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Genetics of ankylosing spondylitis [Genética, HLA-B27 y espondilitis anquilosante: 40 años]

Castro-Santos P.; Gutiérrez M.A.; Díaz-Peña R. (Sociedad Medica de Santiago, 2014)

Genomics and epigenomics in rheumatic diseases: what do they provide in terms of diagnosis and disease management?

Castro-Santos P.; Díaz-Peña R. (Springer London, 2017)

Genetics of rheumatoid arthritis: A new boost is needed in Latin American populations

Castro-Santos P.; Díaz-Peña R. (Elsevier Editora Ltda, 2016)

Variation in the CXCR1 gene (IL8RA) is not associated with susceptibility to chronic periodontitis

Universidade Estadual Paulista (Unesp) (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

Universidade Estadual Paulista (Unesp) (2011-11-04)

Variation in the CXCR1 gene (IL8RA) is not associated with susceptibility to chronic periodontitis

Scarel-Caminaga, Raquel M.; Curtis, Karen M.C.; Renzi, Rivelto; Sogumo, Patrícia M.; Anovazzi, Giovana; Viana, Aline C.; Kim, Yeon J; Orrico, Silvana R.P.; Cirelli, Joni Augusto (2014)

RUNX1 deficiency (familial platelet disorder with predisposition to myeloid leukemia, FPDMM)

Schlegelberger, Brigitte; Heller, Paula Graciela (Elsevier Inc, 2017-04)

In this review, we discuss disease-causing alterations of RUNT-related transcription factor 1 (RUNX1), a master regulator of hematopoietic differentiation. Familial platelet disorder with predisposition to myeloid leukemia ...

Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta

Universidade Estadual de Campinas (UNICAMP); NIH; National Institute for Dental and Craniofacial Research; Universidade Estadual Paulista (Unesp) (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 ...

Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta

Universidade Estadual de Campinas (UNICAMP); NIH; National Institute for Dental and Craniofacial Research; Universidade Estadual Paulista (Unesp) (2007-07-02)

ERAP1 and HLA-C interaction in inflammatory bowel disease in the Spanish population

Castro-Santos P.; Moro-García M.A.; Marcos-Fernández R.; Alonso-Arias R.; Díaz-Peña R. (SAGE Publications Ltd, 2017)

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Genetics of ankylosing spondylitis [Genética, HLA-B27 y espondilitis anquilosante: 40 años]

Genomics and epigenomics in rheumatic diseases: what do they provide in terms of diagnosis and disease management?

Genetics of rheumatoid arthritis: A new boost is needed in Latin American populations

Variation in the CXCR1 gene (IL8RA) is not associated with susceptibility to chronic periodontitis

Variation in the CXCR1 gene (IL8RA) is not associated with susceptibility to chronic periodontitis

Variation in the CXCR1 gene (IL8RA) is not associated with susceptibility to chronic periodontitis

RUNX1 deficiency (familial platelet disorder with predisposition to myeloid leukemia, FPDMM)

Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta

Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta

ERAP1 and HLA-C interaction in inflammatory bowel disease in the Spanish population