I. Pellegrini-Bouiller

Abnormal transduction mechanisms in pituitary adenomas.

A. Barlier, L. Caccavelli, A. Enjalbert, 1997, Hormone research.

Impact of gsp oncogene on the expression of genes coding for Gsalpha, Pit-1, Gi2alpha, and somatostatin receptor 2 in human somatotroph adenomas: involvement in octreotide sensitivity.

A. Barlier, A. J. Zamora, A. Enjalbert, 1999, The Journal of clinical endocrinology and metabolism.

Pit-1 gene expression in human lactotroph and somatotroph pituitary adenomas is correlated to D2 receptor gene expression.

D. Figarella-Branger, A. Barlier, A. Enjalbert, 1996, The Journal of clinical endocrinology and metabolism.

A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency.

A. Barlier, P. Belicar, B. Vialettes, 1996, The Journal of clinical endocrinology and metabolism.

Expression of the members of the Ptx family of transcription factors in human pituitary adenomas.

D. Figarella-Branger, A. J. Zamora, M. Grino, 1999, The Journal of clinical endocrinology and metabolism.

A familial form of congenital hypopituitarism due to a PROP1 mutation in a large kindred: phenotypic and in vitro functional studies.

J. Sarles, A. Barlier, T. Brue, 2004, The Journal of clinical endocrinology and metabolism.

PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency.

C. Teinturier, A. Barlier, J. Chaussain, 2001, The Journal of clinical endocrinology and metabolism.

[Transcription factors of the anterior pituitary and combined hypopituitarism].

T. Brue, A. Enjalbert, S. Vallette, 1999, Annales d'endocrinologie.

Combined pituitary hormone deficiency due to the F135C human Pit-1 (pituitary-specific factor 1) gene mutation: functional and structural correlates.

S. Radovick, T. Brue, A. Enjalbert, 2001, Molecular endocrinology.