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 *

50 related articles for article (PubMed ID: 12510996)

  • 1. Structural hypothalamic defects.
    Dattani M
    J Pediatr Endocrinol Metab; 2002 Dec; 15 Suppl 5():1423-4. PubMed ID: 12510996
    [No Abstract]   [Full Text] [Related]  

  • 2. HESX1 and Septo-Optic Dysplasia.
    Dattani MT; Robinson IC
    Rev Endocr Metab Disord; 2002 Dec; 3(4):289-300. PubMed ID: 12424431
    [No Abstract]   [Full Text] [Related]  

  • 3. Hesx1 gene in midline cerebral defects.
    Antonini SR; Grecco Filho AS; Elias LL; Moreira AC; de Castro M
    J Pediatr; 2001 Nov; 139(5):754. PubMed ID: 11713462
    [No Abstract]   [Full Text] [Related]  

  • 4. Enhanced repression by HESX1 as a cause of hypopituitarism and septooptic dysplasia.
    Cohen RN; Cohen LE; Botero D; Yu C; Sagar A; Jurkiewicz M; Radovick S
    J Clin Endocrinol Metab; 2003 Oct; 88(10):4832-9. PubMed ID: 14557462
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The impact of R53C mutation on the three-dimensional structure, stability, and DNA-binding properties of the human Hesx-1 homeodomain.
    de la Mata I; Garcia JL; González C; Menéndez M; Cañada J; Jiménez-Barbero J; Asensio JL
    Chembiochem; 2002 Aug; 3(8):726-40. PubMed ID: 12203971
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular effects of novel mutations in Hesx1/HESX1 associated with human pituitary disorders.
    Brickman JM; Clements M; Tyrell R; McNay D; Woods K; Warner J; Stewart A; Beddington RS; Dattani M
    Development; 2001 Dec; 128(24):5189-99. PubMed ID: 11748154
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ectopic posterior pituitary lobe and periventricular heterotopia: cerebral malformations with the same underlying mechanism?
    Mitchell LA; Thomas PQ; Zacharin MR; Scheffer IE
    AJNR Am J Neuroradiol; 2002 Oct; 23(9):1475-81. PubMed ID: 12372734
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Septo-optic-pituitary dysplasia.
    Humphreys P
    Handb Clin Neurol; 2008; 87():39-52. PubMed ID: 18809017
    [No Abstract]   [Full Text] [Related]  

  • 9. Septo-optic dysplasia complex: a heterogeneous malformation syndrome.
    Polizzi A; Pavone P; Iannetti P; Manfré L; Ruggieri M
    Pediatr Neurol; 2006 Jan; 34(1):66-71. PubMed ID: 16376284
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel human pathological mutations. Gene symbol: HESX1. Disease: septo-optic dysplasia.
    Mueller OT; Coovadia A
    Hum Genet; 2010 Apr; 127(4):478-9. PubMed ID: 21488242
    [No Abstract]   [Full Text] [Related]  

  • 11. Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse.
    Dattani MT; Martinez-Barbera JP; Thomas PQ; Brickman JM; Gupta R; Mårtensson IL; Toresson H; Fox M; Wales JK; Hindmarsh PC; Krauss S; Beddington RS; Robinson IC
    Nat Genet; 1998 Jun; 19(2):125-33. PubMed ID: 9620767
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Septo-optic dysplasia and other midline defects: the role of transcription factors: HESX1 and beyond.
    McCabe MJ; Alatzoglou KS; Dattani MT
    Best Pract Res Clin Endocrinol Metab; 2011 Feb; 25(1):115-24. PubMed ID: 21396578
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Disruption of SoxB1-dependent Sonic hedgehog expression in the hypothalamus causes septo-optic dysplasia.
    Zhao L; Zevallos SE; Rizzoti K; Jeong Y; Lovell-Badge R; Epstein DJ
    Dev Cell; 2012 Mar; 22(3):585-96. PubMed ID: 22421044
    [TBL] [Abstract][Full Text] [Related]  

  • 14. HESX1: a novel gene implicated in a familial form of septo-optic dysplasia.
    Dattani MT; Martinez-Barbera JP; Thomas PQ; Brickman JM; Gupta R; Wales JK; Hindmarsh PC; Beddington RS; Robinson IC
    Acta Paediatr Suppl; 1999 Dec; 88(433):49-54. PubMed ID: 10626545
    [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. Septo-optic dysplasia.
    Fard MA; Wu-Chen WY; Man BL; Miller NR
    Pediatr Endocrinol Rev; 2010 Sep; 8(1):18-24. PubMed ID: 21037540
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fertility and infertility: genetic contributions from the hypothalamic-pituitary-gonadal axis.
    Achermann JC; Jameson JL
    Mol Endocrinol; 1999 Jun; 13(6):812-8. PubMed ID: 10379880
    [No Abstract]   [Full Text] [Related]  

  • 18. Regulation of hippocampal neuronal differentiation by the basic helix-loop-helix transcription factors HES-1 and MASH-1.
    Castella P; Wagner JA; Caudy M
    J Neurosci Res; 1999 May; 56(3):229-40. PubMed ID: 10336252
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Heritable disorders of pituitary development.
    Parks JS; Brown MR; Hurley DL; Phelps CJ; Wajnrajch MP
    J Clin Endocrinol Metab; 1999 Dec; 84(12):4362-70. PubMed ID: 10599689
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Natural course of septo-optic dysplasia: retrospective analysis of 20 cases].
    León-Gonzalez M; García-Peñas JJ; Puertas-Bordallo D; López-Pino MA; Argente-Oliver J; Cantarín-Extremera V
    Rev Neurol; 2012 Mar; 54(6):321-31. PubMed ID: 22403144
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.