| 1 | CPHD2, PROP1
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| Functional SNPs within the intron 1 of the PROP1 gene contribute to combined growth hormone deficiency (CPHD).
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| Godi M, Mellone S, Tiradani L, Marabese R, Bardelli C, Salerno M, Prodam F, Bellone S, Petri A, Momigliano-Richiardi P, Bona G, Giordano M.
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| J Clin Endocrinol Metab 97(9):E1791-7. doi: 10.1210/jc.2012-1527. Epub 2012 Jun 28.
2012
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| 2 | CPHD2, PROP1
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| Mutations and pituitary morphology in a series of 82 patients with PROP1 gene defects.
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| Obermannova B, Pfaeffle R, Zygmunt-Gorska A, Starzyk J, Verkauskiene R, Smetanina N, Bezlepkina O, Peterkova V, Frisch H, Cinek O, Child CJ, Blum WF, Lebl J.
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| Horm Res Paediatr 76(5):348-54. doi: 10.1159/000332693. Epub 2011 Oct 18.
2011
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| 3 | HESX1, PROP1, TLE1, TLE3
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| Corepressors TLE1 and TLE3 interact with HESX1 and PROP1.
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| Carvalho LR, Brinkmeier ML, Castinetti F, Ellsworth BS, Camper SA.
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| Mol Endocrinol 24(4):754-65. Epub 2010 Feb 24.PMID: 20181723 2010
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| 4 | HESX1, PROP1
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| Pituitary homeodomain transcription factors HESX1 and PROP1 form a heterodimer on the inverted TAAT motif.
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| Kato Y, Kimoto F, Susa T, Nakayama M, Ishikawa A, Kato T.
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| Mol Cell Endocrinol 315(1-2):168-73. doi: 10.1016/j.mce.2009.10.006. Epub 2009 Oct 29.
2010
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| 5 | PROP1
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| Dimeric PROP1 binding to diverse palindromic TAAT sequences promotes its transcriptional activity.
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| Nakayama M, Kato T, Susa T, Sano A, Kitahara K, Kato Y.
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| Mol Cell Endocrinol 307(1-2):36-42. doi: 10.1016/j.mce.2009.03.010. Epub 2009 Mar 28.
2009
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| 6 | PROP1
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| PROP1 coexists with SOX2 and induces PIT1-commitment cells.
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| Yoshida S, Kato T, Susa T, Cai LY, Nakayama M, Kato Y.
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| Biochem Biophys Res Commun 385(1):11-5. doi: 10.1016/j.bbrc.2009.05.027. Epub 2009 May 12.
2009
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| 7 | HES1, PROP1
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| Premature differentiation and aberrant movement of pituitary cells lacking both Hes1 and Prop1.
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| Himes AD, Raetzman LT.
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| Dev Biol 325(1):151-61. doi: 10.1016/j.ydbio.2008.10.010. Epub 2008 Nov 1.
2009
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| 8 | PROP1
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| Comparative genomics reveals functional transcriptional control sequences in the Prop1 gene.
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| Ward RD, Davis SW, Cho M, Esposito C, Lyons RH, Cheng JF, Rubin EM, Rhodes SJ, Raetzman LT, Smith TP, Camper SA.
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| Mamm Genome 18(6-7):521-37. Epub 2007 Jun 8.
2007
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| 9 | HESX1, PROP1, POU1F1, CPHD1, CPHD2, SOPT
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| 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.
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| Rainbow LA, Rees SA, Shaikh MG, Shaw NJ, Cole T, Barrett TG, Kirk JM.
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| Clin Endocrinol (Oxf) 62(2):163-8. 2005
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| 10 | CPHD2, PROP1
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| PROP1 mutations cause progressive deterioration of anterior pituitary function including adrenal insufficiency: a longitudinal analysis.
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| Bottner A, Keller E, Kratzsch J, Stobbe H, Weigel JF, Keller A, Hirsch W, Kiess W, Blum WF, Pfaffle RW.
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| J Clin Endocrinol Metab 89(10):5256-65. 2004
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| 11 | CPHD2, PROP1
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| Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency.
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| Paracchini R, Giordano M, Corrias A, Mellone S, Matarazzo P, Bellone J, Momigliano-Richiardi P, Bona G.
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| Clin Genet 64(2):142-7. 2003
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| 12 | TLE3, AES, TCF4, PROP1
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| TCF and Groucho-related genes influence pituitary growth and development.
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| Brinkmeier ML, Potok MA, Cha KB, Gridley T, Stifani S, Meeldijk J, Clevers H, Camper SA.
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| Mol Endocrinol 17(11):2152-61. Epub 2003 Aug 7. 2003
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| 13 | LHX4, PROP1
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| Lhx4 and Prop1 are required for cell survival and expansion of the pituitary primordia.
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| Raetzman LT, Ward R, Camper SA.
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| Development 129(18):4229-39. 2002
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| 14 | PROP1
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| Functional significance of prop-1 gene expression in pituitary adenomas.
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| Usui T, Nakamura Y, Mizuta H, Murabe H, Muro S, Suda M, Tanaka K, Tanaka I, Shimatsu A, Nakao K.
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| Endocr J 47 Suppl:S85-9. 2000
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| 15 | CPHD2, PROP1
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| Central hypocortisolism as part of combined pituitary hormone deficiency due to mutations of PROP-1 gene.
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| Asteria C, Oliveira JH, Abucham J, Beck-Peccoz P.
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| Eur J Endocrinol 143(3):347-52. 2000
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| 16 | PITX1, PROP1
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| Expression of the pituitary transcription factor Ptx-1, but not that of the trans-activating factor prop-1, is reduced in human corticotroph adenomas and is associated with decreased alpha-subunit secretion.
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| Skelly RH, Korbonits M, Grossman A, Besser GM, Monson JP, Geddes JF, Burrin JM.
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| J Clin Endocrinol Metab 85(7):2537-42. 2000
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| 17 | CPHD2, PROP1
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| Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROP1 gene.
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| Rosenbloom AL, et al.
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| J Clin Endocrinol Metab 84(1):50-7. 1999
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| 18 | CPHD2, PROP1
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| Combined pituitary hormone deficiency in an inbred brazilian kindred associated with a mutation in the PROP-1 gene.
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| Nogueira CR, et al.
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| Mol Genet Metab 67(1):58-61. 1999
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| 19 | CPHD2, PROP1
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| Hot spot in the PROP1 gene responsible for combined pituitary hormone deficiency.
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| Deladoey J, et al.
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| J Clin Endocrinol Metab 84(5):1645-50. 1999
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| 20 | PROP1
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| Prop-1 gene expression in human pituitary tumors.
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| Nakamura S, et al.
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| J Clin Endocrinol Metab 84(7):2581-4 1999
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| 21 | CPHD2, PROP1
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| Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency.
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| Fofanova O, et al.
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| J Clin Endocrinol Metab 83 : 2601-2604. 1998
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| 22 | CPHD2, PROP1
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| Mutations in PROP1 cause familial combined pituitary hormone deficiency.
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| Wu W, et al.
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| Nat Genet 18 : 147. 1998
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| 23 | CPHD2, PROP1
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| The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency.
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| Cogan JD, et al.
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| J Clin Endocrinol Metab 83 : 3346-3349. 1998
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| 24 | CPHD2, PROP1
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| Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitutiion of Arg-->Cys at codon 120 (R120C).
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| Fluck C, et al.
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| J Clin Endocrinol 83 : 3727-3734. 1998
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| 25 | PROP1
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| Human Prop-1 : cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiency.
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| Duquesnoy P, Roy A, Dastot F, Ghali I, Teinturier C, Netchine I, Cacheux V, Hafez M, Salah N, Chaussain JL, Goossens M, Bougneres P, Amselem S.
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| FEBS Lett 437 : 216-220. 1998
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| 26 | PROP1
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| Pituitary lineage determination by the prophet of Pit-1 homeodomain factor defective in ames dwarfism.
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| Sornson MW, et al.
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| Nature 384 : 327-333. 1996
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