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Page 1
Mineralocorticoid receptor mutations differentially affect individual gene expression profiles in pseudohypoaldosteronism type 1.
Fernandes-Rosa FL, Hubert EL, Fagart J, Tchitchek N, Gomes D, Jouanno E, Benecke A, Rafestin-Oblin ME, Jeunemaitre X, Antonini SR, Zennaro MC. Fernandes-Rosa FL, et al. Among authors: antonini sr. J Clin Endocrinol Metab. 2011 Mar;96(3):E519-27. doi: 10.1210/jc.2010-1486. Epub 2010 Dec 15. J Clin Endocrinol Metab. 2011. PMID: 21159846
Recurrence of the R947X mutation in unrelated families with autosomal dominant pseudohypoaldosteronism type 1: evidence for a mutational hot spot in the mineralocorticoid receptor gene.
Fernandes-Rosa FL, de Castro M, Latronico AC, Sippell WG, Riepe FG, Antonini SR. Fernandes-Rosa FL, et al. Among authors: antonini sr. J Clin Endocrinol Metab. 2006 Sep;91(9):3671-5. doi: 10.1210/jc.2006-0605. Epub 2006 Jun 6. J Clin Endocrinol Metab. 2006. PMID: 16757525
Wnt/beta-catenin pathway deregulation in childhood adrenocortical tumors.
Leal LF, Mermejo LM, Ramalho LZ, Martinelli CE Jr, Yunes JA, Seidinger AL, Mastellaro MJ, Cardinalli IA, Brandalise SR, Moreira AC, Tone LG, Scrideli CA, Castro M, Antonini SR. Leal LF, et al. Among authors: antonini sr. J Clin Endocrinol Metab. 2011 Oct;96(10):3106-14. doi: 10.1210/jc.2011-0363. Epub 2011 Aug 17. J Clin Endocrinol Metab. 2011. PMID: 21849527
Altered expression of noncanonical Wnt pathway genes in paediatric and adult adrenocortical tumours.
Mermejo LM, Leal LF, Colli LM, Fragoso MC, Latronico AC, Tone LG, Scrideli CA, Tucci S, Martinelli CE, Yunes JA, Mastellaro MJ, Seidinger AL, Brandalise SR, Moreira AC, Ramalho LN, Antonini SR, Castro M. Mermejo LM, et al. Among authors: antonini sr. Clin Endocrinol (Oxf). 2014 Oct;81(4):503-10. doi: 10.1111/cen.12462. Epub 2014 May 19. Clin Endocrinol (Oxf). 2014. PMID: 24717047
102 results