Jéssica Laís de Oliveira Branquinho Pennacino

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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

Jéssica Laís de Oliveira Branquinho Pennacino in research grants and scholarships supported by FAPESP.

News published in Agência FAPESP Newsletter about the researcher

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Scholarships in Brazil

Ongoing (most recent)

Abstract
Fabry disease (FD) is an inborn error of metabolism caused by mutations in the gene for the enzyme ±-galactosidase A (GLA) located on the X chromosome. These mutations result in deficiency of the enzyme ±-galactosidase A (±-Gal A), causing the accumulation of globotriaosylceramide (Gb3). ±-Gal A deficiency results in pathogenic changes in several organs, including Fabry cardiomyopathy, wi…
Involvement of the kallikrein-kinin system in the pathophysiology of Fabry Disease from patient iPSC-derived cardiomyocytes, BP.PD

Completed (most recent)

Production of recombinant MMP-2, BP.TT

Virtual Library in numbers * Updated data on August 16, 2025

Total / Available in English

1 / 1	Ongoing scholarships in Brazil
1 / 1	Completed scholarships in Brazil
2 / 2	All Scholarships

Associated processes

Most frequent collaborators in research granted by FAPESP

Keywords used by the researcher

Biological Sciences Biology Health Sciences Medicine

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Abstract