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Article

HRPT2 gene alterations in ossifying fibroma of the jaws.

Oral oncology - 1 Aug 2006

Pimenta Flávio Juliano, Gontijo Silveira Letícia Ferreira, Tavares Gabriela Cordeiro, Silva Andreza Campos, Perdigão Paolla Freitas, Castro Wagner Henriques, Gomez Marcus Vinícius, Teh Bin Tean, De Marco Luiz, Gomez Ricardo Santiago

Abstract excerpt

Ossifying fibroma (OF) is a benign neoplasm related to bone characterized by a progressive enlargement of the affected jaw. Recently, the candidate tumor suppressor gene HRPT2 was identified and alterations in this gene were related with the Hyperparathyroidism-jaw tumor syndrome that is characte...

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Identifiers

PMID: 16458039
DOI: 10.1016/j.oraloncology.2005.11.019

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16458039-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

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HRPT2 gene alterations in ossifying fibroma of the jaws.PMID 16458039Read ↗

Assessing the contribution of HRPT2 to the pathogenesis of jaw fibrous dysplasia, ossifying fibroma, and osteosarcoma.Semantic proximity Read ↗

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome.Semantic proximity Read ↗

Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene.Semantic proximity Read ↗

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Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.Semantic proximity Read ↗

Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome.Semantic proximity Read ↗

Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma.Semantic proximity Read ↗

Frequent Large Germline HRPT2 Deletions in a French National Cohort of Patients With Primary HyperparathyroidismSemantic proximity Read ↗

Two cases of multiple ossifying fibromas in the jaws.Semantic proximity Read ↗

A Novel IVS2-1G>A mutation causes aberrant splicing of the HRPT2 gene in a family with hyperparathyroidism-jaw tumor syndrome.Semantic proximity Read ↗

Loss of parafibromin expression in a subset of parathyroid adenomas.Semantic proximity Read ↗

Upregulation of FGFR1 expression is associated with parathyroid carcinogenesis in HPT-JT syndrome due to an HRPT2 splicing mutation.Semantic proximity Read ↗

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