Role of GLI2 in hypopituitarism phenotype

Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects

(2014) Sabrina Soares Paulo et al.   CLINICAL ENDOCRINOLOGY

The role of the sonic hedgehog signalling pathway in patients with midline defects and congenital hypopituitarism

(2014) L.C. Gregory et al.   CLINICAL ENDOCRINOLOGY

Pathogenic mutations inGLI2cause a specific phenotype that is distinct from holoprosencephaly

(2014) Kelly A Bear et al.   JOURNAL OF MEDICAL GENETICS

The Teratogenic Effects of Prenatal Ethanol Exposure Are Exacerbated by Sonic Hedgehog or Gli2 Haploinsufficiency in the Mouse

(2014) Henry W. Kietzman et al.   PLoS One

Functional Characterization of a Heterozygous GLI2 Missense Mutation in Patients With Multiple Pituitary Hormone Deficiency

(2013) G. M. C. Flemming et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Relatively high frequency of non-synonymousGLI2variants in patients with congenital hypopituitarism without holoprosencephaly

(2012) Marcela M. França et al.   CLINICAL ENDOCRINOLOGY

The Role of Sonic Hedgehog-Gli2 Pathway in the Masculinization of External Genitalia

(2011) Shinichi Miyagawa et al.   ENDOCRINOLOGY

Direct and indirect requirements of Shh/Gli signaling in early pituitary development

(2010) Yiwei Wang et al.   DEVELOPMENTAL BIOLOGY

Novel Heterozygous NonsenseGLI2Mutations in Patients with Hypopituitarism and Ectopic Posterior Pituitary Lobe without Holoprosencephaly

(2010) Marcela M. França et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Genetic forms of hypopituitarism and their manifestation in the neonatal period

(2009) Kyriaki S. Alatzoglou et al.   EARLY HUMAN DEVELOPMENT

Genetic Regulation of Pituitary Gland Development in Human and Mouse

(2009) Daniel Kelberman et al.   ENDOCRINE REVIEWS

Heterozygous Orthodenticle Homeobox 2 Mutations Are Associated with Variable Pituitary Phenotype

(2009) Sumito Dateki et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

A Novel Dominant Negative Mutation of OTX2 Associated with Combined Pituitary Hormone Deficiency

(2008) Daniel Diaczok et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM