BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

246 related articles for article (PubMed ID: 11549703)

  • 1. PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency.
    Vallette-Kasic S; Barlier A; Teinturier C; Diaz A; Manavela M; Berthezène F; Bouchard P; Chaussain JL; Brauner R; Pellegrini-Bouiller I; Jaquet P; Enjalbert A; Brue T
    J Clin Endocrinol Metab; 2001 Sep; 86(9):4529-35. PubMed ID: 11549703
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion.
    Agarwal G; Bhatia V; Cook S; Thomas PQ
    J Clin Endocrinol Metab; 2000 Dec; 85(12):4556-61. PubMed ID: 11134108
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Genetic background of inherited multiple pituitary hormone deficiency. Mutations of PROP1 gene in Hungary].
    Halász Z
    Orv Hetil; 2011 Feb; 152(6):221-32. PubMed ID: 21278027
    [TBL] [Abstract][Full Text] [Related]  

  • 4. "Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency.
    Deladoëy J; Flück C; Büyükgebiz A; Kuhlmann BV; Eblé A; Hindmarsh PC; Wu W; Mullis PE
    J Clin Endocrinol Metab; 1999 May; 84(5):1645-50. PubMed ID: 10323394
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene.
    Pernasetti F; Toledo SP; Vasilyev VV; Hayashida CY; Cogan JD; Ferrari C; Lourenço DM; Mellon PL
    J Clin Endocrinol Metab; 2000 Jan; 85(1):390-7. PubMed ID: 10634415
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency.
    Lemos MC; Gomes L; Bastos M; Leite V; Limbert E; Carvalho D; Bacelar C; Monteiro M; Fonseca F; Agapito A; Castro JJ; Regateiro FJ; Carvalheiro M
    Clin Endocrinol (Oxf); 2006 Oct; 65(4):479-85. PubMed ID: 16984240
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg-->Cys at codon 120 (R120C).
    Flück C; Deladoey J; Rutishauser K; Eblé A; Marti U; Wu W; Mullis PE
    J Clin Endocrinol Metab; 1998 Oct; 83(10):3727-34. PubMed ID: 9768691
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene.
    Mendonca BB; Osorio MG; Latronico AC; Estefan V; Lo LS; Arnhold IJ
    J Clin Endocrinol Metab; 1999 Mar; 84(3):942-5. PubMed ID: 10084575
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic screening of combined pituitary hormone deficiency: experience in 195 patients.
    Reynaud R; Gueydan M; Saveanu A; Vallette-Kasic S; Enjalbert A; Brue T; Barlier A
    J Clin Endocrinol Metab; 2006 Sep; 91(9):3329-36. PubMed ID: 16735499
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in PROP1 cause familial combined pituitary hormone deficiency.
    Wu W; Cogan JD; Pfäffle RW; Dasen JS; Frisch H; O'Connell SM; Flynn SE; Brown MR; Mullis PE; Parks JS; Phillips JA; Rosenfeld MG
    Nat Genet; 1998 Feb; 18(2):147-9. PubMed ID: 9462743
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [From gene to disease; POU1F1- and PROP1-mutations in pituitary hormone deficiency].
    Wit JM; Vulsma T; de Vijlder JJ
    Ned Tijdschr Geneeskd; 2001 Dec; 145(50):2425-7. PubMed ID: 11776668
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Four novel mutations of the LHX3 gene cause combined pituitary hormone deficiencies with or without limited neck rotation.
    Pfaeffle RW; Savage JJ; Hunter CS; Palme C; Ahlmann M; Kumar P; Bellone J; Schoenau E; Korsch E; Brämswig JH; Stobbe HM; Blum WF; Rhodes SJ
    J Clin Endocrinol Metab; 2007 May; 92(5):1909-19. PubMed ID: 17327381
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
    Turton JP; Mehta A; Raza J; Woods KS; Tiulpakov A; Cassar J; Chong K; Thomas PQ; Eunice M; Ammini AC; Bouloux PM; Starzyk J; Hindmarsh PC; Dattani MT
    Clin Endocrinol (Oxf); 2005 Jul; 63(1):10-8. PubMed ID: 15963055
    [TBL] [Abstract][Full Text] [Related]  

  • 14. MR imaging of the pituitary gland in children and young adults with congenital combined pituitary hormone deficiency associated with PROP1 mutations.
    Fofanova O; Takamura N; Kinoshita E; Vorontsov A; Vladimirova V; Dedov I; Peterkova V; Yamashita S
    AJR Am J Roentgenol; 2000 Feb; 174(2):555-9. PubMed ID: 10658742
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. A familial form of congenital hypopituitarism due to a PROP1 mutation in a large kindred: phenotypic and in vitro functional studies.
    Reynaud R; Chadli-Chaieb M; Vallette-Kasic S; Barlier A; Sarles J; Pellegrini-Bouiller I; Enjalbert A; Chaieb L; Brue T
    J Clin Endocrinol Metab; 2004 Nov; 89(11):5779-86. PubMed ID: 15531542
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High prevalence of PROP1 defects in Lithuania: phenotypic findings in an ethnically homogenous cohort of patients with multiple pituitary hormone deficiency.
    Navardauskaite R; Dusatkova P; Obermannova B; Pfaeffle RW; Blum WF; Adukauskiene D; Smetanina N; Cinek O; Verkauskiene R; Lebl J
    J Clin Endocrinol Metab; 2014 Jan; 99(1):299-306. PubMed ID: 24178788
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects.
    Lebl J; Vosáhlo J; Pfaeffle RW; Stobbe H; Cerná J; Novotná D; Zapletalová J; Kalvachová B; Hána V; Weiss V; Blum WF
    Eur J Endocrinol; 2005 Sep; 153(3):389-96. PubMed ID: 16131601
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation.
    Riepe FG; Partsch CJ; Blankenstein O; Mönig H; Pfäffle RW; Sippell WG
    J Clin Endocrinol Metab; 2001 Sep; 86(9):4353-7. PubMed ID: 11549674
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations Within the Transcription Factor
    Bulut FD; Özdemir Dilek S; Kotan D; Mengen E; Gürbüz F; Yüksel B
    J Clin Res Pediatr Endocrinol; 2020 Sep; 12(3):261-268. PubMed ID: 31948187
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.