Repair of radiation damage to DNA.

Standard

Repair of radiation damage to DNA. / Willers, H; Dahm-Daphi, Jochen; Powell, S N.

in: BRIT J CANCER, Jahrgang 90, Nr. 7, 7, 2004, S. 1297-1301.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Willers, H, Dahm-Daphi, J & Powell, SN 2004, 'Repair of radiation damage to DNA.', BRIT J CANCER, Jg. 90, Nr. 7, 7, S. 1297-1301. <http://www.ncbi.nlm.nih.gov/pubmed/15054444?dopt=Citation>

APA

Willers, H., Dahm-Daphi, J., & Powell, S. N. (2004). Repair of radiation damage to DNA. BRIT J CANCER, 90(7), 1297-1301. [7]. http://www.ncbi.nlm.nih.gov/pubmed/15054444?dopt=Citation

Vancouver

Willers H, Dahm-Daphi J, Powell SN. Repair of radiation damage to DNA. BRIT J CANCER. 2004;90(7):1297-1301. 7.

Bibtex

@article{b7214a16d1174ce388fce2f1f6e4613d,
title = "Repair of radiation damage to DNA.",
abstract = "DNA double-strand breaks constitute the most dangerous type of DNA damage induced by ionising radiation (IR). Accordingly, the resistance of cells to IR is modulated by three intimately related cellular processes: DNA repair, recombination, and replication. Significant discoveries in this field of research have been made over the last few years. A picture seems to be emerging in which perturbations of recombination in cancer cells are a more widespread cause of genomic instability than previously appreciated. Conversely, such cells may also be more sensitive to certain chemotherapeutic drugs and to IR. Thus, the alterations in recombination that promote carcinogenesis by causing genomic instability may also be the weakness of the tumours that arise in this setting, a concept which could hold great promise for the advancement of cancer treatment in the not too distant future.",
author = "H Willers and Jochen Dahm-Daphi and Powell, {S N}",
year = "2004",
language = "Deutsch",
volume = "90",
pages = "1297--1301",
journal = "BRIT J CANCER",
issn = "0007-0920",
publisher = "NATURE PUBLISHING GROUP",
number = "7",

}

RIS

TY - JOUR

T1 - Repair of radiation damage to DNA.

AU - Willers, H

AU - Dahm-Daphi, Jochen

AU - Powell, S N

PY - 2004

Y1 - 2004

N2 - DNA double-strand breaks constitute the most dangerous type of DNA damage induced by ionising radiation (IR). Accordingly, the resistance of cells to IR is modulated by three intimately related cellular processes: DNA repair, recombination, and replication. Significant discoveries in this field of research have been made over the last few years. A picture seems to be emerging in which perturbations of recombination in cancer cells are a more widespread cause of genomic instability than previously appreciated. Conversely, such cells may also be more sensitive to certain chemotherapeutic drugs and to IR. Thus, the alterations in recombination that promote carcinogenesis by causing genomic instability may also be the weakness of the tumours that arise in this setting, a concept which could hold great promise for the advancement of cancer treatment in the not too distant future.

AB - DNA double-strand breaks constitute the most dangerous type of DNA damage induced by ionising radiation (IR). Accordingly, the resistance of cells to IR is modulated by three intimately related cellular processes: DNA repair, recombination, and replication. Significant discoveries in this field of research have been made over the last few years. A picture seems to be emerging in which perturbations of recombination in cancer cells are a more widespread cause of genomic instability than previously appreciated. Conversely, such cells may also be more sensitive to certain chemotherapeutic drugs and to IR. Thus, the alterations in recombination that promote carcinogenesis by causing genomic instability may also be the weakness of the tumours that arise in this setting, a concept which could hold great promise for the advancement of cancer treatment in the not too distant future.

M3 - SCORING: Zeitschriftenaufsatz

VL - 90

SP - 1297

EP - 1301

JO - BRIT J CANCER

JF - BRIT J CANCER

SN - 0007-0920

IS - 7

M1 - 7

ER -