A MEN1 pancreatic neuroendocrine tumour mouse model, under temporal control

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by occurrence of parathyroid tumours, and neuroendocrine tumours (NETs) of the pancreatic islets and anterior pituitary. The MEN1 gene, encoding menin, is a tumour suppressor, but its precise role in initiatin...

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Bibliographic Details
Main Authors: Lines, K, Nunes, R, Frost, M, Yates, C, Stevenson, M, Thakker, R
Format: Journal article
Language:English
Published: BioScientifica 2017

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