Concepts (154)
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 | 26 | 2022 | 142 | 5.950 |
Why?
|
| Spliceosomes | 17 | 2019 | 45 | 4.320 |
Why?
|
| Saccharomyces cerevisiae Proteins | 16 | 2019 | 276 | 3.410 |
Why?
|
| DEAD-box RNA Helicases | 14 | 2019 | 62 | 3.290 |
Why?
|
| Saccharomyces cerevisiae | 19 | 2017 | 434 | 3.240 |
Why?
|
| RNA Precursors | 13 | 2016 | 69 | 2.620 |
Why?
|
| RNA, Small Nuclear | 10 | 2019 | 32 | 2.600 |
Why?
|
| Adenosine Triphosphatases | 8 | 2019 | 153 | 2.330 |
Why?
|
| RNA Helicases | 8 | 2016 | 35 | 1.810 |
Why?
|
| RNA, Fungal | 9 | 2017 | 42 | 1.750 |
Why?
|
| RNA Splice Sites | 7 | 2016 | 53 | 1.420 |
Why?
|
| Introns | 11 | 2022 | 289 | 1.200 |
Why?
|
| RNA Nucleotidyltransferases | 4 | 2015 | 11 | 0.850 |
Why?
|
| Exons | 7 | 2022 | 450 | 0.830 |
Why?
|
| Alternative Splicing | 1 | 2022 | 201 | 0.800 |
Why?
|
| Base Sequence | 11 | 2022 | 2330 | 0.730 |
Why?
|
| Nucleic Acid Conformation | 10 | 2016 | 332 | 0.710 |
Why?
|
| Ribosomes | 2 | 2009 | 111 | 0.590 |
Why?
|
| RNA | 5 | 2016 | 560 | 0.590 |
Why?
|
| RNA-Directed DNA Polymerase | 1 | 2016 | 16 | 0.570 |
Why?
|
| Nucleotidyltransferases | 1 | 2016 | 29 | 0.570 |
Why?
|
| Adenosine Triphosphate | 4 | 2010 | 314 | 0.560 |
Why?
|
| RNA, Catalytic | 2 | 2014 | 129 | 0.550 |
Why?
|
| Genome, Fungal | 1 | 2015 | 32 | 0.540 |
Why?
|
| RNA Splicing Factors | 6 | 2016 | 27 | 0.540 |
Why?
|
| Endoribonucleases | 1 | 2016 | 92 | 0.530 |
Why?
|
| RNA, Messenger | 3 | 2009 | 1981 | 0.480 |
Why?
|
| Ribonucleoprotein, U5 Small Nuclear | 4 | 2013 | 9 | 0.450 |
Why?
|
| Ribonucleoproteins | 2 | 2013 | 38 | 0.370 |
Why?
|
| Models, Molecular | 9 | 2017 | 1286 | 0.370 |
Why?
|
| Mutation | 11 | 2017 | 3968 | 0.360 |
Why?
|
| Trans-Splicing | 1 | 2008 | 1 | 0.330 |
Why?
|
| Aprotinin | 3 | 1994 | 26 | 0.320 |
Why?
|
| RNA-Binding Proteins | 2 | 2016 | 249 | 0.300 |
Why?
|
| RNA, Double-Stranded | 1 | 2006 | 22 | 0.290 |
Why?
|
| Molecular Sequence Data | 7 | 2015 | 3030 | 0.270 |
Why?
|
| Gene Expression Regulation, Fungal | 2 | 2015 | 61 | 0.240 |
Why?
|
| Ribonucleoprotein, U4-U6 Small Nuclear | 3 | 2013 | 6 | 0.230 |
Why?
|
| Repressor Proteins | 1 | 2006 | 403 | 0.230 |
Why?
|
| Models, Biological | 5 | 2013 | 1749 | 0.230 |
Why?
|
| Ribonucleoproteins, Small Nuclear | 3 | 2009 | 20 | 0.220 |
Why?
|
| Crystallography, X-Ray | 4 | 2017 | 485 | 0.220 |
Why?
|
| Protein Conformation | 5 | 2016 | 881 | 0.210 |
Why?
|
| Protein Binding | 3 | 2019 | 1457 | 0.190 |
Why?
|
| Recombinant Proteins | 4 | 2010 | 1015 | 0.190 |
Why?
|
| Catalysis | 3 | 2013 | 203 | 0.190 |
Why?
|
| Catalytic Domain | 2 | 2017 | 156 | 0.150 |
Why?
|
| Lactococcus lactis | 1 | 2016 | 5 | 0.140 |
Why?
|
| DEAD Box Protein 58 | 1 | 2016 | 11 | 0.140 |
Why?
|
| Clostridiales | 1 | 2016 | 17 | 0.140 |
Why?
|
| Metals | 2 | 2013 | 90 | 0.140 |
Why?
|
| Immunoglobulin Fab Fragments | 1 | 2016 | 81 | 0.140 |
Why?
|
| Binding Sites | 3 | 2017 | 1098 | 0.130 |
Why?
|
| Interferon-beta | 1 | 2016 | 125 | 0.130 |
Why?
|
| Cryoelectron Microscopy | 1 | 2016 | 91 | 0.130 |
Why?
|
| Immunologic Factors | 1 | 2016 | 170 | 0.130 |
Why?
|
| Oligoribonucleotides | 1 | 2014 | 28 | 0.120 |
Why?
|
| Molecular Probes | 1 | 2014 | 35 | 0.120 |
Why?
|
| Guanosine | 1 | 2014 | 29 | 0.120 |
Why?
|
| Recombination, Genetic | 1 | 2016 | 439 | 0.120 |
Why?
|
| Organophosphorus Compounds | 1 | 2014 | 55 | 0.120 |
Why?
|
| Phosphates | 1 | 2014 | 160 | 0.110 |
Why?
|
| Ions | 1 | 2013 | 74 | 0.110 |
Why?
|
| Telomerase | 1 | 2013 | 55 | 0.110 |
Why?
|
| Schizosaccharomyces | 1 | 2013 | 54 | 0.110 |
Why?
|
| Substrate Specificity | 1 | 2013 | 347 | 0.110 |
Why?
|
| RNA, Untranslated | 1 | 2012 | 63 | 0.100 |
Why?
|
| Meiosis | 1 | 2012 | 80 | 0.100 |
Why?
|
| Cell Nucleus | 2 | 2013 | 580 | 0.100 |
Why?
|
| DNA | 1 | 2016 | 1294 | 0.090 |
Why?
|
| Retinitis Pigmentosa | 1 | 2009 | 35 | 0.090 |
Why?
|
| Cytoplasm | 1 | 2010 | 281 | 0.090 |
Why?
|
| RNA, Ribosomal | 1 | 2009 | 60 | 0.080 |
Why?
|
| Plasmids | 1 | 2009 | 287 | 0.080 |
Why?
|
| Disulfides | 3 | 1994 | 64 | 0.080 |
Why?
|
| Ubiquitin | 1 | 2008 | 93 | 0.080 |
Why?
|
| Animals | 5 | 2016 | 26590 | 0.080 |
Why?
|
| Suppression, Genetic | 2 | 2004 | 30 | 0.070 |
Why?
|
| Magnetic Resonance Spectroscopy | 3 | 1994 | 318 | 0.070 |
Why?
|
| Nucleic Acid Heteroduplexes | 1 | 2006 | 11 | 0.070 |
Why?
|
| Guanosine Diphosphate | 1 | 2006 | 19 | 0.070 |
Why?
|
| Ribonucleotides | 1 | 2006 | 13 | 0.070 |
Why?
|
| Guanosine Triphosphate | 1 | 2006 | 38 | 0.070 |
Why?
|
| RNA, Transfer | 1 | 2008 | 151 | 0.070 |
Why?
|
| DNA, Single-Stranded | 1 | 2006 | 92 | 0.070 |
Why?
|
| RNA, Small Nucleolar | 1 | 2006 | 5 | 0.070 |
Why?
|
| Protein Biosynthesis | 1 | 2008 | 378 | 0.070 |
Why?
|
| Humans | 6 | 2022 | 86678 | 0.060 |
Why?
|
| Genes, Lethal | 1 | 2004 | 53 | 0.060 |
Why?
|
| Genes, Fungal | 1 | 2004 | 58 | 0.060 |
Why?
|
| Reverse Transcriptase Polymerase Chain Reaction | 1 | 2006 | 879 | 0.060 |
Why?
|
| Circular Dichroism | 2 | 1994 | 117 | 0.060 |
Why?
|
| Amino Acid Sequence | 3 | 2009 | 2062 | 0.050 |
Why?
|
| Nuclear Magnetic Resonance, Biomolecular | 1 | 2002 | 60 | 0.050 |
Why?
|
| Ribonucleoprotein, U1 Small Nuclear | 1 | 2001 | 2 | 0.050 |
Why?
|
| Neoplasms | 1 | 2016 | 2898 | 0.050 |
Why?
|
| Kinetics | 2 | 2016 | 1513 | 0.050 |
Why?
|
| Protein Structure, Tertiary | 1 | 2002 | 736 | 0.040 |
Why?
|
| Gonadotropin-Releasing Hormone | 1 | 1999 | 103 | 0.040 |
Why?
|
| Antineoplastic Agents, Hormonal | 1 | 1999 | 150 | 0.040 |
Why?
|
| Brachytherapy | 1 | 1999 | 119 | 0.040 |
Why?
|
| RNA Processing, Post-Transcriptional | 1 | 1999 | 105 | 0.040 |
Why?
|
| Temperature | 1 | 1999 | 396 | 0.040 |
Why?
|
| Adenosine Diphosphate | 1 | 2017 | 55 | 0.040 |
Why?
|
| Neoadjuvant Therapy | 1 | 1999 | 318 | 0.040 |
Why?
|
| Nuclear Proteins | 2 | 2013 | 696 | 0.040 |
Why?
|
| Protein Domains | 1 | 2017 | 128 | 0.040 |
Why?
|
| Peptide Library | 1 | 2016 | 84 | 0.040 |
Why?
|
| RNA, Small Untranslated | 1 | 2016 | 14 | 0.040 |
Why?
|
| Actins | 1 | 1999 | 451 | 0.030 |
Why?
|
| Alleles | 1 | 1999 | 1128 | 0.030 |
Why?
|
| Sequence Homology, Amino Acid | 2 | 2009 | 416 | 0.030 |
Why?
|
| Alanine | 1 | 1994 | 85 | 0.030 |
Why?
|
| Cattle | 1 | 1994 | 376 | 0.030 |
Why?
|
| Cysteine | 1 | 1994 | 135 | 0.030 |
Why?
|
| Ribonuclease H | 1 | 2013 | 8 | 0.030 |
Why?
|
| Hydrogen-Ion Concentration | 1 | 1994 | 493 | 0.030 |
Why?
|
| Ligation | 1 | 2013 | 51 | 0.030 |
Why?
|
| Splicing Factor U2AF | 1 | 2013 | 5 | 0.030 |
Why?
|
| Protein Folding | 1 | 1994 | 282 | 0.030 |
Why?
|
| Hydrogen Bonding | 1 | 1992 | 144 | 0.030 |
Why?
|
| Mutagenesis, Site-Directed | 1 | 1992 | 279 | 0.030 |
Why?
|
| Structure-Activity Relationship | 1 | 1992 | 408 | 0.020 |
Why?
|
| In Vitro Techniques | 1 | 1992 | 989 | 0.020 |
Why?
|
| Cell Line, Tumor | 1 | 2016 | 2426 | 0.020 |
Why?
|
| Solutions | 1 | 1990 | 85 | 0.020 |
Why?
|
| Protein Denaturation | 1 | 1990 | 106 | 0.020 |
Why?
|
| Physical Chromosome Mapping | 1 | 2009 | 27 | 0.020 |
Why?
|
| Leucine | 1 | 2009 | 67 | 0.020 |
Why?
|
| Lod Score | 1 | 2009 | 152 | 0.020 |
Why?
|
| Oligonucleotide Array Sequence Analysis | 1 | 2012 | 689 | 0.020 |
Why?
|
| Genes, Dominant | 1 | 2009 | 117 | 0.020 |
Why?
|
| Mice, Inbred C57BL | 1 | 2016 | 3095 | 0.020 |
Why?
|
| Microsatellite Repeats | 1 | 2009 | 145 | 0.020 |
Why?
|
| Genetic Markers | 1 | 2009 | 476 | 0.020 |
Why?
|
| Sulfanilic Acids | 1 | 2008 | 1 | 0.020 |
Why?
|
| Amino Acid Substitution | 1 | 2009 | 339 | 0.020 |
Why?
|
| Water | 1 | 1990 | 277 | 0.020 |
Why?
|
| HeLa Cells | 1 | 2009 | 498 | 0.020 |
Why?
|
| Prostatic Neoplasms | 1 | 1999 | 1721 | 0.020 |
Why?
|
| Mutation, Missense | 1 | 2009 | 276 | 0.020 |
Why?
|
| Ubiquitination | 1 | 2008 | 67 | 0.020 |
Why?
|
| Protein Interaction Domains and Motifs | 1 | 2008 | 86 | 0.020 |
Why?
|
| Transcriptome | 1 | 2012 | 580 | 0.020 |
Why?
|
| Pedigree | 1 | 2009 | 966 | 0.020 |
Why?
|
| Quinolines | 1 | 2008 | 95 | 0.020 |
Why?
|
| Gene Expression Profiling | 1 | 2012 | 1384 | 0.020 |
Why?
|
| Signal Transduction | 1 | 2016 | 3243 | 0.020 |
Why?
|
| Mice | 1 | 2016 | 11356 | 0.010 |
Why?
|
| Yeasts | 1 | 2001 | 49 | 0.010 |
Why?
|
| Combined Modality Therapy | 1 | 1999 | 1686 | 0.010 |
Why?
|
| Male | 2 | 2009 | 40988 | 0.010 |
Why?
|
| Female | 1 | 2009 | 44550 | 0.000 |
Why?
|
| Aged | 1 | 1999 | 18423 | 0.000 |
Why?
|