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Genetics of rheumatoid arthritis: A new boost is needed in Latin American populations
(Elsevier Editora Ltda, 2016)
Genetics of ankylosing spondylitis [Genética, HLA-B27 y espondilitis anquilosante: 40 años]
(Sociedad Medica de Santiago, 2014)
Pathogenesis of preeclampsia: The genetic component
(2012)
Preeclampsia (PE) is one of the main causes of maternal and fetal morbidity and mortality in the world, causing nearly 40% of births delivered before 35 weeks of gestation. PE begins with inadequate trophoblast invasion ...
Variation in the CXCR1 gene (IL8RA) is not associated with susceptibility to chronic periodontitis
(2011-11-04)
Background: The chemokine receptor 1 CXCR-1 (or IL8R-alpha) is a specific receptor for the interleukin 8 (IL-8), which is chemoattractant for neutrophils and has an important role in the inflammatory response. The polymorphism ...
Variation in the CXCR1 gene (IL8RA) is not associated with susceptibility to chronic periodontitis
(2011-11-04)
Background: The chemokine receptor 1 CXCR-1 (or IL8R-alpha) is a specific receptor for the interleukin 8 (IL-8), which is chemoattractant for neutrophils and has an important role in the inflammatory response. The polymorphism ...
Aspectos genéticos do transtorno obsessivo-compulsivo
(Associação Brasileira de Psiquiatria - ABP, 2001-10-01)
Since the first descriptions of obsessive-compulsive disorder (OCD), genetic factors have been implicated in the etiology of the illness. Twin studies show a high concordance rate for monozygotic twins. Family studies found ...
ERAP1 and HLA-C interaction in inflammatory bowel disease in the Spanish population
(SAGE Publications Ltd, 2017)
Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta
(2007-07-02)
Amelogenesis imperfecta (AI) is a genetically heterogeneous group of diseases that result in defective development of tooth enamel. Mutations in several enamel proteins and proteinases have been associated with AI. The ...