Abstract
PORTION OF RESERVE FOR TECHNICAL INFRASTRUCTURE COSTS INSTITUCIONAL SEARCH - YEAR 2018 (AU)
Universidade Estadual de Campinas (UNICAMP). Centro de Hematologia e Hemoterapia (HEMOCENTRO) (Institutional affiliation from the last research proposal) Birthplace: Brazil
graduate at Medicine from Universidade Estadual de Campinas (1993), ph.d. at Clinical Medicine from Universidade Estadual de Campinas (2004) and postdoctoral in Gene Therapy for Hemophilia at Queen's University, Kingston, Canada (2009). Has experience in Medicine, focusing on Hematology, acting on the following subjects: hemophilia, hemostasis, gene therapy, inhibitor. (Source: Lattes Curriculum)
News published in Agência FAPESP Newsletter about the researcher |
More itemsLess items |
TITULO |
Articles published in other media outlets ( ): |
More itemsLess items |
VEICULO: TITULO (DATA) |
VEICULO: TITULO (DATA) |
PORTION OF RESERVE FOR TECHNICAL INFRASTRUCTURE COSTS INSTITUCIONAL SEARCH - YEAR 2018 (AU)
Portion of reserve for technical infrastructure costs institutional search - year 2017. (AU)
Portion of reserve for technical infrastructure costs institucional search - year 2015. (AU)
(Only some records are available in English at this moment)
Polycythemia vera (PV) is the most frequent myeloproliferative neoplasm, characterized by the spontaneous formation of erythroid colonies in vitro, independent of erythropoietin stimulus. It has been recently demonstrated to be associated with the JAK2 V617F point-mutation in the majority of patients. Erythrocytosis is the most common finding in this disease, leading to a series of compli…
Polycythemia vera (PV) is the most frequent myeloproliferative neoplasm, characterized by the spontaneous formation of erythroid colonies in vitro, independent of erythropoietin stimulus. It has been recently demonstrated to be associated with the JAK2 V617F point-mutation in the majority of patients. Erythrocytosis is the most common finding in this disease, leading to a series of compli…
This study was designed to evaluate the adhesive properties in static and under flow conditions of red cells (with or without sickle hemoglobin, Hb S) to endothelial cells from patients with sickle cell disease (HbSS and HbSC). Endothelial cells will be obtained through two different techniques, a) isolation and cultivation of circulating endothelial progenitor cells (Blood outgrowth Endo…
6 / 5 | Completed research grants |
6 / 3 | Completed scholarships in Brazil |
12 / 8 | All research grants and scholarships |
Associated processes |