Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia

Fanconi anemia is a complex disease affecting multiple DNA repair proteins that resolve DNA crosslinks which can block vital processes. Here the authors use parallel genome-wide screens that identify the BLM helicase complex as a suppressor of Fanconi anemia phenotypes.

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Autores principales: Martin Moder, Georgia Velimezi, Michel Owusu, Abdelghani Mazouzi, Marc Wiedner, Joana Ferreira da Silva, Lydia Robinson-Garcia, Fiorella Schischlik, Rastislav Slavkovsky, Robert Kralovics, Michael Schuster, Christoph Bock, Trey Ideker, Stephen P. Jackson, Jörg Menche, Joanna I. Loizou
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/bca0a3f08cd24bcb930f0ad1a08874af
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spelling oai:doaj.org-article:bca0a3f08cd24bcb930f0ad1a08874af2021-12-02T14:42:21ZParallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia10.1038/s41467-017-01439-x2041-1723https://doaj.org/article/bca0a3f08cd24bcb930f0ad1a08874af2017-11-01T00:00:00Zhttps://doi.org/10.1038/s41467-017-01439-xhttps://doaj.org/toc/2041-1723Fanconi anemia is a complex disease affecting multiple DNA repair proteins that resolve DNA crosslinks which can block vital processes. Here the authors use parallel genome-wide screens that identify the BLM helicase complex as a suppressor of Fanconi anemia phenotypes.Martin ModerGeorgia VelimeziMichel OwusuAbdelghani MazouziMarc WiednerJoana Ferreira da SilvaLydia Robinson-GarciaFiorella SchischlikRastislav SlavkovskyRobert KralovicsMichael SchusterChristoph BockTrey IdekerStephen P. JacksonJörg MencheJoanna I. LoizouNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Martin Moder
Georgia Velimezi
Michel Owusu
Abdelghani Mazouzi
Marc Wiedner
Joana Ferreira da Silva
Lydia Robinson-Garcia
Fiorella Schischlik
Rastislav Slavkovsky
Robert Kralovics
Michael Schuster
Christoph Bock
Trey Ideker
Stephen P. Jackson
Jörg Menche
Joanna I. Loizou
Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia
description Fanconi anemia is a complex disease affecting multiple DNA repair proteins that resolve DNA crosslinks which can block vital processes. Here the authors use parallel genome-wide screens that identify the BLM helicase complex as a suppressor of Fanconi anemia phenotypes.
format article
author Martin Moder
Georgia Velimezi
Michel Owusu
Abdelghani Mazouzi
Marc Wiedner
Joana Ferreira da Silva
Lydia Robinson-Garcia
Fiorella Schischlik
Rastislav Slavkovsky
Robert Kralovics
Michael Schuster
Christoph Bock
Trey Ideker
Stephen P. Jackson
Jörg Menche
Joanna I. Loizou
author_facet Martin Moder
Georgia Velimezi
Michel Owusu
Abdelghani Mazouzi
Marc Wiedner
Joana Ferreira da Silva
Lydia Robinson-Garcia
Fiorella Schischlik
Rastislav Slavkovsky
Robert Kralovics
Michael Schuster
Christoph Bock
Trey Ideker
Stephen P. Jackson
Jörg Menche
Joanna I. Loizou
author_sort Martin Moder
title Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia
title_short Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia
title_full Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia
title_fullStr Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia
title_full_unstemmed Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia
title_sort parallel genome-wide screens identify synthetic viable interactions between the blm helicase complex and fanconi anemia
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/bca0a3f08cd24bcb930f0ad1a08874af
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