Last Updated: 09/26/2026
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Found 14 publications
Embryonic stem cell factor FOXD3 (Genesis) defects in gastrointestinal stromal tumors.
Journal: Endocrine-related cancer
Published: March 13, 2023
PRKACB variants in skeletal disease or adrenocortical hyperplasia: effects on protein kinase A.
Journal: Endocrine-related cancer
Published: August 21, 2020
A phosphodiesterase 11 (Pde11a) knockout mouse expressed functional but reduced Pde11a: Phenotype and impact on adrenocortical function.
Journal: Molecular and cellular endocrinology
Published: July 11, 2020
Insulin-like growth factor 2 (IGF2) expression in adrenocortical disease due to PRKAR1A mutations compared to other benign adrenal tumors.
Journal: Endocrine
Published: May 31, 2020
Brentuximab vedotin as monotherapy for unresectable breast implant-associated anaplastic large cell lymphoma.
Journal: Clinical case reports
Published: December 01, 2018
Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentations.
Journal: European journal of endocrinology
Published: May 01, 2015
Is IGSF1 involved in human pituitary tumor formation?
Journal: Endocrine-related cancer
Published: December 21, 2014
Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation.
Journal: The New England journal of medicine
Published: December 04, 2014
Clinical and molecular genetics of the phosphodiesterases (PDEs).
Journal: Endocrine reviews
Published: December 07, 2013
Deletions of the PRKAR1A locus at 17q24.2-q24.3 in Carney complex: genotype-phenotype correlations and implications for genetic testing.
Journal: The Journal of clinical endocrinology and metabolism
Published: October 31, 2013
Phosphodiesterase 11A (PDE11A) gene defects in patients with acth-independent macronodular adrenal hyperplasia (AIMAH): functional variants may contribute to genetic susceptibility of bilateral adrenal tumors.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 22, 2012
KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome.
Journal: Endocrine-related cancer
Published: February 11, 2012
Last Updated: 09/26/2026