CV Lattes
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Universidade Estadual de Campinas (UNICAMP). Centro de Hematologia e Hemoterapia (HEMOCENTRO) (Institutional affiliation from the last research proposal) Birthplace: Brazil
Graduated in Biological Sciences from the Faculty of Philosophy, Sciences and Languages of Ribeirão Preto - University of São Paulo (2002). Held the master's and doctorate in Basic and Applied Immunology by the Ribeirão Preto Medical School - University of São Paulo, with emphasis on the study of Neuroimmunology (2005 and 2009). Postdoctoral developed in the Department of Pathology and Immunology of Washinghton University in St. Louis, MO, USA, under the supervision of Dr. Marco Colonna in the study of the functions of plasmacytoid dendritic cells (from 2013 to 2015). She is currently a postdoctoral fellow by the Ribeirão Preto Medical School - University of São Paulo, under the supervision of Dr. João Santana da Silva, where investigates the role of dendritic cells and their PRRs in Coxsackie virus infection. She has experience in the area of Immunology, with emphasis on infectious diseases (coxsackievirus, LCMV, Plasmodium berghei and Trypanosoma cruzi) and cellular immunity. (Source: Lattes Curriculum)
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Sickle cell anemia (SCA) is one of the most common hemoglobinopathies in the world. Patients with SCA present reduced quality of life due to complications resulting from the change in the shape and physical properties of erythrocytes. These complications consist of chronic hemolytic anemia, pain crisis, organ dysfunction, susceptibility to infections, among others. SCA can be considered a…
Sickle Cell Anemia (SCA) is one of the most common hemoglobinopathies in the world. Patients with SCA present reduced quality of life due to complications resulting from the change in the shape and physical properties of erythrocytes. These complications consist of chronic Hemolytic Anemia, pain crisis, organ dysfunction, susceptibility to infections, among others. SCA can be considered a…
Sickle cell disease is a hereditary disease of high relevance worldwide caused by a mutation in the gene that encodes the b subunit of hemoglobin, which forms an anomalous hemoglobin (HbS), which polymerizes during deoxygenation, forming sickle-shaped erythrocytes. This condition can lead to several clinical complications, most of which are associated with episodes of vaso-occlusion, a ph…
Sickle cell anemia (SCA) is one of the most common hemoglobinopathies in the world. Patients with SCA present reduced quality of life due to complications resulting from the change in the shape and physical properties of erythrocytes. These complications consist of chronic hemolytic anemia, pain crisis, organ dysfunction, susceptibility to infections, among others. SCA can be considered a…
(Only some records are available in English at this moment)
Sickle cell anemia (SCA) is one of the most common hemoglobinopathies in the world. Patients with SCA present reduced quality of life due to complications resulting from the change in the shape and physical properties of erythrocytes. These complications consist of chronic hemolytic anemia, pain crisis, organ dysfunction, susceptibility to infections, among others. SCA can be considered a…
Sickle cell anemia (SCA) is one of the most common hemoglobinopathies around the world. Patients affected by SCA have a reduced quality of life due to complications resulting from changes in the shape and physical properties of erythrocytes. These complications consist of chronic hemolytic anemia, pain crises, organ dysfunction, susceptibility to infections, among others. It is also known…
Sickle cell anemia (SCA) is one of the most common hemoglobinopathies around the world. Patients affected by SCA have a reduced quality of life due to complications resulting from changes in the shape and physical properties of erythrocytes. These complications consist of chronic hemolytic anemia, pain crises, organ dysfunction, susceptibility to infections, among others. Patients with SC…
(Only some records are available in English at this moment)
Sickle Cell Anemia (SCA) is a genetic disorder caused by a mutation in the beta globin chain, leading to the production of hemoglobin S. This event causes red blood cells to sickle during deoxygenation, increasing hemolysis and reducing cell lifespan. Hemolysis occurs both in the spleen and intravascularly, releasing damage-associated molecular patterns (DAMPs) that trigger inflammation a…
The development of the distinct subsets of dendritic cells (DCs) from monocytes and bone marrow precursors during homeostasis is mediated by the different transcription factors expressed and the cytokines present in the microenvironment. A number of these cytokines and their receptors is up-regulated upon infection, which can influence the expansion and the differentiation of the preforme…
| 2 / 2 | Ongoing grants |
| 4 / 4 | Ongoing scholarships in Brazil |
| 5 / 5 | Completed scholarships in Brazil |
| 2 / 2 | Completed scholarships abroad |
| 13 / 13 | All research grants and scholarships |
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