A dual enzyme system composed of a polyester hydrolase and a carboxylesterase enhances the biocatalytic degradation of polyethylene terephthalate films
Barth, Markus, Honak, Annett, Oeser, Thorsten, Wei, Ren, Belisário-Ferrari, Matheus R, Then, Johannes, Schmidt, Juliane, Zimmermann, Wolfgang
Published in Biotechnology journal (01.08.2016)
Published in Biotechnology journal (01.08.2016)
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Ca2+ and Mg2+ binding site engineering increases the degradation of polyethylene terephthalate films by polyester hydrolases from Thermobifida fusca
Then, Johannes, Wei, Ren, Oeser, Thorsten, Barth, Markus, Belisário-Ferrari, Matheus R, Schmidt, Juliane, Zimmermann, Wolfgang
Published in Biotechnology journal (01.04.2015)
Published in Biotechnology journal (01.04.2015)
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CETP gene polymorphisms and haplotypes are explanatory variables for HDL cholesterol level in sickle cell disease
Cruz, N R C, Valente, T N S, Ferreira, F O, Macedo, L R, Belisário, A R, Silva, C M da, Oliveira, N S, Gomides, A F F, Velloso-Rodrigues, C
Published in Brazilian journal of medical and biological research (01.01.2024)
Published in Brazilian journal of medical and biological research (01.01.2024)
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Co-inheritance of a-thalassemia dramatically decreases the risk of acute splenic sequestration in a large cohort of newborns with hemoglobin SC
Rezende, Paulo V, Belisário, André R, Oliveira, Érica L, Almeida, Jéssica A, Oliveira, Larissa M M, Muniz, Maristela B S R, Viana, Marcos B
Published in Haematologica (Roma) (01.07.2019)
Published in Haematologica (Roma) (01.07.2019)
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Clinical and hematological profile in a newborn cohort with hemoglobin SC
Rezende, Paulo V., Santos, Millane V., Campos, Gustavo F., Vieira, Laura L.M., Souza, Maristela B., Belisário, André R., Silva, Celia M., Viana, Marcos B.
Published in Jornal de pediatria (01.11.2018)
Published in Jornal de pediatria (01.11.2018)
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Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics
Belisário, André R., Carneiro-Proietti, Anna B., Sabino, Ester Cerdeira, Araújo, Aderson, Loureiro, Paula, Máximo, Cláudia, Flor-Park, Miriam V., Rodrigues, Daniela D.O.W., Ozahata, Mina Cintho, McClure, Christopher, Mota, Rosimere Afonso, Gomes Moura, Isabel C., Custer, Brian, Kelly, Shannon
Published in Hemoglobin (02.01.2020)
Published in Hemoglobin (02.01.2020)
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INTERACTION BETWEEN HAPLOTYPES OF BCL11A AND HBS1L-MYB, MAJOR QUANTITATIVE TRAIT LOCI FOR FETAL HEMOGLOBIN (HBF) LEVELS, AND INCIDENCE OF CLINICAL PHENOTYPES IN CHILDREN WITH SICKLE CELL ANEMIA
Sillva, NF, Oliveira, LN, Belisário, AR, Viana, MB, Luizon, MR, Sales, RR
Published in Hematology, Transfusion and Cell Therapy (01.10.2024)
Published in Hematology, Transfusion and Cell Therapy (01.10.2024)
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BCL11A POLYMORPHISMS ASSOCIATED WITH INCREASED FETAL HEMOGLOBIN IN RESPONSE TO HYDROXYUREA TREATMENT IN A COHORT OF PEDIATRIC PATIENTS WITH SICKLE CELL ANEMIA
Nogueira, BL, Sales, RR, Belisário, AR, Faria, G, Mendes, F, Viana, MB, Luizon, MR
Published in Hematology, Transfusion and Cell Therapy (01.10.2021)
Published in Hematology, Transfusion and Cell Therapy (01.10.2021)
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CHRONIC KIDNEY DISEASE IN BRAZILIAN ADULTS WITH SICKLE CELL DISEASE: RESULTS FROM THE REDS-III MULTICENTER COHORT STUDY
Belisário, AR, Silva, ACSE, Moura, ICG, Carneiro-Proietti, AB, Sabino, EC, Loureiro, P, Máximo, C, Flor-Park, MV, Rodrigues, DOW, Ozahata, MC, Mota, RA, Dinardo, CL, Kelly, S, Custer, B
Published in Hematology, Transfusion and Cell Therapy (01.10.2021)
Published in Hematology, Transfusion and Cell Therapy (01.10.2021)
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Low urinary levels of angiotensin‐converting enzyme 2 may contribute to albuminuria in children with sickle cell anaemia
Belisário, André R., Vieira, Érica L. M., Almeida, Jéssica A., Mendes, Fabíola G., Miranda, Aline S., Rezende, Paulo V., Viana, Marcos B., Simões e Silva, Ana C.
Published in British journal of haematology (01.04.2019)
Published in British journal of haematology (01.04.2019)
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