USP8 Somatic Mutations in Cushing’s Disease and Silent Corticotropinomas

Background: Somatic mutations in the ubiquitin-specific peptidase 8 (USP8) gene have been described in Cushing’s disease (CD). These mutations increase proopiomelanocortin transcription resulting in ACTH production and seem to correlate with somatostatin receptor type 5 (SST5) expression. Aims: Scre...

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Detalles Bibliográficos
Autores principales: Lamback, Elisa Baranski, Lima, Carlos Henrique de Azeredo, Miranda, Renan Lyra, Guterres, Alexandro, Andreiuolo, Felipe, Wildemberg, Luiz Eduardo Armondi, Gadelha, Monica Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Neuroendocrinology and Pituitary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090680/
http://dx.doi.org/10.1210/jendso/bvab048.1328

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090680/
http://dx.doi.org/10.1210/jendso/bvab048.1328

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