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Genetics of ankylosing spondylitis [Genética, HLA-B27 y espondilitis anquilosante: 40 años]
(Sociedad Medica de Santiago, 2014)
RUNX1 deficiency (familial platelet disorder with predisposition to myeloid leukemia, FPDMM)
(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 ...
Genetic and Household Determinants of Predisposition to Human Hookworm Infection in a Brazilian Community
(University of Chicago Press, 2018)
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 ...
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 ...
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 ...