Marcia Aparecida Silva Graminha
CV Lattes
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ORCID
Universidade Estadual Paulista (UNESP). Campus de Araraquara. Faculdade de Ciências Farmacêuticas (FCFAR) (Institutional affiliation from the last research proposal) Birthplace: Brazil
graduate at Ciências Biológica from Universidade de São Paulo (1994), master's at Genetics from Universidade de São Paulo (1998) and ph.d. at Genética from Universidade de São Paulo (2002). Has experience in Genetics, focusing on Molecular Genetics and of Microorganisms, acting on the following subjects: bioinformatics, gene expression regulation, fungi, aspergillus nidulans and drug resistance. (Source: Lattes Curriculum)
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- Project for the Reserva Técnica Institucional of the School of Pharmaceutical Sciences - UNESP/Araraquara, AP.RT.INST
- Therapeutics for leishmaniasis: from screening to the study of mechanisms of action, a contribution to the discovery of new antileishmanial molecules, AP.R
- Leishmaniasis: from screening to the study of mechanisms of action, a contribution to the discovery of new bioactive molecules, AP.R
(Only some records are available in English at this moment)
- Target characterization on the surface of Leishmania infantum using the Li1 peptide, capable of inhibiting parasite internalization into host cells: assessment of Leishmania-macrophage interaction and extension of investigations to Leishmania braziliensis, BP.MS
- Cell-penetrating peptides (CPPs) bioconjugated to mimetic peptides containing nitroimidazooxazole and nitroimidazoxazine cores: development of bioconjugates active against cutaneous leishmaniasis, BP.DR
- Bioconjugation to the R8 peptide as an innovative strategy against Leishmania amazonensis: inhibition of cysteine protease B., BP.IC
(Only some records are available in English at this moment)
- ANTILEISHMANIAL PEPTIDES: PLANNING, SYNTHESIS, CHEMICAL AND BIOLOGICAL CHARACTERIZATION OF NEW SYNTHETIC PEPTIDES DIRECTED TO THE MCU (MITOCHONDRIAL CALCIUM UNIPORTER) MOLECULAR TARGET OF LEISHMANIA, BP.IC
- Identification of peptides capable of inhibiting the internalization process of Leishmania braziliensis promastigotes in differentiated macrophage cells., BP.IC
- Characterization of Leishmania infantum - macrophage interaction: Identification of binding proteins in L. infantum through synthetic peptides selected by phage display technique, BP.IC
(Only some records are available in English at this moment)
- New insight into the mechanism of action of CP2 in Leishmania: analysis of calcium homeostasis and the respiratory chain, BE.EP.PD
- Natural and/or bioinorganinc compounds as possible LiTOP1B inhibitors: an evaluation, BE.PQ
- Proteomic analysis of Leishmania mexicana by permeabilization of different cell membranes with digitonin, BE.EP.IC
(Only some records are available in English at this moment)