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pubmed-article:11443921pubmed:dateCreated2001-7-10lld:pubmed
pubmed-article:11443921pubmed:abstractTextAllelic deletions along the short arm of human chromosome 3 were mapped in 57 pairs of DNA samples from tumor and normal tissue of renal carcinoma patients in order to locate potential tumor suppressor genes. Twenty highly polymorphic microsatellite markers were used for deletion mapping. Allelic deletions were found in most of the samples (91%). Extended terminal deletions (56%) prevailed over shorter internal and multiple deletions and dominated (65%) in the most aggressive histopathological kidney cancer subtype, clear-cell carcinoma. Frequency analysis of loss of heterozygosity allowed detection of the human chromosome 3 regions most essential for renal carcinomas: the region adjacent to the gene VHL (3p26-p25), the region of homozygous deletions AP20 (3p22-p21.33), and a new region between markers D3S2420 and D3S2409 (3p21.31, 2.2 Mbp).lld:pubmed
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pubmed-article:11443921pubmed:authorpubmed-author:LoginovV IVIlld:pubmed
pubmed-article:11443921pubmed:authorpubmed-author:BazovI VIVlld:pubmed
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pubmed-article:11443921pubmed:volume35lld:pubmed
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pubmed-article:11443921pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:11443921pubmed:articleTitle[Mapping allelic deletions on the short arm of human chromosome 3 in kidney neoplasms].lld:pubmed
pubmed-article:11443921pubmed:affiliationbazov@yahoo.comlld:pubmed
pubmed-article:11443921pubmed:publicationTypeJournal Articlelld:pubmed
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