Tod Mitchell Woolf, Ph.D.
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?
|
|---|
| Deoxyribonucleases | 1 | 2017 | 209 | 0.510 |
Why?
|
| Oligonucleotides, Antisense | 4 | 1996 | 457 | 0.310 |
Why?
|
| RNA | 6 | 2011 | 2709 | 0.230 |
Why?
|
| Clinical Trials as Topic | 1 | 2017 | 8002 | 0.180 |
Why?
|
| RNA-Induced Silencing Complex | 2 | 2011 | 52 | 0.180 |
Why?
|
| RNA, Catalytic | 2 | 1996 | 52 | 0.150 |
Why?
|
| Oligonucleotides | 2 | 2011 | 563 | 0.140 |
Why?
|
| Ribonuclease H | 2 | 1995 | 50 | 0.140 |
Why?
|
| Oocytes | 2 | 1992 | 1165 | 0.130 |
Why?
|
| RNA Interference | 3 | 2011 | 2816 | 0.130 |
Why?
|
| Dystrophin | 1 | 1995 | 281 | 0.110 |
Why?
|
| RNA Editing | 1 | 1995 | 149 | 0.110 |
Why?
|
| Pharmacogenetics | 1 | 1998 | 675 | 0.110 |
Why?
|
| Drug Design | 1 | 1998 | 1044 | 0.110 |
Why?
|
| Genetic Engineering | 1 | 2017 | 930 | 0.090 |
Why?
|
| Thionucleotides | 1 | 1990 | 107 | 0.090 |
Why?
|
| Embryo, Nonmammalian | 2 | 1990 | 904 | 0.090 |
Why?
|
| RNA, Messenger | 7 | 2011 | 12747 | 0.080 |
Why?
|
| DNA Repair | 1 | 1998 | 2041 | 0.080 |
Why?
|
| RNA, Small Interfering | 2 | 2011 | 3412 | 0.080 |
Why?
|
| RNA, Double-Stranded | 1 | 2010 | 290 | 0.080 |
Why?
|
| Ribonuclease III | 1 | 2010 | 267 | 0.070 |
Why?
|
| Xenopus | 3 | 1995 | 709 | 0.070 |
Why?
|
| DNA | 1 | 1998 | 7189 | 0.060 |
Why?
|
| Genetic Variation | 1 | 1998 | 6567 | 0.050 |
Why?
|
| Mutation | 2 | 1998 | 30004 | 0.050 |
Why?
|
| Gene Silencing | 2 | 2011 | 1495 | 0.050 |
Why?
|
| Inhibins | 2 | 1993 | 211 | 0.050 |
Why?
|
| Nucleic Acid Conformation | 2 | 2011 | 896 | 0.040 |
Why?
|
| Gene Targeting | 1 | 2003 | 838 | 0.040 |
Why?
|
| Molecular Sequence Data | 6 | 1996 | 17598 | 0.040 |
Why?
|
| Structure-Activity Relationship | 2 | 1996 | 3057 | 0.040 |
Why?
|
| Mesoderm | 2 | 1993 | 673 | 0.040 |
Why?
|
| Base Sequence | 4 | 1995 | 12404 | 0.040 |
Why?
|
| Trans-Activators | 2 | 1997 | 2846 | 0.040 |
Why?
|
| Neurotoxins | 1 | 1997 | 240 | 0.030 |
Why?
|
| Molecular Weight | 2 | 1996 | 2171 | 0.030 |
Why?
|
| Animals | 10 | 2017 | 168089 | 0.030 |
Why?
|
| Codon, Terminator | 1 | 1995 | 124 | 0.030 |
Why?
|
| Cell Survival | 2 | 1997 | 5778 | 0.030 |
Why?
|
| RNA Splicing | 1 | 1998 | 896 | 0.030 |
Why?
|
| Adenosine Deaminase | 1 | 1995 | 250 | 0.030 |
Why?
|
| Gastrula | 1 | 1993 | 82 | 0.030 |
Why?
|
| Embryonic Induction | 1 | 1993 | 151 | 0.030 |
Why?
|
| Blastocyst | 2 | 1993 | 432 | 0.030 |
Why?
|
| RNA Probes | 1 | 1992 | 111 | 0.030 |
Why?
|
| Drug Delivery Systems | 1 | 2003 | 2223 | 0.020 |
Why?
|
| Xenopus laevis | 2 | 1993 | 962 | 0.020 |
Why?
|
| Ovarian Follicle | 1 | 1993 | 244 | 0.020 |
Why?
|
| Blotting, Northern | 1 | 1992 | 1545 | 0.020 |
Why?
|
| Central Nervous System | 1 | 1997 | 1333 | 0.020 |
Why?
|
| RNA, Small Untranslated | 1 | 2010 | 77 | 0.020 |
Why?
|
| Fibronectins | 1 | 1992 | 724 | 0.020 |
Why?
|
| Endoribonucleases | 1 | 1990 | 227 | 0.020 |
Why?
|
| Oligopeptides | 1 | 1993 | 1179 | 0.020 |
Why?
|
| Kinetics | 1 | 1995 | 6312 | 0.020 |
Why?
|
| Humans | 9 | 2017 | 761222 | 0.020 |
Why?
|
| HeLa Cells | 1 | 2011 | 3073 | 0.010 |
Why?
|
| Models, Genetic | 1 | 1995 | 3430 | 0.010 |
Why?
|
| Proto-Oncogene Proteins | 1 | 1996 | 4513 | 0.010 |
Why?
|
| Proteins | 1 | 1997 | 5993 | 0.010 |
Why?
|
| Peptides | 1 | 1993 | 4353 | 0.010 |
Why?
|
| Activins | 2 | 1993 | 210 | 0.010 |
Why?
|
| Cells, Cultured | 2 | 2011 | 18927 | 0.010 |
Why?
|
| Models, Biological | 1 | 1995 | 9458 | 0.010 |
Why?
|
| Gene Expression Regulation | 1 | 1996 | 11855 | 0.010 |
Why?
|
| Neurons | 1 | 1997 | 9429 | 0.010 |
Why?
|
| Proto-Oncogene Proteins c-myb | 1 | 1996 | 78 | 0.010 |
Why?
|
| Cell Line | 1 | 2010 | 15545 | 0.010 |
Why?
|
| Rats, Sprague-Dawley | 2 | 1997 | 8164 | 0.010 |
Why?
|
| Carbohydrates | 1 | 1996 | 389 | 0.010 |
Why?
|
| Notochord | 1 | 1993 | 37 | 0.010 |
Why?
|
| In Situ Hybridization | 1 | 1997 | 1900 | 0.010 |
Why?
|
| Hedgehog Proteins | 1 | 1997 | 769 | 0.010 |
Why?
|
| Substrate Specificity | 1 | 1996 | 1768 | 0.010 |
Why?
|
| Protein Sorting Signals | 1 | 1993 | 275 | 0.010 |
Why?
|
| Rats | 2 | 1997 | 23705 | 0.010 |
Why?
|
| Amino Acid Sequence | 2 | 1993 | 13402 | 0.010 |
Why?
|
| Brain Chemistry | 1 | 1993 | 959 | 0.010 |
Why?
|
| Cell Division | 1 | 1996 | 4451 | 0.010 |
Why?
|
| Eye | 1 | 1993 | 713 | 0.010 |
Why?
|
| Mice | 2 | 2010 | 81330 | 0.000 |
Why?
|
| Female | 4 | 1996 | 392552 | 0.000 |
Why?
|
| Cloning, Molecular | 1 | 1990 | 4167 | 0.000 |
Why?
|
| Swine | 1 | 1990 | 5909 | 0.000 |
Why?
|
| Transcription, Genetic | 1 | 1990 | 7571 | 0.000 |
Why?
|
| Brain | 1 | 1993 | 27094 | 0.000 |
Why?
|