Concepts (148)
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?
|
---|
Adenosine | 12 | 2012 | 78 | 1.480 |
Why?
|
Receptor, Adenosine A1 | 8 | 2012 | 10 | 1.440 |
Why?
|
Myocardium | 7 | 2012 | 275 | 1.260 |
Why?
|
Myocardial Contraction | 6 | 2012 | 88 | 1.260 |
Why?
|
Myocytes, Cardiac | 5 | 2012 | 96 | 0.990 |
Why?
|
Protein Kinase C-epsilon | 5 | 2012 | 12 | 0.890 |
Why?
|
Heart | 4 | 2012 | 282 | 0.850 |
Why?
|
Receptor, Adenosine A2A | 3 | 2008 | 17 | 0.840 |
Why?
|
Receptors, Adrenergic, beta | 3 | 2008 | 20 | 0.580 |
Why?
|
Rats | 14 | 2016 | 1980 | 0.570 |
Why?
|
Aging | 3 | 2012 | 743 | 0.560 |
Why?
|
Heart Ventricles | 3 | 2008 | 261 | 0.560 |
Why?
|
Type C Phospholipases | 3 | 2015 | 33 | 0.440 |
Why?
|
Adrenergic beta-Agonists | 3 | 2008 | 32 | 0.410 |
Why?
|
S-Adenosylhomocysteine | 1 | 2012 | 3 | 0.410 |
Why?
|
Adenosine Deaminase | 1 | 2012 | 19 | 0.400 |
Why?
|
Rats, Sprague-Dawley | 8 | 2012 | 622 | 0.370 |
Why?
|
Protein Phosphatase 2 | 2 | 2008 | 10 | 0.360 |
Why?
|
HSP27 Heat-Shock Proteins | 1 | 2010 | 3 | 0.340 |
Why?
|
Adenylyl Cyclases | 3 | 2007 | 21 | 0.340 |
Why?
|
Calcium Signaling | 2 | 2008 | 158 | 0.330 |
Why?
|
Protein Kinase C | 2 | 2015 | 103 | 0.330 |
Why?
|
Coatomer Protein | 1 | 2009 | 1 | 0.320 |
Why?
|
p38 Mitogen-Activated Protein Kinases | 1 | 2010 | 149 | 0.320 |
Why?
|
Receptors, Adrenergic, beta-1 | 2 | 2012 | 7 | 0.310 |
Why?
|
Membrane Proteins | 4 | 2012 | 894 | 0.300 |
Why?
|
Receptors, Adenosine A2 | 1 | 2007 | 4 | 0.290 |
Why?
|
Isoproterenol | 5 | 2012 | 36 | 0.290 |
Why?
|
Phenethylamines | 4 | 2008 | 10 | 0.290 |
Why?
|
GTP-Binding Proteins | 1 | 2007 | 82 | 0.280 |
Why?
|
Receptors, Purinergic P1 | 2 | 2004 | 12 | 0.270 |
Why?
|
Animals | 16 | 2016 | 20612 | 0.250 |
Why?
|
Ischemic Preconditioning, Myocardial | 1 | 2005 | 23 | 0.240 |
Why?
|
Myocardial Reperfusion Injury | 1 | 2005 | 28 | 0.240 |
Why?
|
Phosphoprotein Phosphatases | 1 | 2005 | 41 | 0.240 |
Why?
|
Rats, Inbred F344 | 3 | 2012 | 53 | 0.220 |
Why?
|
Signal Transduction | 5 | 2015 | 3027 | 0.200 |
Why?
|
Mice, Inbred C57BL | 4 | 2010 | 3387 | 0.180 |
Why?
|
Xanthines | 3 | 2012 | 8 | 0.170 |
Why?
|
Phosphorylation | 3 | 2010 | 937 | 0.160 |
Why?
|
Adenosine A1 Receptor Agonists | 2 | 2009 | 2 | 0.160 |
Why?
|
Adenosine A2 Receptor Agonists | 2 | 2008 | 7 | 0.150 |
Why?
|
Mice, Knockout | 3 | 2010 | 2104 | 0.150 |
Why?
|
Cyclic AMP-Dependent Protein Kinases | 3 | 2012 | 93 | 0.150 |
Why?
|
Precipitin Tests | 2 | 2007 | 77 | 0.120 |
Why?
|
Presynaptic Terminals | 2 | 2007 | 37 | 0.120 |
Why?
|
Male | 9 | 2012 | 29546 | 0.120 |
Why?
|
Adenosine A1 Receptor Antagonists | 3 | 2012 | 5 | 0.120 |
Why?
|
DNA, Mitochondrial | 1 | 2016 | 87 | 0.120 |
Why?
|
Nerve Growth Factor | 1 | 2015 | 5 | 0.120 |
Why?
|
Coronary Vessels | 1 | 2016 | 118 | 0.120 |
Why?
|
Cells, Cultured | 2 | 2010 | 2154 | 0.120 |
Why?
|
Apolipoproteins E | 1 | 2015 | 109 | 0.110 |
Why?
|
Metabolic Syndrome | 1 | 2016 | 142 | 0.110 |
Why?
|
Mice | 4 | 2010 | 10815 | 0.110 |
Why?
|
Estrenes | 2 | 2015 | 9 | 0.110 |
Why?
|
Pyrrolidinones | 2 | 2015 | 11 | 0.110 |
Why?
|
Mitogen-Activated Protein Kinases | 1 | 2015 | 216 | 0.110 |
Why?
|
Adenosine Deaminase Inhibitors | 1 | 2012 | 1 | 0.100 |
Why?
|
Tubercidin | 1 | 2012 | 2 | 0.100 |
Why?
|
Adrenergic Antagonists | 1 | 2012 | 3 | 0.100 |
Why?
|
Mitochondria | 1 | 2016 | 370 | 0.100 |
Why?
|
Perfusion | 1 | 2012 | 73 | 0.100 |
Why?
|
Sodium Chloride | 1 | 2012 | 63 | 0.100 |
Why?
|
Adenine | 1 | 2012 | 50 | 0.100 |
Why?
|
Hydrolases | 1 | 2012 | 82 | 0.090 |
Why?
|
Protein Kinase Inhibitors | 2 | 2012 | 187 | 0.090 |
Why?
|
GTP-Binding Protein alpha Subunits, Gi-Go | 1 | 2010 | 15 | 0.080 |
Why?
|
Inositol 1,4,5-Trisphosphate | 1 | 2010 | 27 | 0.080 |
Why?
|
Sarcomeres | 1 | 2010 | 51 | 0.080 |
Why?
|
Phosphodiesterase Inhibitors | 1 | 2009 | 27 | 0.080 |
Why?
|
Models, Animal | 1 | 2010 | 235 | 0.080 |
Why?
|
Calcium | 2 | 2010 | 574 | 0.080 |
Why?
|
Immunoprecipitation | 1 | 2009 | 126 | 0.080 |
Why?
|
Dose-Response Relationship, Drug | 2 | 2008 | 863 | 0.080 |
Why?
|
Benzophenanthridines | 1 | 2008 | 2 | 0.080 |
Why?
|
Thionucleotides | 1 | 2008 | 38 | 0.080 |
Why?
|
Antibodies | 1 | 2009 | 182 | 0.070 |
Why?
|
Tyrosine | 1 | 2008 | 93 | 0.070 |
Why?
|
Cyclic AMP | 1 | 2008 | 143 | 0.070 |
Why?
|
Membranes | 1 | 2007 | 18 | 0.070 |
Why?
|
Guanosine Diphosphate | 1 | 2007 | 19 | 0.070 |
Why?
|
Enzyme Activation | 1 | 2008 | 380 | 0.070 |
Why?
|
Purinergic P1 Receptor Agonists | 2 | 2004 | 6 | 0.070 |
Why?
|
Immunohistochemistry | 1 | 2009 | 890 | 0.070 |
Why?
|
Pituitary Gland, Posterior | 1 | 2007 | 17 | 0.070 |
Why?
|
Enzyme Inhibitors | 2 | 2007 | 373 | 0.070 |
Why?
|
Exocytosis | 1 | 2007 | 60 | 0.070 |
Why?
|
Neuropeptides | 1 | 2007 | 82 | 0.060 |
Why?
|
Okadaic Acid | 1 | 2005 | 9 | 0.060 |
Why?
|
Age Factors | 1 | 2009 | 1556 | 0.060 |
Why?
|
Peptides | 1 | 2008 | 576 | 0.060 |
Why?
|
Myocardial Ischemia | 1 | 2005 | 116 | 0.060 |
Why?
|
Norepinephrine | 1 | 2004 | 103 | 0.060 |
Why?
|
Luminescent Proteins | 1 | 2004 | 128 | 0.050 |
Why?
|
Electric Stimulation | 1 | 2004 | 140 | 0.050 |
Why?
|
Cell Death | 1 | 2005 | 284 | 0.050 |
Why?
|
Rabbits | 1 | 2004 | 332 | 0.050 |
Why?
|
Alkaline Phosphatase | 1 | 2003 | 46 | 0.050 |
Why?
|
Time Factors | 2 | 2008 | 3749 | 0.050 |
Why?
|
Green Fluorescent Proteins | 1 | 2004 | 364 | 0.050 |
Why?
|
Oligonucleotide Array Sequence Analysis | 1 | 2003 | 298 | 0.050 |
Why?
|
Transfection | 1 | 2004 | 691 | 0.050 |
Why?
|
Inosine | 1 | 2002 | 4 | 0.050 |
Why?
|
Cell Hypoxia | 1 | 2002 | 42 | 0.050 |
Why?
|
Cellular Senescence | 1 | 2002 | 110 | 0.040 |
Why?
|
Protein Biosynthesis | 1 | 2003 | 317 | 0.040 |
Why?
|
Gene Expression | 1 | 2004 | 838 | 0.040 |
Why?
|
Fibroblasts | 1 | 2002 | 392 | 0.040 |
Why?
|
Gene Expression Profiling | 1 | 2003 | 769 | 0.040 |
Why?
|
Proteins | 1 | 2003 | 751 | 0.040 |
Why?
|
RNA, Messenger | 1 | 2003 | 1534 | 0.030 |
Why?
|
Rats, Zucker | 1 | 2016 | 7 | 0.030 |
Why?
|
DNA Fragmentation | 1 | 2016 | 35 | 0.030 |
Why?
|
Vasodilation | 1 | 2016 | 36 | 0.030 |
Why?
|
Isothiuronium | 1 | 2015 | 1 | 0.030 |
Why?
|
Chromones | 1 | 2015 | 20 | 0.030 |
Why?
|
Maleimides | 1 | 2015 | 9 | 0.030 |
Why?
|
NG-Nitroarginine Methyl Ester | 1 | 2015 | 29 | 0.030 |
Why?
|
PC12 Cells | 1 | 2015 | 26 | 0.030 |
Why?
|
Reactive Oxygen Species | 1 | 2016 | 224 | 0.030 |
Why?
|
Nitric Oxide Synthase Type II | 1 | 2015 | 70 | 0.030 |
Why?
|
Morpholines | 1 | 2015 | 89 | 0.030 |
Why?
|
Indoles | 1 | 2015 | 110 | 0.030 |
Why?
|
Oxidative Stress | 1 | 2016 | 294 | 0.030 |
Why?
|
DNA Damage | 1 | 2016 | 285 | 0.030 |
Why?
|
Proto-Oncogene Proteins c-akt | 1 | 2015 | 202 | 0.030 |
Why?
|
Adrenergic beta-1 Receptor Agonists | 1 | 2012 | 1 | 0.030 |
Why?
|
Colforsin | 1 | 2012 | 24 | 0.020 |
Why?
|
Organ Culture Techniques | 1 | 2012 | 69 | 0.020 |
Why?
|
Isoquinolines | 1 | 2012 | 33 | 0.020 |
Why?
|
Promoter Regions, Genetic | 1 | 2015 | 672 | 0.020 |
Why?
|
Sulfonamides | 1 | 2012 | 126 | 0.020 |
Why?
|
Protein Transport | 1 | 2012 | 402 | 0.020 |
Why?
|
Transcription, Genetic | 1 | 2015 | 875 | 0.020 |
Why?
|
Intracellular Signaling Peptides and Proteins | 1 | 2012 | 336 | 0.020 |
Why?
|
Disease Models, Animal | 1 | 2016 | 2178 | 0.020 |
Why?
|
Feedback | 1 | 2007 | 89 | 0.020 |
Why?
|
Feedback, Physiological | 1 | 2007 | 60 | 0.020 |
Why?
|
Hypothalamus | 1 | 2007 | 132 | 0.020 |
Why?
|
Synaptic Transmission | 1 | 2007 | 150 | 0.020 |
Why?
|
Adenosine Triphosphate | 1 | 2007 | 292 | 0.010 |
Why?
|
Adenosine Triphosphatases | 1 | 2007 | 257 | 0.010 |
Why?
|
In Vitro Techniques | 1 | 2004 | 487 | 0.010 |
Why?
|
Chromatography, High Pressure Liquid | 1 | 2002 | 231 | 0.010 |
Why?
|
Cell Line | 1 | 2002 | 2039 | 0.010 |
Why?
|
Lung | 1 | 2002 | 939 | 0.010 |
Why?
|
Humans | 1 | 2002 | 62866 | 0.000 |
Why?
|