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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… 
National Institutes of Health

Related topics

Related topics

12 relations
Blood supply aspectsIn BloodMicrobiologicalProcess of secretion

Narrower (4)

Cancer of JawGigantiform Cementoma, FamilialHyperparathyroidism-Jaw Tumor SyndromeMandibular Neoplasms

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2010
Highly Cited
2010
Differential expression of microRNAs in human parathyroid carcinomas compared with normal parathyroid tissue.
Parathyroid carcinoma (PaC) is a rare cause of primary hyperparathyroidism. Though the loss of the oncosuppressor CDC73/HRPT2… 
Highly Cited
2009
Highly Cited
2009
Accuracy of combined protein gene product 9.5 and parafibromin markers for immunohistochemical diagnosis of parathyroid carcinoma.
CONTEXT Parafibromin, encoded by HRPT2, is the first marker with significant benefit in the diagnosis of parathyroid carcinoma… 
Highly Cited
2006
Highly Cited
2006
Loss of Nuclear Expression of Parafibromin Distinguishes Parathyroid Carcinomas and Hyperparathyroidism-Jaw Tumor (HPT-JT) Syndrome-related Adenomas From Sporadic Parathyroid Adenomas and…
Parathyroid carcinoma is notoriously difficult to diagnose with confidence in borderline cases. Commonly there is a long lag time… 
Highly Cited
2005
Highly Cited
2005
The Parafibromin Tumor Suppressor Protein Is Part of a Human Paf1 Complex
ABSTRACT Parafibromin, the product of the HRPT2 (hyperparathyroidism-jaw tumor syndrome 2) tumor suppressor gene, is the human… 
Highly Cited
2005
Highly Cited
2005
The HRPT2 Tumor Suppressor Gene Product Parafibromin Associates with Human PAF1 and RNA Polymerase II
ABSTRACT Inactivation of the HRPT2 tumor suppressor gene is associated with the pathogenesis of the hereditary… 
Highly Cited
2005
Highly Cited
2005
Uterine tumours are a phenotypic manifestation of the hyperparathyroidism‐jaw tumour syndrome
The hyperparathyroidism‐jaw tumour (HPT‐JT) syndrome is an autosomal dominant disorder characterized by parathyroid tumours… 
Highly Cited
2004
Highly Cited
2004
Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors.
We investigated the involvement of the HRPT2 gene by loss of heterozygosity analysis and direct sequencing in a kindred with… 
Highly Cited
2004
Highly Cited
2004
Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome.
Familial isolated hyperparathyroidism (FIHP) can result occasionally from the incomplete expression of a syndromic form of… 
Review
2002
Review
2002
Hyperparathyroidism in hereditary syndromes: special expressions and special managements.
Hyperparathyroidism (HPT) in its hereditary variants assumes special forms, has special associations, and requires special… 
Highly Cited
1995
Highly Cited
1995
Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31.
The syndrome of hereditary hyperparathyroidism and jaw tumors (HPT-JT) is characterized by inheritance, in an autosomal dominant… 
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