Search Results - "Silva, M.F.B."

Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review by Campello, C P, Lima-Silva, M F B, Lima, E L S de, Nunes, G R S, Silva, H A M, Dellalibera, E, Britto, L R P B de, Lemos, C A A, Muniz, M T C

“…Vocal fold leukoplakia (VFL) has a risk of malignant transformation. Therefore, patients can have symptoms such as dysphonia, vocal strain, difficulty…”
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EXPANDED POLYSTYRENE USANDO ÓLEO DE SOJA RESIDUAL by Da Silva, M.F.B, de Campos, A, Ferreira, D.C, Rocha, V.C, Lemos, D.A, Goncalves, J.C.S.I, Poleto, C, da Luz, M.S

“…The current work presents a simple method for recycling waste expanded polystyrene (EPS), using waste cooking soybean oil (WCSO). The process of polystyrene…”
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Advances in methods for characterization of hepatic urea cycle enzymatic activity in HepaRG cells using UPLC-MS/MS by Moedas, M.F., Adam, A.A.A., Farelo, M.A., IJlst, L., Chamuleau, R.A.F.M., Hoekstra, R., Wanders, R.J.A., Silva, M.F.B.

“…Current methodologies for the assessment of urea cycle (UC) enzymatic activity are insufficient to accurately evaluate this pathway in biological specimens…”
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NAD depletion and mitochondrial protein hyperacetylation: New insights on liver toxicity and drug-induced effects in vivo by Moedas, M., Van Chruchten, A., IJlst, L., Castro, R., Houtkooper, R.H., Wanders, R.J.A., Silva, M.F.B.

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EXPANDED POLYSTYRENE USANDO ÓLEO DE SOJA RESIDUAL by Da Silva, M.F.B, Campos, A., de, Ferreira, D.C, Rocha, V.C, Lemos, D.A, Goncalves, J.C.S.I, Poleto, C, Luz, M.S., da

“…The current work presents a simple method for recycling waste expanded polystyrene (EPS), using waste cooking soybean oil (WCSO). The process of polystyrene…”
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Retrospective study of the medium-chain acyl-CoA dehydrogenase deficiency in Portugal by Ventura, F.V., Leandro, P., Luz, A., Rivera, I.A., Silva, M.F.B., Ramos, R., Rocha, H., Lopes, A., Fonseca, H., Gaspar, A., Diogo, L., Martins, E., Leão-Teles, E., Vilarinho, L., Tavares de Almeida, I.

“…Medium‐chain acyl‐CoA dehydrogenase deficiency (MCADD) is the commonest genetic defect of mitochondrial fatty acid β‐oxidation. About 60% of MCADD patients are…”
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