Associated Papers
The mutational landscape of ARMC5 in Primary Bilateral Macronodular Adrenal Hyperplasia: an update.
Bouys L et al.
Orphanet Journal of Rare Diseases, 2025
Primary bilateral macronodular adrenal hyperplasia: definitely a genetic disease.
Cavalcante IP et al.
Nature Reviews. Endocrinology, 2022
ARMC5-CUL3 E3 ligase targets full-length SREBF in adrenocortical tumors.
Okuno Y et al.
Jci Insight, 2022
Genetics of primary bilateral macronodular adrenal hyperplasia: a model for early diagnosis of Cushing's syndrome?
Drougat L et al.
European Journal of Endocrinology, 2015
ARMC5 Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences.
Espiard S et al.
The Journal of Clinical Endocrinology and Metabolism, 2015
Aberrant transcriptional regulations in cancers: genome, transcriptome and epigenome analysis of lung adenocarcinoma cell lines.
Suzuki A et al.
Nucleic Acids Research, 2014
25378332 (PubMed )
Supplement: supp_gku885_nar-02466-x-2014-File008.zip › Supplemenatry_TableS9.xlsx › TableS9A
ARMC5 mutations in macronodular adrenal hyperplasia with Cushing's syndrome.
Assié G et al.
The New England Journal of Medicine, 2013
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