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Empagliflozin reduces arrhythmogenic effects in rat neonatal and human iPSC-derived cardiomyocytes and improves cytosolic calcium handling at least partially independent of NHE1.
Silva Dos Santos D, Turaça LT, Coutinho KCDS, Barbosa RAQ, Polidoro JZ, Kasai-Brunswick TH, Campos de Carvalho AC, Girardi ACC. Silva Dos Santos D, et al. Among authors: turaca lt. Sci Rep. 2023 May 29;13(1):8689. doi: 10.1038/s41598-023-35944-5. Sci Rep. 2023. PMID: 37248416 Free PMC article.
Integrated molecular, biochemical, and physiological assessment unravels key extraction method mediated influences on rat neonatal cardiomyocytes.
Jensen L, Neri E, Bassaneze V, De Almeida Oliveira NC, Dariolli R, Turaça LT, Levy D, Veronez D, Ferraz MSA, Alencar AM, Bydlowski SP, Cestari IA, Krieger JE. Jensen L, et al. Among authors: turaca lt. J Cell Physiol. 2018 Jul;233(7):5420-5430. doi: 10.1002/jcp.26380. Epub 2018 Jan 19. J Cell Physiol. 2018. PMID: 29219187
Kinin-B2 receptor activity determines the differentiation fate of neural stem cells.
Trujillo CA, Negraes PD, Schwindt TT, Lameu C, Carromeu C, Muotri AR, Pesquero JB, Cerqueira DM, Pillat MM, de Souza HD, Turaça LT, Abreu JG, Ulrich H. Trujillo CA, et al. Among authors: turaca lt. J Biol Chem. 2012 Dec 28;287(53):44046-61. doi: 10.1074/jbc.M112.407197. Epub 2012 Nov 6. J Biol Chem. 2012. PMID: 23132855 Free PMC article.
New mutations in the GLA gene in Brazilian families with Fabry disease.
Turaça LT, Pessoa JG, Motta FL, Muñoz Rojas MV, Müller KB, Lourenço CM, Junior Marques W, D'Almeida V, Martins AM, Pesquero JB. Turaça LT, et al. J Hum Genet. 2012 Jun;57(6):347-51. doi: 10.1038/jhg.2012.32. Epub 2012 May 3. J Hum Genet. 2012. PMID: 22551898
Correlation between GLA variants and alpha-Galactosidase A profile in dried blood spot: an observational study in Brazilian patients.
Varela P, Mastroianni Kirsztajn G, Motta FL, Martin RP, Turaça LT, Ferrer HLF, Gomes CP, Nicolicht P, Mara Marins M, Pessoa JG, Braga MC, D'Almeida V, Martins AM, Pesquero JB. Varela P, et al. Among authors: turaca lt. Orphanet J Rare Dis. 2020 Jan 29;15(1):30. doi: 10.1186/s13023-019-1274-3. Orphanet J Rare Dis. 2020. PMID: 31996269 Free PMC article.
Novel GAA mutations in patients with Pompe disease.
Turaça LT, de Faria DO, Kyosen SO, Teixeira VD, Motta FL, Pessoa JG, Rodrigues E Silva M, de Almeida SS, D'Almeida V, Munoz Rojas MV, Martins AM, Pesquero JB. Turaça LT, et al. Gene. 2015 Apr 25;561(1):124-31. doi: 10.1016/j.gene.2015.02.023. Epub 2015 Feb 12. Gene. 2015. PMID: 25681614
11 results