1.260 |
Why?
|
Substrate Specificity | 32 | 2013 | 149 | 1.190 |
Why?
|
Malates | 14 | 2007 | 16 | 1.160 |
Why?
|
Ascaris | 20 | 2002 | 20 | 1.130 |
Why?
|
Alanine | 13 | 2010 | 40 | 1.060 |
Why?
|
Glutamic Acid | 7 | 2012 | 50 | 1.020 |
Why?
|
Transaminases | 4 | 2009 | 10 | 0.970 |
Why?
|
Acetyltransferases | 8 | 2006 | 36 | 0.970 |
Why?
|
Haemophilus influenzae | 6 | 2012 | 66 | 0.970 |
Why?
|
Recombinant Proteins | 18 | 2012 | 408 | 0.960 |
Why?
|
Catalytic Domain | 14 | 2017 | 77 | 0.920 |
Why?
|
Enzyme Inhibitors | 13 | 2017 | 247 | 0.900 |
Why?
|
Animals | 85 | 2013 | 9962 | 0.880 |
Why?
|
Niacinamide | 3 | 2008 | 12 | 0.880 |
Why?
|
Amino Acid Sequence | 23 | 2010 | 674 | 0.880 |
Why?
|
Cysteine | 15 | 2013 | 67 | 0.860 |
Why?
|
Acid-Base Equilibrium | 4 | 2012 | 10 | 0.860 |
Why?
|
Aspartic Acid | 8 | 2008 | 52 | 0.850 |
Why?
|
Histidine | 9 | 2012 | 50 | 0.850 |
Why?
|
Ketoglutaric Acids | 4 | 2011 | 16 | 0.850 |
Why?
|
Spectrometry, Fluorescence | 18 | 2010 | 63 | 0.840 |
Why?
|
Serine | 18 | 2009 | 48 | 0.830 |
Why?
|
Molecular Sequence Data | 21 | 2010 | 1036 | 0.820 |
Why?
|
Helminth Proteins | 4 | 2008 | 15 | 0.810 |
Why?
|
Amino Acid Substitution | 12 | 2015 | 102 | 0.790 |
Why?
|
Magnetic Resonance Spectroscopy | 13 | 2011 | 176 | 0.750 |
Why?
|
Serine O-Acetyltransferase | 8 | 2012 | 8 | 0.730 |
Why?
|
Pyridines | 5 | 2009 | 99 | 0.730 |
Why?
|
Deuterium Exchange Measurement | 8 | 2015 | 17 | 0.720 |
Why?
|
Protons | 6 | 2007 | 54 | 0.710 |
Why?
|
Enzymes | 6 | 2011 | 22 | 0.700 |
Why?
|
Oxidation-Reduction | 19 | 2011 | 354 | 0.690 |
Why?
|
Circular Dichroism | 17 | 2008 | 43 | 0.650 |
Why?
|
Acetyl Coenzyme A | 8 | 2011 | 18 | 0.640 |
Why?
|
Molecular Structure | 12 | 2011 | 239 | 0.640 |
Why?
|
Spectrophotometry, Ultraviolet | 13 | 2011 | 54 | 0.630 |
Why?
|
Enzyme Activation | 20 | 2010 | 262 | 0.600 |
Why?
|
Magnesium | 11 | 2007 | 40 | 0.600 |
Why?
|
Schiff Bases | 13 | 2010 | 13 | 0.590 |
Why?
|
Hyphomicrobium | 3 | 2009 | 3 | 0.580 |
Why?
|
Carboxy-Lyases | 3 | 2009 | 6 | 0.580 |
Why?
|
Mutation, Missense | 2 | 2015 | 67 | 0.570 |
Why?
|
Isoenzymes | 10 | 2013 | 86 | 0.560 |
Why?
|
Coenzymes | 3 | 2009 | 9 | 0.530 |
Why?
|
gamma-Glutamyltransferase | 5 | 2017 | 18 | 0.520 |
Why?
|
Diphosphates | 7 | 2008 | 12 | 0.510 |
Why?
|
Protein Binding | 14 | 2013 | 631 | 0.500 |
Why?
|
Protein Kinases | 8 | 2010 | 143 | 0.490 |
Why?
|
Sheep | 10 | 2006 | 97 | 0.490 |
Why?
|
Mathematics | 27 | 2004 | 42 | 0.490 |
Why?
|
Sulfonamides | 4 | 2013 | 69 | 0.480 |
Why?
|
Phosphates | 4 | 2009 | 30 | 0.470 |
Why?
|
Metals | 3 | 2009 | 39 | 0.470 |
Why?
|
Tyrosine | 3 | 2009 | 90 | 0.460 |
Why?
|
Solvents | 10 | 2009 | 38 | 0.460 |
Why?
|
Gluconates | 3 | 2006 | 11 | 0.460 |
Why?
|
Protein Structure, Secondary | 10 | 2017 | 130 | 0.450 |
Why?
|
Candida | 6 | 1998 | 19 | 0.440 |
Why?
|
Nursing Staff | 2 | 2013 | 7 | 0.430 |
Why?
|
Fructosediphosphates | 8 | 2006 | 8 | 0.420 |
Why?
|
Adenosine Diphosphate | 6 | 2010 | 27 | 0.400 |
Why?
|
Mutation | 6 | 2010 | 820 | 0.400 |
Why?
|
Enzyme Stability | 9 | 2012 | 30 | 0.390 |
Why?
|
Quinones | 2 | 2009 | 23 | 0.390 |
Why?
|
Thermus thermophilus | 1 | 2011 | 7 | 0.380 |
Why?
|
Spectrophotometry | 12 | 2007 | 34 | 0.380 |
Why?
|
Fumarates | 4 | 2003 | 16 | 0.370 |
Why?
|
Needs Assessment | 1 | 2011 | 53 | 0.370 |
Why?
|
Tritium | 9 | 2000 | 17 | 0.370 |
Why?
|
Pseudomonas putida | 3 | 2006 | 3 | 0.370 |
Why?
|
Propionibacterium | 6 | 1994 | 12 | 0.360 |
Why?
|
Quality Improvement | 1 | 2011 | 112 | 0.350 |
Why?
|
Mass Screening | 1 | 2011 | 141 | 0.350 |
Why?
|
Oxidoreductases | 5 | 1998 | 56 | 0.350 |
Why?
|
Base Sequence | 6 | 2012 | 573 | 0.350 |
Why?
|
Adenosine Triphosphate | 12 | 2006 | 115 | 0.340 |
Why?
|
Nuclear Magnetic Resonance, Biomolecular | 5 | 2010 | 55 | 0.340 |
Why?
|
Biochemistry | 1 | 2009 | 10 | 0.340 |
Why?
|
Structure-Activity Relationship | 14 | 2011 | 200 | 0.330 |
Why?
|
Crystallography, X-Ray | 12 | 2017 | 214 | 0.330 |
Why?
|
Hydrogen Bonding | 6 | 2008 | 39 | 0.330 |
Why?
|
HIV Infections | 1 | 2011 | 146 | 0.330 |
Why?
|
Dihydrouracil Dehydrogenase (NADP) | 6 | 2004 | 9 | 0.330 |
Why?
|
Protein Structure, Tertiary | 7 | 2008 | 283 | 0.330 |
Why?
|
Diamines | 1 | 2009 | 5 | 0.330 |
Why?
|
Nucleotides | 1 | 2009 | 20 | 0.330 |
Why?
|
Periodicals as Topic | 1 | 2009 | 50 | 0.320 |
Why?
|
Career Mobility | 1 | 2008 | 7 | 0.320 |
Why?
|
Health Facility Environment | 1 | 2008 | 4 | 0.320 |
Why?
|
Tryptophan Synthase | 3 | 2007 | 4 | 0.320 |
Why?
|
Potassium | 1 | 2008 | 41 | 0.310 |
Why?
|
Job Satisfaction | 1 | 2008 | 24 | 0.310 |
Why?
|
Ambulatory Care | 1 | 2008 | 58 | 0.310 |
Why?
|
Apoenzymes | 3 | 2011 | 6 | 0.310 |
Why?
|
Binding, Competitive | 12 | 2013 | 62 | 0.310 |
Why?
|
Escherichia coli | 7 | 2003 | 328 | 0.300 |
Why?
|
Drug Resistance, Bacterial | 1 | 2008 | 39 | 0.300 |
Why?
|
Fructosephosphates | 8 | 2008 | 8 | 0.300 |
Why?
|
Accidental Falls | 1 | 2007 | 31 | 0.290 |
Why?
|
Attitude of Health Personnel | 1 | 2008 | 139 | 0.290 |
Why?
|
Cardiovascular Diseases | 1 | 2011 | 346 | 0.290 |
Why?
|
Manganese | 6 | 2006 | 22 | 0.290 |
Why?
|
Carbon Isotopes | 9 | 2002 | 43 | 0.280 |
Why?
|
Models, Theoretical | 9 | 2013 | 129 | 0.280 |
Why?
|
DNA Primers | 4 | 2012 | 143 | 0.270 |
Why?
|
Bacillus anthracis | 1 | 2008 | 146 | 0.270 |
Why?
|
Phosphofructokinases | 1 | 2006 | 1 | 0.270 |
Why?
|
2-Aminoadipic Acid | 1 | 2006 | 2 | 0.260 |
Why?
|
Malonates | 1 | 2005 | 1 | 0.260 |
Why?
|
Blood Glucose | 1 | 2007 | 300 | 0.260 |
Why?
|
Sulfur | 2 | 2010 | 33 | 0.260 |
Why?
|
Methionine | 2 | 2005 | 37 | 0.260 |
Why?
|
Fungi | 1 | 2006 | 50 | 0.250 |
Why?
|
Breast Neoplasms | 1 | 2011 | 441 | 0.250 |
Why?
|
Arginine | 4 | 2007 | 39 | 0.250 |
Why?
|
Colorado | 3 | 2011 | 47 | 0.250 |
Why?
|
Oxygen | 1 | 2006 | 218 | 0.250 |
Why?
|
Diabetes Mellitus | 1 | 2007 | 207 | 0.250 |
Why?
|
Alcohols | 1 | 2005 | 11 | 0.240 |
Why?
|
Allosteric Regulation | 9 | 2005 | 18 | 0.240 |
Why?
|
alpha-Cyclodextrins | 1 | 2004 | 3 | 0.240 |
Why?
|
Oligopeptides | 5 | 2010 | 95 | 0.240 |
Why?
|
Lyases | 5 | 2010 | 5 | 0.240 |
Why?
|
Anions | 2 | 2001 | 15 | 0.240 |
Why?
|
Pyruvates | 5 | 2009 | 11 | 0.240 |
Why?
|
Isotope Labeling | 8 | 1988 | 30 | 0.230 |
Why?
|
Chlorides | 2 | 2001 | 13 | 0.230 |
Why?
|
Enterobacteriaceae | 3 | 2000 | 8 | 0.230 |
Why?
|
Ligands | 5 | 2007 | 168 | 0.230 |
Why?
|
Iron | 2 | 2004 | 103 | 0.230 |
Why?
|
Amidohydrolases | 3 | 2005 | 11 | 0.220 |
Why?
|
Diethyl Pyrocarbonate | 4 | 2006 | 4 | 0.220 |
Why?
|
Cyclic AMP | 3 | 1992 | 80 | 0.220 |
Why?
|
Humans | 23 | 2017 | 26842 | 0.220 |
Why?
|
Plants | 5 | 2010 | 64 | 0.210 |
Why?
|
Sulfhydryl Compounds | 5 | 2011 | 29 | 0.210 |
Why?
|
Thiadiazoles | 3 | 2013 | 3 | 0.210 |
Why?
|
Thermodynamics | 4 | 2011 | 86 | 0.200 |
Why?
|
Sequence Homology, Amino Acid | 4 | 2008 | 130 | 0.200 |
Why?
|
Cations, Divalent | 5 | 2005 | 14 | 0.200 |
Why?
|
Sequence Alignment | 3 | 2009 | 110 | 0.200 |
Why?
|
Cattle | 13 | 2005 | 383 | 0.190 |
Why?
|
Glutamine | 3 | 2010 | 32 | 0.190 |
Why?
|
Dimerization | 5 | 2006 | 75 | 0.190 |
Why?
|
Oxaloacetates | 4 | 2004 | 5 | 0.190 |
Why?
|
Phosphoadenosine Phosphosulfate | 3 | 2010 | 3 | 0.190 |
Why?
|
Aspartate Ammonia-Lyase | 2 | 1995 | 2 | 0.190 |
Why?
|
Viscosity | 3 | 2012 | 37 | 0.190 |
Why?
|
Drug Design | 2 | 2013 | 62 | 0.190 |
Why?
|
Models, Biological | 6 | 2013 | 446 | 0.190 |
Why?
|
Isotopes | 2 | 1998 | 9 | 0.180 |
Why?
|
Glycine | 3 | 2011 | 31 | 0.180 |
Why?
|
Arylsulfotransferase | 2 | 2010 | 2 | 0.180 |
Why?
|
Swine | 8 | 2009 | 220 | 0.180 |
Why?
|
L-Serine Dehydratase | 1 | 1999 | 1 | 0.170 |
Why?
|
Oxaloacetic Acid | 3 | 2007 | 8 | 0.170 |
Why?
|
Allosteric Site | 5 | 2003 | 11 | 0.170 |
Why?
|
Decarboxylation | 5 | 2002 | 5 | 0.170 |
Why?
|
Plants, Medicinal | 4 | 1994 | 17 | 0.170 |
Why?
|
Fabaceae | 4 | 1994 | 14 | 0.170 |
Why?
|
Recombinant Fusion Proteins | 3 | 2010 | 228 | 0.170 |
Why?
|
Formates | 4 | 2000 | 20 | 0.170 |
Why?
|
Protein Structure, Quaternary | 3 | 2010 | 26 | 0.170 |
Why?
|
2-Aminoadipate Transaminase | 2 | 2011 | 3 | 0.160 |
Why?
|
Conserved Sequence | 3 | 2008 | 54 | 0.160 |
Why?
|
Imines | 3 | 2011 | 21 | 0.160 |
Why?
|
Bacteria | 3 | 2013 | 263 | 0.160 |
Why?
|
Alcohol Dehydrogenase | 3 | 1998 | 6 | 0.160 |
Why?
|
Oxidants | 1 | 1998 | 30 | 0.160 |
Why?
|
Hydrogen | 1 | 1998 | 56 | 0.150 |
Why?
|
Cations, Monovalent | 2 | 2008 | 4 | 0.150 |
Why?
|
Microspectrophotometry | 1 | 1998 | 1 | 0.150 |
Why?
|
Acetylation | 3 | 2005 | 36 | 0.150 |
Why?
|
Phosphorylation | 9 | 2009 | 560 | 0.150 |
Why?
|
Diazooxonorleucine | 1 | 2017 | 1 | 0.140 |
Why?
|
Adenosine Monophosphate | 4 | 1999 | 20 | 0.140 |
Why?
|
Tricarboxylic Acids | 2 | 2007 | 5 | 0.140 |
Why?
|
Sulfides | 6 | 2001 | 38 | 0.140 |
Why?
|
Glutamate Dehydrogenase | 3 | 1988 | 4 | 0.140 |
Why?
|
Surveys and Questionnaires | 3 | 2013 | 918 | 0.140 |
Why?
|
Middle Aged | 4 | 2013 | 6818 | 0.130 |
Why?
|
Multienzyme Complexes | 2 | 2010 | 29 | 0.130 |
Why?
|
Carboxylic Acids | 2 | 2000 | 17 | 0.130 |
Why?
|
Phosphorus Isotopes | 2 | 2011 | 6 | 0.130 |
Why?
|
Phosphoric Monoester Hydrolases | 3 | 2000 | 48 | 0.120 |
Why?
|
Phenylalanine | 2 | 2005 | 23 | 0.120 |
Why?
|
Sodium | 2 | 2005 | 47 | 0.120 |
Why?
|
Thiocyanates | 2 | 1993 | 19 | 0.120 |
Why?
|
Fungal Proteins | 3 | 2004 | 72 | 0.120 |
Why?
|
Carbon Radioisotopes | 7 | 2008 | 19 | 0.120 |
Why?
|
L-Lactate Dehydrogenase | 2 | 1993 | 19 | 0.120 |
Why?
|
Biocatalysis | 2 | 2012 | 22 | 0.120 |
Why?
|
Metals, Rare Earth | 1 | 1994 | 1 | 0.120 |
Why?
|
Education, Nursing, Graduate | 1 | 2013 | 4 | 0.110 |
Why?
|
Molecular Weight | 4 | 2005 | 118 | 0.110 |
Why?
|
Students, Nursing | 1 | 2013 | 13 | 0.110 |
Why?
|
Phosphopeptides | 1 | 1993 | 11 | 0.110 |
Why?
|
Hydro-Lyases | 2 | 2006 | 8 | 0.110 |
Why?
|
Sulfates | 3 | 2008 | 86 | 0.110 |
Why?
|
Protein Denaturation | 2 | 2011 | 28 | 0.110 |
Why?
|
Nitrobenzenes | 2 | 2010 | 4 | 0.110 |
Why?
|
Monitoring, Physiologic | 1 | 2013 | 54 | 0.110 |
Why?
|
Muscles | 3 | 1996 | 70 | 0.100 |
Why?
|
Point Mutation | 2 | 2011 | 60 | 0.100 |
Why?
|
Hydroxylamine | 3 | 2009 | 9 | 0.100 |
Why?
|
Disulfides | 4 | 2010 | 33 | 0.100 |
Why?
|
Isomerism | 3 | 1999 | 12 | 0.100 |
Why?
|
Acetates | 3 | 1999 | 44 | 0.100 |
Why?
|
Intracellular Signaling Peptides and Proteins | 3 | 2010 | 276 | 0.100 |
Why?
|
Stereoisomerism | 5 | 2000 | 45 | 0.100 |
Why?
|
Blood Pressure | 1 | 2013 | 351 | 0.100 |
Why?
|
DNA, Fungal | 1 | 2011 | 6 | 0.100 |
Why?
|
Aged | 3 | 2013 | 5166 | 0.100 |
Why?
|
Fluorescence | 3 | 2003 | 48 | 0.100 |
Why?
|
Hypercholesterolemia | 1 | 2011 | 17 | 0.100 |
Why?
|
Carboxypeptidase B2 | 1 | 2011 | 1 | 0.090 |
Why?
|
Plasminogen | 1 | 2011 | 8 | 0.090 |
Why?
|
Enzyme Assays | 1 | 2011 | 6 | 0.090 |
Why?
|
Fibrin | 1 | 2011 | 17 | 0.090 |
Why?
|
Fibrinolysis | 1 | 2011 | 21 | 0.090 |
Why?
|
Fibrinolysin | 1 | 2011 | 15 | 0.090 |
Why?
|
Pyruvic Acid | 4 | 2000 | 15 | 0.090 |
Why?
|
Female | 5 | 2013 | 14462 | 0.090 |
Why?
|
Oncology Nursing | 1 | 2011 | 9 | 0.090 |
Why?
|
Adult | 3 | 2013 | 7382 | 0.090 |
Why?
|
Radioisotope Dilution Technique | 6 | 1990 | 14 | 0.090 |
Why?
|
Life Style | 1 | 2011 | 83 | 0.090 |
Why?
|
Patient Education as Topic | 1 | 2011 | 87 | 0.090 |
Why?
|
Amino Acid Oxidoreductases | 2 | 1988 | 4 | 0.090 |
Why?
|
Acrylates | 1 | 2010 | 2 | 0.090 |
Why?
|
Mitochondria | 5 | 2002 | 333 | 0.090 |
Why?
|
Computer Simulation | 2 | 2010 | 221 | 0.090 |
Why?
|
Smoking Prevention | 1 | 2011 | 87 | 0.090 |
Why?
|
Quality of Health Care | 1 | 2011 | 77 | 0.090 |
Why?
|
Patient Satisfaction | 1 | 2011 | 89 | 0.090 |
Why?
|
Chromatography, High Pressure Liquid | 3 | 2004 | 128 | 0.090 |
Why?
|
Comorbidity | 1 | 2011 | 252 | 0.090 |
Why?
|
Models, Structural | 2 | 2005 | 13 | 0.090 |
Why?
|
Cytosol | 2 | 2005 | 47 | 0.090 |
Why?
|
Biopsy | 1 | 2011 | 199 | 0.090 |
Why?
|
Amidines | 1 | 2010 | 8 | 0.090 |
Why?
|
Hydrolases | 1 | 2010 | 11 | 0.090 |
Why?
|
Health Services Accessibility | 1 | 2011 | 90 | 0.090 |
Why?
|
Chickens | 4 | 1994 | 59 | 0.080 |
Why?
|
Osmosis | 1 | 2009 | 7 | 0.080 |
Why?
|
Oxalates | 1 | 1989 | 3 | 0.080 |
Why?
|
Cloning, Molecular | 4 | 2011 | 205 | 0.080 |
Why?
|
Mitogen-Activated Protein Kinases | 1 | 2009 | 83 | 0.080 |
Why?
|
Dose-Response Relationship, Drug | 3 | 2011 | 586 | 0.080 |
Why?
|
Tryptophan | 4 | 2003 | 39 | 0.080 |
Why?
|
Anti-Bacterial Agents | 1 | 2013 | 496 | 0.080 |
Why?
|
In Vitro Techniques | 5 | 2010 | 238 | 0.080 |
Why?
|
Risk Assessment | 1 | 2011 | 586 | 0.080 |
Why?
|
Nursing Evaluation Research | 1 | 2008 | 7 | 0.080 |
Why?
|
Salaries and Fringe Benefits | 1 | 2008 | 6 | 0.080 |
Why?
|
Health Maintenance Organizations | 1 | 2008 | 9 | 0.080 |
Why?
|
Nursing Methodology Research | 1 | 2008 | 14 | 0.080 |
Why?
|
Education, Nursing, Continuing | 1 | 2008 | 7 | 0.080 |
Why?
|
Total Quality Management | 1 | 2008 | 11 | 0.080 |
Why?
|
Nurse's Role | 1 | 2008 | 17 | 0.080 |
Why?
|
Sulfotransferases | 1 | 2008 | 8 | 0.080 |
Why?
|
Professional Competence | 1 | 2008 | 36 | 0.080 |
Why?
|
Glyoxylates | 1 | 1988 | 1 | 0.080 |
Why?
|
Dihydropteroate Synthase | 1 | 2008 | 1 | 0.080 |
Why?
|
4-Aminobenzoic Acid | 1 | 2008 | 1 | 0.080 |
Why?
|
Pterins | 1 | 2008 | 1 | 0.080 |
Why?
|
Triose-Phosphate Isomerase | 1 | 2008 | 1 | 0.080 |
Why?
|
Magnesium Compounds | 1 | 2008 | 2 | 0.080 |
Why?
|
Phosphoric Acids | 1 | 2008 | 2 | 0.080 |
Why?
|
Glycerolphosphate Dehydrogenase | 1 | 2008 | 2 | 0.080 |
Why?
|
Fructose-Bisphosphate Aldolase | 1 | 2008 | 4 | 0.080 |
Why?
|
Leadership | 1 | 2008 | 49 | 0.080 |
Why?
|
Probability | 1 | 2008 | 75 | 0.080 |
Why?
|
Phosphotransferases (Alcohol Group Acceptor) | 2 | 1999 | 27 | 0.080 |
Why?
|
Male | 6 | 2013 | 12871 | 0.080 |
Why?
|
Amino Acids | 3 | 1999 | 80 | 0.080 |
Why?
|
Phosphotransferases | 1 | 2008 | 15 | 0.080 |
Why?
|
Benzoates | 1 | 1988 | 30 | 0.080 |
Why?
|
Coenzyme A | 2 | 2006 | 10 | 0.070 |
Why?
|
Program Evaluation | 1 | 2008 | 162 | 0.070 |
Why?
|
Frail Elderly | 1 | 2007 | 15 | 0.070 |
Why?
|
Analysis of Variance | 1 | 2008 | 388 | 0.070 |
Why?
|
Hydrophobic and Hydrophilic Interactions | 1 | 2007 | 43 | 0.070 |
Why?
|
Protein Subunits | 1 | 2007 | 40 | 0.070 |
Why?
|
Isocitrates | 1 | 2007 | 3 | 0.070 |
Why?
|
Metabolic Networks and Pathways | 1 | 2007 | 46 | 0.070 |
Why?
|
Asparagine | 1 | 2006 | 7 | 0.070 |
Why?
|
Hexosediphosphates | 1 | 1986 | 1 | 0.070 |
Why?
|
Sugar Phosphates | 1 | 1986 | 1 | 0.070 |
Why?
|
Motivation | 1 | 2008 | 207 | 0.070 |
Why?
|
Glutathione | 3 | 2013 | 68 | 0.070 |
Why?
|
Glycosides | 1 | 2006 | 8 | 0.070 |
Why?
|
Threonine | 1 | 2006 | 21 | 0.070 |
Why?
|
Calorimetry | 1 | 2006 | 12 | 0.070 |
Why?
|
Electrophoresis, Polyacrylamide Gel | 2 | 2004 | 165 | 0.070 |
Why?
|
Logistic Models | 1 | 2007 | 397 | 0.070 |
Why?
|
Molecular Probes | 2 | 1996 | 13 | 0.070 |
Why?
|
Crystallization | 2 | 1998 | 47 | 0.060 |
Why?
|
Aspartate Aminotransferases | 2 | 1999 | 20 | 0.060 |
Why?
|
Rats | 7 | 2009 | 1545 | 0.060 |
Why?
|
Case-Control Studies | 1 | 2007 | 702 | 0.060 |
Why?
|
Acyl Coenzyme A | 1 | 2005 | 12 | 0.060 |
Why?
|
Guanosine Triphosphate | 2 | 1982 | 29 | 0.060 |
Why?
|
Feedback, Physiological | 1 | 2005 | 9 | 0.060 |
Why?
|
Myocardium | 3 | 1996 | 171 | 0.060 |
Why?
|
Sulfhydryl Reagents | 1 | 1984 | 3 | 0.060 |
Why?
|
Ammonia-Lyases | 1 | 1984 | 1 | 0.060 |
Why?
|
Cyclodextrins | 1 | 2004 | 4 | 0.060 |
Why?
|
Electron-Transferring Flavoproteins | 1 | 2004 | 1 | 0.060 |
Why?
|
Testis | 3 | 2000 | 39 | 0.060 |
Why?
|
Glycosylphosphatidylinositols | 1 | 2004 | 8 | 0.060 |
Why?
|
Transglutaminases | 1 | 2004 | 8 | 0.060 |
Why?
|
Biotin | 1 | 2004 | 25 | 0.060 |
Why?
|
Computers | 4 | 1990 | 29 | 0.060 |
Why?
|
2,6-Dichloroindophenol | 1 | 2004 | 2 | 0.060 |
Why?
|
Protein Renaturation | 1 | 2004 | 4 | 0.060 |
Why?
|
Candida albicans | 1 | 2004 | 44 | 0.060 |
Why?
|
Young Adult | 1 | 2011 | 2582 | 0.060 |
Why?
|
Time Factors | 4 | 2010 | 1562 | 0.060 |
Why?
|
Molecular Chaperones | 1 | 2004 | 49 | 0.060 |
Why?
|
Macromolecular Substances | 3 | 1993 | 52 | 0.060 |
Why?
|
Signal Transduction | 1 | 2010 | 1344 | 0.060 |
Why?
|
Pyrimidines | 1 | 2004 | 121 | 0.060 |
Why?
|
Restriction Mapping | 2 | 2005 | 20 | 0.050 |
Why?
|
Dihydroorotase | 1 | 2003 | 1 | 0.050 |
Why?
|
Membrane Glycoproteins | 1 | 2004 | 143 | 0.050 |
Why?
|
Tartrates | 1 | 2002 | 2 | 0.050 |
Why?
|
Horses | 3 | 1994 | 34 | 0.050 |
Why?
|
Glucosephosphate Dehydrogenase | 3 | 1998 | 5 | 0.050 |
Why?
|
Evolution, Molecular | 1 | 2003 | 80 | 0.050 |
Why?
|
Dialysis | 2 | 1995 | 4 | 0.050 |
Why?
|
Risk Factors | 1 | 2007 | 2010 | 0.050 |
Why?
|
Sodium Azide | 2 | 2000 | 2 | 0.050 |
Why?
|
Spectrum Analysis | 1 | 2002 | 29 | 0.050 |
Why?
|
Genes, Bacterial | 1 | 2002 | 106 | 0.050 |
Why?
|
Norleucine | 1 | 2001 | 1 | 0.050 |
Why?
|
Nitrogen Isotopes | 4 | 1988 | 19 | 0.050 |
Why?
|
Creatine Kinase | 1 | 1981 | 13 | 0.050 |
Why?
|
DNA-Binding Proteins | 1 | 2005 | 482 | 0.050 |
Why?
|
Drug Evaluation, Preclinical | 2 | 2013 | 57 | 0.050 |
Why?
|
Retrospective Studies | 1 | 2007 | 2432 | 0.050 |
Why?
|
Hydrolysis | 2 | 2011 | 58 | 0.040 |
Why?
|
Phenol | 2 | 2010 | 7 | 0.040 |
Why?
|
Electron Spin Resonance Spectroscopy | 2 | 1997 | 35 | 0.040 |
Why?
|
Genetic Vectors | 1 | 2000 | 107 | 0.040 |
Why?
|
Valine | 1 | 1999 | 12 | 0.040 |
Why?
|
Phosphofructokinase-2 | 4 | 2000 | 11 | 0.040 |
Why?
|
Fluorometry | 1 | 1999 | 7 | 0.040 |
Why?
|
Consensus Sequence | 1 | 1998 | 17 | 0.040 |
Why?
|
Electron Transport | 1 | 1998 | 29 | 0.040 |
Why?
|
Chromatography, Thin Layer | 1 | 1998 | 18 | 0.040 |
Why?
|
Phosphorus Radioisotopes | 2 | 1988 | 6 | 0.040 |
Why?
|
Mutagenesis, Insertional | 1 | 1998 | 37 | 0.040 |
Why?
|
Organic Chemistry Phenomena | 1 | 1998 | 1 | 0.040 |
Why?
|
Formate Dehydrogenases | 1 | 1998 | 5 | 0.040 |
Why?
|
Chemistry, Organic | 1 | 1998 | 4 | 0.040 |
Why?
|
Fluorescence Polarization | 1 | 1997 | 8 | 0.040 |
Why?
|
Chemical Phenomena | 3 | 1987 | 21 | 0.040 |
Why?
|
Rabbits | 2 | 1993 | 272 | 0.040 |
Why?
|
Uracil | 2 | 1997 | 10 | 0.040 |
Why?
|
Genes, Helminth | 1 | 1997 | 9 | 0.040 |
Why?
|
Chromatography, Liquid | 1 | 1997 | 73 | 0.040 |
Why?
|
Hydroxylamines | 2 | 1987 | 6 | 0.030 |
Why?
|
Alcaligenes | 1 | 1996 | 1 | 0.030 |
Why?
|
Chemistry | 2 | 1987 | 10 | 0.030 |
Why?
|
Spin Labels | 1 | 1996 | 19 | 0.030 |
Why?
|
Energy Transfer | 1 | 1996 | 7 | 0.030 |
Why?
|
Solutions | 1 | 1996 | 31 | 0.030 |
Why?
|
Gene Expression | 1 | 1998 | 406 | 0.030 |
Why?
|
Luminescent Measurements | 1 | 1996 | 30 | 0.030 |
Why?
|
Cold Temperature | 1 | 1996 | 34 | 0.030 |
Why?
|
Pyridoxal | 1 | 1995 | 1 | 0.030 |
Why?
|
Guanidine | 1 | 1995 | 3 | 0.030 |
Why?
|
Guanidines | 1 | 1995 | 6 | 0.030 |
Why?
|
Cyclic AMP-Dependent Protein Kinases | 1 | 1996 | 33 | 0.030 |
Why?
|
Poly Adenosine Diphosphate Ribose | 1 | 1995 | 1 | 0.030 |
Why?
|
Titrimetry | 1 | 1995 | 6 | 0.030 |
Why?
|
Nitrobenzoates | 1 | 1995 | 7 | 0.030 |
Why?
|
Poly(ADP-ribose) Polymerases | 1 | 1995 | 22 | 0.030 |
Why?
|
Succinates | 1 | 1995 | 9 | 0.030 |
Why?
|
Succinic Acid | 1 | 1995 | 10 | 0.030 |
Why?
|
Chromatography, Agarose | 2 | 1996 | 3 | 0.030 |
Why?
|
Oxygen Isotopes | 2 | 1988 | 8 | 0.030 |
Why?
|
Bacillus subtilis | 2 | 1988 | 23 | 0.030 |
Why?
|
Species Specificity | 2 | 1986 | 186 | 0.030 |
Why?
|
Tartronates | 2 | 2003 | 2 | 0.030 |
Why?
|
Cobalt | 1 | 1994 | 18 | 0.030 |
Why?
|
Chromatography, Ion Exchange | 1 | 1993 | 13 | 0.030 |
Why?
|
Regression Analysis | 1 | 1994 | 209 | 0.030 |
Why?
|
beta-Alanine | 1 | 1993 | 12 | 0.030 |
Why?
|
X-Ray Diffraction | 1 | 1993 | 41 | 0.030 |
Why?
|
Ethanol | 2 | 1993 | 118 | 0.030 |
Why?
|
NIH 3T3 Cells | 1 | 2013 | 44 | 0.030 |
Why?
|
Potassium Chloride | 1 | 1992 | 10 | 0.030 |
Why?
|
Piperidones | 1 | 1993 | 32 | 0.030 |
Why?
|
Zinc | 1 | 1993 | 57 | 0.030 |
Why?
|
Mutant Proteins | 1 | 2012 | 25 | 0.020 |
Why?
|
Genes, Fungal | 1 | 2011 | 7 | 0.020 |
Why?
|
Protein Kinase Inhibitors | 1 | 1992 | 143 | 0.020 |
Why?
|
Cadmium | 1 | 1991 | 14 | 0.020 |
Why?
|
Leukotriene C4 | 1 | 2011 | 2 | 0.020 |
Why?
|
Cyclohexanols | 2 | 1981 | 5 | 0.020 |
Why?
|
Cyclohexanones | 2 | 1981 | 4 | 0.020 |
Why?
|
Dipeptidases | 1 | 2011 | 5 | 0.020 |
Why?
|
Naphthols | 1 | 2010 | 6 | 0.020 |
Why?
|
DNA | 1 | 1993 | 365 | 0.020 |
Why?
|
Glycoside Hydrolases | 2 | 2004 | 4 | 0.020 |
Why?
|
Isocitrate Dehydrogenase | 2 | 1981 | 20 | 0.020 |
Why?
|
Alanine Dehydrogenase | 2 | 1988 | 2 | 0.020 |
Why?
|
Electrodes | 1 | 1990 | 71 | 0.020 |
Why?
|
Cells, Cultured | 1 | 2013 | 970 | 0.020 |
Why?
|
Protein-Arginine Deiminases | 1 | 2010 | 4 | 0.020 |
Why?
|
Peptides | 1 | 2012 | 280 | 0.020 |
Why?
|
Acids | 1 | 2010 | 16 | 0.020 |
Why?
|
Glycerol | 1 | 2009 | 16 | 0.020 |
Why?
|
Half-Life | 1 | 2009 | 32 | 0.020 |
Why?
|
Drug Combinations | 1 | 2009 | 50 | 0.020 |
Why?
|
Software | 1 | 1990 | 121 | 0.020 |
Why?
|
Sodium Chloride | 1 | 2009 | 65 | 0.020 |
Why?
|
Haplorhini | 1 | 2009 | 15 | 0.020 |
Why?
|
Combinatorial Chemistry Techniques | 1 | 2009 | 11 | 0.020 |
Why?
|
MAP Kinase Signaling System | 1 | 2009 | 93 | 0.020 |
Why?
|
Stress, Physiological | 1 | 2009 | 90 | 0.020 |
Why?
|
Peptide Fragments | 2 | 2005 | 197 | 0.020 |
Why?
|
Arthritis, Rheumatoid | 1 | 2010 | 132 | 0.020 |
Why?
|
Computational Biology | 1 | 2010 | 150 | 0.020 |
Why?
|
Glucose-6-Phosphate Isomerase | 1 | 1988 | 4 | 0.020 |
Why?
|
Mandelic Acids | 1 | 1988 | 2 | 0.020 |
Why?
|
Carbohydrate Dehydrogenases | 1 | 1988 | 1 | 0.020 |
Why?
|
Sugar Alcohol Dehydrogenases | 1 | 1988 | 2 | 0.020 |
Why?
|
Indicators and Reagents | 1 | 1988 | 26 | 0.020 |
Why?
|
Pseudomonas | 1 | 1988 | 13 | 0.020 |
Why?
|
Aldehyde Reductase | 1 | 1988 | 7 | 0.020 |
Why?
|
Nucleoside Deaminases | 1 | 1987 | 1 | 0.020 |
Why?
|
Adenosine Deaminase | 1 | 1987 | 5 | 0.020 |
Why?
|
Borates | 1 | 1987 | 1 | 0.020 |
Why?
|
Diacetyl | 1 | 1987 | 1 | 0.020 |
Why?
|
Placenta | 1 | 1988 | 74 | 0.020 |
Why?
|
Cell Line | 1 | 2009 | 672 | 0.020 |
Why?
|
Mice | 2 | 2013 | 4406 | 0.020 |
Why?
|
Carbohydrates | 1 | 1986 | 15 | 0.020 |
Why?
|
Glutathione Transferase | 1 | 2005 | 30 | 0.020 |
Why?
|
Algorithms | 1 | 1988 | 419 | 0.020 |
Why?
|
Ethylmaleimide | 1 | 1984 | 6 | 0.020 |
Why?
|
Dithionitrobenzoic Acid | 1 | 1984 | 3 | 0.020 |
Why?
|
Ammonia | 1 | 1984 | 18 | 0.020 |
Why?
|
Entamoeba histolytica | 1 | 1984 | 2 | 0.020 |
Why?
|
Streptavidin | 1 | 2004 | 11 | 0.010 |
Why?
|
Biophysics | 1 | 2004 | 14 | 0.010 |
Why?
|
Subcellular Fractions | 1 | 2004 | 19 | 0.010 |
Why?
|
Pichia | 1 | 2004 | 5 | 0.010 |
Why?
|
Biophysical Phenomena | 1 | 2004 | 9 | 0.010 |
Why?
|
Amines | 1 | 2004 | 13 | 0.010 |
Why?
|
Precipitin Tests | 1 | 2004 | 47 | 0.010 |
Why?
|
Proline | 1 | 2004 | 11 | 0.010 |
Why?
|
Open Reading Frames | 1 | 2004 | 38 | 0.010 |
Why?
|
GTP-Binding Proteins | 1 | 2004 | 43 | 0.010 |
Why?
|
Guinea Pigs | 1 | 2004 | 73 | 0.010 |
Why?
|
Glycosylation | 1 | 2004 | 69 | 0.010 |
Why?
|
Phosphatidylinositols | 1 | 2004 | 24 | 0.010 |
Why?
|
Cell Adhesion | 1 | 2004 | 133 | 0.010 |
Why?
|
Cell Wall | 1 | 2004 | 64 | 0.010 |
Why?
|
Hexokinase | 1 | 1983 | 16 | 0.010 |
Why?
|
Acrylamide | 1 | 2003 | 2 | 0.010 |
Why?
|
Protein Folding | 1 | 2003 | 47 | 0.010 |
Why?
|
Saccharomyces | 1 | 2003 | 1 | 0.010 |
Why?
|
Dictyostelium | 1 | 2003 | 5 | 0.010 |
Why?
|
Dimethylformamide | 1 | 1983 | 1 | 0.010 |
Why?
|
Maleates | 1 | 1983 | 1 | 0.010 |
Why?
|
Pyridoxamine | 1 | 1983 | 1 | 0.010 |
Why?
|
Inosine Triphosphate | 1 | 1982 | 1 | 0.010 |
Why?
|
Drosophila melanogaster | 1 | 2003 | 61 | 0.010 |
Why?
|
Blotting, Western | 1 | 2004 | 503 | 0.010 |
Why?
|
Epithelial Cells | 1 | 2004 | 240 | 0.010 |
Why?
|
Arabidopsis | 1 | 2003 | 65 | 0.010 |
Why?
|
Glutamates | 1 | 1982 | 14 | 0.010 |
Why?
|
Temperature | 1 | 1983 | 207 | 0.010 |
Why?
|
Columbidae | 1 | 1981 | 1 | 0.010 |
Why?
|
Trifluoroethanol | 1 | 1981 | 2 | 0.010 |
Why?
|
Phosphocreatine | 1 | 1981 | 22 | 0.010 |
Why?
|
Amides | 1 | 1981 | 18 | 0.010 |
Why?
|
Fumarate Hydratase | 1 | 1980 | 4 | 0.010 |
Why?
|
Phylogeny | 1 | 2003 | 461 | 0.010 |
Why?
|
Affinity Labels | 1 | 1999 | 4 | 0.010 |
Why?
|
Mass Spectrometry | 1 | 1999 | 186 | 0.010 |
Why?
|
ortho-Aminobenzoates | 1 | 1997 | 2 | 0.010 |
Why?
|
Flavins | 1 | 1997 | 2 | 0.010 |
Why?
|
Indoles | 1 | 1998 | 98 | 0.010 |
Why?
|
Ammonium Sulfate | 1 | 1996 | 3 | 0.010 |
Why?
|
Flavoproteins | 1 | 1996 | 5 | 0.010 |
Why?
|
Chemical Fractionation | 1 | 1996 | 9 | 0.010 |
Why?
|
Adenosine Diphosphate Ribose | 1 | 1995 | 3 | 0.010 |
Why?
|
Thymus Gland | 1 | 1995 | 53 | 0.010 |
Why?
|
Gene Library | 1 | 1993 | 45 | 0.010 |
Why?
|
Crystallography | 1 | 1992 | 6 | 0.010 |
Why?
|
Buffers | 1 | 1991 | 24 | 0.010 |
Why?
|
Chromatography, Gel | 1 | 1991 | 36 | 0.010 |
Why?
|
Isoelectric Point | 1 | 1988 | 7 | 0.000 |
Why?
|
Glucuronates | 1 | 1988 | 3 | 0.000 |
Why?
|
Glucuronic Acid | 1 | 1988 | 10 | 0.000 |
Why?
|
Vitamin K | 1 | 1988 | 39 | 0.000 |
Why?
|
Intestinal Mucosa | 1 | 1987 | 186 | 0.000 |
Why?
|
Pregnancy | 1 | 1988 | 1130 | 0.000 |
Why?
|
Glucose | 1 | 1983 | 191 | 0.000 |
Why?
|
Chemistry, Physical | 1 | 1981 | 13 | 0.000 |
Why?
|
Aldehyde Oxidoreductases | 1 | 1979 | 9 | 0.000 |
Why?
|