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Lauro Thiago Turaca

Explore the profile of Lauro Thiago Turaca including associated specialties, affiliations and a list of published articles. Areas
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Articles 6
Citations 39
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Recent Articles
1.
Silva Dos Santos D, Turaca L, Coutinho K, Barbosa R, Polidoro J, Kasai-Brunswick T, et al.
Sci Rep . 2023 May; 13(1):8689. PMID: 37248416
The antidiabetic agent class of sodium-glucose cotransporter 2 (SGLT2) inhibitors confer unprecedented cardiovascular benefits beyond glycemic control, including reducing the risk of fatal ventricular arrhythmias. However, the impact of SGLT2...
2.
Munoz J, Dariolli R, da Silva C, Neri E, Valadao I, Turaca L, et al.
Stem Cell Res Ther . 2022 Sep; 13(1):437. PMID: 36056380
Background: Human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CM) are a promising disease model, even though hiPSC-CMs cultured for extended periods display an undifferentiated transcriptional landscape. MiRNA-target gene interactions contribute to fine-tuning...
3.
Ribeiro da Silva A, Neri E, Turaca L, Dariolli R, Fonseca-Alaniz M, Santos-Miranda A, et al.
Sci Rep . 2020 Oct; 10(1):16163. PMID: 32999360
Cardiac fibroblasts are present throughout the myocardium and are enriched in the microenvironment surrounding the ventricular conduction system (VCS). Several forms of arrhythmias are linked to VCS abnormalities, but it...
4.
Turaca L, de Faria D, Kyosen S, Teixeira V, Motta F, Pessoa J, et al.
Gene . 2015 Feb; 561(1):124-31. PMID: 25681614
Pompe disease is an autosomal recessive disorder linked to GAA gene that leads to a multi-system intralysosomal accumulation of glycogen. Mutation identification in the GAA gene can be very important...
5.
Chaves K, Turaca L, Bosco Pesquero J, Mennecier G, Dagli M, Chammas R, et al.
Biomed Pharmacother . 2012 Aug; 66(6):464-8. PMID: 22920414
Tumor cells induce the disruption of homeostasis between cellular and extracellular compartments to favor tumor progression. The expression of fibronectin (FN), a matrix glycoprotein, is increased in several carcinoma cell...
6.
Turaca L, Pessoa J, Motta F, Munoz Rojas M, Muller K, Lourenco C, et al.
J Hum Genet . 2012 May; 57(6):347-51. PMID: 22551898
Fabry disease (FD) is an X-linked inborn error of glycosphingolipid catabolism that results from mutations in the alpha-galactosidase A (GLA) gene. Evaluating the enzymatic activity in male individuals usually performs...