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M F Sonati

Explore the profile of M F Sonati including associated specialties, affiliations and a list of published articles. Areas
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Articles 44
Citations 172
Followers 0
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Recent Articles
1.
Soler A, Pedroso G, Geraldo A, Albuquerque D, Costa F, Santos M, et al.
Int J Lab Hematol . 2024 Apr; 46(4):747-750. PMID: 38566588
No abstract available.
2.
Chenou F, Albuquerque D, Leonardo D, Domingos I, Bezerra M, Araujo A, et al.
Biochem Genet . 2020 Apr; 58(4):580-594. PMID: 32277314
The impaired bioavailability of endogenous nitric oxide (NO) in sickle cell anemia (SCA) may be influenced by polymorphisms in the endothelial nitric oxide synthase gene (eNOS). We compared allelic/genotypic frequencies...
3.
Pedroso G, Fernandes P, Jorge S, Nascimento P, Lima P, Grigoleto M, et al.
Ann Hematol . 2019 Nov; 98(12):2853-2855. PMID: 31712880
No abstract available.
4.
Jorge S, Lanaro C, Albuquerque D, Nascimento P, Pedroso G, Oliveira S, et al.
Ann Hematol . 2019 Jun; 98(9):2253-2255. PMID: 31253996
No abstract available.
5.
Ferreira R, Mota N, Pedroso G, Kimura E, Geraldo A, Santos M, et al.
Int J Lab Hematol . 2018 Jun; 40(5):e96-e98. PMID: 29851275
No abstract available.
6.
Jorge S, Bringas M, Petruk A, Arrar M, Marti M, Skaf M, et al.
Arch Biochem Biophys . 2017 Dec; 637:73-78. PMID: 29199120
Human hemoglobin (Hb) Coimbra (βAsp99Glu) is one of the seven βAsp99 Hb variants described to date. All βAsp99 substitutions result in increased affinity for O and decreased heme-heme cooperativity and...
7.
Mota N, Kimura E, Ferreira R, Albuquerque D, Ribeiro D, Santos M, et al.
Int J Lab Hematol . 2017 Mar; 39(4):e106-e109. PMID: 28318097
No abstract available.
8.
Zaccariotto T, Lanaro C, Albuquerque D, Santos M, Bezerra M, Cunha F, et al.
Genet Mol Res . 2012 Dec; 11(4):3861-8. PMID: 23212325
Phosphatidylinositol phosphate kinases (PIPKs) are enzymes that participate in diverse intracellular signaling pathways. They are classified into 3 functionally distinct subfamilies - PIPKI (α, β, γ), PIPKII (α, β, γ),...
9.
Da Luz J, Lopez P, Kimura E, Albuquerque D, Costa F, Sans M, et al.
Int J Lab Hematol . 2012 Aug; 35(1):111-4. PMID: 22898041
We describe here a new frameshift mutation of β-thalassemia in a Uruguayan family with Italian ancestry [β48 (-T); HBB:c.146delT]. This frameshift results in formation of premature stop codon (TGA) 40 ...
10.
Suemasu C, Kimura E, Oliveira D, Bezerra M, Araujo A, Costa F, et al.
Braz J Med Biol Res . 2010 Dec; 44(1):16-22. PMID: 21180887
Alpha-thalassemia is the most common inherited disorder of hemoglobin synthesis. Genomic deletions involving the alpha-globin gene cluster on chromosome 16p13.3 are the most frequent molecular causes of the disease. Although...