Zobrazeno 1 - 10 of 36 pro vyhledávání: '"Edis Belini Junior"'
1
Akademický článek
Yeast enhancement by mass mating and selective pressure for the integrated production process of first and second-generation ethanol
Autor: Elisangela de Souza Miranda Muynarsk, Renata Maria Christofoleti-Furlan, Brigitte Sthepani Orozco Colonia, Edis Belini Junior, Danilo Grünig Humberto da Silva, Luiz Carlos Basso
Publikováno v: Revista Brasileira de Ciências Ambientais, Vol 59, Pp e2141-e2141 (2024)
A produção de etanol de segunda geração é uma tecnologia de aplicação mundial com potencial para substituir os combustíveis fósseis e contribuir para a sustentabilidade. A incorporação da produção de etanol de segunda geração nas biorr
Externí odkaz: https://doaj.org/article/bfe74b71760146d98671a687da9d9f04
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2
Akademický článek
Incidence of hemoglobinopathies and spatialization of newborns with sickle cell trait in Mato Grosso do Sul, Brazil
Autor: Priscila de Matos Cândido-Bacani, Patrícia Medeiros Silva Grilo, Vanessa da Silveira Ramos, Michelly Zanchin, Indiara Correia Pereira, Josaine Sousa Palmieri Oliveira, Vitor Matheus Bacani, Edis Belini Junior
Publikováno v: Einstein (São Paulo), Vol 20 (2022)
ABSTRACT Objective To evaluate the incidence of variant hemoglobins of newborn samples from the Neonatal Screening Center in the state of Mato Grosso do Sul, Brazil, and to analyze the distribution and spatial autocorrelation of newborns with sickle
Externí odkaz: https://doaj.org/article/e3b3b2da4082444dbbb9f20890dc51a4
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3
Akademický článek
The influence of hydroxyurea on oxidative stress in sickle cell anemia
Autor: Lidiane de Souza Torres, Danilo Grünig Humberto da Silva, Edis Belini Junior, Eduardo Alves de Almeida, Clarisse Lopes de Castro Lobo, Rodolfo Delfini Cançado, Milton Artur Ruiz, Claudia Regina Bonini-Domingos
Publikováno v: Revista Brasileira de Hematologia e Hemoterapia, Vol 34, Iss 6, Pp 421-425 (2012)
OBJECTIVE: The oxidative stress in 20 sickle cell anemia patients taking hydroxyurea and 13 sickle cell anemia patients who did not take hydroxyurea was compared with a control group of 96 individuals without any hemoglobinopathy. METHODS: Oxidative
Externí odkaz: https://doaj.org/article/44f4c89b7eeb4f669650897092bdb838
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4
Akademický článek
Perfil de beta talassemia heterozigota obtido a partir de análise data mining em banco de dados The profile of beta thalassemia obtained by data mining analysis in a database
Autor: Ana L. B. Domingos, Lucas A. Granzotto, Edis Belini Junior, Thiago Y. K. Oliveira, Ana C. B. Domingos, Claudia R. Bonini-Domingos
Publikováno v: Revista Brasileira de Hematologia e Hemoterapia, Vol 32, Iss 1, Pp 78-79 (2010)
Variations in the phenotypic expression of heterozygous beta thalassemia reflect the formation of different populations. To better understand the profile of heterozygous beta-thalassemia of the Brazilian population, we aimed at establishing parameter
Externí odkaz: https://doaj.org/article/133c19512f1541eb98c5dc67fceb47c6
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5
Akademický článek
The relationship between of ACE I/D and the MTHFR C677T polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of Brazilian obese patients
Autor: Flavio Fontes Pirozzi, Edis Belini Junior, Jessika Viviani Okumura, Mariana Salvarani, Claudia Regina Bonini-Domingos, Milton Artur Ruiz
Publikováno v: Archives of Endocrinology and Metabolism, Vol 62, Iss 1, Pp 21-26
ABSTRACT Objectives This study aimed to evaluate the frequencies of the angiotensin converting enzyme (ACE) gene insertion/deletion (I/D) and methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphisms in obese patients with and without type
Externí odkaz: https://doaj.org/article/96b1010e31c24ee5bfa4cbeb8b33e8aa
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6
Akademický článek
Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia
Autor: Diego A. Pereira-Martins, Igor F. Domingos, Edis Belini-Junior, Juan L. Coelho-Silva, Isabel Weinhäuser, Aderson S. Araújo, Clarisse L. Lobo, Claudia R. Bonini-Domingos, Marcos A. Bezerra, Antonio R. Lucena-Araujo
Publikováno v: Hematology, Transfusion and Cell Therapy, Vol 43, Iss 3, Pp 243-248 (2021)
Introduction: Sickle cell anemia (SCA) is a Mendelian disorder with a heterogeneous clinical course. The reasons for this phenotypic diversity are not entirely established, but it is known that high fetal hemoglobin levels lead to a milder course of
Externí odkaz: https://doaj.org/article/b4f7b9e9364742d191c10f93c9d5a4c7
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7
Contribuição genética para o entendimento da fisiopatologia da doença de crohn / Genetic contribution to understanding the pathophysiology of crohn's disease
Autor: Luís Fernando Lipka Insfran, Paulo Roberto da Silva Couto, Edis Belini Junior
Publikováno v: Brazilian Journal of Health Review; Vol. 5 No. 2 (2022); 6265-6278
Brazilian Journal of Health Review; v. 5 n. 2 (2022); 6265-6278
Brazilian Journal of Health Review
Federação das Indústrias do Estado do Paraná (FIEP)
instacron:BJRH
A Doença de Crohn (DC) integra o grupo das Doenças Inflamatórias Intestinais (DII) e apresenta aspectos multifatoriais, os quais dificultam a correta compreensão de sua fisiopatologia. Apesar de forte componente genético de susceptibilidade, com
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e382374ceb5503ab03872a706085df1
https://ojs.brazilianjournals.com.br/ojs/index.php/BJHR/article/view/46235
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9
Atypical β-S haplotypes: classification and genetic modulation in patients with sickle cell anemia
Autor: Patrícia P. Nascimento, Gisele Cristine de Souza Carrocini, Lidiane de Souza Torres, Edis Belini-Junior, Danilo Grünig Humberto da Silva, Jéssika Viviani Okumura, Claudia Regina Bonini-Domingos, Clarisse Lopes de Castro Lobo, Larissa Paola Rodrigues Venancio
Publikováno v: Journal of Human Genetics. 64:239-248
β-S globin haplotype (βS haplotype) characterization in sickle cell anemia (SCA) patients is important because it assists individualized treatment. However, the patient with atypical haplotypes do not present detailed studies such as clinical and l
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d44028fe2ac86a8e02115f60727ee29
https://doi.org/10.1038/s10038-018-0554-4
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10
COMPLICAÇÕES DA COVID-19 EM PESSOAS COM DOENÇA FALCIFORME: REVISÃO TEÓRICA
Autor: Patricia Medeiros Silva Grilo, Giovanna da Silva Parente, Lucimeire Silva, Aline Russomano de Gouvêa, Edis Belini Junior
Publikováno v: Anais do Congresso Brasileiro de Imunologia On-line.
Introdução: A Doença Falciforme (DF), afecção genética caracterizada por anemia hemolítica crônica e inflamatória, tem a presença da Hemoglobina S e pode apresentar diferentes genótipos. Devido a fisiopatologia complexa da DF, as pessoas a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::131a082ae711a705210ca1a2c899d7a5
https://doi.org/10.51161/rems/1019
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