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STUDY OF PTPN22 GENE POLYMORPHISM IN WOMEN WITH ENDOMETRIOSIS

Grant number: 09/01960-2
Support Opportunities:Scholarships in Brazil - Scientific Initiation
Start date: August 01, 2009
End date: July 31, 2011
Field of knowledge:Health Sciences - Medicine - Medical Clinics
Principal Investigator:Caio Parente Barbosa
Grantee:Juliana Souto Teles
Host Institution: Faculdade de Medicina do ABC (FMABC). Organização Social de Saúde. Fundação do ABC. Santo André , SP, Brazil
News published in Agência FAPESP Newsletter about the scholarship:
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VEICULO: TITULO (DATA)
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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)
VILARINO, FABIA LIMA; BIANCO, BIANCA; LERNER, TATIANA GOBERSTEIN; TELES, JULIANA SOUTO; MAFRA, FERNANDA ABANI; CHRISTOFOLINI, DENISE MARIA; BARBOSA, CAIO PARENTE. Analysis of vitamin D receptor gene polymorphisms in women with and without endometriosis. HUMAN IMMUNOLOGY, v. 72, n. 4, p. 359-363, . (10/01104-6, 09/01960-2, 10/00459-5)
CHRISTOFOLINI, DENISE MARIA; TELES, JULIANA SOUTO; VILARINO, FABIA LIMA; ANDRE, GUSTAVO MENDONCA; BIANCO, BIANCA; BARBOSA, CAIO PARENTE. COMT polymorphism and the risk of endometriosis-related infertility. Gynecological Endocrinology, v. 27, n. 12, p. 1099-1102, . (09/01960-2)