CV Lattes
Universidade Estadual Paulista (UNESP). Campus de Botucatu. Instituto de Biociências (IBB) (Institutional affiliation from the last research proposal) Birthplace: Brazil
Graduating in Nutrition from Universidade Estadual Paulista - UNESP campus in Botucatu. Conducted Scientific Initiation (CI) activity at the Department of Structural and Functional Biology, focusing on biomarkers for Duchenne Muscular Dystrophy with Scientific Initiation scholarship process nº 2018/25598-0 by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) (2019/2020). Conducted Research Internship Abroad with Research Internship Abroad Scholarship (BEPE - FAPESP #2019/20162-1), at the University of Washington - Seattle, WA - USA, focusing on gene therapy, metabolome and Duchenne Muscular Dystrophy (2019 -2020). Performs virtual outpatient care activity in the e-Care Sentinela University Extension Program, assisting patients with Post-Covid Syndrome (2022-current). Was student representative of the Nutrition Course Council (CONUTRI) at UNESP Botucatu campus (2019-2020, 2020-2021, 2021-2022). He carried out an Extracurricular Volunteer Internship activity at the Post-Covid-19 Multiprofessional Outpatient Clinic at the Pulmonary Function Laboratory of the Hospital das Clínicas of the Faculty of Medicine of Botucatu (HCFMB)(2021-2022). Performed Volunteer Extracurricular Internship at the HCFMB Prenatal Hypertension Outpatient Clinic (2021-2022). Was president of the Study Group on Transgender Health (GESTRANS) of the Botucatu Institute of Biosciences (IBB) of UNESP in Botucatu (2021). Was Research Director of the Academic League in Health and Sports Performance (LiSPE) of UNESP in Botucatu (2021). (Source: Lattes Curriculum)
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Biomarkers are cellular, structural and biochemical components that can be used as parameters to evaluate the presence and progression of a disease. Duchenne muscular dystrophy (DMD) is a progressive degenerative disease that affects skeletal and cardiac muscles leading the patient to death. In DMD, the absence of the protein dystrophin results in sarcolemmal fragility, deficiency in its …
Duchenne Muscular Dystrophy (DMD) is an X chromosome-linked and the most common hereditary muscular disease in childhood. Mutation in the DMD gene leads to the absence of dystrophin, a subsarcolemmal protein, which is part of dystrophin-glycoproteins complex (DGC). The mdx mice, DMD model, shows the first signs of degeneration around 20 days of age and around 26 months of age shows typica…
| 1 / 1 | Completed scholarships in Brazil |
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