A Blood-Based Polyamine Signature Associated With Disease Progression in Patients With Multiple Endocrine Neoplasia Type 1-Related Duodenopancreatic Neuroendocrine Tumors

Background: Multiple Endocrine Neoplasia Type 1 (MEN1) is a rare inherited autosomal dominant disease predisposing patients to endocrine tumors. MEN1 can be genetically diagnosed at an early age. Patients are prone to develop benign parathyroid tumors then multifocal duodenopancreatic neuroendocrine...

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Detalles Bibliográficos
Autores principales: Fahrmann, Johannes F, Pieterman, Carolina, Wasylishen, Amanda R, Peterson, Christine B, Halperin, Daniel M, Agarwal, Sunita Kishore, Blau, Jenny, Del Rivero, Jaydira, Nilubol, Naris, Walter, Mary F, Welch, James M, Weinstein, Lee Scott, van Treijen, Mark, Valk, Gerlof D, Vriens, Menno R, Perrier, Nancy D, Hanash, Samir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Tumor Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265731/
http://dx.doi.org/10.1210/jendso/bvab048.2064

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