Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
---|
Nucleosomes | 55 | 2024 | 184 | 10.630 |
Why?
|
Histones | 62 | 2024 | 457 | 10.540 |
Why?
|
Saccharomyces cerevisiae Proteins | 49 | 2024 | 425 | 9.910 |
Why?
|
Chromatin Assembly and Disassembly | 35 | 2024 | 229 | 8.530 |
Why?
|
Chromatin | 54 | 2023 | 599 | 7.930 |
Why?
|
Saccharomyces cerevisiae | 44 | 2024 | 540 | 7.680 |
Why?
|
Adenosine Triphosphatases | 23 | 2024 | 253 | 4.790 |
Why?
|
Transcription, Genetic | 31 | 2023 | 841 | 3.860 |
Why?
|
Transcription Factors | 39 | 2024 | 1471 | 3.580 |
Why?
|
DNA Repair | 19 | 2017 | 242 | 3.570 |
Why?
|
Heterochromatin | 8 | 2024 | 84 | 3.120 |
Why?
|
Adenosine Triphosphate | 22 | 2022 | 289 | 2.990 |
Why?
|
Chromosomal Proteins, Non-Histone | 13 | 2024 | 168 | 2.370 |
Why?
|
Genomic Instability | 7 | 2020 | 53 | 2.340 |
Why?
|
DNA Breaks, Double-Stranded | 9 | 2019 | 78 | 2.290 |
Why?
|
DNA-Binding Proteins | 31 | 2020 | 1151 | 2.270 |
Why?
|
DNA | 27 | 2022 | 805 | 2.010 |
Why?
|
Sirtuins | 5 | 2023 | 26 | 1.850 |
Why?
|
Nuclear Proteins | 17 | 2015 | 750 | 1.820 |
Why?
|
Silent Information Regulator Proteins, Saccharomyces cerevisiae | 5 | 2018 | 14 | 1.670 |
Why?
|
DNA Helicases | 12 | 2017 | 187 | 1.540 |
Why?
|
Multienzyme Complexes | 4 | 2016 | 76 | 1.430 |
Why?
|
Gene Expression Regulation, Fungal | 11 | 2020 | 125 | 1.380 |
Why?
|
Exosome Multienzyme Ribonuclease Complex | 2 | 2021 | 5 | 1.270 |
Why?
|
DNA Damage | 10 | 2014 | 279 | 1.270 |
Why?
|
DNA, Fungal | 9 | 2019 | 57 | 1.120 |
Why?
|
Histone Acetyltransferases | 10 | 2015 | 56 | 1.100 |
Why?
|
Protein Processing, Post-Translational | 7 | 2017 | 258 | 1.090 |
Why?
|
Recombination, Genetic | 5 | 2009 | 238 | 1.020 |
Why?
|
Biochemistry | 5 | 2010 | 50 | 0.960 |
Why?
|
Cell Cycle | 4 | 2019 | 382 | 0.930 |
Why?
|
Protein Binding | 21 | 2024 | 1555 | 0.920 |
Why?
|
Exodeoxyribonucleases | 2 | 2014 | 28 | 0.890 |
Why?
|
Epigenesis, Genetic | 5 | 2024 | 357 | 0.880 |
Why?
|
Acetyltransferases | 8 | 2004 | 24 | 0.870 |
Why?
|
Acetylation | 11 | 2020 | 112 | 0.840 |
Why?
|
DNA Replication | 7 | 2017 | 228 | 0.840 |
Why?
|
Replication Origin | 2 | 2020 | 35 | 0.820 |
Why?
|
ATPases Associated with Diverse Cellular Activities | 3 | 2020 | 25 | 0.810 |
Why?
|
Transcriptional Activation | 4 | 2020 | 188 | 0.810 |
Why?
|
Cell Nucleus | 10 | 2020 | 608 | 0.790 |
Why?
|
Recombinant Proteins | 8 | 2021 | 689 | 0.790 |
Why?
|
RNA Stability | 1 | 2023 | 97 | 0.790 |
Why?
|
Gene Silencing | 7 | 2024 | 378 | 0.790 |
Why?
|
Drosophila | 3 | 2009 | 421 | 0.750 |
Why?
|
Models, Molecular | 14 | 2014 | 1128 | 0.750 |
Why?
|
Homeostasis | 3 | 2023 | 346 | 0.750 |
Why?
|
Fungal Proteins | 7 | 2010 | 144 | 0.710 |
Why?
|
Animals | 39 | 2021 | 19649 | 0.640 |
Why?
|
Drosophila Proteins | 6 | 2021 | 679 | 0.600 |
Why?
|
Nucleic Acid Conformation | 8 | 2010 | 234 | 0.580 |
Why?
|
Chromatography, Affinity | 4 | 2010 | 48 | 0.560 |
Why?
|
Promoter Regions, Genetic | 9 | 2017 | 650 | 0.560 |
Why?
|
Models, Genetic | 4 | 2015 | 255 | 0.520 |
Why?
|
Xenopus laevis | 7 | 2019 | 67 | 0.510 |
Why?
|
DNA, Single-Stranded | 1 | 2017 | 100 | 0.510 |
Why?
|
Rad51 Recombinase | 4 | 2013 | 26 | 0.510 |
Why?
|
Gene Expression Regulation | 5 | 2007 | 1552 | 0.500 |
Why?
|
Histone Deacetylases | 4 | 2019 | 61 | 0.490 |
Why?
|
Genetic Techniques | 3 | 2010 | 39 | 0.480 |
Why?
|
Trans-Activators | 4 | 2010 | 300 | 0.470 |
Why?
|
DNA Polymerase III | 1 | 2014 | 28 | 0.470 |
Why?
|
Ubiquitin | 3 | 2011 | 97 | 0.460 |
Why?
|
RNA, Messenger | 4 | 2023 | 1465 | 0.440 |
Why?
|
Genome, Fungal | 3 | 2021 | 40 | 0.430 |
Why?
|
RecQ Helicases | 1 | 2013 | 9 | 0.430 |
Why?
|
DNA End-Joining Repair | 1 | 2013 | 23 | 0.420 |
Why?
|
Protein Multimerization | 3 | 2024 | 169 | 0.420 |
Why?
|
Polymerase Chain Reaction | 6 | 2014 | 495 | 0.420 |
Why?
|
Nucleosome Assembly Protein 1 | 2 | 2009 | 2 | 0.400 |
Why?
|
Genome | 2 | 2013 | 257 | 0.400 |
Why?
|
Histone Code | 2 | 2019 | 26 | 0.390 |
Why?
|
Molecular Chaperones | 2 | 2016 | 99 | 0.390 |
Why?
|
Chromosomes | 3 | 2015 | 135 | 0.380 |
Why?
|
Histone-Lysine N-Methyltransferase | 4 | 2015 | 29 | 0.380 |
Why?
|
Protein Structure, Tertiary | 8 | 2007 | 656 | 0.360 |
Why?
|
Yeasts | 4 | 2003 | 51 | 0.360 |
Why?
|
Chromosomes, Fungal | 3 | 2020 | 35 | 0.350 |
Why?
|
Lysine | 4 | 2019 | 75 | 0.350 |
Why?
|
RNA Polymerase II | 6 | 2016 | 72 | 0.350 |
Why?
|
Dictyostelium | 1 | 2010 | 10 | 0.340 |
Why?
|
Ubiquitin-Protein Ligases | 3 | 2009 | 210 | 0.340 |
Why?
|
Cell Cycle Proteins | 3 | 2009 | 384 | 0.340 |
Why?
|
DNA Primers | 5 | 2014 | 289 | 0.330 |
Why?
|
Chromosomal Instability | 1 | 2009 | 20 | 0.330 |
Why?
|
Recombinational DNA Repair | 1 | 2009 | 19 | 0.330 |
Why?
|
Ultracentrifugation | 3 | 2015 | 28 | 0.330 |
Why?
|
Electrophoretic Mobility Shift Assay | 6 | 2013 | 64 | 0.320 |
Why?
|
DNA Footprinting | 5 | 2013 | 17 | 0.320 |
Why?
|
Chromatography, Ion Exchange | 1 | 2009 | 25 | 0.320 |
Why?
|
Humans | 36 | 2023 | 59366 | 0.320 |
Why?
|
Electrophoresis, Polyacrylamide Gel | 7 | 2014 | 178 | 0.310 |
Why?
|
Methylation | 5 | 2015 | 124 | 0.310 |
Why?
|
Protein Conformation | 6 | 2016 | 763 | 0.310 |
Why?
|
Polyamines | 1 | 2007 | 11 | 0.280 |
Why?
|
Galactokinase | 1 | 2007 | 3 | 0.280 |
Why?
|
Molecular Biology | 3 | 2013 | 66 | 0.270 |
Why?
|
RNA, Untranslated | 2 | 2019 | 101 | 0.270 |
Why?
|
Cell Extracts | 6 | 2010 | 25 | 0.250 |
Why?
|
Plasmids | 8 | 2013 | 279 | 0.250 |
Why?
|
Cullin Proteins | 1 | 2005 | 8 | 0.250 |
Why?
|
Chromatin Immunoprecipitation | 4 | 2012 | 145 | 0.250 |
Why?
|
Embryonic Stem Cells | 2 | 2017 | 151 | 0.250 |
Why?
|
Adaptation, Physiological | 1 | 2006 | 117 | 0.250 |
Why?
|
Deoxyribonuclease I | 4 | 2013 | 40 | 0.240 |
Why?
|
Protein Subunits | 3 | 2013 | 165 | 0.240 |
Why?
|
Fenfluramine | 1 | 2005 | 4 | 0.240 |
Why?
|
Schizosaccharomyces pombe Proteins | 1 | 2005 | 73 | 0.230 |
Why?
|
Protamine Kinase | 1 | 2004 | 2 | 0.230 |
Why?
|
Phosphorylation | 7 | 2013 | 883 | 0.230 |
Why?
|
Gene Expression Regulation, Enzymologic | 2 | 2009 | 128 | 0.220 |
Why?
|
Templates, Genetic | 3 | 2010 | 21 | 0.220 |
Why?
|
Transcription Factor TFIID | 3 | 2017 | 10 | 0.210 |
Why?
|
Tyrosine | 1 | 2003 | 92 | 0.210 |
Why?
|
Binding Sites | 8 | 2017 | 881 | 0.210 |
Why?
|
Enzymes | 1 | 2003 | 33 | 0.210 |
Why?
|
Recombinant Fusion Proteins | 3 | 2010 | 490 | 0.210 |
Why?
|
Nucleic Acid Heteroduplexes | 1 | 2003 | 15 | 0.210 |
Why?
|
HeLa Cells | 9 | 2010 | 526 | 0.210 |
Why?
|
Catalysis | 2 | 2019 | 152 | 0.200 |
Why?
|
Kinetics | 5 | 2008 | 751 | 0.190 |
Why?
|
Fluorescence | 1 | 2022 | 83 | 0.190 |
Why?
|
Cytoplasm | 1 | 2023 | 270 | 0.190 |
Why?
|
Repressor Proteins | 2 | 2017 | 331 | 0.180 |
Why?
|
Phosphorus Radioisotopes | 4 | 2013 | 14 | 0.180 |
Why?
|
Cytidine Deaminase | 1 | 2002 | 84 | 0.180 |
Why?
|
Blotting, Western | 5 | 2015 | 583 | 0.180 |
Why?
|
Genes, Fungal | 3 | 2007 | 56 | 0.180 |
Why?
|
Regulatory Sequences, Nucleic Acid | 1 | 2021 | 96 | 0.180 |
Why?
|
Dimerization | 2 | 2013 | 144 | 0.170 |
Why?
|
Signal Transduction | 1 | 2010 | 2903 | 0.170 |
Why?
|
Molecular Sequence Data | 5 | 2012 | 1951 | 0.170 |
Why?
|
HSP90 Heat-Shock Proteins | 2 | 2020 | 64 | 0.170 |
Why?
|
Telomerase | 2 | 2010 | 31 | 0.160 |
Why?
|
Time Factors | 7 | 2007 | 3615 | 0.160 |
Why?
|
DNA Repair Enzymes | 3 | 2005 | 37 | 0.160 |
Why?
|
Micrococcal Nuclease | 3 | 2009 | 13 | 0.160 |
Why?
|
Saccharomycetales | 2 | 2010 | 17 | 0.160 |
Why?
|
Mutation | 5 | 2015 | 2456 | 0.160 |
Why?
|
Insecta | 2 | 2009 | 37 | 0.160 |
Why?
|
RNA, Fungal | 1 | 2019 | 38 | 0.160 |
Why?
|
Euchromatin | 2 | 2017 | 16 | 0.160 |
Why?
|
Exosomes | 1 | 2019 | 44 | 0.150 |
Why?
|
Cell Line | 4 | 2017 | 1983 | 0.150 |
Why?
|
Amino Acid Sequence | 4 | 2005 | 1553 | 0.150 |
Why?
|
TATA-Binding Protein Associated Factors | 1 | 2017 | 18 | 0.140 |
Why?
|
Cells, Cultured | 3 | 2015 | 2092 | 0.140 |
Why?
|
Macromolecular Substances | 3 | 2003 | 160 | 0.140 |
Why?
|
Multiprotein Complexes | 2 | 2010 | 153 | 0.130 |
Why?
|
Magnesium | 2 | 2010 | 52 | 0.130 |
Why?
|
Protein Kinases | 3 | 2002 | 142 | 0.130 |
Why?
|
Image Processing, Computer-Assisted | 2 | 2015 | 651 | 0.130 |
Why?
|
Chickens | 4 | 2006 | 90 | 0.130 |
Why?
|
Eukaryotic Cells | 2 | 2014 | 57 | 0.130 |
Why?
|
Polyadenylation | 1 | 2016 | 45 | 0.130 |
Why?
|
Phosphoproteins | 1 | 2017 | 211 | 0.130 |
Why?
|
Alternative Splicing | 1 | 2016 | 122 | 0.120 |
Why?
|
Mutagenesis, Site-Directed | 2 | 2013 | 248 | 0.120 |
Why?
|
Transcriptional Elongation Factors | 1 | 2015 | 11 | 0.120 |
Why?
|
Protein Methyltransferases | 2 | 2006 | 14 | 0.120 |
Why?
|
Rosaniline Dyes | 1 | 2014 | 2 | 0.120 |
Why?
|
Protein Folding | 3 | 2010 | 260 | 0.120 |
Why?
|
Oligonucleotide Array Sequence Analysis | 2 | 2009 | 294 | 0.120 |
Why?
|
Mutation Rate | 1 | 2014 | 19 | 0.120 |
Why?
|
Hydrolysis | 2 | 2005 | 140 | 0.120 |
Why?
|
Microscopy, Electron | 1 | 2015 | 247 | 0.120 |
Why?
|
Molecular Imaging | 1 | 2015 | 46 | 0.120 |
Why?
|
Microscopy, Atomic Force | 1 | 2014 | 30 | 0.120 |
Why?
|
DNA Mismatch Repair | 1 | 2014 | 31 | 0.110 |
Why?
|
S Phase | 2 | 2008 | 74 | 0.110 |
Why?
|
Xenopus Proteins | 2 | 2006 | 35 | 0.110 |
Why?
|
Mutant Proteins | 1 | 2014 | 103 | 0.110 |
Why?
|
Monte Carlo Method | 1 | 2014 | 87 | 0.110 |
Why?
|
Cell Division | 2 | 2009 | 443 | 0.110 |
Why?
|
Peptide Fragments | 2 | 2008 | 400 | 0.110 |
Why?
|
Escherichia coli | 3 | 2014 | 695 | 0.110 |
Why?
|
Sequence Alignment | 2 | 2005 | 288 | 0.110 |
Why?
|
Biological Assay | 2 | 2010 | 56 | 0.110 |
Why?
|
Iodine Radioisotopes | 2 | 2003 | 50 | 0.110 |
Why?
|
Isotope Labeling | 4 | 2013 | 68 | 0.100 |
Why?
|
Ku Autoantigen | 1 | 2013 | 4 | 0.100 |
Why?
|
Ribonucleases | 1 | 2013 | 31 | 0.100 |
Why?
|
Antigens, Nuclear | 1 | 2013 | 19 | 0.100 |
Why?
|
Biocatalysis | 1 | 2013 | 45 | 0.100 |
Why?
|
Transcription Initiation Site | 1 | 2013 | 49 | 0.100 |
Why?
|
Oligonucleotides | 1 | 2014 | 215 | 0.100 |
Why?
|
Protein Stability | 1 | 2013 | 85 | 0.100 |
Why?
|
Point Mutation | 1 | 2013 | 160 | 0.100 |
Why?
|
G1 Phase | 1 | 2013 | 55 | 0.100 |
Why?
|
Reverse Transcriptase Polymerase Chain Reaction | 3 | 2015 | 527 | 0.100 |
Why?
|
Genomics | 3 | 2009 | 319 | 0.100 |
Why?
|
Substrate Specificity | 1 | 2013 | 333 | 0.100 |
Why?
|
Regulatory Elements, Transcriptional | 1 | 2012 | 37 | 0.100 |
Why?
|
DNA Mutational Analysis | 1 | 2012 | 188 | 0.090 |
Why?
|
Cell Wall | 1 | 2012 | 115 | 0.090 |
Why?
|
Mitosis | 1 | 2013 | 208 | 0.090 |
Why?
|
Cloning, Molecular | 1 | 2012 | 381 | 0.090 |
Why?
|
Electrophoresis, Agar Gel | 1 | 2010 | 16 | 0.090 |
Why?
|
Potassium Permanganate | 1 | 2010 | 1 | 0.090 |
Why?
|
DNA Polymerase II | 1 | 2010 | 8 | 0.090 |
Why?
|
Mediator Complex | 1 | 2010 | 13 | 0.090 |
Why?
|
Stress, Physiological | 1 | 2012 | 185 | 0.090 |
Why?
|
Guanosine | 1 | 2010 | 10 | 0.090 |
Why?
|
Cell Fractionation | 1 | 2009 | 32 | 0.080 |
Why?
|
Sirtuin 2 | 1 | 2009 | 6 | 0.080 |
Why?
|
Computational Biology | 1 | 2012 | 333 | 0.080 |
Why?
|
Sulfuric Acid Esters | 1 | 2009 | 6 | 0.080 |
Why?
|
Alkylating Agents | 1 | 2009 | 10 | 0.080 |
Why?
|
Magnesium Chloride | 2 | 2006 | 5 | 0.080 |
Why?
|
Telomere-Binding Proteins | 1 | 2009 | 6 | 0.080 |
Why?
|
Algorithms | 1 | 2014 | 974 | 0.080 |
Why?
|
Epitopes | 1 | 2010 | 286 | 0.080 |
Why?
|
Microscopy | 1 | 2009 | 90 | 0.080 |
Why?
|
Electrophoresis, Gel, Pulsed-Field | 1 | 2008 | 9 | 0.070 |
Why?
|
Hydroxyurea | 1 | 2008 | 20 | 0.070 |
Why?
|
Gene Deletion | 3 | 2016 | 293 | 0.070 |
Why?
|
Alleles | 2 | 2006 | 411 | 0.070 |
Why?
|
Editorial Policies | 1 | 2007 | 52 | 0.070 |
Why?
|
Multigene Family | 1 | 2007 | 92 | 0.070 |
Why?
|
DNA Methylation | 1 | 2009 | 271 | 0.070 |
Why?
|
Publishing | 1 | 2007 | 89 | 0.070 |
Why?
|
Amino Acid Substitution | 2 | 2010 | 234 | 0.070 |
Why?
|
Genome, Human | 1 | 2008 | 224 | 0.070 |
Why?
|
Molecular Structure | 1 | 2007 | 374 | 0.070 |
Why?
|
Research | 1 | 2007 | 188 | 0.060 |
Why?
|
DNA, Ribosomal | 2 | 2004 | 29 | 0.060 |
Why?
|
HMGN1 Protein | 1 | 2005 | 3 | 0.060 |
Why?
|
Centromere | 1 | 2006 | 38 | 0.060 |
Why?
|
Phosphoprotein Phosphatases | 1 | 2005 | 41 | 0.060 |
Why?
|
Methyltransferases | 1 | 2005 | 52 | 0.060 |
Why?
|
Casein Kinase II | 1 | 2005 | 16 | 0.060 |
Why?
|
Blotting, Southern | 1 | 2005 | 52 | 0.060 |
Why?
|
Conserved Sequence | 1 | 2005 | 170 | 0.060 |
Why?
|
Serine | 1 | 2005 | 83 | 0.060 |
Why?
|
Amino Acid Motifs | 1 | 2005 | 149 | 0.060 |
Why?
|
RNA-Binding Proteins | 2 | 2012 | 386 | 0.060 |
Why?
|
Immunoprecipitation | 1 | 2005 | 113 | 0.060 |
Why?
|
DNA Restriction Enzymes | 3 | 2011 | 35 | 0.060 |
Why?
|
Schizosaccharomyces | 1 | 2005 | 104 | 0.060 |
Why?
|
Glucose | 1 | 2007 | 445 | 0.060 |
Why?
|
Radioisotope Dilution Technique | 1 | 2003 | 1 | 0.050 |
Why?
|
Mice | 2 | 2015 | 10294 | 0.050 |
Why?
|
Indicators and Reagents | 1 | 2003 | 51 | 0.050 |
Why?
|
Rad52 DNA Repair and Recombination Protein | 1 | 2003 | 2 | 0.050 |
Why?
|
Replication Protein A | 1 | 2003 | 13 | 0.050 |
Why?
|
Deoxyribodipyrimidine Photo-Lyase | 1 | 2003 | 1 | 0.050 |
Why?
|
Chromatography, High Pressure Liquid | 1 | 2004 | 225 | 0.050 |
Why?
|
Membrane Proteins | 1 | 2009 | 850 | 0.050 |
Why?
|
Models, Chemical | 1 | 2004 | 136 | 0.050 |
Why?
|
Microscopy, Electron, Scanning Transmission | 1 | 2003 | 2 | 0.050 |
Why?
|
Cell Proliferation | 1 | 2007 | 941 | 0.050 |
Why?
|
Xenopus | 1 | 2003 | 54 | 0.050 |
Why?
|
Molecular Weight | 1 | 2003 | 184 | 0.050 |
Why?
|
Models, Biological | 3 | 2006 | 1143 | 0.050 |
Why?
|
Rec A Recombinases | 1 | 2003 | 35 | 0.050 |
Why?
|
CHO Cells | 1 | 2003 | 189 | 0.050 |
Why?
|
APOBEC-1 Deaminase | 1 | 2002 | 2 | 0.050 |
Why?
|
CDC28 Protein Kinase, S cerevisiae | 1 | 2002 | 4 | 0.050 |
Why?
|
Ultraviolet Rays | 1 | 2003 | 127 | 0.050 |
Why?
|
RNA, Ribosomal, 5S | 1 | 2002 | 4 | 0.050 |
Why?
|
Cricetinae | 1 | 2003 | 366 | 0.050 |
Why?
|
Mi-2 Nucleosome Remodeling and Deacetylase Complex | 1 | 2002 | 17 | 0.050 |
Why?
|
Acetyl Coenzyme A | 1 | 2002 | 22 | 0.050 |
Why?
|
Salts | 1 | 2002 | 15 | 0.050 |
Why?
|
Polycomb Repressive Complex 1 | 1 | 2002 | 31 | 0.050 |
Why?
|
CDC2 Protein Kinase | 1 | 2002 | 33 | 0.050 |
Why?
|
Autoradiography | 2 | 2013 | 53 | 0.050 |
Why?
|
Sea Urchins | 1 | 2002 | 35 | 0.050 |
Why?
|
Enterocytes | 1 | 2002 | 24 | 0.050 |
Why?
|
Carbon | 1 | 2022 | 45 | 0.050 |
Why?
|
Interferon-beta | 1 | 2002 | 76 | 0.050 |
Why?
|
Temperature | 1 | 2003 | 295 | 0.050 |
Why?
|
High Mobility Group Proteins | 1 | 2021 | 20 | 0.050 |
Why?
|
Cryoelectron Microscopy | 1 | 2023 | 187 | 0.050 |
Why?
|
Structure-Activity Relationship | 1 | 2002 | 365 | 0.050 |
Why?
|
Autoantigens | 1 | 2002 | 129 | 0.050 |
Why?
|
alpha 1-Antitrypsin | 1 | 2002 | 87 | 0.050 |
Why?
|
Whole Genome Sequencing | 1 | 2021 | 63 | 0.040 |
Why?
|
Larva | 1 | 2021 | 132 | 0.040 |
Why?
|
Mutagenesis | 1 | 2021 | 129 | 0.040 |
Why?
|
Microfilament Proteins | 1 | 2021 | 108 | 0.040 |
Why?
|
Hydrogen-Ion Concentration | 1 | 2022 | 450 | 0.040 |
Why?
|
Myo-Inositol-1-Phosphate Synthase | 1 | 2020 | 1 | 0.040 |
Why?
|
Peptides | 1 | 2004 | 549 | 0.040 |
Why?
|
Protein Domains | 1 | 2020 | 140 | 0.040 |
Why?
|
Myosin Heavy Chains | 1 | 2020 | 42 | 0.040 |
Why?
|
Base Sequence | 2 | 2013 | 1302 | 0.040 |
Why?
|
Gene Expression Profiling | 1 | 2002 | 718 | 0.040 |
Why?
|
Cytoskeletal Proteins | 1 | 2020 | 196 | 0.040 |
Why?
|
Actins | 1 | 2020 | 259 | 0.040 |
Why?
|
TATA-Box Binding Protein | 1 | 2017 | 10 | 0.040 |
Why?
|
Antibodies | 2 | 2010 | 179 | 0.040 |
Why?
|
In Vitro Techniques | 2 | 2010 | 471 | 0.030 |
Why?
|
Drosophila melanogaster | 1 | 2021 | 481 | 0.030 |
Why?
|
Poly dA-dT | 1 | 2016 | 7 | 0.030 |
Why?
|
Cell Differentiation | 1 | 2002 | 1304 | 0.030 |
Why?
|
Transfection | 1 | 2017 | 675 | 0.030 |
Why?
|
Histone Chaperones | 1 | 2015 | 7 | 0.030 |
Why?
|
Genotype | 1 | 2017 | 617 | 0.030 |
Why?
|
Calibration | 1 | 2015 | 67 | 0.030 |
Why?
|
Protein Biosynthesis | 1 | 2016 | 297 | 0.030 |
Why?
|
RNA Interference | 1 | 2017 | 590 | 0.030 |
Why?
|
Phenotype | 1 | 2017 | 1137 | 0.030 |
Why?
|
Polynucleotide 5'-Hydroxyl-Kinase | 1 | 2013 | 2 | 0.030 |
Why?
|
Open Reading Frames | 1 | 2013 | 80 | 0.030 |
Why?
|
Phosphoric Monoester Hydrolases | 1 | 2013 | 47 | 0.030 |
Why?
|
MADS Domain Proteins | 1 | 2012 | 2 | 0.030 |
Why?
|
Dose-Response Relationship, Drug | 2 | 2005 | 805 | 0.020 |
Why?
|
Consensus Sequence | 1 | 2012 | 29 | 0.020 |
Why?
|
Mitogen-Activated Protein Kinases | 1 | 2012 | 205 | 0.020 |
Why?
|
Cross-Linking Reagents | 1 | 2011 | 117 | 0.020 |
Why?
|
Reproducibility of Results | 1 | 2015 | 1559 | 0.020 |
Why?
|
Resins, Synthetic | 1 | 2010 | 2 | 0.020 |
Why?
|
Hemagglutinins | 1 | 2010 | 17 | 0.020 |
Why?
|
Chemical Fractionation | 1 | 2010 | 13 | 0.020 |
Why?
|
Microspheres | 1 | 2010 | 55 | 0.020 |
Why?
|
Sequence Analysis, DNA | 1 | 2012 | 394 | 0.020 |
Why?
|
Mass Spectrometry | 1 | 2012 | 295 | 0.020 |
Why?
|
Electrophoresis, Gel, Two-Dimensional | 1 | 2009 | 39 | 0.020 |
Why?
|
Subcellular Fractions | 1 | 2009 | 68 | 0.020 |
Why?
|
Staining and Labeling | 1 | 2010 | 124 | 0.020 |
Why?
|
Guanosine Triphosphate | 1 | 2010 | 50 | 0.020 |
Why?
|
Restriction Mapping | 1 | 2009 | 51 | 0.020 |
Why?
|
Protein Interaction Mapping | 1 | 2009 | 67 | 0.020 |
Why?
|
Crystallography, X-Ray | 1 | 2010 | 424 | 0.020 |
Why?
|
CCCTC-Binding Factor | 1 | 2008 | 40 | 0.020 |
Why?
|
Enzyme Inhibitors | 1 | 2010 | 347 | 0.020 |
Why?
|
Tandem Repeat Sequences | 1 | 2006 | 26 | 0.020 |
Why?
|
Optical Tweezers | 1 | 2006 | 8 | 0.020 |
Why?
|
Genetic Vectors | 1 | 2013 | 808 | 0.020 |
Why?
|
Stress, Mechanical | 1 | 2006 | 110 | 0.020 |
Why?
|
Molecular Probes | 1 | 2006 | 29 | 0.020 |
Why?
|
DNA-Activated Protein Kinase | 1 | 2005 | 12 | 0.020 |
Why?
|
Protein Phosphatase 2 | 1 | 2005 | 10 | 0.020 |
Why?
|
Ataxia Telangiectasia Mutated Proteins | 1 | 2005 | 42 | 0.020 |
Why?
|
Sodium Dodecyl Sulfate | 1 | 2005 | 30 | 0.020 |
Why?
|
NFI Transcription Factors | 1 | 2004 | 7 | 0.010 |
Why?
|
Mammary Tumor Virus, Mouse | 1 | 2004 | 7 | 0.010 |
Why?
|
Tumor Suppressor Proteins | 1 | 2005 | 194 | 0.010 |
Why?
|
Receptors, Progesterone | 1 | 2004 | 108 | 0.010 |
Why?
|
Fibroblasts | 1 | 2005 | 377 | 0.010 |
Why?
|
Progesterone | 1 | 2004 | 158 | 0.010 |
Why?
|
Precipitin Tests | 1 | 2002 | 76 | 0.010 |
Why?
|
Birds | 1 | 2002 | 8 | 0.010 |
Why?
|
Alanine | 1 | 2002 | 49 | 0.010 |
Why?
|