Zobrazeno 1 - 10
of 34
pro vyhledávání: '"J F Eliason"'
Autor:
K Helfer-Guarnori, P Vassilakos, N de Quay, X Albe, N Odartchenko, J F Eliason, J C Givel, L Suardet
Publikováno v:
Cancer. 66:1168-1175
In a prospective study, the DNA content of Feulgen-stained nuclei obtained from fresh samples of 211 colorectal adenocarcinomas was evaluated by means of image analysis. The DNA histogram classification took into account aneuploidy and S-phase fracti
Autor:
Z, Bacso, J F, Eliason
Publikováno v:
Cytometry. 45(3)
Phosphatidylserine (PS) binding by annexin V (AV) is an early membrane marker of apoptosis. Using laser scanning cytometry (LSC) and the comet assay, we showed that the DNA of AV(+) cells is so highly fragmented that it cannot be quantified by the co
Publikováno v:
Cancer research. 60(16)
Jurkat leukemia cells induced to undergo apoptosis by treatment with an antibody against the Fas receptor have two annexin V (AV)-binding subpopulations: (a) single-positive cells that bind AV but not propidium iodide (PI); and (b) double-positive ce
Publikováno v:
European journal of cancer (Oxford, England : 1990). (12)
Interferon-alpha (IFN-alpha) enhances the activity of the 5-fluorouracil (5-FU) prodrug 5'-deoxy-5-fluorouridine (5'-dFUrd) in colorectal cancer cells in vitro by upregulating the enzyme pyrimidine nucleoside phosphorylase (PNPase), which is responsi
Publikováno v:
Cancer research. 53
A novel arotinoid, 4-((2-(p-[(E)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl- 2-naphthyl)propenyl]phenoxy))ethyl))-morpholine, was tested in rats bearing established chemically induced mammary tumors. At a dose of 0.35 mmol/kg/day of 4-((2-(p-[(E)-2-(5
Publikováno v:
Cancer research. 52(13)
We have established 3 new human colorectal cancer cell lines (LS411N, LS513, and LS1034) from clinical biopsy samples. These lines are tumorigenic and grow s.c. as adenocarcinomas in nude mouse xenografts. Specific marker chromosomes are observed in
Publikováno v:
Updates in Colo-Proctology ISBN: 9783540553274
Fluoropyrimidines are commonly used in clinical oncology, but their strong dose-dependent toxicity limits therapeutic application. The synthetic derivative 5′-deoxy-5-fluorouridine (5′-dFUrd) [1] has raised marked interest due to a higher therape
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a15abf4bbd067b938ea8d335817fdcf6
https://doi.org/10.1007/978-3-642-51680-1_14
https://doi.org/10.1007/978-3-642-51680-1_14
Publikováno v:
European journal of cancer (Oxford, England : 1990). 28(2-3)
The biological activity of 5'-deoxy-5-fluorouridine (5'-dFUrd) depends upon intracellular enzymatic cleavage by pyrimidine phosphorylase to form 5-fluorouracil (5-FU). Interferon-alpha 2a (IFN-alpha) effect was analysed alone and combined with 5-FU o
Publikováno v:
Journal of Clinical Oncology. 27:4035-4035
4035 Background: Current guidance for postoperative clinical management of stages I/II CRC patients (pts) is suboptimal. We hypothesized that a molecular prognostic test using primary CRC tissue would better predict the chances of tumor R within 3 ye
Autor:
X, Albe, P, Vassilakos, K, Helfer-Guarnori, J C, Givel, N, de Quay, L, Suardet, J F, Eliason, N, Odartchenko
Publikováno v:
Cancer. 66(6)
In a prospective study, the DNA content of Feulgen-stained nuclei obtained from fresh samples of 211 colorectal adenocarcinomas was evaluated by means of image analysis. The DNA histogram classification took into account aneuploidy and S-phase fracti