Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Michael B. Dilling"'
Autor:
Leonid Metelitsa, Ross Durland, Michael B. Dilling, Anne C. DiSante, Christine E. Flynn, Venkat Selvamanickam
Publikováno v:
Technology & Innovation. 21:169-177
Collaborations between academia and industry are growing in scope, duration, and sophistication. The best collaborations recognize the unique strengths and skill sets of both parties and are structured to leverage what each party does best. In many c
Autor:
Corrie E.M. Gidding, Glen S. Germain, Michael B. Dilling, Tiny G. J. Meeuwsen-de Boer, Richard A. Ashmun, Siebold S. N. de Graaf, Karen A. Veverka, Willem A. Kamps, Peter J. Houghton
Publikováno v:
Cancer Chemotherapy and Pharmacology, 45, 1, pp. 21-30
Cancer Chemotherapy and Pharmacology, 45, 21-30
Cancer Chemotherapy and Pharmacology, 45, 21-30
Purpose: Recombinant human insulin-like growth factor I (rhIGF-I) has been reported to ameliorate vincristine-induced neuropathy, the dose-limiting side effect of this antimitotic anticancer drug. However, rhIGF-I also might have adverse effects, as
Autor:
Hajime Hosoi, Takuma Shikata, Robert T. Abraham, Mary K. Danks, Michael B. Dilling, John C. Lawrence, Aleksander Sekulic, Linda N. Liu, Peter J. Houghton
Publikováno v:
Molecular Pharmacology. 54:815-824
Rapamycin is a potent cytostatic agent that arrests cells in the G1 phase of the cell cycle. The relationships between cellular sensitivity to rapamycin, drug accumulation, expression of mammalian target of rapamycin (mTOR), and inhibition of growth
Autor:
Franklin C. Harwood, Peter J. Houghton, Lili Shu, Michael B. Dilling, Shile Huang, Hidenori Ichijo, John Easton
Publikováno v:
Molecular cell. 11(6)
Under serum-free conditions, rapamycin, an inhibitor of mammalian target of rapamycin (mTOR), induces apoptosis of cells lacking functional p53. Cells expressing wild-type p53 or p21(Cip1)arrest in G1 and remain viable. In cells lacking functional p5
Autor:
Peter J. Houghton, Xiongwen Zhang, Michael B. Dilling, Glen S. Germain, Franklin C. Harwood, Lorina Dudkin, Arun L. Jayaraman
Publikováno v:
The Journal of biological chemistry. 277(16)
To determine whether inhibition of either the ribosomal p70 S6 kinase or eukaryotic initiation factor (eIF) 4E pathways downstream of the mammalian target of rapamycin, mTOR, contributes to rapamycin-induced growth arrest, clones of Rh30 rhabdomyosar