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
Graduado em Farmácia pela Universidade do Sagrado Coração (2008). Possui Mestrado em Farmacologia (2013), pelo Programa de Pós-Graduação em Farmacologia Escola Paulista de Medicina - Universidade Federal de São Paulo. Atualmente Doutorando em Farmacologia pelo mesmo Programa de Pós-Graduação (EPM-UNIFESP), onde desenvolve estudos sobre mecanismos de morte celular, autofagia e mitofagia, ambos ligados a sinalização mediada pelo íon cálcio, em um modelo celular que superexpressa permanentemente a proteína alfa-sinucleína. (Source: Lattes Curriculum)
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Parkinson's Disease (PD) is the second neurodegenerative disorder most common. One of most know neuronal alteration described in PD is the protein aggregation, as consequence of failure in degradation of oxidates and malformed proteins. The cellular process that acts in the degradation of protein aggregates is the autophagy, which have been extensively investigated due its role in the the…
The main pathological feature of Parkinson's disease (PD) is the presence of intracitoplasmatic protein aggregates called Lewy Bodies, whose main component is the protein alpha-synuclein on its fibrilar conformation. In the 1990's, two mutations in the gene that encodes alpha-synuclein (SNCA) were described. These mutations lead to transcription of mutant proteins, A30P and A53T, both of …
The main pathological hallmark of Parkinson's disease (PD) is the presence of aggregates formed by the protein alpha-synuclein called Lewy Bodies. Two point mutations on alpha-synuclein gene (SNCA) lead to the formation of mutated proteins, A30P and A53T, both related to familial Parkinson's disease. According to several evidences, alpha-synuclein binds to mitochondrial complex I, promoti…
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