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Article

Allelic loss from chromosome 11 in parathyroid tumors.

Cancer research - 15 Dec 1992

Friedman E, De Marco L, Gejman P V, Norton J A, Bale A E, Aurbach G D, Spiegel A M, Marx S J

Abstract excerpt

Parathyroid tumors may occur in a sporadic fashion or, more rarely, as part of a familial syndrome (such as familial multiple endocrine neoplasia type I). The MENI gene has been mapped by linkage analysis to chromosome 11 at band q11-q13, and presumably acts as a tumor suppressor gene. In the present study, which is an extension of our previous studies, we examined 41 parathyroid tumors from patients with...

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PMID: 1360870

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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Allelic loss from chromosome 11 in parathyroid tumors.PMID 1360870Read ↗

Putative parathyroid tumor suppressor on 1p: independent molecular mechanisms of tumorigenesis from 11q allelic loss.Semantic proximity Read ↗

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Allelic loss on chromosome 11 in hereditary and sporadic tumors related to familial multiple endocrine neoplasia type 1.Semantic proximity Read ↗

Multiple endocrine neoplasia type 1 (MEN1): LOH studies in a affected family and in sporadic cases.Semantic proximity Read ↗

Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors.Semantic proximity Read ↗

Multiple allelic deletions and intratumoral genetic heterogeneity in men1 pancreatic tumors.Semantic proximity Read ↗

Allelic deletions on chromosome 11q13 in multiple endocrine neoplasia type 1-associated and sporadic gastrinomas and pancreatic endocrine tumors.Semantic proximity Read ↗

Localization of the multiple endocrine neoplasia type I (MEN1) gene based on tumor loss of heterozygosity analysis.Semantic proximity Read ↗

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