In tumor cells regulation of DNA double strand break repair through EGF receptor involves both NHEJ and HR and is independent of p53 and K-Ras status.
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In tumor cells regulation of DNA double strand break repair through EGF receptor involves both NHEJ and HR and is independent of p53 and K-Ras status. / Myllynen, Laura; Rieckmann, Thorsten; Dahm-Daphi, Jochen; Kasten-Pisula, Ulla; Petersen, Cordula; Dikomey, Ekkehard; Kriegs, Malte.
in: RADIOTHER ONCOL, Jahrgang 101, Nr. 1, 1, 2011, S. 147-151.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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TY - JOUR
T1 - In tumor cells regulation of DNA double strand break repair through EGF receptor involves both NHEJ and HR and is independent of p53 and K-Ras status.
AU - Myllynen, Laura
AU - Rieckmann, Thorsten
AU - Dahm-Daphi, Jochen
AU - Kasten-Pisula, Ulla
AU - Petersen, Cordula
AU - Dikomey, Ekkehard
AU - Kriegs, Malte
PY - 2011
Y1 - 2011
N2 - The purpose of this study was to examine whether the epidermal growth factor receptor (EGFR) may be used as a general target to modulate DNA double strand break (DSB) repair in tumor cells.
AB - The purpose of this study was to examine whether the epidermal growth factor receptor (EGFR) may be used as a general target to modulate DNA double strand break (DSB) repair in tumor cells.
M3 - SCORING: Journal article
VL - 101
SP - 147
EP - 151
JO - RADIOTHER ONCOL
JF - RADIOTHER ONCOL
SN - 0167-8140
IS - 1
M1 - 1
ER -