Association of the M1V PRKAR1A Mutation with Primary Pigmented Nodular Adrenocortical Disease in Two Large Families

Ítems similars

• MicroRNA Signature of Primary Pigmented Nodular Adrenocortical Disease: Clinical Correlations and Regulation of Wnt Signaling
  per: Iliopoulos, Dimitrios, et al.
  Publicat: (2009)
• Integrated Genomic Analysis of Nodular Tissue in Macronodular Adrenocortical Hyperplasia: Progression of Tumorigenesis in a Disorder Associated with Multiple Benign Lesions
  per: Almeida, Madson Q., et al.
  Publicat: (2011)
• In Vitro Studies of Novel PRKAR1A Mutants that Extend the Predicted RIα Protein Sequence into the 3′-Untranslated Open Reading Frame: Proteasomal Degradation Leads to RIα Haploinsufficiency and Carney Complex
  per: Patronas, Yianna, et al.
  Publicat: (2012)
• Detection of somatic β-catenin mutations in primary pigmented nodular adrenocortical disease (PPNAD)
  per: Tadjine, Mimi, et al.
  Publicat: (2008)
• Abnormalities of cAMP signaling are present in adrenocortical lesions associated with ACTH-independent Cushing syndrome despite the absence of mutations in known genes
  per: Bimpaki, Eirini I., et al.
  Publicat: (2009)