Talita C B Pereira
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Explore the profile of Talita C B Pereira including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
114
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Recent Articles
1.
Effting P, Thirupathi A, Muller A, Pereira B, Sepa-Kishi D, Marqueze L, et al.
Nutrients
. 2022 Jun;
14(11).
PMID: 35683979
This study investigates whether ladder climbing (LC), as a model of resistance exercise, can reverse whole-body and skeletal muscle deleterious metabolic and inflammatory effects of high-fat (HF) diet-induced obesity in...
2.
Costa K, Pereira T, Valente C, Pissinate K, Soares J, Cruz F, et al.
Colloids Surf B Biointerfaces
. 2019 Feb;
177:58-67.
PMID: 30711760
Nanomaterials have been attracting attention due to the wide range of applications in nanomedicine. Polypyrrole (PPy), a conductive polymer, has been employed in the biomedical field due to its stimulus-responsive...
3.
Pereira P, Machado G, Danesi G, Canevese F, Reddy V, Pereira T, et al.
J Neurosci
. 2015 Dec;
35(49):16272-81.
PMID: 26658875
Significance Statement: Itch is the most common symptom of the skin and is related to noncutaneous diseases. It severely impairs patients' quality of life when it becomes chronic and there...
4.
Scaini G, Morais M, Furlanetto C, Kist L, Pereira T, Schuck P, et al.
Neurochem Res
. 2015 Feb;
40(5):885-93.
PMID: 25681161
Maple syrup urine disease (MSUD) is caused by an inborn error in metabolism resulting from a deficiency in the branched-chain α-keto acid dehydrogenase complex activity. This blockage leads to accumulation...
5.
Conterato G, Quatrin A, Somacal S, Ruviaro A, Vicentini J, Augusti P, et al.
Basic Clin Pharmacol Toxicol
. 2013 Dec;
114(6):476-84.
PMID: 24345272
Renal thioredoxin reductase-1 (TrxR-1) activity is stimulated at lead doses lower than that necessary to inhibit δ-aminolevulinate dehydratase activity (δ-ALA-D), which is a classical early biomarker of lead effects. Thus,...
6.
Ferreira G, Scaini G, Jeremias I, Carvalho-Silva M, Goncalves C, Pereira T, et al.
Mol Neurobiol
. 2013 Oct;
49(2):734-40.
PMID: 24091827
Tyrosinemia type II, which is also known as Richner-Hanhart syndrome, is an inborn error of metabolism that is due to a block in the transamination reaction that converts tyrosine to...
7.
Scaini G, Mello-Santos L, Furlanetto C, Jeremias I, Mina F, Schuck P, et al.
Mol Neurobiol
. 2013 Apr;
48(3):581-9.
PMID: 23559405
Maple syrup urine disease (MSUD) is a neurometabolic disorder caused by deficiency of the activity of the mitochondrial enzyme complex branched-chain α-keto acid dehydrogenase leading to accumulation of the branched-chain...
8.
Ferreira G, Carvalho-Silva M, Goncalves C, Vieira J, Scaini G, Ghedim F, et al.
Neurochem Int
. 2012 Oct;
61(8):1370-4.
PMID: 23046746
Tyrosinemia is a rare genetic disease caused by mutations on genes that codify enzymes responsible for tyrosine metabolism. Considering that tyrosinemics patients usually present symptoms associated with central nervous system...
9.
Scaini G, de Rochi N, Jeremias I, Deroza P, Zugno A, Pereira T, et al.
Mol Neurobiol
. 2012 Feb;
45(2):279-86.
PMID: 22328136
Maple syrup urine disease is an inherited metabolic disease predominantly characterized by neurological dysfunction. However, the mechanisms underlying the neuropathology of this disease are still not defined. Therefore, the aim...
10.
Amado L, Garcia M, Pereira T, Yunes J, Bogo M, Monserrat J
Comp Biochem Physiol C Toxicol Pharmacol
. 2011 May;
154(3):146-53.
PMID: 21586338
This paper evaluated the chemoprotective effect of lipoic acid (LA) against microcystin (MC) toxicity in carp Cyprinus carpio. To determine the LA dose and the time necessary for the induction...