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Analysis of modulator genes in the nonclassical 21-hydroxylase deficiency phenotype

Grant number: 08/51624-6
Support Opportunities:Scholarships in Brazil - Master
Start date: August 01, 2008
End date: July 31, 2010
Field of knowledge:Health Sciences - Medicine - Medical Clinics
Principal Investigator:Tania Aparecida Sartori Sanchez Bachega
Grantee:Vivian Moura Massari
Host Institution: Faculdade de Medicina (FM). Universidade de São Paulo (USP). São Paulo , SP, Brazil
Associated research grant:05/04726-0 - Molecular characterization of congenital endocrine diseases that affect growth and development, AP.TEM
News published in Agência FAPESP Newsletter about the scholarship:
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Scientific publications
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
MOURA-MASSARI, V. O.; BUGANO, D. D. G.; MARCONDES, J. A. M.; GOMES, L. G.; MENDONCA, B. B.; BACHEGA, T. A. S. S.. CYP21A2 Genotypes do not Predict the Severity of Hyperandrogenic Manifestations in the Nonclassical Form of Congenital Adrenal Hyperplasia. Hormone and Metabolic Research, v. 45, n. 4, p. 301-307, . (08/51624-6, 05/04726-0)
MOURA-MASSARI, VIVIAN OLIVEIRA; CUNHA, FLAVIA SIQUEIRA; GOMES, LARISSA GARCIA; DINIZ GOMES, DIOGO BUGANO; MIGUEL MARCONDES, JOSE ANTONIO; MADUREIRA, GUIOMAR; DE MENDONCA, BERENICE BILHARINHO; SARTORI SANCHEZ BACHEGA, TANIA A.. The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene. PLoS One, v. 11, n. 2, . (14/07878-4, 08/51624-6, 05/04726-0)