Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized in man by parathyroid, pancreatic, pituitary and adrenal tumours. The MEN1 gene encodes a 610-amino acid protein (menin) which is a tumour suppressor. To investigate the in vivo role of menin, we developed a m...

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Foilsithe in:Endocr Relat Cancer
Main Authors: Harding, Brian, Lemos, Manuel C, Reed, Anita A C, Walls, Gerard V, Jeyabalan, Jeshmi, Bowl, Michael R, Tateossian, Hilda, Sullivan, Nicky, Hough, Tertius, Fraser, William D, Ansorge, Olaf, Cheeseman, Michael T, Thakker, Rajesh V
Formáid: Artigo
Teanga:Inglês
Foilsithe: Society for Endocrinology 2009
Ábhair:
Regular Papers
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4439740/
https://ncbi.nlm.nih.gov/pubmed/19620250
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1677/ERC-09-0082
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