The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in a large cohort of children and adolescents with pituitary adenomas

অনুরূপ উপাদানগুলি

• THE GROWTH HORMONE RECEPTOR (GHR) POLYMORPHISM IN GROWTH-RETARDED CHILDREN WITH CUSHING DISEASE: LACK OF ASSOCIATION WITH GROWTH AND MEASURES OF THE SOMATOTROPIC AXIS
  অনুযায়ী: Drori-Herishanu, Limor, অন্যান্য
  প্রকাশিত: (2009)
• Association of the M1V PRKAR1A Mutation with Primary Pigmented Nodular Adrenocortical Disease in Two Large Families
  অনুযায়ী: Pereira, Alberto M., অন্যান্য
  প্রকাশিত: (2010)
• An Intronic Mutation is Associated with Prolactinoma in a Young Boy, Decreased Penetrance in his Large Family, and Variable Effects on MEN1 mRNA and Protein
  অনুযায়ী: Drori-Herishanu, L., অন্যান্য
  প্রকাশিত: (2009)
• Prkar1a haploinsufficiency ameliorates the growth hormone excess phenotype in Aip-deficient mice
  অনুযায়ী: Schernthaner-Reiter, Marie Helene, অন্যান্য
  প্রকাশিত: (2020)
• Frequent Phosphodiesterase 11A Gene (PDE11A) Defects in Patients with Carney Complex (CNC) Caused by PRKAR1A Mutations: PDE11A May Contribute to Adrenal and Testicular Tumors in CNC as a Modifier of the Phenotype
  অনুযায়ী: Libé, Rossella, অন্যান্য
  প্রকাশিত: (2011)