Mair Churchill
Concepts (413)
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?
|
---|
DNA | 39 | 2023 | 1388 | 3.380 |
Why?
| Histones | 14 | 2023 | 552 | 2.740 |
Why?
| High Mobility Group Proteins | 17 | 2012 | 50 | 2.420 |
Why?
| DNA-Binding Proteins | 21 | 2019 | 1346 | 2.120 |
Why?
| Mitochondrial Proteins | 6 | 2019 | 226 | 1.860 |
Why?
| Bacterial Proteins | 17 | 2018 | 759 | 1.850 |
Why?
| Transcription Factors | 14 | 2019 | 1570 | 1.600 |
Why?
| Molecular Chaperones | 9 | 2023 | 174 | 1.500 |
Why?
| DNA, Mitochondrial | 4 | 2019 | 187 | 1.420 |
Why?
| Chromatin Assembly Factor-1 | 3 | 2023 | 9 | 1.350 |
Why?
| Acyl-Butyrolactones | 5 | 2014 | 10 | 1.350 |
Why?
| Cell Cycle Proteins | 8 | 2014 | 565 | 1.320 |
Why?
| Ligases | 7 | 2011 | 32 | 1.250 |
Why?
| Histone Chaperones | 3 | 2012 | 14 | 1.240 |
Why?
| Molecular Sequence Data | 42 | 2016 | 2873 | 1.210 |
Why?
| Models, Molecular | 31 | 2015 | 1435 | 1.200 |
Why?
| Nucleosomes | 7 | 2018 | 131 | 1.140 |
Why?
| Chromatin Assembly and Disassembly | 3 | 2018 | 93 | 1.120 |
Why?
| Amino Acid Sequence | 34 | 2016 | 2073 | 1.070 |
Why?
| Repressor Proteins | 5 | 2018 | 377 | 0.990 |
Why?
| Protein Binding | 24 | 2019 | 1975 | 0.990 |
Why?
| Quorum Sensing | 7 | 2018 | 72 | 0.950 |
Why?
| DNA Damage | 3 | 2023 | 357 | 0.940 |
Why?
| Saccharomyces cerevisiae Proteins | 6 | 2012 | 348 | 0.860 |
Why?
| 4-Butyrolactone | 7 | 2012 | 19 | 0.800 |
Why?
| Pseudomonas aeruginosa | 6 | 2018 | 305 | 0.790 |
Why?
| Binding Sites | 24 | 2014 | 1224 | 0.780 |
Why?
| Cytosine | 2 | 2019 | 46 | 0.700 |
Why?
| CpG Islands | 1 | 2019 | 119 | 0.670 |
Why?
| Nucleic Acid Conformation | 18 | 2015 | 670 | 0.660 |
Why?
| Protein Structure, Tertiary | 14 | 2012 | 823 | 0.650 |
Why?
| Protein Multimerization | 6 | 2019 | 161 | 0.630 |
Why?
| Crystallography, X-Ray | 11 | 2015 | 422 | 0.570 |
Why?
| Transcription, Genetic | 5 | 2019 | 1323 | 0.560 |
Why?
| Base Sequence | 23 | 2012 | 2160 | 0.560 |
Why?
| Signal Transduction | 9 | 2018 | 4713 | 0.560 |
Why?
| DNA Methylation | 2 | 2019 | 503 | 0.530 |
Why?
| Drosophila Proteins | 5 | 2014 | 171 | 0.530 |
Why?
| Sequence Alignment | 9 | 2015 | 336 | 0.500 |
Why?
| Promoter Regions, Genetic | 5 | 2019 | 1158 | 0.500 |
Why?
| Gram-Negative Bacteria | 3 | 2010 | 70 | 0.490 |
Why?
| Mutation, Missense | 4 | 2017 | 300 | 0.480 |
Why?
| Chromatin | 5 | 2018 | 442 | 0.480 |
Why?
| Drosophila melanogaster | 11 | 2010 | 200 | 0.480 |
Why?
| Receptors, Progesterone | 4 | 2011 | 325 | 0.470 |
Why?
| Protein Conformation | 12 | 2015 | 848 | 0.460 |
Why?
| Mitochondria | 1 | 2019 | 786 | 0.450 |
Why?
| Lipase | 1 | 2013 | 70 | 0.440 |
Why?
| Site-Specific DNA-Methyltransferase (Adenine-Specific) | 2 | 2003 | 4 | 0.430 |
Why?
| Insect Proteins | 4 | 2000 | 31 | 0.410 |
Why?
| Saccharomyces cerevisiae | 3 | 2012 | 495 | 0.410 |
Why?
| Trans-Activators | 6 | 2018 | 373 | 0.400 |
Why?
| Sequence Homology, Amino Acid | 9 | 2012 | 372 | 0.390 |
Why?
| Animals | 45 | 2022 | 33390 | 0.380 |
Why?
| Transcriptional Activation | 2 | 2011 | 349 | 0.360 |
Why?
| Crystallization | 7 | 2011 | 146 | 0.360 |
Why?
| Mutation | 12 | 2016 | 3457 | 0.300 |
Why?
| Protein Structure, Secondary | 9 | 2011 | 338 | 0.300 |
Why?
| Gene Expression Regulation, Bacterial | 6 | 2014 | 279 | 0.290 |
Why?
| Transferases | 1 | 2006 | 27 | 0.290 |
Why?
| Recombination, Genetic | 3 | 2003 | 173 | 0.290 |
Why?
| HMG-Box Domains | 3 | 2015 | 3 | 0.290 |
Why?
| Substrate Specificity | 6 | 2022 | 371 | 0.280 |
Why?
| HMGB1 Protein | 3 | 2015 | 49 | 0.280 |
Why?
| Yersinia pestis | 1 | 2006 | 34 | 0.270 |
Why?
| Adenine | 3 | 2008 | 223 | 0.260 |
Why?
| Endopeptidases | 2 | 2022 | 73 | 0.250 |
Why?
| Nucleoproteins | 2 | 1994 | 28 | 0.250 |
Why?
| Bacteria | 2 | 2011 | 757 | 0.240 |
Why?
| Porifera | 2 | 2014 | 8 | 0.240 |
Why?
| Gene Silencing | 2 | 2023 | 177 | 0.230 |
Why?
| Protein Conformation, alpha-Helical | 1 | 2023 | 15 | 0.230 |
Why?
| Virulence | 3 | 2018 | 240 | 0.230 |
Why?
| RNA, Ribosomal, 5S | 3 | 1990 | 4 | 0.210 |
Why?
| Pantoea | 1 | 2001 | 2 | 0.210 |
Why?
| Rhenium | 1 | 2001 | 9 | 0.210 |
Why?
| Capsid Proteins | 1 | 2022 | 70 | 0.210 |
Why?
| Capsid | 1 | 2022 | 77 | 0.210 |
Why?
| Virus Assembly | 1 | 2022 | 67 | 0.210 |
Why?
| Bacteriophage lambda | 1 | 2022 | 81 | 0.210 |
Why?
| HMGB Proteins | 3 | 2008 | 15 | 0.200 |
Why?
| Recombinant Proteins | 7 | 2008 | 1308 | 0.200 |
Why?
| Adenosine | 1 | 2003 | 211 | 0.200 |
Why?
| RNA, Ribosomal | 3 | 1990 | 158 | 0.200 |
Why?
| Rhodobacter sphaeroides | 1 | 2000 | 6 | 0.190 |
Why?
| Cyclin A | 2 | 2011 | 15 | 0.190 |
Why?
| Mammals | 1 | 2022 | 253 | 0.190 |
Why?
| Structure-Activity Relationship | 4 | 2013 | 522 | 0.190 |
Why?
| Ligands | 2 | 2018 | 567 | 0.190 |
Why?
| Protein Interaction Domains and Motifs | 2 | 2013 | 138 | 0.190 |
Why?
| Centrosome | 2 | 2011 | 59 | 0.190 |
Why?
| DNA, Single-Stranded | 2 | 1991 | 114 | 0.180 |
Why?
| Archaeal Proteins | 1 | 2000 | 49 | 0.180 |
Why?
| Burkholderia | 2 | 2009 | 13 | 0.180 |
Why?
| DNA Repair | 2 | 1991 | 198 | 0.180 |
Why?
| Humans | 26 | 2019 | 118983 | 0.170 |
Why?
| Oligodeoxyribonucleotides | 3 | 2016 | 139 | 0.170 |
Why?
| Xenopus Proteins | 2 | 2012 | 67 | 0.170 |
Why?
| Sea Urchins | 2 | 2016 | 7 | 0.170 |
Why?
| Entropy | 2 | 2011 | 35 | 0.160 |
Why?
| Electrophoretic Mobility Shift Assay | 2 | 2012 | 76 | 0.160 |
Why?
| Pseudomonas Infections | 2 | 2011 | 193 | 0.160 |
Why?
| Mutagenesis, Site-Directed | 4 | 2016 | 364 | 0.150 |
Why?
| Nuclear Proteins | 3 | 2012 | 597 | 0.150 |
Why?
| Gene Deletion | 3 | 2013 | 361 | 0.150 |
Why?
| Operon | 2 | 2007 | 62 | 0.150 |
Why?
| Deuterium | 2 | 2011 | 78 | 0.140 |
Why?
| Serum Response Factor | 1 | 2016 | 31 | 0.140 |
Why?
| Xenopus | 3 | 2010 | 104 | 0.140 |
Why?
| DNA Primers | 3 | 2012 | 533 | 0.130 |
Why?
| Gas Chromatography-Mass Spectrometry | 2 | 2006 | 135 | 0.130 |
Why?
| Polymerase Chain Reaction | 2 | 1999 | 1012 | 0.130 |
Why?
| Models, Biological | 2 | 2013 | 1715 | 0.130 |
Why?
| Gene Expression Regulation | 4 | 2016 | 2446 | 0.130 |
Why?
| Neurodevelopmental Disorders | 1 | 2016 | 116 | 0.130 |
Why?
| Rhodobacteraceae | 1 | 2014 | 1 | 0.130 |
Why?
| PTEN Phosphohydrolase | 1 | 2016 | 143 | 0.130 |
Why?
| Hemagglutinins, Viral | 1 | 1994 | 6 | 0.130 |
Why?
| Sumoylation | 1 | 2014 | 16 | 0.130 |
Why?
| Urinary Bladder Neoplasms | 1 | 2017 | 211 | 0.130 |
Why?
| Escherichia coli | 4 | 2008 | 758 | 0.130 |
Why?
| SUMO-1 Protein | 1 | 2014 | 21 | 0.130 |
Why?
| Protein Interaction Mapping | 2 | 2012 | 104 | 0.130 |
Why?
| Genes, Retinoblastoma | 1 | 1994 | 9 | 0.120 |
Why?
| CREB-Binding Protein | 1 | 2014 | 28 | 0.120 |
Why?
| Immunoglobulin Fab Fragments | 1 | 1994 | 69 | 0.120 |
Why?
| Symbiosis | 1 | 2014 | 63 | 0.120 |
Why?
| Chromatography, Liquid | 3 | 2011 | 355 | 0.120 |
Why?
| Mutant Proteins | 2 | 2013 | 100 | 0.120 |
Why?
| Myocytes, Smooth Muscle | 1 | 2016 | 238 | 0.120 |
Why?
| Base Composition | 3 | 1990 | 77 | 0.120 |
Why?
| Thermodynamics | 4 | 2012 | 392 | 0.120 |
Why?
| Neoplasms, Radiation-Induced | 1 | 1994 | 66 | 0.120 |
Why?
| Chromatography, Reverse-Phase | 1 | 2013 | 25 | 0.120 |
Why?
| Glycolipids | 1 | 2013 | 37 | 0.120 |
Why?
| Tandem Mass Spectrometry | 3 | 2011 | 421 | 0.120 |
Why?
| Phospholipases | 1 | 2013 | 14 | 0.120 |
Why?
| Heparan Sulfate Proteoglycans | 1 | 2013 | 21 | 0.110 |
Why?
| Thymine | 2 | 2008 | 12 | 0.110 |
Why?
| Locomotion | 1 | 2013 | 83 | 0.110 |
Why?
| Dendritic Cells | 1 | 2016 | 442 | 0.110 |
Why?
| Histone Deacetylase Inhibitors | 1 | 2014 | 200 | 0.110 |
Why?
| Hydrolysis | 1 | 2013 | 176 | 0.110 |
Why?
| Roseobacter | 1 | 2012 | 1 | 0.110 |
Why?
| Amino Acid Substitution | 3 | 2012 | 276 | 0.110 |
Why?
| DNA, Bacterial | 2 | 2011 | 314 | 0.110 |
Why?
| rho Guanine Nucleotide Dissociation Inhibitor beta | 1 | 2012 | 4 | 0.110 |
Why?
| Fimbriae Proteins | 2 | 2013 | 15 | 0.110 |
Why?
| Cholesterol, HDL | 1 | 2013 | 199 | 0.110 |
Why?
| Immunoglobulin G | 1 | 2016 | 788 | 0.100 |
Why?
| Protein Kinase C-alpha | 1 | 2012 | 43 | 0.100 |
Why?
| Crystallography | 2 | 2006 | 25 | 0.100 |
Why?
| Dimerization | 3 | 2006 | 183 | 0.100 |
Why?
| rac1 GTP-Binding Protein | 1 | 2012 | 58 | 0.100 |
Why?
| Response Elements | 2 | 2011 | 82 | 0.100 |
Why?
| Magnetic Resonance Spectroscopy | 5 | 2007 | 508 | 0.100 |
Why?
| Hydrogen Bonding | 3 | 2000 | 146 | 0.100 |
Why?
| Xenopus laevis | 2 | 2011 | 128 | 0.100 |
Why?
| Circular Dichroism | 1 | 2011 | 139 | 0.100 |
Why?
| Staining and Labeling | 1 | 2012 | 146 | 0.100 |
Why?
| Markov Chains | 1 | 2011 | 118 | 0.100 |
Why?
| Ultraviolet Rays | 2 | 1991 | 381 | 0.100 |
Why?
| Cholesterol | 1 | 2013 | 375 | 0.100 |
Why?
| Carbodiimides | 1 | 2011 | 4 | 0.100 |
Why?
| Catalytic Domain | 2 | 2003 | 206 | 0.100 |
Why?
| Spectrometry, Fluorescence | 1 | 2012 | 173 | 0.100 |
Why?
| Cyclin E | 1 | 2011 | 21 | 0.100 |
Why?
| B-Lymphocytes | 1 | 2016 | 770 | 0.100 |
Why?
| Protein Stability | 1 | 2011 | 164 | 0.100 |
Why?
| Enzyme Activation | 1 | 2013 | 828 | 0.100 |
Why?
| Genetic Association Studies | 1 | 2013 | 371 | 0.100 |
Why?
| Antibodies, Viral | 1 | 1994 | 542 | 0.100 |
Why?
| Cell Survival | 2 | 1991 | 1047 | 0.100 |
Why?
| Metalloproteins | 1 | 1990 | 5 | 0.100 |
Why?
| Genes | 2 | 1990 | 231 | 0.100 |
Why?
| Hydroxides | 5 | 1990 | 26 | 0.090 |
Why?
| DNA, Ribosomal | 1 | 1990 | 79 | 0.090 |
Why?
| Immunity, Innate | 1 | 2016 | 745 | 0.090 |
Why?
| Protein Processing, Post-Translational | 1 | 2012 | 408 | 0.090 |
Why?
| Alleles | 1 | 2013 | 832 | 0.090 |
Why?
| Myocytes, Cardiac | 1 | 2014 | 472 | 0.090 |
Why?
| Biofilms | 1 | 2012 | 231 | 0.090 |
Why?
| Bayes Theorem | 1 | 2011 | 344 | 0.090 |
Why?
| Models, Genetic | 2 | 1994 | 595 | 0.090 |
Why?
| Chemoreceptor Cells | 1 | 2010 | 54 | 0.090 |
Why?
| Nasal Mucosa | 1 | 2010 | 97 | 0.090 |
Why?
| Light | 1 | 1991 | 342 | 0.080 |
Why?
| Burkholderia mallei | 1 | 2008 | 7 | 0.080 |
Why?
| Fluorescence Resonance Energy Transfer | 2 | 2016 | 183 | 0.080 |
Why?
| Peptide Fragments | 2 | 2007 | 702 | 0.080 |
Why?
| Receptors, G-Protein-Coupled | 1 | 2010 | 200 | 0.080 |
Why?
| Amino Acid Motifs | 2 | 2011 | 200 | 0.080 |
Why?
| Pseudomonas | 1 | 2007 | 27 | 0.080 |
Why?
| Genotype | 1 | 2013 | 1882 | 0.080 |
Why?
| Fimbriae, Bacterial | 1 | 2007 | 26 | 0.080 |
Why?
| Static Electricity | 3 | 2004 | 121 | 0.080 |
Why?
| Taste | 1 | 2010 | 218 | 0.080 |
Why?
| Adenocarcinoma | 1 | 1994 | 812 | 0.080 |
Why?
| Free Radicals | 5 | 1990 | 104 | 0.080 |
Why?
| Vaccines, Synthetic | 1 | 2007 | 128 | 0.070 |
Why?
| Cell Cycle | 1 | 2010 | 550 | 0.070 |
Why?
| Cricetinae | 3 | 2011 | 263 | 0.070 |
Why?
| Alanine | 1 | 2006 | 102 | 0.070 |
Why?
| Hydroxyl Radical | 4 | 1990 | 94 | 0.070 |
Why?
| Proteins | 2 | 1995 | 938 | 0.070 |
Why?
| Nuclear Magnetic Resonance, Biomolecular | 3 | 2009 | 240 | 0.070 |
Why?
| Acetylation | 3 | 2014 | 217 | 0.070 |
Why?
| Receptors, Cell Surface | 1 | 2007 | 367 | 0.070 |
Why?
| Gene Expression Regulation, Fungal | 2 | 2012 | 67 | 0.070 |
Why?
| Molecular Structure | 2 | 2007 | 459 | 0.060 |
Why?
| Polymorphism, Single Nucleotide | 1 | 2013 | 2062 | 0.060 |
Why?
| Acyl Carrier Protein | 1 | 2004 | 2 | 0.060 |
Why?
| Kinetics | 3 | 2004 | 1625 | 0.060 |
Why?
| Phosphorylation | 3 | 2013 | 1634 | 0.060 |
Why?
| Nucleic Acid Heteroduplexes | 2 | 1997 | 8 | 0.060 |
Why?
| Microtubule-Associated Proteins | 1 | 2005 | 188 | 0.060 |
Why?
| Crossing Over, Genetic | 1 | 2003 | 1 | 0.060 |
Why?
| Colorado | 1 | 2013 | 4196 | 0.060 |
Why?
| Amino Acids | 2 | 2005 | 465 | 0.060 |
Why?
| Phosphoproteins | 1 | 2005 | 308 | 0.060 |
Why?
| Chlorine | 1 | 2003 | 55 | 0.060 |
Why?
| Serogroup | 1 | 2022 | 34 | 0.050 |
Why?
| HMGB2 Protein | 1 | 2002 | 4 | 0.050 |
Why?
| Inflammation | 1 | 2013 | 2566 | 0.050 |
Why?
| DNA Mutational Analysis | 2 | 2016 | 381 | 0.050 |
Why?
| Neoplasm Proteins | 1 | 2005 | 401 | 0.050 |
Why?
| Proteolysis | 1 | 2022 | 146 | 0.050 |
Why?
| Models, Chemical | 1 | 2003 | 274 | 0.050 |
Why?
| CHO Cells | 2 | 2011 | 143 | 0.050 |
Why?
| DNA-Cytosine Methylases | 1 | 2000 | 2 | 0.050 |
Why?
| Receptors, Estrogen | 1 | 2004 | 387 | 0.050 |
Why?
| Lung Neoplasms | 1 | 1994 | 2220 | 0.050 |
Why?
| Cricetulus | 2 | 2011 | 98 | 0.050 |
Why?
| HEK293 Cells | 2 | 2014 | 625 | 0.050 |
Why?
| Protein Folding | 1 | 2022 | 250 | 0.050 |
Why?
| S-Adenosylmethionine | 1 | 2000 | 49 | 0.050 |
Why?
| Nitrogen Isotopes | 1 | 2000 | 55 | 0.050 |
Why?
| Receptors, Cytoplasmic and Nuclear | 1 | 2002 | 195 | 0.050 |
Why?
| Carbon Isotopes | 1 | 2000 | 115 | 0.050 |
Why?
| Nucleotides | 1 | 2000 | 112 | 0.050 |
Why?
| Disulfides | 2 | 1997 | 91 | 0.050 |
Why?
| Mice | 6 | 2016 | 15520 | 0.050 |
Why?
| Catalysis | 1 | 2000 | 295 | 0.040 |
Why?
| Rats, Sprague-Dawley | 2 | 2016 | 2478 | 0.040 |
Why?
| Anti-Bacterial Agents | 1 | 2009 | 1510 | 0.040 |
Why?
| Chromatography, Ion Exchange | 1 | 1999 | 51 | 0.040 |
Why?
| Mice, Inbred BALB C | 2 | 2009 | 1206 | 0.040 |
Why?
| Cell Line | 3 | 2010 | 2708 | 0.040 |
Why?
| Chromosomes | 1 | 1999 | 87 | 0.040 |
Why?
| COS Cells | 2 | 2009 | 184 | 0.040 |
Why?
| Cytochromes c | 1 | 1998 | 64 | 0.040 |
Why?
| Mice, Transgenic | 2 | 2016 | 2025 | 0.040 |
Why?
| Electrophoresis | 1 | 1997 | 26 | 0.040 |
Why?
| Cloning, Molecular | 1 | 1999 | 546 | 0.040 |
Why?
| Chromosomal Proteins, Non-Histone | 1 | 1998 | 103 | 0.040 |
Why?
| Fungal Proteins | 1 | 1998 | 130 | 0.040 |
Why?
| Muscidae | 1 | 1996 | 1 | 0.040 |
Why?
| DNA Nucleotidyltransferases | 1 | 1996 | 11 | 0.040 |
Why?
| Methionine | 1 | 1997 | 145 | 0.040 |
Why?
| Water | 1 | 2000 | 425 | 0.040 |
Why?
| Rats | 2 | 2016 | 5394 | 0.040 |
Why?
| Ataxia | 1 | 2016 | 38 | 0.040 |
Why?
| Strabismus | 1 | 2016 | 27 | 0.040 |
Why?
| Fluorescence | 2 | 2010 | 159 | 0.040 |
Why?
| United Kingdom | 1 | 2016 | 236 | 0.030 |
Why?
| Transfection | 2 | 2012 | 890 | 0.030 |
Why?
| Electrophoresis, Polyacrylamide Gel | 3 | 2010 | 332 | 0.030 |
Why?
| DNA Transposable Elements | 1 | 1996 | 102 | 0.030 |
Why?
| Syndrome | 1 | 2016 | 344 | 0.030 |
Why?
| Protein Kinases | 1 | 1998 | 310 | 0.030 |
Why?
| Canada | 1 | 2016 | 340 | 0.030 |
Why?
| Fushi Tarazu Transcription Factors | 1 | 1995 | 5 | 0.030 |
Why?
| Intellectual Disability | 1 | 2016 | 136 | 0.030 |
Why?
| Face | 1 | 2016 | 165 | 0.030 |
Why?
| Age of Onset | 1 | 2016 | 467 | 0.030 |
Why?
| Gene Order | 1 | 2014 | 28 | 0.030 |
Why?
| Adjuvants, Immunologic | 1 | 2016 | 207 | 0.030 |
Why?
| Binding, Competitive | 1 | 1995 | 205 | 0.030 |
Why?
| Binding Sites, Antibody | 1 | 1994 | 38 | 0.030 |
Why?
| Antibody Formation | 1 | 2016 | 276 | 0.030 |
Why?
| Antigen-Antibody Reactions | 1 | 1994 | 51 | 0.030 |
Why?
| Hemagglutinin Glycoproteins, Influenza Virus | 1 | 1994 | 20 | 0.030 |
Why?
| Protein Biosynthesis | 2 | 2014 | 397 | 0.030 |
Why?
| Biocatalysis | 1 | 2014 | 64 | 0.030 |
Why?
| Neutrons | 1 | 1994 | 5 | 0.030 |
Why?
| Plasmids | 2 | 2004 | 355 | 0.030 |
Why?
| Oxidation-Reduction | 1 | 1997 | 940 | 0.030 |
Why?
| Tyrosine | 1 | 1995 | 233 | 0.030 |
Why?
| Molecular Weight | 3 | 2005 | 343 | 0.030 |
Why?
| Mass Spectrometry | 1 | 1997 | 681 | 0.030 |
Why?
| Recombinant Fusion Proteins | 3 | 2004 | 653 | 0.030 |
Why?
| Crosses, Genetic | 1 | 1994 | 138 | 0.030 |
Why?
| Inverted Repeat Sequences | 1 | 2013 | 11 | 0.030 |
Why?
| Developmental Disabilities | 1 | 2016 | 247 | 0.030 |
Why?
| Transcription Factor TFIIIA | 2 | 1990 | 5 | 0.030 |
Why?
| Methods | 2 | 1990 | 67 | 0.030 |
Why?
| Genetic Loci | 1 | 2014 | 281 | 0.030 |
Why?
| Checkpoint Kinase 2 | 1 | 2012 | 23 | 0.030 |
Why?
| Muscle, Smooth, Vascular | 1 | 2016 | 457 | 0.030 |
Why?
| Conserved Sequence | 2 | 2007 | 219 | 0.030 |
Why?
| Histone Deacetylases | 1 | 2014 | 198 | 0.030 |
Why?
| Drosophila | 1 | 2014 | 140 | 0.030 |
Why?
| Lysine | 1 | 2014 | 248 | 0.030 |
Why?
| Epitopes | 1 | 1994 | 443 | 0.030 |
Why?
| HeLa Cells | 1 | 2014 | 583 | 0.030 |
Why?
| Tetradecanoylphorbol Acetate | 1 | 2012 | 155 | 0.030 |
Why?
| Animals, Newborn | 1 | 2014 | 806 | 0.030 |
Why?
| Enzyme-Linked Immunosorbent Assay | 1 | 1994 | 827 | 0.030 |
Why?
| Point Mutation | 1 | 2012 | 228 | 0.030 |
Why?
| Serine | 1 | 2012 | 138 | 0.030 |
Why?
| Netropsin | 1 | 1991 | 1 | 0.030 |
Why?
| Homeodomain Proteins | 1 | 1995 | 469 | 0.020 |
Why?
| Temperature | 2 | 2004 | 622 | 0.020 |
Why?
| Cyclin-Dependent Kinase 2 | 1 | 2011 | 32 | 0.020 |
Why?
| Dose-Response Relationship, Radiation | 1 | 1991 | 129 | 0.020 |
Why?
| S Phase | 1 | 2011 | 74 | 0.020 |
Why?
| G1 Phase | 1 | 2011 | 68 | 0.020 |
Why?
| Distamycins | 1 | 1990 | 1 | 0.020 |
Why?
| Models, Structural | 1 | 1990 | 38 | 0.020 |
Why?
| Molecular Conformation | 1 | 1991 | 146 | 0.020 |
Why?
| Dactinomycin | 1 | 1990 | 24 | 0.020 |
Why?
| Edetic Acid | 1 | 1990 | 47 | 0.020 |
Why?
| Cell Line, Tumor | 1 | 2017 | 2851 | 0.020 |
Why?
| X-Ray Diffraction | 1 | 1990 | 86 | 0.020 |
Why?
| Heterotrimeric GTP-Binding Proteins | 1 | 2010 | 16 | 0.020 |
Why?
| Guanine | 1 | 1990 | 75 | 0.020 |
Why?
| Trigeminal Nerve | 1 | 2010 | 28 | 0.020 |
Why?
| Quaternary Ammonium Compounds | 1 | 2010 | 46 | 0.020 |
Why?
| Cyclin-Dependent Kinase Inhibitor p27 | 1 | 2010 | 69 | 0.020 |
Why?
| Burkholderia Infections | 1 | 2009 | 5 | 0.020 |
Why?
| Fibroblasts | 1 | 2014 | 842 | 0.020 |
Why?
| Leucine Zippers | 1 | 2009 | 16 | 0.020 |
Why?
| Immunoprecipitation | 1 | 2010 | 161 | 0.020 |
Why?
| Mice, Knockout | 1 | 2016 | 2680 | 0.020 |
Why?
| Ovary | 1 | 1991 | 205 | 0.020 |
Why?
| Spermatozoa | 1 | 1989 | 91 | 0.020 |
Why?
| Protein Structure, Quaternary | 1 | 2009 | 116 | 0.020 |
Why?
| TRPM Cation Channels | 1 | 2010 | 68 | 0.020 |
Why?
| Cyclin-Dependent Kinases | 1 | 2010 | 111 | 0.020 |
Why?
| Sequence Deletion | 1 | 2009 | 171 | 0.020 |
Why?
| Hydroxylation | 1 | 1988 | 26 | 0.020 |
Why?
| Cell Differentiation | 1 | 2016 | 1753 | 0.020 |
Why?
| Microscopy, Fluorescence | 1 | 2010 | 412 | 0.020 |
Why?
| Phenazines | 1 | 2007 | 9 | 0.020 |
Why?
| Chromatography, Thin Layer | 1 | 2007 | 23 | 0.020 |
Why?
| Cells, Cultured | 1 | 2016 | 4080 | 0.020 |
Why?
| Antibodies, Monoclonal | 1 | 1994 | 1285 | 0.020 |
Why?
| Sequence Homology, Nucleic Acid | 1 | 2007 | 155 | 0.020 |
Why?
| Zinc | 1 | 1990 | 262 | 0.020 |
Why?
| Deoxyribonuclease I | 3 | 1995 | 36 | 0.020 |
Why?
| Antigens, Bacterial | 1 | 2007 | 116 | 0.020 |
Why?
| Blotting, Western | 1 | 2010 | 1195 | 0.020 |
Why?
| DNA Footprinting | 2 | 1996 | 28 | 0.020 |
Why?
| Infant, Newborn | 1 | 2016 | 5255 | 0.020 |
Why?
| Ultracentrifugation | 1 | 2005 | 49 | 0.020 |
Why?
| Chromatography, Gel | 1 | 2005 | 133 | 0.020 |
Why?
| Aurora Kinase B | 1 | 2005 | 9 | 0.020 |
Why?
| Aurora Kinases | 1 | 2005 | 28 | 0.020 |
Why?
| Immunohistochemistry | 1 | 2010 | 1691 | 0.020 |
Why?
| Male | 4 | 2016 | 57808 | 0.020 |
Why?
| Immunization | 1 | 2007 | 412 | 0.020 |
Why?
| Sequence Analysis, DNA | 1 | 2007 | 755 | 0.020 |
Why?
| Macromolecular Substances | 1 | 2004 | 202 | 0.020 |
Why?
| Mice, Inbred C57BL | 1 | 1994 | 4908 | 0.020 |
Why?
| Zinc Fingers | 1 | 2004 | 46 | 0.010 |
Why?
| Chromatography, High Pressure Liquid | 1 | 2005 | 490 | 0.010 |
Why?
| Estrogen Receptor beta | 1 | 2004 | 37 | 0.010 |
Why?
| Glutathione Transferase | 1 | 2004 | 97 | 0.010 |
Why?
| Calcium | 1 | 2010 | 1171 | 0.010 |
Why?
| Calorimetry | 1 | 2003 | 59 | 0.010 |
Why?
| Infant | 1 | 2016 | 8293 | 0.010 |
Why?
| Survival Rate | 1 | 2007 | 1720 | 0.010 |
Why?
| Estrogen Receptor alpha | 1 | 2004 | 126 | 0.010 |
Why?
| Peptides | 1 | 2008 | 879 | 0.010 |
Why?
| Female | 4 | 2016 | 61574 | 0.010 |
Why?
| Dose-Response Relationship, Drug | 1 | 2004 | 1947 | 0.010 |
Why?
| Hydro-Lyases | 1 | 1998 | 4 | 0.010 |
Why?
| Sex-Determining Region Y Protein | 1 | 1998 | 2 | 0.010 |
Why?
| Cytochrome c Group | 1 | 1998 | 37 | 0.010 |
Why?
| Adolescent | 1 | 2016 | 18479 | 0.010 |
Why?
| Lymphoid Enhancer-Binding Factor 1 | 1 | 1998 | 8 | 0.010 |
Why?
| Precipitin Tests | 1 | 1998 | 94 | 0.010 |
Why?
| Acetyltransferases | 1 | 1998 | 21 | 0.010 |
Why?
| beta-Galactosidase | 1 | 1998 | 65 | 0.010 |
Why?
| Yeasts | 1 | 1998 | 52 | 0.010 |
Why?
| DNA Restriction Enzymes | 2 | 1988 | 53 | 0.010 |
Why?
| Histone Acetyltransferases | 1 | 1998 | 53 | 0.010 |
Why?
| Child | 1 | 2016 | 19129 | 0.010 |
Why?
| Transposases | 1 | 1996 | 9 | 0.010 |
Why?
| Manganese Compounds | 1 | 1996 | 4 | 0.010 |
Why?
| Chlorides | 1 | 1996 | 137 | 0.010 |
Why?
| Cross-Linking Reagents | 1 | 1995 | 186 | 0.010 |
Why?
| Oligonucleotides | 1 | 1995 | 140 | 0.010 |
Why?
| Solutions | 1 | 1994 | 156 | 0.010 |
Why?
| RNA, Messenger | 2 | 1993 | 2657 | 0.010 |
Why?
| Software | 1 | 1998 | 613 | 0.010 |
Why?
| Phylogeny | 1 | 1996 | 816 | 0.010 |
Why?
| Larva | 1 | 1993 | 213 | 0.010 |
Why?
| Chromosome Mapping | 1 | 1993 | 510 | 0.010 |
Why?
| Diethyl Pyrocarbonate | 1 | 1990 | 2 | 0.010 |
Why?
| Electrophoresis, Agar Gel | 1 | 1990 | 25 | 0.010 |
Why?
| Endonucleases | 1 | 1990 | 31 | 0.010 |
Why?
| Magnesium | 1 | 1990 | 150 | 0.010 |
Why?
| Copper | 1 | 1990 | 102 | 0.010 |
Why?
| Computer Simulation | 1 | 1994 | 922 | 0.010 |
Why?
| Purines | 1 | 1990 | 161 | 0.010 |
Why?
| Iron | 1 | 1990 | 248 | 0.010 |
Why?
| Nucleotide Mapping | 1 | 1988 | 4 | 0.010 |
Why?
| Chromosome Deletion | 1 | 1988 | 95 | 0.000 |
Why?
| Viral Regulatory and Accessory Proteins | 1 | 1987 | 28 | 0.000 |
Why?
| Oocytes | 1 | 1988 | 190 | 0.000 |
Why?
| Indicators and Reagents | 1 | 1987 | 100 | 0.000 |
Why?
| Viral Proteins | 1 | 1987 | 296 | 0.000 |
Why?
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