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Author Title [ Type(Asc)] Year
Filters: Author is Cruz, E.  [Clear All Filters]
Journal Article
Fernandez, L., Rodriguez, S., Huang, H., Chora, A., et al. (2008). Tumor necrosis factor-α and endothelial cells modulate Notch signaling in the bone marrow microenvironment during inflammation. Experimental Hematology, 36(5), 545 - 558.e1.
Cruz, E., Vieira, J., Almeida, S., Lacerda, R., et al. (2006). A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: Relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload. BMC Medical Genetics, 7.
Vieira, J., Cardoso, C. S., Pinto, J., Patil, K., et al. (2007). A putative gene located at the MHC class I region around the D6S105 marker contributes to the setting of CD8+ T-lymphocyte numbers in humans. International Journal of Immunogenetics, 34(5), 359 - 367.
Cruz, E., Whittington, C., Krikler, S. H., Mascarenhas, C., et al. (2008). A new 500 kb haplotype associated with high CD8+ T-lymphocyte numbers predicts a less severe expression of hereditary hemochromatosis. BMC medical genetics, 9, 97.
Costa, M., Cruz, E., Oliveira, S., Benes, V., et al. (2015). Lymphocyte gene expression signatures from patients and mouse models of hereditary hemochromatosis reveal a function of hfe as a negative regulator of cd8+ t-Lymphocyte activation and differentiation in vivo. PLoS ONE, 10(4).
MacEdo, M. F., Cruz, E., Lacerda, R., Porto, G., & De Sousa, M. (2005). Low serum transferrin levels in HFE C282Y homozygous subjects are associated with low CD8+ T lymphocyte numbers. Blood Cells, Molecules, and Diseases, 35(3), 319 - 325.
MacEdo, M. F., Porto, G., Costa, M., Vieira, C. P., et al. (2010). Low numbers of CD8 + T lymphocytes in hereditary haemochromatosis are explained by a decrease of the most mature CD8 + effector memory T cells. Clinical and Experimental Immunology, 159(3), 363 - 371.
Cruz, E., Vieira, J., Gonçalves, R., Alves, H., et al. (2004). Involvement of the Major Histocompatibility Complex region in the regulation regulation of circulating CD8+ T-cell numbers in humans. Tissue Antigens, 64(1), 25 - 34.
Cruz, E., Porto, G., Morais, S., Campos, M., & De Sousa, M. (2005). HFE mutations in the pathobiology of hemophilic arthropathy [1]. Blood, 105(8), 3381 - 3382.
Cardoso, C. S., Araújo, H. C., Cruz, E., Afonso, A., et al. (2006). Haemochromatosis gene (HFE) mutations in viral-associated neoplasia: Linkage to cervical cancer. Biochemical and Biophysical Research Communications, 341(1), 232 - 238.
Porto, G., Cruz, E., Miranda, H. P., Porto, B., et al. (2004). Growth hormone (GH)-induced reconstitution of CD8+ CD28+ T lymphocytes in a rare case of severe lymphopenia associated with Juvenile Haemochromatosis and Turner's syndrome. Clinical Endocrinology, 61(4), 437 - 440.
Cruz, E., Melo, G., Lacerda, R., Almeida, S., & Porto, G. (2006). The CD8+ T-lymphocyte profile as a modifier of iron overload in HFE hemochromatosis: An update of clinical and immunological data from 70 C282Y homozygous subjects. Blood Cells, Molecules, and Diseases, 37(1), 33 - 39.

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