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...
Main Authors: | , , , , , |
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Format: | Journal article |
Language: | English |
Published: |
BioScientifica
2017
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