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PUBMED FOR HANDHELDS

Journal Abstract Search


202 related items for PubMed ID: 24483153

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  • 4. Functional characterization of the hGRαT556I causing Chrousos syndrome.
    Nicolaides NC, Skyrla E, Vlachakis D, Psarra AM, Moutsatsou P, Sertedaki A, Kossida S, Charmandari E.
    Eur J Clin Invest; 2016 Jan; 46(1):42-9. PubMed ID: 26541474
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  • 6. Primary generalized familial and sporadic glucocorticoid resistance (Chrousos syndrome) and hypersensitivity.
    Charmandari E, Kino T, Chrousos GP.
    Endocr Dev; 2013 Jan; 24():67-85. PubMed ID: 23392096
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  • 8. Pathophysiology of Glucocorticoid Signaling.
    Vitellius G, Trabado S, Bouligand J, Delemer B, Lombès M.
    Ann Endocrinol (Paris); 2018 Jun; 79(3):98-106. PubMed ID: 29685454
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  • 9. A novel point mutation in the amino terminal domain of the human glucocorticoid receptor (hGR) gene enhancing hGR-mediated gene expression.
    Charmandari E, Ichijo T, Jubiz W, Baid S, Zachman K, Chrousos GP, Kino T.
    J Clin Endocrinol Metab; 2008 Dec; 93(12):4963-8. PubMed ID: 18827003
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  • 10. A novel point mutation in helix 10 of the human glucocorticoid receptor causes generalized glucocorticoid resistance by disrupting the structure of the ligand-binding domain.
    Nader N, Bachrach BE, Hurt DE, Gajula S, Pittman A, Lescher R, Kino T.
    J Clin Endocrinol Metab; 2010 May; 95(5):2281-5. PubMed ID: 20335448
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  • 11. Further characterization of human glucocorticoid receptor mutants, R477H and G679S, associated with primary generalized glucocorticoid resistance.
    Ruiz M, Hedman E, Gåfvels M, Eggertsen G, Werner S, Wahrenberg H, Wikström AC.
    Scand J Clin Lab Invest; 2013 Apr; 73(3):203-7. PubMed ID: 23391271
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  • 12. A novel, C-terminal dominant negative mutation of the GR causes familial glucocorticoid resistance through abnormal interactions with p160 steroid receptor coactivators.
    Vottero A, Kino T, Combe H, Lecomte P, Chrousos GP.
    J Clin Endocrinol Metab; 2002 Jun; 87(6):2658-67. PubMed ID: 12050230
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  • 13. A NOVEL GLUCOCORTICOID RECEPTOR MUTATION IN PRIMARY GENERALIZED GLUCOCORTICOID RESISTANCE DISEASE.
    Ma L, Tan X, Li J, Long Y, Xiao Z, De J, Ren Y, Tian H, Chen T.
    Endocr Pract; 2020 Jun 02; 26(6):651-659. PubMed ID: 32045292
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  • 14. Functional characterization of the natural human glucocorticoid receptor (hGR) mutants hGRalphaR477H and hGRalphaG679S associated with generalized glucocorticoid resistance.
    Charmandari E, Kino T, Ichijo T, Zachman K, Alatsatianos A, Chrousos GP.
    J Clin Endocrinol Metab; 2006 Apr 02; 91(4):1535-43. PubMed ID: 16449337
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  • 15. Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance.
    Nicolaides N, Lamprokostopoulou A, Sertedaki A, Charmandari E.
    Hormones (Athens); 2016 Apr 02; 15(1):23-34. PubMed ID: 27086682
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  • 16. Primary generalized glucocorticoid resistance and hypersensitivity: the end-organ involvement in the stress response.
    Charmandari E.
    Sci Signal; 2012 Oct 02; 5(244):pt5. PubMed ID: 23033539
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  • 17. Glucocorticoid Resistance.
    Nicolaides NC, Charmandari E.
    Exp Suppl; 2019 Oct 02; 111():85-102. PubMed ID: 31588529
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  • 18. [Primary Generalized Glucocorticoid Resistance: a case report].
    Larina II, Makazan NV, Ivashchenko KV, Platonova NM, Orlova EM, Kareva MA, Sozaeva LS, Yukina MY, Tulpakov AN, Dukhanin AS, Shimanovskii NL, Troshina EA.
    Probl Endokrinol (Mosk); 2024 Feb 28; 70(1):30-37. PubMed ID: 38433539
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  • 19. Single Nucleotide Variations of the Human GR Gene Manifested as Pathologic Mutations or Polymorphisms.
    Kino T.
    Endocrinology; 2018 Jul 01; 159(7):2506-2519. PubMed ID: 29762667
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  • 20. Natural glucocorticoid receptor mutants causing generalized glucocorticoid resistance: molecular genotype, genetic transmission, and clinical phenotype.
    Charmandari E, Kino T, Souvatzoglou E, Vottero A, Bhattacharyya N, Chrousos GP.
    J Clin Endocrinol Metab; 2004 Apr 01; 89(4):1939-49. PubMed ID: 15070967
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