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Journal Abstract Search

279 related items for PubMed ID: 14561704

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  • 3. 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
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  • 4. 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
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  • 5. Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism.
    Sajedi E, Gaston-Massuet C, Signore M, Andoniadou CL, Kelberman D, Castro S, Etchevers HC, Gerrelli D, Dattani MT, Martinez-Barbera JP.
    Dis Model Mech; 2008 Dec; 1(4-5):241-54. PubMed ID: 19093031
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  • 8. Molecular genetics of septo-optic dysplasia.
    Dattani ML, Martinez-Barbera J, Thomas PQ, Brickman JM, Gupta R, Wales JK, Hindmarsh PC, Beddington RS, Robinson IC.
    Horm Res; 2000 Dec; 53 Suppl 1():26-33. PubMed ID: 10895039
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  • 9. Temporal regulation of a paired-like homeodomain repressor/TLE corepressor complex and a related activator is required for pituitary organogenesis.
    Dasen JS, Martinez Barbera JP, Herman TS, Connell SO, Olson L, Ju B, Tollkuhn J, Baek SH, Rose DW, Rosenfeld MG.
    Genes Dev; 2001 Dec 01; 15(23):3193-207. PubMed ID: 11731482
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  • 10. HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype.
    Fang Q, Benedetti AF, Ma Q, Gregory L, Li JZ, Dattani M, Sadeghi-Nejad A, Arnhold IJ, Mendonca BB, Camper SA, Carvalho LR.
    Clin Endocrinol (Oxf); 2016 Sep 01; 85(3):408-14. PubMed ID: 27000987
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  • 11. 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 01; 128(24):5189-99. PubMed ID: 11748154
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  • 12. A novel homozygous HESX1 mutation causes panhypopituitarism without midline defects and optic nerve anomalies.
    Durmaz B, Cogulu O, Dizdarer C, Stobbe H, Pfaeffle R, Ozkinay F.
    J Pediatr Endocrinol Metab; 2011 Dec 01; 24(9-10):779-82. PubMed ID: 22145475
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  • 13. 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 01; 23(9):1475-81. PubMed ID: 12372734
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  • 14. Hesx1 homeodomain protein represses transcription as a monomer and antagonises transactivation of specific sites as a homodimer.
    Quirk J, Brown P.
    J Mol Endocrinol; 2002 Jun 01; 28(3):193-205. PubMed ID: 12063185
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  • 15. Transcription factors regulating pituitary development.
    Parks JS, Brown MR.
    Growth Horm IGF Res; 1999 Jun 01; 9 Suppl B():2-8; discussion 8-11. PubMed ID: 10549299
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  • 16. HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism.
    McNay DE, Turton JP, Kelberman D, Woods KS, Brauner R, Papadimitriou A, Keller E, Keller A, Haufs N, Krude H, Shalet SM, Dattani MT.
    J Clin Endocrinol Metab; 2007 Feb 01; 92(2):691-7. PubMed ID: 17148560
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  • 17. A novel mutation in HESX1 causes combined pituitary hormone deficiency without septo optic dysplasia phenotypes.
    Takagi M, Takahashi M, Ohtsu Y, Sato T, Narumi S, Arakawa H, Hasegawa T.
    Endocr J; 2016 Apr 25; 63(4):405-10. PubMed ID: 26781211
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  • 18. 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 25; 62(2):163-8. PubMed ID: 15670191
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  • 19. The homeobox protein Six3 interacts with the Groucho corepressor and acts as a transcriptional repressor in eye and forebrain formation.
    Kobayashi M, Nishikawa K, Suzuki T, Yamamoto M.
    Dev Biol; 2001 Apr 15; 232(2):315-26. PubMed ID: 11401394
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  • 20. Heritable disorders of pituitary development.
    Parks JS, Brown MR, Hurley DL, Phelps CJ, Wajnrajch MP.
    J Clin Endocrinol Metab; 1999 Dec 15; 84(12):4362-70. PubMed ID: 10599689
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