An uncommon phenotype with familial central hypogonadism caused by a novel PROP1 gene mutant truncated in the transactivation domainREYNAUD, Rachel; BARLIER, Anne; VALLETTE-KASIC, Sophie et al.The Journal of clinical endocrinology and metabolism. 2005, Vol 90, Num 8, pp 4880-4887, issn 0021-972X, 8 p.Article

Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletionABRAO, M. G; LEITE, M. V; CARVALHO, L. R et al.Clinical endocrinology (Oxford. Print). 2006, Vol 65, Num 3, pp 294-300, issn 0300-0664, 7 p.Article

PROP1 gene analysis in portuguese patients with combined pituitary hormone deficiencyLEMOS, Manuel C; GOMES, Leonor; CASTRO, Joao J et al.Clinical endocrinology (Oxford. Print). 2006, Vol 65, Num 4, pp 479-485, issn 0300-0664, 7 p.Article

Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defectsLEBL, Jan; VOSAHLO, Jan; BLUM, Werner F et al.European journal of endocrinology. 2005, Vol 153, Num 3, pp 389-396, issn 0804-4643, 8 p.Article

A novel PROP1 gene mutation (157delA) in Japanese siblings with combined anterior pituitary hormone deficiencyTATSUMI, Ke-Ita; KIKUCHI, Kiyoshi; TSUMURA, Kumi et al.Clinical endocrinology (Oxford. Print). 2004, Vol 61, Num 5, pp 635-640, issn 0300-0664, 6 p.Article

Two new PROP1 gene mutations responsible for compound pituitary hormone deficiencyPARACCHINI, R; GIORDANO, M; CORRIAS, A et al.Clinical genetics. 2003, Vol 64, Num 2, pp 142-147, issn 0009-9163, 6 p.Article

A familial form of congenital hypopituitarism due to a PROP1 mutation in a large kindred: Phenotypic and in vitro functional studiesREYNAUD, Rachel; CHADLI-CHAIEB, Molka; VALLETTE-KASIC, Sophie et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 11, pp 5779-5786, issn 0021-972X, 8 p.Article

Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD)KELBERMAN, D; TURTON, J. P. G; WOODS, K. S et al.Clinical endocrinology (Oxford. Print). 2009, Vol 70, Num 1, pp 96-103, issn 0300-0664, 8 p.Article

Ovulation induction and successful pregnancy outcome in two patients with Prop1 gene mutationsVOUTETAKIS, Antonis; SERTEDAKI, Amalia; LIVADAS, Sarantis et al.Fertility and sterility. 2004, Vol 82, Num 2, pp 454-457, issn 0015-0282, 4 p.Article

Cloning, characterization, and physical mapping of the canine Prop-1 gene (PROP 1): exclusion as a candidate for combined pituitary hormone deficiency in German shepherd dogsLANTINGA-VAN LEEUWEN, I. S; KOOISTRA, H. S; MOL, J. A et al.Cytogenetics and cell genetics. 2000, Vol 88, Num 1-2, pp 140-144, issn 0301-0171Article

High Prevalence of PROP1 Defects in Lithuania: Phenotypic Findings in an Ethnically Homogenous Cohort of Patients With Multiple Pituitary Hormone DeficiencyNAVARDAUSKAITE, Ruta; DUSATKOVA, Petra; OBERMANNOVA, Barbora et al.The Journal of clinical endocrinology and metabolism. 2014, Vol 99, Num 1, pp 299-306, issn 0021-972X, 8 p.Article

Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROP1 geneROSENBLOOM, A. L; SELMAN ALMONTE, A; BROWN, M. R et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 1, pp 50-57, issn 0021-972XArticle

A New Chalcone Derivative (E)-3-(4-Methoxyphenyl)-2-methyl-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one Suppresses Prostate Cancer Involving p53-mediated Cell Cycle Arrests and ApoptosisYONG ZHANG; SRINIVASAN, Balasubramanian; CHENGGUO XING et al.Anticancer research. 2012, Vol 32, Num 9, pp 3689-3698, issn 0250-7005, 10 p.Article

Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasiaRAINBOW, L. A; REES, S. A; SHAIKH, M. G et al.Clinical endocrinology (Oxford. Print). 2005, Vol 62, Num 2, pp 163-168, issn 0300-0664, 6 p.Article

Hot spot in the PROP1 gene responsible for combined pituitary hormone deficiencyDELADOËY, J; FLÜCK, C; BÜYÜKGEBIZ, A et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 5, pp 1645-1650, issn 0021-972XArticle