Juliana S Teles

No ORCID on file · 5 papers in corpus
article 2012
Genetic association study of polymorphisms FOXP3 and FCRL3 in women with endometriosis
Fertility and sterility ·doi:10.1016/j.fertnstert.2012.01.125

ObjectiveTo consider a possible cumulative effect of two genetic polymorphisms (FOXP3 C-2383T/rs3761549 and FCRL3 C-169T/rs7528684) that were previously shown to be associated with endometriosis.DesignGenetic association study.SettingHuman …

article 2011
Analysis of FOXP3 polymorphisms in infertile women with and without endometriosis
Fertility and sterility ·doi:10.1016/j.fertnstert.2011.03.033

ObjectiveTo evaluate FOXP3 polymorphisms (rs3761549, rs3761548, rs2232368, rs2232366, and rs2280883) in a group of infertile women with and without endometriosis and controls.DesignCase control study.SettingHuman Reproduction Outpatient Cli…

article 2011
Association of FCRL3 −169T/C polymorphism with endometriosis and identification of a protective haplotype against the development of the disease in Brazilian population
Human immunology ·doi:10.1016/j.humimm.2011.05.005

An aberrant immunologic mechanism has been suggested to be involved in the pathogenesis of endometriosis. Fc receptor-like 3 gene (FCRL3) has been proposed as a novel autoimmune predisposing factor. The authors have hypothesized a possible …

article 2011
Association of FCRL3 C-169T promoter single-nucleotide polymorphism with idiopathic infertility and infertility-related endometriosis
Journal of Reproductive Immunology ·doi:10.1016/j.jri.2011.02.007

An aberrant immunological mechanism is thought to be involved in the pathogenesis of endometriosis. The present study aimed to determine whether there is a relationship between endometriosis and/or infertility and the FCRL3 C-169T polymorph…

article 2010
ORIGINAL ARTICLE: PTPN22 C1858T Polymorphism in Women with Endometriosis
American journal of reproductive immunology (New York, N.Y. : 1989) ·doi:10.1111/j.1600-0897.2009.00797.x

PROBLEM: Endometriosis has been suggested to be an autoimmune disease and recently, an allelic variation of the PTPN22 (C1858T) gene was revealed to be associated with the development of autoimmunity. The aim of the study was to determine t…