CV Lattes
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Universidade Estadual Paulista (UNESP). Campus de São José do Rio Preto. Instituto de Biociências, Letras e Ciências Exatas (IBILCE) (Institutional affiliation from the last research proposal) Birthplace: Brazil
Graduation at Licenciatura Em Ciências Biológicas from Universidade Estadual Paulista Júlio de Mesquita Filho (1982), graduation at Ciências Biológicas Esino de Primeiro Grau from Universidade Estadual Paulista Júlio de Mesquita Filho (1983), master's at Genetics from Universidade Estadual Paulista Júlio de Mesquita Filho (1990) and doctorate at Genetics from Universidade Estadual Paulista Júlio de Mesquita Filho (1993). He is currently professor assistente doutor at Universidade Estadual Paulista Júlio de Mesquita Filho. Has experience in Genetics, focusing on Human and Medical Genetics, acting on the following subjects: diagnóstico laboratorial, diversidade genética, polimorfismo, hemoglobinopatias and prevenção. (Source: Lattes Curriculum)
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AbstractSickle cell disease (SCD) is an inherited hemolytic anemia whose pathophysiology is driven by polymerization of the hemoglobin S (Hb S), leading to hemolysis and vaso-occlusive events. Inflammation is a fundamental component in these processes and a continuous inflammatory stimulus can lead to tissue damages. Thus, pro-resolving pathways emerge in order to restore the homeostasis.…
Hemoglobinopathies are inherited hematological diseases of monogenic origin and autosomal recessive transmission. The term sickle disease (SCD) is used to represent a group of genetic disorders characterized by the presence of HbS, either in homozygosis, characterized by sickle cell anemia (SCA) recognized as the condition of greatest clinical significance within the group, or by its pres…
Sickle Cell Anemia (SCA), characterized by the presence of Hb S in homozygous, presents physiopathological events as hemolysis and vaso-occlusion, leading to ischemia-reperfusion injury with consequent clinical manifestations such as acute chest syndrome (ACS), crises of pain and priapism. These manifestations can be aggravated by genetic polymorphisms involved in some metabolic pathways …
Sickle cell disease (SCD) is the hemolytic anemias group with presence of hemoglobin S (Hb S), and includes sickle cell anemia, thalassemia interactions and associations with other hemoglobin variants. The interaction of HbS with beta-thalassemia (Hb S²-thalassemia) involves combinations that can result in variable phenotypes depending on the type of mutation for inherited beta thalassemi…
(Only some records are available in English at this moment)
Human activities have been considered the main causes of climate change (CC) observed in the world and effects of increases temperature, acidification and salinity in marine water bodies have been reported in benthonic fish. In the fish Solea senegalensis, for example, the water temperature is a basic abiotic factor that regulates its physiology and metabolism, since it inhabits coastal a…
| 5 / 2 | Completed research grants |
| 20 / 17 | Completed scholarships in Brazil |
| 1 / 1 | Completed scholarships abroad |
| 26 / 20 | All research grants and scholarships |
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