4.8 Editorial Material

Breaking Up Just Got Easier to Do

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CELL
卷 138, 期 1, 页码 20-22

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CELL PRESS
DOI: 10.1016/j.cell.2009.06.039

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  1. NIGMS NIH HHS [R01 GM041784-21, R01 GM041784] Funding Source: Medline

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The SLX4 protein functions as a platform for catalytic subunits of structure-specific endonucleases. Findings reported in Cell (Fekairi et al., 2009; Svendsen et al., 2009) and in Molecular Cell (Andersen et al., 2009; Mu oz et al., 2009) now identify the human SLX4 and show that in association with the SLX1 endonuclease it directs the symmetric cleavage and resolution of Holliday junctions.

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