Concepts (159)
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?
|
|---|
| RNA Splicing | 27 | 2024 | 158 | 5.380 |
Why?
|
| Spliceosomes | 18 | 2024 | 48 | 4.030 |
Why?
|
| Saccharomyces cerevisiae Proteins | 16 | 2019 | 301 | 2.990 |
Why?
|
| DEAD-box RNA Helicases | 14 | 2019 | 71 | 2.890 |
Why?
|
| Saccharomyces cerevisiae | 19 | 2017 | 460 | 2.860 |
Why?
|
| RNA Precursors | 13 | 2016 | 73 | 2.310 |
Why?
|
| RNA, Small Nuclear | 10 | 2019 | 36 | 2.290 |
Why?
|
| Adenosine Triphosphatases | 8 | 2019 | 155 | 2.060 |
Why?
|
| RNA Helicases | 8 | 2016 | 36 | 1.600 |
Why?
|
| RNA, Fungal | 9 | 2017 | 43 | 1.540 |
Why?
|
| RNA Splice Sites | 8 | 2024 | 58 | 1.310 |
Why?
|
| Introns | 13 | 2024 | 304 | 1.300 |
Why?
|
| RNA Nucleotidyltransferases | 5 | 2024 | 12 | 0.960 |
Why?
|
| Alternative Splicing | 2 | 2024 | 219 | 0.890 |
Why?
|
| Exons | 8 | 2024 | 454 | 0.780 |
Why?
|
| Base Sequence | 11 | 2022 | 2342 | 0.660 |
Why?
|
| Nucleic Acid Conformation | 10 | 2016 | 349 | 0.620 |
Why?
|
| RNA | 5 | 2016 | 597 | 0.520 |
Why?
|
| Ribosomes | 2 | 2009 | 116 | 0.520 |
Why?
|
| RNA-Directed DNA Polymerase | 1 | 2016 | 16 | 0.500 |
Why?
|
| Adenosine Triphosphate | 4 | 2010 | 323 | 0.500 |
Why?
|
| Nucleotidyltransferases | 1 | 2016 | 32 | 0.500 |
Why?
|
| RNA, Catalytic | 2 | 2014 | 134 | 0.490 |
Why?
|
| Genome, Fungal | 1 | 2015 | 35 | 0.480 |
Why?
|
| Endoribonucleases | 1 | 2016 | 93 | 0.470 |
Why?
|
| RNA Splicing Factors | 6 | 2016 | 29 | 0.470 |
Why?
|
| RNA, Messenger | 4 | 2024 | 2057 | 0.450 |
Why?
|
| Ribonucleoprotein, U5 Small Nuclear | 4 | 2013 | 9 | 0.400 |
Why?
|
| Models, Molecular | 9 | 2017 | 1364 | 0.330 |
Why?
|
| Ribonucleoproteins | 2 | 2013 | 37 | 0.320 |
Why?
|
| Mutation | 11 | 2017 | 4326 | 0.310 |
Why?
|
| RNA-Binding Proteins | 3 | 2024 | 294 | 0.300 |
Why?
|
| Trans-Splicing | 1 | 2008 | 1 | 0.290 |
Why?
|
| Aprotinin | 3 | 1994 | 25 | 0.290 |
Why?
|
| RNA, Double-Stranded | 1 | 2006 | 26 | 0.260 |
Why?
|
| Molecular Sequence Data | 7 | 2015 | 3047 | 0.240 |
Why?
|
| Nonsense Mediated mRNA Decay | 1 | 2024 | 9 | 0.220 |
Why?
|
| Gene Expression Regulation, Fungal | 2 | 2015 | 65 | 0.210 |
Why?
|
| Models, Biological | 5 | 2013 | 1801 | 0.200 |
Why?
|
| Ribonucleoprotein, U4-U6 Small Nuclear | 3 | 2013 | 6 | 0.200 |
Why?
|
| Ribonucleoproteins, Small Nuclear | 3 | 2009 | 20 | 0.200 |
Why?
|
| Repressor Proteins | 1 | 2006 | 445 | 0.200 |
Why?
|
| Crystallography, X-Ray | 4 | 2017 | 520 | 0.190 |
Why?
|
| Protein Conformation | 5 | 2016 | 925 | 0.180 |
Why?
|
| Recombinant Proteins | 4 | 2010 | 1024 | 0.170 |
Why?
|
| Protein Binding | 3 | 2019 | 1544 | 0.170 |
Why?
|
| Catalysis | 3 | 2013 | 213 | 0.160 |
Why?
|
| Catalytic Domain | 2 | 2017 | 162 | 0.130 |
Why?
|
| Lactococcus lactis | 1 | 2016 | 5 | 0.130 |
Why?
|
| DEAD Box Protein 58 | 1 | 2016 | 11 | 0.130 |
Why?
|
| Clostridiales | 1 | 2016 | 18 | 0.120 |
Why?
|
| Metals | 2 | 2013 | 100 | 0.120 |
Why?
|
| Immunoglobulin Fab Fragments | 1 | 2016 | 86 | 0.120 |
Why?
|
| Binding Sites | 3 | 2017 | 1155 | 0.120 |
Why?
|
| Interferon-beta | 1 | 2016 | 126 | 0.120 |
Why?
|
| Cryoelectron Microscopy | 1 | 2016 | 113 | 0.120 |
Why?
|
| Immunologic Factors | 1 | 2016 | 179 | 0.110 |
Why?
|
| Oligoribonucleotides | 1 | 2014 | 27 | 0.110 |
Why?
|
| Recombination, Genetic | 1 | 2016 | 444 | 0.110 |
Why?
|
| Molecular Probes | 1 | 2014 | 37 | 0.110 |
Why?
|
| Guanosine | 1 | 2014 | 30 | 0.110 |
Why?
|
| Organophosphorus Compounds | 1 | 2014 | 53 | 0.100 |
Why?
|
| Phosphates | 1 | 2014 | 165 | 0.100 |
Why?
|
| Ions | 1 | 2013 | 78 | 0.100 |
Why?
|
| Telomerase | 1 | 2013 | 68 | 0.100 |
Why?
|
| Schizosaccharomyces | 1 | 2013 | 56 | 0.100 |
Why?
|
| Substrate Specificity | 1 | 2013 | 364 | 0.090 |
Why?
|
| RNA, Untranslated | 1 | 2012 | 69 | 0.090 |
Why?
|
| Meiosis | 1 | 2012 | 84 | 0.090 |
Why?
|
| Cell Nucleus | 2 | 2013 | 618 | 0.090 |
Why?
|
| DNA | 1 | 2016 | 1328 | 0.080 |
Why?
|
| Retinitis Pigmentosa | 1 | 2009 | 36 | 0.080 |
Why?
|
| Cytoplasm | 1 | 2010 | 286 | 0.080 |
Why?
|
| RNA, Ribosomal | 1 | 2009 | 71 | 0.070 |
Why?
|
| Plasmids | 1 | 2009 | 289 | 0.070 |
Why?
|
| Disulfides | 3 | 1994 | 65 | 0.070 |
Why?
|
| Humans | 8 | 2024 | 94647 | 0.070 |
Why?
|
| Ubiquitin | 1 | 2008 | 96 | 0.070 |
Why?
|
| HeLa Cells | 2 | 2024 | 520 | 0.070 |
Why?
|
| Animals | 5 | 2016 | 28587 | 0.070 |
Why?
|
| Suppression, Genetic | 2 | 2004 | 30 | 0.070 |
Why?
|
| Magnetic Resonance Spectroscopy | 3 | 1994 | 321 | 0.070 |
Why?
|
| Nucleic Acid Heteroduplexes | 1 | 2006 | 11 | 0.060 |
Why?
|
| Guanosine Diphosphate | 1 | 2006 | 19 | 0.060 |
Why?
|
| Ribonucleotides | 1 | 2006 | 13 | 0.060 |
Why?
|
| Guanosine Triphosphate | 1 | 2006 | 38 | 0.060 |
Why?
|
| DNA, Single-Stranded | 1 | 2006 | 95 | 0.060 |
Why?
|
| RNA, Transfer | 1 | 2008 | 168 | 0.060 |
Why?
|
| RNA, Small Nucleolar | 1 | 2006 | 8 | 0.060 |
Why?
|
| Protein Biosynthesis | 1 | 2008 | 389 | 0.060 |
Why?
|
| Genes, Lethal | 1 | 2004 | 53 | 0.050 |
Why?
|
| Genes, Fungal | 1 | 2004 | 60 | 0.050 |
Why?
|
| Reverse Transcriptase Polymerase Chain Reaction | 1 | 2006 | 898 | 0.050 |
Why?
|
| Circular Dichroism | 2 | 1994 | 118 | 0.050 |
Why?
|
| Amino Acid Sequence | 3 | 2009 | 2093 | 0.050 |
Why?
|
| HEK293 Cells | 1 | 2024 | 690 | 0.050 |
Why?
|
| Nuclear Magnetic Resonance, Biomolecular | 1 | 2002 | 64 | 0.050 |
Why?
|
| Ribonucleoprotein, U1 Small Nuclear | 1 | 2001 | 2 | 0.040 |
Why?
|
| Kinetics | 2 | 2016 | 1560 | 0.040 |
Why?
|
| Neoplasms | 1 | 2016 | 3205 | 0.040 |
Why?
|
| Quantitative Trait Loci | 1 | 2024 | 632 | 0.040 |
Why?
|
| Protein Structure, Tertiary | 1 | 2002 | 748 | 0.040 |
Why?
|
| Gonadotropin-Releasing Hormone | 1 | 1999 | 105 | 0.040 |
Why?
|
| Antineoplastic Agents, Hormonal | 1 | 1999 | 152 | 0.040 |
Why?
|
| Brachytherapy | 1 | 1999 | 124 | 0.040 |
Why?
|
| RNA Processing, Post-Transcriptional | 1 | 1999 | 118 | 0.030 |
Why?
|
| Temperature | 1 | 1999 | 416 | 0.030 |
Why?
|
| Adenosine Diphosphate | 1 | 2017 | 60 | 0.030 |
Why?
|
| Nuclear Proteins | 2 | 2013 | 755 | 0.030 |
Why?
|
| Genome-Wide Association Study | 1 | 2024 | 1742 | 0.030 |
Why?
|
| Peptide Library | 1 | 2016 | 84 | 0.030 |
Why?
|
| Protein Domains | 1 | 2017 | 160 | 0.030 |
Why?
|
| RNA, Small Untranslated | 1 | 2016 | 15 | 0.030 |
Why?
|
| Neoadjuvant Therapy | 1 | 1999 | 440 | 0.030 |
Why?
|
| Gene Expression Regulation | 1 | 2024 | 2041 | 0.030 |
Why?
|
| Actins | 1 | 1999 | 473 | 0.030 |
Why?
|
| Alleles | 1 | 1999 | 1153 | 0.030 |
Why?
|
| Sequence Homology, Amino Acid | 2 | 2009 | 423 | 0.030 |
Why?
|
| Alanine | 1 | 1994 | 84 | 0.030 |
Why?
|
| Cattle | 1 | 1994 | 386 | 0.030 |
Why?
|
| Cysteine | 1 | 1994 | 145 | 0.030 |
Why?
|
| Ribonuclease H | 1 | 2013 | 8 | 0.030 |
Why?
|
| Hydrogen-Ion Concentration | 1 | 1994 | 506 | 0.030 |
Why?
|
| Ligation | 1 | 2013 | 53 | 0.030 |
Why?
|
| Splicing Factor U2AF | 1 | 2013 | 5 | 0.030 |
Why?
|
| Protein Folding | 1 | 1994 | 294 | 0.020 |
Why?
|
| Hydrogen Bonding | 1 | 1992 | 153 | 0.020 |
Why?
|
| Mutagenesis, Site-Directed | 1 | 1992 | 283 | 0.020 |
Why?
|
| Structure-Activity Relationship | 1 | 1992 | 437 | 0.020 |
Why?
|
| In Vitro Techniques | 1 | 1992 | 1008 | 0.020 |
Why?
|
| Solutions | 1 | 1990 | 86 | 0.020 |
Why?
|
| Protein Denaturation | 1 | 1990 | 109 | 0.020 |
Why?
|
| Cell Line, Tumor | 1 | 2016 | 2755 | 0.020 |
Why?
|
| Physical Chromosome Mapping | 1 | 2009 | 28 | 0.020 |
Why?
|
| Oligonucleotide Array Sequence Analysis | 1 | 2012 | 701 | 0.020 |
Why?
|
| Leucine | 1 | 2009 | 60 | 0.020 |
Why?
|
| Lod Score | 1 | 2009 | 153 | 0.020 |
Why?
|
| Genes, Dominant | 1 | 2009 | 116 | 0.020 |
Why?
|
| Microsatellite Repeats | 1 | 2009 | 149 | 0.020 |
Why?
|
| Mice, Inbred C57BL | 1 | 2016 | 3452 | 0.020 |
Why?
|
| Genetic Markers | 1 | 2009 | 477 | 0.020 |
Why?
|
| Amino Acid Substitution | 1 | 2009 | 338 | 0.020 |
Why?
|
| Sulfanilic Acids | 1 | 2008 | 1 | 0.020 |
Why?
|
| Prostatic Neoplasms | 1 | 1999 | 1790 | 0.020 |
Why?
|
| Water | 1 | 1990 | 298 | 0.020 |
Why?
|
| Mutation, Missense | 1 | 2009 | 296 | 0.020 |
Why?
|
| Ubiquitination | 1 | 2008 | 79 | 0.020 |
Why?
|
| Protein Interaction Domains and Motifs | 1 | 2008 | 89 | 0.020 |
Why?
|
| Quinolines | 1 | 2008 | 89 | 0.020 |
Why?
|
| Pedigree | 1 | 2009 | 976 | 0.020 |
Why?
|
| Transcriptome | 1 | 2012 | 749 | 0.020 |
Why?
|
| Gene Expression Profiling | 1 | 2012 | 1518 | 0.020 |
Why?
|
| Signal Transduction | 1 | 2016 | 3578 | 0.010 |
Why?
|
| Mice | 1 | 2016 | 12428 | 0.010 |
Why?
|
| Yeasts | 1 | 2001 | 50 | 0.010 |
Why?
|
| Combined Modality Therapy | 1 | 1999 | 1756 | 0.010 |
Why?
|
| Male | 2 | 2009 | 45142 | 0.010 |
Why?
|
| Female | 1 | 2009 | 49310 | 0.000 |
Why?
|
| Aged | 1 | 1999 | 20601 | 0.000 |
Why?
|