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… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1995-2018
0246819952018

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
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)
Is this relevant?
2006
2006
OBJECTIVE To investigate two patients with the hyperparathyroidism-jaw tumour (HPT-JT) syndrome and three patients with familial… (More)
Is this relevant?
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)
  • table 1
  • figure 1
  • figure 2
  • table 2
  • table 3
Is this relevant?
2004
2004
We investigated the involvement of the HRPT2 gene by loss of heterozygosity analysis and direct sequencing in a kindred with… (More)
  • figure 1
  • table 2
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
2004
2004
A Villablanca, A Calender, L Forsberg, A Höög, J-D Cheng, D Petillo, C Bauters, K Kahnoski, T Ebeling, P Salmela, A-L Richardson… (More)
  • figure 1
  • table 1
  • table 2
  • figure 2
  • table 3
Is this relevant?
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)
Is this relevant?
Highly Cited
2003
Highly Cited
2003
BACKGROUND Hyperparathyroidism is a common endocrinopathy characterised by the formation of parathyroid tumours. In this study… (More)
Is this relevant?
2001
2001
The hyperparathyroidism-jaw tumour (HPT-JT) syndrome is an autosomal dominant disease characterized by the occurrence of… (More)
Is this relevant?
1996
1996
Hereditary hyperparathyroidism-jaw tumor syndrome (HPT-JT) is an autosomal dominant disease (OMIM 145001) that has recently been… (More)
Is this relevant?
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)
Is this relevant?