Analysis of SRY gene regulation by SP1 and WT1 proteins

• Grant number: 08/03168-1
• Support Opportunities: Scholarships in Brazil - Post-Doctoral
• Start date: January 01, 2009
• End date: December 31, 2010
• Field of knowledge: Health Sciences - Medicine - Medical Clinics
• Principal Investigator: Maricilda Palandi de Mello
• Grantee: Fernanda Caroline Soardi
• Host Institution: Centro de Biologia Molecular e Engenharia Genética (CBMEG). Universidade Estadual de Campinas (UNICAMP). Campinas , SP, Brazil

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)

FABBRI, HELENA CAMPOS; RIBEIRO DE ANDRADE, JULIANA GABRIEL; SOARDI, FERNANDA CAROLINE; DE CALAIS, FLAVIA LEME; PETROLI, REGINALDO JOSE; MACIEL-GUERRA, ANDREA TREVAS; GUERRA-JUNIOR, GIL; DE MELLO, MARICILDA PALANDI. The novel p.Cys65Tyr mutation in NR5A1 gene in three 46,XY siblings with normal testosterone levels and their mother with primary ovarian insufficiency. BMC MEDICAL GENETICS, v. 15, JAN 10 2014. (09/08320-9, 08/01964-5, 08/03168-1, 11/02865-3)

CUNHA, J. L.; SOARDI, F. C.; BERNARDI, R. D.; OLIVEIRA, L. E. C.; BENEDETTI, C. E.; GUERRA-JUNIOR, G.; MACIEL-GUERRA, A. T.; DE MELLO, M. P.. The novel p.E89K mutation in the SRY gene inhibits DNA binding and causes the 46,XY disorder of sex development. Brazilian Journal of Medical and Biological Research, v. 44, n. 4, p. 361-365, APR 2011. (08/03168-1, 07/00900-0)