Research Topics
Genomes and GenesSpecies | T W SchulteSummaryAffiliation: National Institutes of Health Country: USA Publications
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Publications
Expression of PAX3 in Ewing's sarcoma family of tumorsT W Schulte
Clinical Pharmacology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA
Biochem Mol Med 60:121-6. 1997..We found expression of PAX3 in most, but not all, of the specimens analyzed, including cell lines and patient material...
Destabilization of Raf-1 by geldanamycin leads to disruption of the Raf-1-MEK-mitogen-activated protein kinase signalling pathwayT W Schulte
Clinical Pharmacology Branch, National Cancer Institute, Bethesda, Maryland 20892, USA
Mol Cell Biol 16:5839-45. 1996..Thus, we demonstrate that interaction between HSP90 and Raf-1 is a sine qua non for Raf stability and function as a signal transducer and that the effects observed cannot be attributed to a general impairment of protein kinase function...
Geldanamycin-induced destabilization of Raf-1 involves the proteasomeT W Schulte
Medicine Branch, National Cancer Institute, Bethesda, Maryland 20892, USA
Biochem Biophys Res Commun 239:655-9. 1997..Signaling through this pathway was inhibited by GA, concomitant with loss of Raf-1 protein, but was restored if Raf-1 was protected from GA-induced degradation by proteasome inhibitors...
Antibiotic radicicol binds to the N-terminal domain of Hsp90 and shares important biologic activities with geldanamycinT W Schulte
Medicine Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA
Cell Stress Chaperones 3:100-8. 1998..Radicicol thus represents a structurally unique antibiotic, and the first non-benzoquinone ansamycin, capable of binding to Hsp90 and interfering with its function...
The benzoquinone ansamycin 17-allylamino-17-demethoxygeldanamycin binds to HSP90 and shares important biologic activities with geldanamycinT W Schulte
Medicine Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892 1928, USA
Cancer Chemother Pharmacol 42:273-9. 1998..We therefore examined the biologic effects of 17-allylamino-17-demethoxygeldanamycin (17-AG), an ansamycin derivative with lower in vivo toxicity than GA...
