Concepedia

A novel CDC73 gene mutation in an Italian family with hyperparathyroidism-jaw tumour (HPT-JT) syndrome

Maria Grazia Chiofalo, Angelo Sparaneo, Massimiliano Chetta, Renato Franco, Filomena Baorda, Luigia Cinque, Matteo Granatiero, Leonardo D’Agruma, Luciano Pezzullo, Alfredo Scillitani,

Cellular Oncology · 2014 · 18 citations · 18 references

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References

18

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome

John D. Carpten, Christiane M. Robbins, Andrea Villablanca et al. · Nature Genetics · 2002 · 749 citations

, , +11

Somatic and Germ-Line Mutations of the<i>HRPT2</i>Gene in Sporadic Parathyroid Carcinoma

Trisha M. Shattuck, Stiina Välimäki, Takao Obara et al. · New England Journal of Medicine · 2003 · 597 citations

, , +16

Parafibromin/Hyrax Activates Wnt/Wg Target Gene Transcription by Direct Association with β-catenin/Armadillo

Christian Mosimann, George Hausmann, Konrad Basler · Cell · 2006 · 310 citations · Full text

, , +12

The Parafibromin Tumor Suppressor Protein Is Part of a Human Paf1 Complex

Orit Rozenblatt–Rosen, Christina M. Hughes, Suraj Nannepaga et al. · Molecular and Cellular Biology · 2005 · 284 citations · Full text

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Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome.

Charles E. Jackson, R A Norum, Scott B. Boyd et al. · PubMed · 1990 · 212 citations

, , +16