G2-delay after irradiation with alpha-particles as studied in synchronized cultures and by the bromodeoxyuridine-33258H technique.

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G2-delay after irradiation with alpha-particles as studied in synchronized cultures and by the bromodeoxyuridine-33258H technique. / Hieber, L; Beck-Bornholdt, Hans-Peter; Lücke-Huhle, C.

In: Cytometry, Vol. 2, No. 3, 3, 1981, p. 175-178.

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@article{29a16740e24b43a6ab84b4233568f687,
title = "G2-delay after irradiation with alpha-particles as studied in synchronized cultures and by the bromodeoxyuridine-33258H technique.",
abstract = "Division delay of mouse L-929 fibroblasts after alpha-irradiation is due to a pronounced lengthening of their G2-phase. Experiments on synchronously and asynchronously growing cultures revealed a cell cycle phase-dependent sensitivity of this effect: Cells irradiated in G2 or at the G1/S border suffered a longer G2-delay than cells irradiated at mid- or late-S. Progression through G2 was nearly normal at doses up to 0.3 Gy if cells were exposed during G1 phase.",
author = "L Hieber and Hans-Peter Beck-Bornholdt and C L{\"u}cke-Huhle",
year = "1981",
language = "Deutsch",
volume = "2",
pages = "175--178",
number = "3",

}

RIS

TY - JOUR

T1 - G2-delay after irradiation with alpha-particles as studied in synchronized cultures and by the bromodeoxyuridine-33258H technique.

AU - Hieber, L

AU - Beck-Bornholdt, Hans-Peter

AU - Lücke-Huhle, C

PY - 1981

Y1 - 1981

N2 - Division delay of mouse L-929 fibroblasts after alpha-irradiation is due to a pronounced lengthening of their G2-phase. Experiments on synchronously and asynchronously growing cultures revealed a cell cycle phase-dependent sensitivity of this effect: Cells irradiated in G2 or at the G1/S border suffered a longer G2-delay than cells irradiated at mid- or late-S. Progression through G2 was nearly normal at doses up to 0.3 Gy if cells were exposed during G1 phase.

AB - Division delay of mouse L-929 fibroblasts after alpha-irradiation is due to a pronounced lengthening of their G2-phase. Experiments on synchronously and asynchronously growing cultures revealed a cell cycle phase-dependent sensitivity of this effect: Cells irradiated in G2 or at the G1/S border suffered a longer G2-delay than cells irradiated at mid- or late-S. Progression through G2 was nearly normal at doses up to 0.3 Gy if cells were exposed during G1 phase.

M3 - SCORING: Zeitschriftenaufsatz

VL - 2

SP - 175

EP - 178

IS - 3

M1 - 3

ER -