Concepts (136)
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?
|
|---|
| Newcastle disease virus | 27 | 2013 | 86 | 4.920 |
Why?
|
| HN Protein | 24 | 2013 | 57 | 4.090 |
Why?
|
| Viral Fusion Proteins | 19 | 2014 | 74 | 3.670 |
Why?
|
| Virus Internalization | 9 | 2014 | 99 | 2.320 |
Why?
|
| Receptors, Virus | 14 | 2013 | 82 | 1.840 |
Why?
|
| Membrane Fusion | 11 | 2012 | 77 | 1.740 |
Why?
|
| Nipah Virus | 4 | 2013 | 5 | 1.300 |
Why?
|
| Measles virus | 4 | 2011 | 9 | 1.000 |
Why?
|
| Hemagglutinins, Viral | 7 | 2008 | 19 | 0.900 |
Why?
|
| Viral Proteins | 6 | 2019 | 261 | 0.900 |
Why?
|
| Polysaccharides | 4 | 2019 | 147 | 0.850 |
Why?
|
| Viral Envelope Proteins | 4 | 2013 | 111 | 0.820 |
Why?
|
| Antibodies, Monoclonal | 12 | 2005 | 858 | 0.670 |
Why?
|
| Neuraminidase | 6 | 2004 | 49 | 0.540 |
Why?
|
| N-Acetylneuraminic Acid | 4 | 2011 | 53 | 0.530 |
Why?
|
| Cricetinae | 11 | 2013 | 376 | 0.490 |
Why?
|
| Ephrin-B2 | 2 | 2012 | 6 | 0.490 |
Why?
|
| Virus Attachment | 3 | 2011 | 23 | 0.480 |
Why?
|
| Cell Line | 13 | 2012 | 2017 | 0.430 |
Why?
|
| Molecular Sequence Data | 15 | 2012 | 1983 | 0.430 |
Why?
|
| Cell Fusion | 4 | 2012 | 45 | 0.430 |
Why?
|
| Amino Acid Substitution | 6 | 2013 | 252 | 0.420 |
Why?
|
| Recombinant Fusion Proteins | 4 | 2011 | 502 | 0.420 |
Why?
|
| Protein Multimerization | 1 | 2013 | 171 | 0.400 |
Why?
|
| Protein Binding | 7 | 2014 | 1566 | 0.400 |
Why?
|
| Ephrin-B3 | 1 | 2012 | 1 | 0.390 |
Why?
|
| Hendra Virus | 1 | 2012 | 1 | 0.390 |
Why?
|
| Paramyxovirinae | 1 | 2011 | 2 | 0.380 |
Why?
|
| Measles | 1 | 2011 | 8 | 0.370 |
Why?
|
| Parainfluenza Virus 3, Human | 2 | 2004 | 5 | 0.370 |
Why?
|
| Binding Sites | 3 | 2011 | 873 | 0.360 |
Why?
|
| Mutation | 5 | 2007 | 2471 | 0.340 |
Why?
|
| Animals | 25 | 2019 | 19767 | 0.340 |
Why?
|
| Interferons | 1 | 2009 | 63 | 0.320 |
Why?
|
| Virulence Factors | 1 | 2009 | 84 | 0.320 |
Why?
|
| Mutation, Missense | 2 | 2014 | 180 | 0.310 |
Why?
|
| Mutagenesis, Site-Directed | 7 | 2008 | 258 | 0.310 |
Why?
|
| Amino Acid Sequence | 12 | 2006 | 1589 | 0.310 |
Why?
|
| Glycoproteins | 2 | 2019 | 194 | 0.240 |
Why?
|
| Respirovirus | 2 | 1995 | 3 | 0.240 |
Why?
|
| Metapneumovirus | 2 | 2014 | 6 | 0.220 |
Why?
|
| Structure-Activity Relationship | 7 | 2005 | 376 | 0.200 |
Why?
|
| Mutant Proteins | 2 | 2013 | 106 | 0.180 |
Why?
|
| Protein Structure, Tertiary | 3 | 2007 | 665 | 0.170 |
Why?
|
| Protein Conformation | 4 | 2005 | 774 | 0.160 |
Why?
|
| Mononegavirales | 1 | 2019 | 2 | 0.160 |
Why?
|
| Antigens, Viral | 4 | 1997 | 133 | 0.160 |
Why?
|
| Glycosylation | 4 | 2019 | 135 | 0.150 |
Why?
|
| Epitopes | 5 | 2005 | 296 | 0.140 |
Why?
|
| Base Sequence | 6 | 2005 | 1313 | 0.140 |
Why?
|
| Henipavirus Infections | 2 | 2013 | 3 | 0.130 |
Why?
|
| Chick Embryo | 5 | 1993 | 50 | 0.120 |
Why?
|
| Integrin alphaV | 1 | 2014 | 2 | 0.110 |
Why?
|
| Integrin alpha5beta1 | 1 | 2014 | 5 | 0.110 |
Why?
|
| Paramyxoviridae Infections | 1 | 2014 | 7 | 0.110 |
Why?
|
| Membrane Fusion Proteins | 1 | 2013 | 1 | 0.110 |
Why?
|
| Dimerization | 2 | 2005 | 146 | 0.110 |
Why?
|
| Kidney | 2 | 2012 | 397 | 0.110 |
Why?
|
| Neutralization Tests | 3 | 2005 | 125 | 0.100 |
Why?
|
| Electrophoretic Mobility Shift Assay | 1 | 2013 | 64 | 0.100 |
Why?
|
| Cysteine | 3 | 2008 | 109 | 0.100 |
Why?
|
| Disulfides | 2 | 2008 | 63 | 0.100 |
Why?
|
| Protein Interaction Mapping | 1 | 2013 | 72 | 0.100 |
Why?
|
| Cell Membrane | 2 | 2011 | 492 | 0.100 |
Why?
|
| Models, Molecular | 2 | 2008 | 1137 | 0.100 |
Why?
|
| Guinea Pigs | 1 | 2011 | 103 | 0.090 |
Why?
|
| Vero Cells | 1 | 2011 | 76 | 0.090 |
Why?
|
| Cells, Cultured | 5 | 1994 | 2101 | 0.090 |
Why?
|
| Virulence | 2 | 2014 | 189 | 0.090 |
Why?
|
| Chickens | 1 | 2009 | 91 | 0.080 |
Why?
|
| Membrane Cofactor Protein | 1 | 2008 | 3 | 0.080 |
Why?
|
| Electrophoresis, Polyacrylamide Gel | 2 | 2001 | 183 | 0.070 |
Why?
|
| Viruses | 1 | 1988 | 79 | 0.070 |
Why?
|
| Lung | 1 | 2012 | 842 | 0.070 |
Why?
|
| Sequence Homology, Amino Acid | 1 | 2007 | 359 | 0.070 |
Why?
|
| Humans | 7 | 2019 | 60138 | 0.070 |
Why?
|
| HeLa Cells | 1 | 2007 | 531 | 0.060 |
Why?
|
| Hemagglutination Inhibition Tests | 1 | 2005 | 9 | 0.060 |
Why?
|
| Binding Sites, Antibody | 1 | 2005 | 29 | 0.060 |
Why?
|
| COS Cells | 1 | 2005 | 175 | 0.060 |
Why?
|
| Virus Replication | 1 | 2006 | 307 | 0.060 |
Why?
|
| Oligosaccharides | 1 | 2004 | 63 | 0.050 |
Why?
|
| Sequence Deletion | 1 | 2004 | 114 | 0.050 |
Why?
|
| Protein Folding | 2 | 1997 | 261 | 0.050 |
Why?
|
| Giant Cells | 1 | 2003 | 17 | 0.050 |
Why?
|
| Brain | 1 | 2012 | 1493 | 0.050 |
Why?
|
| Oligodeoxyribonucleotides | 2 | 1995 | 243 | 0.050 |
Why?
|
| Temperature | 1 | 2003 | 299 | 0.050 |
Why?
|
| Recombinant Proteins | 1 | 2004 | 697 | 0.050 |
Why?
|
| Child | 1 | 2011 | 4335 | 0.050 |
Why?
|
| Precipitin Tests | 1 | 2001 | 79 | 0.050 |
Why?
|
| Sialic Acids | 2 | 1992 | 46 | 0.050 |
Why?
|
| Antibodies, Viral | 2 | 1992 | 305 | 0.040 |
Why?
|
| Genes, Reporter | 1 | 1999 | 243 | 0.040 |
Why?
|
| Blotting, Western | 1 | 1999 | 598 | 0.040 |
Why?
|
| Peptide Mapping | 1 | 1997 | 29 | 0.030 |
Why?
|
| Restriction Mapping | 1 | 1995 | 53 | 0.030 |
Why?
|
| Hemadsorption | 1 | 1994 | 1 | 0.030 |
Why?
|
| DNA Primers | 1 | 1995 | 293 | 0.030 |
Why?
|
| Substrate Specificity | 1 | 1995 | 325 | 0.030 |
Why?
|
| Sigmodontinae | 1 | 2014 | 13 | 0.030 |
Why?
|
| Conserved Sequence | 1 | 1994 | 172 | 0.030 |
Why?
|
| Protein Structure, Secondary | 1 | 1994 | 254 | 0.030 |
Why?
|
| Chymotrypsin | 1 | 1993 | 27 | 0.030 |
Why?
|
| Cricetulus | 1 | 2013 | 102 | 0.030 |
Why?
|
| Amino Acid Motifs | 1 | 2014 | 153 | 0.030 |
Why?
|
| CHO Cells | 1 | 2013 | 190 | 0.030 |
Why?
|
| Hydrolysis | 1 | 1993 | 139 | 0.030 |
Why?
|
| Hot Temperature | 1 | 1993 | 127 | 0.030 |
Why?
|
| Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase | 1 | 1992 | 2 | 0.030 |
Why?
|
| Mutagenesis | 1 | 1992 | 131 | 0.020 |
Why?
|
| Hydrogen-Ion Concentration | 1 | 1993 | 434 | 0.020 |
Why?
|
| DNA Mutational Analysis | 1 | 2012 | 196 | 0.020 |
Why?
|
| Periodic Acid | 1 | 1991 | 2 | 0.020 |
Why?
|
| In Vitro Techniques | 1 | 1992 | 472 | 0.020 |
Why?
|
| Virion | 1 | 1992 | 123 | 0.020 |
Why?
|
| Recombination, Genetic | 1 | 2012 | 237 | 0.020 |
Why?
|
| Solubility | 1 | 1991 | 176 | 0.020 |
Why?
|
| RNA, Viral | 1 | 2012 | 265 | 0.020 |
Why?
|
| Sequence Analysis, DNA | 1 | 2012 | 398 | 0.020 |
Why?
|
| Genetic Variation | 1 | 1992 | 367 | 0.020 |
Why?
|
| Genotype | 1 | 2012 | 643 | 0.020 |
Why?
|
| Fibroblasts | 1 | 1992 | 370 | 0.020 |
Why?
|
| Rats | 1 | 2014 | 1918 | 0.020 |
Why?
|
| Binding, Competitive | 1 | 1989 | 100 | 0.020 |
Why?
|
| Phenotype | 1 | 1992 | 1158 | 0.020 |
Why?
|
| Poliovirus | 1 | 1988 | 5 | 0.020 |
Why?
|
| Peptides | 1 | 1991 | 551 | 0.020 |
Why?
|
| Capsid | 1 | 1988 | 89 | 0.020 |
Why?
|
| Kinetics | 1 | 1988 | 738 | 0.020 |
Why?
|
| Models, Biological | 1 | 1988 | 1143 | 0.010 |
Why?
|
| Female | 1 | 2014 | 31249 | 0.010 |
Why?
|
| Molecular Weight | 1 | 1987 | 189 | 0.000 |
Why?
|
| Protein Precursors | 1 | 1988 | 74 | 0.000 |
Why?
|
| Peptide Hydrolases | 1 | 1988 | 80 | 0.000 |
Why?
|
| Oxidation-Reduction | 1 | 1987 | 305 | 0.000 |
Why?
|