CV Lattes
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Universidade Federal de São Paulo (UNIFESP). Campus São Paulo. Escola Paulista de Medicina (EPM) (Institutional affiliation from the last research proposal) Birthplace: Brazil
Postdoctoral Researcher in Biological Sciences at the Federal University of São Paulo (UNIFESP) (2023), working on the project "In vitro models for studying the neurophysiopathology of Fabry disease." Ph.D. in Biological Sciences (Molecular Biology) from UNIFESP (2022), Masters in Biological Sciences (Molecular Biology) from UNIFESP (2016), and Bachelors in Biomedicine from the University José do Rosário Vellano (2013). I have extensive experience in Biochemistry, with an emphasis on Molecular Biology and Human Genetics, focusing on the cellular and molecular study of inborn errors of metabolism and lysosomal storage diseases. I have broad expertise in cell culture techniques (cell lines and primary cells), induced pluripotent stem cells (iPSCs), 2D culture and 3D bioprinting, as well as working with blood-brain barrier models. Advanced experience in confocal microscopy and various genetics and molecular biology techniques. (Source: Lattes Curriculum)
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Fabry disease (FD) is an inborn error of metabolism caused by mutations in the GLA gene located on the X chromosome. Defects in this gene lead to the deficiency of ±-galactosidase A (±-Gal A), an enzyme responsible for degrading glycosphingolipids, mainly globotriaosylceramide (Gb3). ±-Gal A is present in all tissues, and its deficiency results in a progressive multisystem disease. FD cov…
Fabry disease (FD) is an inborn error of metabolism caused by mutations in the GLA gene located on the X chromosome. Defects in this gene lead to ±-galactosidase A (±-Gal A) deficiency, an enzyme responsible for degrading glycosphingolipids, mainly globotriaosylceramide (Gb3). ±-Gal A is present in all tissues, and its deficiency results in progressive multisystem disease. SCD covers a wi…
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