S. Igreja

MicroRNA miR-107 is overexpressed in pituitary adenomas and inhibits the expression of aryl hydrocarbon receptor-interacting protein in vitro.

M. Korbonits, A. Grossman, H. Chahal, 2012, American journal of physiology. Endocrinology and metabolism.

Assessment of p27 (cyclin‐dependent kinase inhibitor 1B) and aryl hydrocarbon receptor‐interacting protein (AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectable MEN1 gene mutations

R. Quinton, M. Korbonits, S. Akker, 2009, Clinical endocrinology.

Correction of a Cystic Fibrosis Splicing Mutation by Antisense Oligonucleotides

Hugo M. Botelho, L. Clarke, M. Amaral, 2016, Human mutation.

Somatostatin analogs modulate AIP in somatotroph adenomas: the role of the ZAC1 pathway.

M. Korbonits, S. Schulz, A. Grossman, 2012, The Journal of clinical endocrinology and metabolism.

The role of the aryl hydrocarbon receptor-interacting protein gene in familial and sporadic pituitary adenomas.

Julian R. E. Davis, D. Berney, R. Quinton, 2008, The Journal of clinical endocrinology and metabolism.

MicroRNA miR-107 is overexpressed in pituitary adenomas and in vitro inhibits 1 the expression of aryl hydrocarbon receptor-interacting protein (AIP)

M. Korbonits, A. Grossman, H. Chahal, 2012 .

Characterization of Aryl Hydrocarbon Receptor Interacting Protein (AIP) Mutations in Familial Isolated Pituitary Adenoma Families

U. Srirangalingam, S. Ellard, M. Korbonits, 2010, Human mutation.

Assessing the residual CFTR gene expression in human nasal epithelium cells bearing CFTR splicing mutations causing cystic fibrosis

M. Amaral, A. Ramalho, T. Casals, 2013, European Journal of Human Genetics.

AMP‐activated protein kinase mediates glucocorticoid‐ induced metabolic changes: a novel mechanism in Cushing's syndrome

G. Arnaldi, M. Korbonits, M. Christ-Crain, 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

mRNA‐based detection of rare CFTR mutations improves genetic diagnosis of cystic fibrosis in populations with high genetic heterogeneity

A. Ramalho, V. Felício, S. Igreja, 2017, Clinical genetics.