Zobrazeno 1 - 10
of 38
pro vyhledávání: '"S D Reich"'
Autor:
J. Schindler, G. Hebert, Y. Nishida, J. Balzer, John M. Kirkwood, T. Trautman, Marc S. Ernstoff, S D Reich, C. A. Davis, S. A. Rudnick
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 8(6)
Interferon-gamma (IFN gamma), as produced by recombinant DNA technology, has shown a wide range of immunomodulatory activity in vitro and in vivo. Clinical studies have attempted to establish a dose-response relationship to define optimal dosage rang
Autor:
A P Mazar, Mark R. Middleton, C Hayward, S A Lowndes, S D Reich, A Timms, A Adams, Adrian L. Harris
Publikováno v:
Web of Science
2065 Background: Copper chelation reduces the secretion of many angiogenic factors and reduces tumour growth and microvascular density in animal models. ATN-224 is a second generation analogue of ammonium tetrathiomolybdate, which reportedly can stab
Autor:
Mark R. Middleton, Chris Jones, Heidi Steinfeldt, R Kaufman, Alan Hilary Calvert, J. Evans, Ruth Plummer, L Robson, S. D. Reich, Richard K. Wilson
Publikováno v:
Journal of Clinical Oncology. 23:3065-3065
3065 Background: AG-014699 inhibits poly(ADP-ribose) polymerase (PARP) is a key enzyme in DNA repair. AG-014699 sensitizes cancer cells to DNA damaging drugs such as TMZ. AG-014699 is the first PARP inhibitor to be evaluated in cancer patients. Metho
Autor:
S. D. Reich, F. Robert, M. Amantea, William R. Dinwoodie, Daniel M. Sullivan, M. Zhang, M. Bishop, Christopher R. Garrett
Publikováno v:
Journal of Clinical Oncology. 22:3075-3075
3075 Background: AG2037 is a rationally designed, novel inhibitor of GARFT, which is an essential enzyme in the de novo synthesis of purines, a critical process for cell growth. Methods: The primary objectives of these studies were to determine the m
Autor:
Merrill S. Kies, Hope S. Rugo, G. Wilding, S. D. Reich, Glenn Liu, Roy S. Herbst, John W. Park, T. M. McShane, Heidi Steinfeldt, Yazdi K. Pithavala
Publikováno v:
Journal of Clinical Oncology. 22:2503-2503
2503 Background: AG-013736 is a potent and selective inhibitor of VEGF and PDGF receptor tyrosine kinases with broad preclinical activity in xenograft models of solid tumors. Methods: The primary objective was to determine maximum tolerated dose (MTD
Autor:
C. A. Davis, John M. Kirkwood, J Balser, S D Reich, T. Trautman, P Witman, S. A. Rudnick, Marc S. Ernstoff
Publikováno v:
Journal of Clinical Oncology. 5:1804-1810
Thirty patients with documented metastatic melanoma were randomly assigned to receive recombinant DNA-produced gamma-interferon (specific activity approximately, 20 MU/mg) intravenously (IV) over either two or 24 hours at dosages of 3, 30, 300, 1,000
Publikováno v:
Cancer treatment reports. 67(2)
Autor:
S D, Reich, N R, Bachur
Publikováno v:
Cancer research. 36(10)
Adriamycin dosage should be reduced in patients with impaired liver function, since adriamycin disposition is influenced by liver metabolism and biliary excretion. It follows that drugs that increase the metabolism or excretory capacity of the liver
Autor:
S D, Reich
Publikováno v:
Cancer nursing. 4(6)
Autor:
S D, Reich
Publikováno v:
Cancer nursing. 5(6)