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CDC73 wt Allele

Known as: Hyperparathyroidism 2 (with Jaw Tumor) Gene, C1orf28, HPT-JT 
Human CDC73 wild-type allele is located in the vicinity of 1q25 and is approximately 132 kb in length. This allele, which encodes parafibromin… 
National Institutes of Health

Papers overview

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Review
2016
Review
2016
  • R. Thakker
  • Journal of internal medicine
  • 2016
  • Corpus ID: 26615079
Primary hyperparathyroidism (PHPT), due to parathyroid tumours, may occur as part of a complex syndrome or as an isolated… 
Review
2010
Review
2010
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… 
Highly Cited
2005
Highly Cited
2005
The hyperparathyroidism‐jaw tumour (HPT‐JT) syndrome is an autosomal dominant disorder characterized by parathyroid tumours… 
Highly Cited
2004
Highly Cited
2004
Purpose: A reliable method for diagnosing parathyroid carcinoma has remained elusive over the years, resulting in its under… 
Highly Cited
2004
Highly Cited
2004
Familial hyperparathyroidism is not uncommon in clinical endocrine practice. It encompasses a spectrum of disorders including… 
Highly Cited
2003
Highly Cited
2003
BACKGROUND We looked for mutations of the HRPT2 gene, which encodes the parafibromin protein, in sporadic parathyroid carcinoma… 
2003
2003
Primary hyperparathyroidism is a state of excess secretion of parathyroid hormone and hypercalcemia, often with skeletal and… 
Highly Cited
1998
Highly Cited
1998
Approximately 70 families with familial isolated hyperparathyroidism (FIHP) have been reported. Whether it is a separate entity… 
Highly Cited
1995
Highly Cited
1995
The syndrome of hereditary hyperparathyroidism and jaw tumors (HPT-JT) is characterized by inheritance, in an autosomal dominant…