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pubmed-article:14676120pubmed:abstractTextClinical and experimental evidence suggest that the p33ING1b candidate tumor suppressor functionally cooperates with p53 in controlling biochemical and biological functions. Because p53 is frequently mutated in brain tumors and the ING1 locus maps to a site of which the loss is associated with gliomas, we analyzed the mutation and expression profiles of ING1B in human brain tumors. Here we present the first report of ING1 expression and mutation analyses in human brain tumor samples and malignant glioma cell lines.lld:pubmed
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pubmed-article:14676120pubmed:articleTitleAltered subcellular localization and low frequency of mutations of ING1 in human brain tumors.lld:pubmed
pubmed-article:14676120pubmed:affiliationDepartment of Medical Biochemistry and Southern Alberta Cancer Research Center, The University of Calgary, Calgary, Alberta, Canada.lld:pubmed
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