Zobrazeno 1 - 6
of 6
pro vyhledávání: '"J. J. Casciari"'
Publikováno v:
Scopus-Elsevier
Six rodent cell lines (36B10 rat glioma cells, 9L rat gliosarcoma cells, V79 Chinese hamster lung fibroblasts, EMT6/UW and EMT6/Ro mouse mammary sarcoma cells, and RIF-1 mouse fibrosarcoma cells) were tested for growth in cylindrical threads of Matri
Publikováno v:
Medical Physics. 22:1127-1139
[F-18]fluoromisonidazole (FMISO), a positron-emitting nitroimidazole, binds preferentially to hypoxic cells. It has been used to image hypoxia in human tumors with positron emission tomography (PET). In order to quantify tumor oxygenation status from
Autor:
J J, Casciari, J S, Rasey
Publikováno v:
Radiation research. 141(1)
Fluoromisonidazole [1-(2-nitroimidazolyl)-2-hydroxy-3-fluoropropane, FMISO] shows promise as a hypoxia imaging agent: it binds preferentially to anoxic cells in monolayers in vitro and accumulates in radiobiologically hypoxic tumors in vivo. The mult
Autor:
G V, Martin, J H, Caldwell, M M, Graham, J R, Grierson, K, Kroll, M J, Cowan, T K, Lewellen, J S, Rasey, J J, Casciari, K A, Krohn
Publikováno v:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 33(12)
Fluoromisonidazole (FMISO) is metabolically trapped in viable cells as a function of reduced cellular pO2. Therefore [18F]-FMISO is potentially useful for evaluating patients with hypoxic but viable myocardium. The goal of this study was to investiga
Autor:
J. J. Casciari, J. S. Rasey
Publikováno v:
Radiation Research. 141:28
Fluoromisonidazole [1-(2-nitroimidazolyl)-2-hydroxy-3-fluoropropane, FMISO] shows promise as a hypoxia imaging agent: it binds preferentially to anoxic cells in monolayers in vitro and accumulates in radiobiologically hypoxic tumors in vivo. The mult
Publikováno v:
Cancer research. 48(14)
In order to understand the role of glucose limitations in controlling multicellular tumor spheroid growth, knowledge of the glucose diffusion coefficient is essential. The effective diffusivity of glucose in spheroids of rodent and human tumor cell l