These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

341 related articles for article (PubMed ID: 15519252)

  • 1. Pituitary hormone deficiencies due to transcription factor gene alterations.
    Reynaud R; Saveanu A; Barlier A; Enjalbert A; Brue T
    Growth Horm IGF Res; 2004 Dec; 14(6):442-8. PubMed ID: 15519252
    [TBL] [Abstract][Full Text] [Related]  

  • 2. LHX3 and LHX4 transcription factors in pituitary development and disease.
    Colvin SC; Mullen RD; Pfaeffle RW; Rhodes SJ
    Pediatr Endocrinol Rev; 2009 Jan; 6 Suppl 2():283-90. PubMed ID: 19337183
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Pituitary transcription factors: from congenital deficiencies to gene therapy.
    Quentien MH; Barlier A; Franc JL; Pellegrini I; Brue T; Enjalbert A
    J Neuroendocrinol; 2006 Sep; 18(9):633-42. PubMed ID: 16879162
    [TBL] [Abstract][Full Text] [Related]  

  • 5. GH transcription factors.
    Pfaffle RW; Kim C; Blankenstein O; Kentrup H
    J Pediatr Endocrinol Metab; 1999 Apr; 12 Suppl 1():311-7. PubMed ID: 10698595
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. PROP1, HESX1, POU1F1, LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency.
    de Graaff LC; Argente J; Veenma DC; Drent ML; Uitterlinden AG; Hokken-Koelega AC
    Horm Res Paediatr; 2010; 73(5):363-71. PubMed ID: 20389107
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. Genetic disorders of the pituitary.
    Cohen LE
    Curr Opin Endocrinol Diabetes Obes; 2012 Feb; 19(1):33-9. PubMed ID: 22157402
    [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. Molecular analysis of LHX3 and PROP-1 in pituitary hormone deficiency patients with posterior pituitary ectopia.
    Sloop KW; Walvoord EC; Showalter AD; Pescovitz OH; Rhodes SJ
    J Clin Endocrinol Metab; 2000 Aug; 85(8):2701-8. PubMed ID: 10946868
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pituitary transcription factors in the aetiology of combined pituitary hormone deficiency.
    Pfäffle R; Klammt J
    Best Pract Res Clin Endocrinol Metab; 2011 Feb; 25(1):43-60. PubMed ID: 21396574
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Clinical and genetic aspects of combined pituitary hormone deficiencies].
    Castinetti F; Reynaud R; Saveanu A; Quentien MH; Albarel F; Barlier A; Enjalbert A; Brue T
    Ann Endocrinol (Paris); 2008 Feb; 69(1):7-17. PubMed ID: 18291347
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Genetic aspects of growth hormone deficiency].
    Reynaud R; Castinetti F; Galon-Faure N; Albarel-Loy F; Saveanu A; Quentien MH; Jullien N; Khammar A; Enjalbert A; Barlier A; Brue T
    Arch Pediatr; 2011 Jun; 18(6):696-706. PubMed ID: 21497494
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. Pathophysiology of syndromic combined pituitary hormone deficiency due to a LHX3 defect in light of LHX3 and LHX4 expression during early human development.
    Sobrier ML; Attié-Bitach T; Netchine I; Encha-Razavi F; Vekemans M; Amselem S
    Gene Expr Patterns; 2004 Dec; 5(2):279-84. PubMed ID: 15567726
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Basic science and clinical research advances in the pituitary transcription factors: Pit-1 and Prop-1.
    Kerr J; Wood W; Ridgway EC
    Curr Opin Endocrinol Diabetes Obes; 2008 Aug; 15(4):359-63. PubMed ID: 18594277
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cellular determination in the anterior pituitary gland: PIT-1 and PROP-1 mutations as causes of human combined pituitary hormone deficiency.
    Rodriguez R; Andersen B
    Minerva Endocrinol; 2003 Jun; 28(2):123-33. PubMed ID: 12717343
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular basis of pituitary development defects.
    Turki ZM; Hamaoui RB; Ben Slama C
    Tunis Med; 2007 Dec; 85(12):999-1003. PubMed ID: 19170376
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.