May 1, 2024

A long‐term prognosis study of human USP8‐mutated ACTH‐secreting pituitary neuroendocrine tumours

Puntos clave

Los puntos clave no están disponibles para este artículo en este momento.

Resumen

Somatic variants in the ubiquitin-specific protease 8 (USP8) gene are the most common genetic cause of Cushing disease. We aimed to explore the relationship between clinical outcomes and USP8 status in a single centre.

Me gusta

Guardar

Cite This Study

Miao et al. (Wed,) studied this question.

synapsesocial.com/papers/68e6c052b6db6435876403e4 https://doi.org/https://doi.org/10.1111/cen.15065

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1<i>P53</i> gene mutation in an atypical corticotroph adenoma with Cushing's disease2008 · 56 citations
2RETRACTED: <i>KMT2C</i> Mutations in Diffuse-Type Gastric Adenocarcinoma Promote Epithelial-to-Mesenchymal Transition2018 · 95 citations
3MLL3 suppresses tumorigenesis through regulating TNS3 enhancer activity2021 · 32 citations
4Long-term results after microsurgery for Cushing disease: experience with 426 primary operations over 35 years2008 · 205 citations
5SETD2 variation correlates with tumor mutational burden and MSI along with improved response to immunotherapy2023 · 20 citations

Me gusta

Guardar