Global gene expression in neuroendocrine tumors from patients with the MEN1 syndrome

BACKGROUND: Multiple Endocrine Neoplasia type 1 (MEN1, OMIM 131100) is an autosomal dominant disorder characterized by endocrine tumors of the parathyroids, pancreatic islets and pituitary. The disease is caused by the functional loss of the tumor suppressor protein menin, coded by the MEN1 gene. Th...

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Detalles Bibliográficos
Autores principales: Dilley, William G, Kalyanaraman, Somasundaram, Verma, Sulekha, Cobb, J Perren, Laramie, Jason M, Lairmore, Terry C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC549185/
https://www.ncbi.nlm.nih.gov/pubmed/15691381
http://dx.doi.org/10.1186/1476-4598-4-9

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