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- Preclinical and Early Clinical Development of PTC596, a Novel . . .
AbstractPTC596 is an investigational small-molecule tubulin-binding agent Unlike other tubulin-binding agents, PTC596 is orally bioavailable and is not a P-glycoprotein substrate So as to characterize PTC596 to position the molecule for optimal clinical development, the interactions of PTC596 with tubulin using crystallography, its spectrum of preclinical in vitro anticancer activity, and
- Preclinical and Early Clinical Development of PTC596, a Novel . . .
PTC596 is an investigational small-molecule tubulin-binding agent Unlike other tubulin-binding agents, PTC596 is orally bioavailable and is not a P-glycoprotein substrate So as to characterize PTC596 to position the molecule for optimal clinical development, the interactions of PTC596 with tubulin …
- Differential Binding of Inorganic Particles to MARCO - PMC
Only TiO 2 required divalent cations (viz , Ca +2 and or Mg +2) for binding to MARCO, and results from competitive binding studies supported the notion that TiO 2 and both the silica particles bound to different motifs in SRCR domain of MARCO
- Phase 1 results of PTC596, a novel small molecule targeting . . .
A phase I trial of selective PI3K inhibitor taselisib (tas) plus palbociclib (palb) with and without endocrine therapy incorporating pharmacodynamic (PD) studies in patients (pts) with advanced cancers Phase 1 study of the p53-MDM2 inhibitor AMG 232 combined with trametinib plus dabrafenib or
- Brännström Ott Moa - AbeBooks
Tälja köksredskap by Brännström Ott, Moa and a great selection of related books, art and collectibles available now at AbeBooks com
- Differential Binding of Inorganic Particles to MARCO - PMC
Only TiO 2 required divalent cations (viz , Ca +2 and or Mg +2) for binding to MARCO, and results from competitive binding studies supported the notion that TiO 2 and both the silica particles bound to different motifs in SRCR domain of MARCO
- New Insights into the Cell Biology of the Marginal Zone of . . .
The ligand‐binding specificities of SIGNR1 are therefore quite similar to the ones described for DC‐SIGN, based on the presence of the EPN sequence motif in the carbohydrate recognizing domain (CRD)
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