
doi: 10.1242/jcs.01311
pmid: 15371520
Central to the pathways that induce cell growth in mammals is the murine target of rapamycin (mTOR), a multi-domain, 298 kDa, evolutionarily-conserved Ser/Thr kinase that is inhibited by the drug rapamycin ([Schmelzle and Hall, 2000][1]). mTOR exerts its effects by phosphorylating eukaryotic
Enzyme Activation, Phosphatidylinositol 3-Kinases, Multiprotein Complexes, Proto-Oncogene Proteins, TOR Serine-Threonine Kinases, Animals, Protein Serine-Threonine Kinases, Protein Kinases, Proto-Oncogene Proteins c-akt, Signal Transduction
Enzyme Activation, Phosphatidylinositol 3-Kinases, Multiprotein Complexes, Proto-Oncogene Proteins, TOR Serine-Threonine Kinases, Animals, Protein Serine-Threonine Kinases, Protein Kinases, Proto-Oncogene Proteins c-akt, Signal Transduction
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 57 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
