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6. The role of CBP/p300 interactions and Pit-1 dimerization in the pathophysiological mechanism of combined pituitary hormone deficiency. Cohen RN; Brue T; Naik K; Houlihan CA; Wondisford FE; Radovick S J Clin Endocrinol Metab; 2006 Jan; 91(1):239-47. PubMed ID: 16263824 [TBL] [Abstract][Full Text] [Related]
7. A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency. Pellegrini-Bouiller I; Bélicar P; Barlier A; Gunz G; Charvet JP; Jaquet P; Brue T; Vialettes B; Enjalbert A J Clin Endocrinol Metab; 1996 Aug; 81(8):2790-6. PubMed ID: 8768831 [TBL] [Abstract][Full Text] [Related]
8. Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia. Pfäffle RW; DiMattia GE; Parks JS; Brown MR; Wit JM; Jansen M; Van der Nat H; Van den Brande JL; Rosenfeld MG; Ingraham HA Science; 1992 Aug; 257(5073):1118-21. PubMed ID: 1509263 [TBL] [Abstract][Full Text] [Related]
9. Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter? Dattani MT Clin Endocrinol (Oxf); 2005 Aug; 63(2):121-30. PubMed ID: 16060904 [TBL] [Abstract][Full Text] [Related]
10. Combined pituitary hormone deficiency due to the F135C human Pit-1 (pituitary-specific factor 1) gene mutation: functional and structural correlates. Vallette-Kasic S; Pellegrini-Bouiller I; Sampieri F; Gunz G; Diaz A; Radovick S; Enjalbert A; Brue T Mol Endocrinol; 2001 Mar; 15(3):411-20. PubMed ID: 11222742 [TBL] [Abstract][Full Text] [Related]
13. Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred. Nogueira CR; Leite CC; Chedid EP; Liberman B; Pimentel-Filho FR; Kopp P; Medeiros-Neto GA J Endocrinol Invest; 1997 Nov; 20(10):629-33. PubMed ID: 9438923 [TBL] [Abstract][Full Text] [Related]
14. A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency. Radovick S; Nations M; Du Y; Berg LA; Weintraub BD; Wondisford FE Science; 1992 Aug; 257(5073):1115-8. PubMed ID: 1509262 [TBL] [Abstract][Full Text] [Related]
15. 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 dysplasia. Rainbow LA; Rees SA; Shaikh MG; Shaw NJ; Cole T; Barrett TG; Kirk JM Clin Endocrinol (Oxf); 2005 Feb; 62(2):163-8. PubMed ID: 15670191 [TBL] [Abstract][Full Text] [Related]
16. Magnetic resonance imaging of the hypothalamus-pituitary unit in childrensuspected of hypopituitarism: who, how and when toinvestigate. Maghnie M; Ghirardello S; Genovese E J Endocrinol Invest; 2004 May; 27(5):496-509. PubMed ID: 15279086 [TBL] [Abstract][Full Text] [Related]
17. Role of Pit-1 in the gene expression of growth hormone, prolactin, and thyrotropin. Cohen LE; Wondisford FE; Radovick S Endocrinol Metab Clin North Am; 1996 Sep; 25(3):523-40. PubMed ID: 8879985 [TBL] [Abstract][Full Text] [Related]
18. Thyrotropin (TSH) beta-subunit gene expression--an example for the complex regulation of pituitary hormone genes. Steinfelder HJ; Wondisford FE Exp Clin Endocrinol Diabetes; 1997; 105(4):196-203. PubMed ID: 9285205 [TBL] [Abstract][Full Text] [Related]
19. [Congenital hypopituitarism: when should transcription factor gene screenings be performed?]. Reynaud R; Barlier A; Chadli-Chaieb M; Saveanu A; Simonin G; Enjalbert A; Brue T Presse Med; 2004 Mar; 33(6):400-5. PubMed ID: 15105786 [TBL] [Abstract][Full Text] [Related]
20. A tissue-specific enhancer confers Pit-1-dependent morphogen inducibility and autoregulation on the pit-1 gene. Rhodes SJ; Chen R; DiMattia GE; Scully KM; Kalla KA; Lin SC; Yu VC; Rosenfeld MG Genes Dev; 1993 Jun; 7(6):913-32. PubMed ID: 8504933 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]