Cyclin-dependent kinase inhibitor 1B (CDKN1B) gene variants in AIP mutation-negative familial isolated pituitary adenoma kindreds

High prevalence of AIP gene mutations following focused screening in young patients with sporadic pituitary macroadenomas

(2011) Maria A Tichomirowa et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype

(2011) Diego Ojeda et al.   FERTILITY AND STERILITY

Somatic Mutation and Germline Sequence Abnormalities inCDKN1B, Encoding p27Kip1, in Sporadic Parathyroid Adenomas

(2011) Jessica Costa-Guda et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Characterization of aryl hydrocarbon receptor interacting protein (AIP) mutations in familial isolated pituitary adenoma families

(2010) Susana Igreja et al.   HUMAN MUTATION

A novel germline CDKN1B mutation causing multiple endocrine tumors: clinical, genetic and functional characterization

(2010) Sara Molatore et al.   HUMAN MUTATION

Clinical Characteristics and Therapeutic Responses in Patients with Germ-LineAIPMutations and Pituitary Adenomas: An International Collaborative Study

(2010) Adrian F. Daly et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

p27kip1: A New Multiple Endocrine Neoplasia Gene?

(2010) Ilaria Marinoni et al.   NEUROENDOCRINOLOGY

Prevalence of pituitary adenomas: a community-based, cross-sectional study in Banbury (Oxfordshire, UK)

(2009) Alberto Fernandez et al.   CLINICAL ENDOCRINOLOGY

Rare Germline Mutations in Cyclin-Dependent Kinase Inhibitor Genes in Multiple Endocrine Neoplasia Type 1 and Related States

(2009) Sunita K. Agarwal et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Post-translational regulation of the tumor suppressor p27KIP1

(2008) J. Vervoorts et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Assessment ofp27(cyclin-dependent kinase inhibitor 1B) and aryl hydrocarbon receptor-interacting protein (AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectableMEN1gene mutations

(2008) Susana Igreja et al.   CLINICAL ENDOCRINOLOGY