RNF138 joins the HR team

Research output: Contribution to journal › Journal article › Research › peer-review

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RNF138 joins the HR team. / Bekker-Jensen, Simon; Mailand, Niels.

In: Nature Cell Biology, Vol. 17, No. 11, 10.2015, p. 1375-7.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Bekker-Jensen, S & Mailand, N 2015, 'RNF138 joins the HR team', Nature Cell Biology, vol. 17, no. 11, pp. 1375-7. https://doi.org/10.1038/ncb3262

APA

Bekker-Jensen, S., & Mailand, N. (2015). RNF138 joins the HR team. Nature Cell Biology, 17(11), 1375-7. https://doi.org/10.1038/ncb3262

Vancouver

Bekker-Jensen S, Mailand N. RNF138 joins the HR team. Nature Cell Biology. 2015 Oct;17(11):1375-7. https://doi.org/10.1038/ncb3262

Author

Bekker-Jensen, Simon ; Mailand, Niels. / RNF138 joins the HR team. In: Nature Cell Biology. 2015 ; Vol. 17, No. 11. pp. 1375-7.

Bibtex

@article{b53eba9c225b4d5fbae5bc7099f6e19d,
title = "RNF138 joins the HR team",
abstract = "Two studies show that the E3 ubiquitin ligase RNF138 is recruited to DNA double-strand break sites, where it ubiquitylates key repair factors to promote DNA-end resection and homologous recombination. These findings add insights into the multilayered regulatory mechanisms underlying DNA double-strand break repair pathway choice in mammalian cells.",
author = "Simon Bekker-Jensen and Niels Mailand",
year = "2015",
month = oct,
doi = "10.1038/ncb3262",
language = "English",
volume = "17",
pages = "1375--7",
journal = "Nature Cell Biology",
issn = "1465-7392",
publisher = "nature publishing group",
number = "11",

}

RIS

TY - JOUR

T1 - RNF138 joins the HR team

AU - Bekker-Jensen, Simon

AU - Mailand, Niels

PY - 2015/10

Y1 - 2015/10

N2 - Two studies show that the E3 ubiquitin ligase RNF138 is recruited to DNA double-strand break sites, where it ubiquitylates key repair factors to promote DNA-end resection and homologous recombination. These findings add insights into the multilayered regulatory mechanisms underlying DNA double-strand break repair pathway choice in mammalian cells.

AB - Two studies show that the E3 ubiquitin ligase RNF138 is recruited to DNA double-strand break sites, where it ubiquitylates key repair factors to promote DNA-end resection and homologous recombination. These findings add insights into the multilayered regulatory mechanisms underlying DNA double-strand break repair pathway choice in mammalian cells.

U2 - 10.1038/ncb3262

DO - 10.1038/ncb3262

M3 - Journal article

C2 - 26515018

VL - 17

SP - 1375

EP - 1377

JO - Nature Cell Biology

JF - Nature Cell Biology

SN - 1465-7392

IS - 11

ER -

ID: 152956640