Genetic Analyses of the<i>HRPT2</i>Gene in Primary Hyperparathyroidism: Germline and Somatic Mutations in Familial and Sporadic Parathyroid Tumors
Filomena Cetani(University of Pisa), Claudio Marcocci(University of Pisa), Aldo Pinchera, Elena Ambrogini(University of Pisa), Luisella Cianferotti(University of Florence), Elena Pardi(University of Pisa), Giada Dipollina(University of Pisa), Simona Borsari(University of Pisa), Paolo Viacava(University of Pisa), Elisabetta Gazzerro(Istituto Giannina Gaslini), Giacomo Colussi(Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda), Piero Berti(University of Pisa), Paolo Miccoli(University of Pisa)
Cited by 256
Related Papers
Bone Morphogenetic Proteins, Their Antagonists, and the Skeleton
|Endocrine Reviews|2003|859
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
|Nature|2012|631
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis
|Nature Genetics|1998|502
Surgery or Surveillance for Mild Asymptomatic Primary Hyperparathyroidism: A Prospective, Randomized Clinical Trial
|The Journal of Clinical Endocrinology & Metabolism|2007|406
Bone morphogenetic proteins induce the expression of noggin, which limits their activity in cultured rat osteoblasts.
|Journal of Clinical Investigation|1998|346