Search details
1.
KDM1A inactivation causes hereditary food-dependent Cushing syndrome.
Genet Med
; 24(2): 374-383, 2022 02.
Article
in English
| MEDLINE | ID: mdl-34906447
2.
ARMC5 mutations in macronodular adrenal hyperplasia with Cushing's syndrome.
N Engl J Med
; 369(22): 2105-14, 2013 Nov 28.
Article
in English
| MEDLINE | ID: mdl-24283224
3.
Impact of Morphology in the Genotype and Phenotype Correlation of Bilateral Macronodular Adrenocortical Disease (BMAD): A Series of Clinicopathologically Well-Characterized 35 Cases.
Endocr Pathol
; 34(2): 179-199, 2023 Jun.
Article
in English
| MEDLINE | ID: mdl-36864263
4.
NF-κB signaling activation and roles in thyroid cancers: implication of MAP3K14/NIK.
Oncogenesis
; 12(1): 55, 2023 Nov 16.
Article
in English
| MEDLINE | ID: mdl-37973791
5.
Tumor suppressor gene ARMC5 controls adrenal redox state through NRF1 turnover.
Endocr Relat Cancer
; 29(11): 615-624, 2022 11 01.
Article
in English
| MEDLINE | ID: mdl-36040830
6.
Transcriptome in paraffin samples for the diagnosis and prognosis of adrenocortical carcinoma.
Eur J Endocrinol
; 186(6): 607-617, 2022 Apr 21.
Article
in English
| MEDLINE | ID: mdl-35266879
7.
Identification of glucocorticoid-related molecular signature by whole blood methylome analysis.
Eur J Endocrinol
; 186(2): 297-308, 2022 Jan 13.
Article
in English
| MEDLINE | ID: mdl-34914631
8.
Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene ARMC5 in 352 unselected patients.
Eur J Endocrinol
; 187(1): 123-134, 2022 May 24.
Article
in English
| MEDLINE | ID: mdl-35521700
9.
Whole blood methylome-derived features to discriminate endocrine hypertension.
Clin Epigenetics
; 14(1): 142, 2022 11 03.
Article
in English
| MEDLINE | ID: mdl-36329530
10.
Genomic classification of benign adrenocortical lesions.
Endocr Relat Cancer
; 28(1): 79-95, 2021 01.
Article
in English
| MEDLINE | ID: mdl-33151900
11.
Cullin 3 targets the tumor suppressor gene ARMC5 for ubiquitination and degradation.
Endocr Relat Cancer
; 27(4): 221-230, 2020 04.
Article
in English
| MEDLINE | ID: mdl-32023208
12.
Intratumor heterogeneity of prognostic DNA-based molecular markers in adrenocortical carcinoma.
Endocr Connect
; 9(7): 705-714, 2020 Jul.
Article
in English
| MEDLINE | ID: mdl-32698135
13.
Pangenomic Classification of Pituitary Neuroendocrine Tumors.
Cancer Cell
; 37(1): 123-134.e5, 2020 01 13.
Article
in English
| MEDLINE | ID: mdl-31883967
14.
MET overexpression and activation favors invasiveness in a model of anaplastic thyroid cancer.
Oncotarget
; 10(23): 2320-2334, 2019 Mar 19.
Article
in English
| MEDLINE | ID: mdl-31040922
15.
Value of Molecular Classification for Prognostic Assessment of Adrenocortical Carcinoma.
JAMA Oncol
; 5(10): 1440-1447, 2019 Oct 01.
Article
in English
| MEDLINE | ID: mdl-31294750
16.
Differential expression of parathyroid hormone-related protein in adrenocortical tumors: autocrine/paracrine effects on the growth and signaling pathways in H295R cells.
Cancer Epidemiol Biomarkers Prev
; 17(9): 2275-85, 2008 Sep.
Article
in English
| MEDLINE | ID: mdl-18768493
17.
Germline inactivating mutations of the aryl hydrocarbon receptor-interacting protein gene in a large cohort of sporadic acromegaly: mutations are found in a subset of young patients with macroadenomas.
Eur J Endocrinol
; 157(1): 1-8, 2007 Jul.
Article
in English
| MEDLINE | ID: mdl-17609395
18.
Mutations of beta-catenin in adrenocortical tumors: activation of the Wnt signaling pathway is a frequent event in both benign and malignant adrenocortical tumors.
Cancer Res
; 65(17): 7622-7, 2005 Sep 01.
Article
in English
| MEDLINE | ID: mdl-16140927
19.
ARMC5 mutation in a Portuguese family with primary bilateral macronodular adrenal hyperplasia (PBMAH).
Endocrinol Diabetes Metab Case Rep
; 20172017.
Article
in English
| MEDLINE | ID: mdl-28458897
20.
DUSP5 and DUSP6, two ERK specific phosphatases, are markers of a higher MAPK signaling activation in BRAF mutated thyroid cancers.
PLoS One
; 12(9): e0184861, 2017.
Article
in English
| MEDLINE | ID: mdl-28910386