Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity

Werner syndrome (WS) is a human premature aging disorder characterized by chromosomal instability. The cellular defects of WS presumably reflect compromised or aberrant function of a DNA metabolic pathway that under normal circumstances confers stability to the genome. We report a novel interaction...

Täydet tiedot

Bibliografiset tiedot

Julkaisussa:	EMBO J
Päätekijät:	Brosh, Robert M., von Kobbe, Cayetano, Sommers, Joshua A., Karmakar, Parimal, Opresko, Patricia L., Piotrowski, Jason, Dianova, Irina, Dianov, Grigory L., Bohr, Vilhelm A.
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	Nature Publishing Group 2001
Aiheet:	Article
Linkit:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC125684/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11598021/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/emboj/20.20.5791
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