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http://purl.uniprot.org/citations/18316586http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18316586http://www.w3.org/2000/01/rdf-schema#comment"CDC25A is a critical regulator of cell cycle progression and checkpoint response. Overexpression of this cyclin-dependent kinase phosphatase occurs often in human cancers. Our recent genetic studies in the mouse indicate that restricting CDC25A can limit tumorigenesis induced by the HER2/neu-RAS oncogenic pathway without compromising normal cell division or viability. These findings offer a sound foundation to justify development of CDC25A inhibitors for antitumor therapy."xsd:string
http://purl.uniprot.org/citations/18316586http://purl.org/dc/terms/identifier"doi:10.1158/0008-5472.can-07-5983"xsd:string
http://purl.uniprot.org/citations/18316586http://purl.uniprot.org/core/author"Ray D."xsd:string
http://purl.uniprot.org/citations/18316586http://purl.uniprot.org/core/author"Kiyokawa H."xsd:string
http://purl.uniprot.org/citations/18316586http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18316586http://purl.uniprot.org/core/name"Cancer Res"xsd:string
http://purl.uniprot.org/citations/18316586http://purl.uniprot.org/core/pages"1251-1253"xsd:string
http://purl.uniprot.org/citations/18316586http://purl.uniprot.org/core/title"CDC25A phosphatase: a rate-limiting oncogene that determines genomic stability."xsd:string
http://purl.uniprot.org/citations/18316586http://purl.uniprot.org/core/volume"68"xsd:string
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