miR-3156-5p is downregulated in serum of MEN1 patients and regulates expression of MORF4L2

Multiple endocrine neoplasia type 1 (MEN1), caused by mutations in the MEN1 gene encoding menin, is an autosomal dominant disorder characterised by the combined occurrence of parathyroid, pituitary and pancreatic neuroendocrine tumours (NETs). Development of these tumours is associated with wide var...

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Detalles Bibliográficos
Autores principales: Kooblall, Kreepa G, Stokes, Victoria J, Shariq, Omair A, English, Katherine A, Stevenson, Mark, Broxholme, John, Wright, Benjamin, Lockstone, Helen E, Buck, David, Grozinsky-Glasberg, Simona, Yates, Christopher J, Thakker, Rajesh V, Lines, Kate E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9422251/
https://www.ncbi.nlm.nih.gov/pubmed/35900839
http://dx.doi.org/10.1530/ERC-22-0045

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