Jaw Neoplasms

Known as: Jaw Neoplasms [Disease/Finding], Jaw neoplasm, Neoplasm, Jaw 
Cancers or tumors of the MAXILLA or MANDIBLE unspecified. For neoplasms of the maxilla, MAXILLARY NEOPLASMS is available and of the mandible… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1950-2017
0102019502016

Papers overview

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2010
2010
Parathyroid carcinoma (PaC) is a rare cause of primary hyperparathyroidism. Though the loss of the oncosuppressor CDC73/HRPT2… (More)
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2008
2008
Parafibromin, a transcription factor associated with the PAF complex, is encoded by the HRPT2 gene, mutations of which cause the… (More)
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2008
2008
Parafibromin is a tumor suppressor protein encoded by HRPT2, a gene recently implicated in the hereditary hyperparathyroidism-jaw… (More)
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Highly Cited
2006
Highly Cited
2006
Parathyroid carcinoma is notoriously difficult to diagnose with confidence in borderline cases. Commonly there is a long lag time… (More)
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Highly Cited
2005
Highly Cited
2005
Inactivation of the HRPT2 tumor suppressor gene is associated with the pathogenesis of the hereditary hyperparathyroidism-jaw… (More)
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Highly Cited
2005
Highly Cited
2005
Parafibromin, the product of the HRPT2 (hyperparathyroidism-jaw tumor syndrome 2) tumor suppressor gene, is the human homologue… (More)
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Highly Cited
2004
Highly Cited
2004
PURPOSE A reliable method for diagnosing parathyroid carcinoma has remained elusive over the years, resulting in its under… (More)
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Highly Cited
2004
Highly Cited
2004
We investigated the involvement of the HRPT2 gene by loss of heterozygosity analysis and direct sequencing in a kindred with… (More)
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Highly Cited
2003
Highly Cited
2003
BACKGROUND We looked for mutations of the HRPT2 gene, which encodes the parafibromin protein, in sporadic parathyroid carcinoma… (More)
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Highly Cited
1995
Highly Cited
1995
The syndrome of hereditary hyperparathyroidism and jaw tumors (HPT-JT) is characterized by inheritance, in an autosomal dominant… (More)
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