Mbl2
Mostrando 1-12 de 93 artigos, teses e dissertações.
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1. O que é a Síndrome de Wolff-Parkinson-White?
A síndrome de Wolff-Parkinson-White (WPW) é uma doença congênita gerando taquicardias e arritmias, que reduzem a eficiência do coração. As manifestações clínicas incluem sudorese, dor no peito, cefaleia, dificuldades respiratórias, letargia, sensação de desmaio, perda de apetite, palpitações rápidas e visíveis no tórax, incluindo insufic
Núcleo de Telessaúde HC UFMG. Publicado em: 12/06/2023
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2. Polimorfismo do gene da lectina ligante de manose e seu efeito em desfechos de curto prazo em bebês prematuros
Resumo Objetivo: A lectina ligante de manose (MBL, do inglês mannose-binding lectin), que pertence à família das colectinas, é um reagente de fase aguda que ativa o sistema complemento. Este estudo teve como objetivo investigar o efeito do polimorfismo do gene MBL2 em desfechos de curto prazo em prematuros. Método: Este estudo prospectivo incluiu cria
J. Pediatr. (Rio J.). Publicado em: 2020-08
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3. Activity of ceftolozane-tazobactam and comparators against gram-negative bacilli: Results from the study for monitoring antimicrobial resistance trends (SMART – Brazil; 2016–2017)
Abstract Multi-drug resistant Gram-negative bacilli (GNB) have been reported as cause of serious hospital-acquired infections worldwide. The aim of this study was to investigate the in vitro activity of ceftolozane-tazobactam compared to other agents against GNB isolated from patients admitted to Brazilian medical centers between the years 2016 and 2017. Pre
Braz J Infect Dis. Publicado em: 2020-08
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4. Association between MBL2 haplotypes and dengue severity in children from Rio de Janeiro, Brazil
BACKGROUND Dengue is an arthropod-borne viral disease with a majority of asymptomatic individuals and clinical manifestations varying from mild fever to severe and potentially lethal forms. An increasing number of genetic studies have outlined the association between host genetic variations and dengue severity. Genes associated to viral recognition and ent
Mem. Inst. Oswaldo Cruz. Publicado em: 23/05/2019
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5. Mannose-Binding Lectin 2 (MBL2) combined genotypes deficiency is associated with susceptibility for Oral Lichen Planus
Abstract Oral Lichen Planus (OLP) is an oral inflammatory condition, mediated by host immune system reaction, presenting basal membrane damages with inflammatory lesions in the mouth and/or skin. In this study, the role of functional polymorphisms in the MBL2 gene, encoding for Mannose-Binding Protein C (MBP-C), a member of the innate immune response and an
Genet. Mol. Biol.. Publicado em: 21/02/2019
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6. CTLA-4 gene polymorphisms are associated with obesity in Turner Syndrome
Abstract Turner syndrome (TS) is characterized by a set of clinical conditions, including autoimmune/inflammatory diseases and infectious conditions, that can compromise a patient’s quality of life. Here we assessed polymorphisms in CTLA-4 +49A/G (rs231775), PTPN22 +1858G/A (rs2476601), and MBL2 -550 (H/L) (rs11003125), -221(X/Y) (rs7096206) and exon 1 (A/
Genet. Mol. Biol.. Publicado em: 29/11/2018
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7. Periodontal parameters in prediabetes, type 2 diabetes mellitus, and non-diabetic patients
Abstract The aim of the present study was to compare the clinical and radiographic periodontal parameters in prediabetes, type 2 diabetes mellitus (T2DM), and non-diabetic patients. Forty-one patients with prediabetes (Group 1), 43 patients with T2DM (Group 2), and 41 controls (Group 3) were included. Demographic data were recorded using a questionnaire. Ful
Braz. oral res.. Publicado em: 06/08/2018
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8. Níveis circulantes da lectina ligadora de manose (MBL) na degeneração macular relacionada à idade
RESUMO Objetivos: Avaliar se as concentrações séricas da lectina ligante de manose da via das lectinas do sistema complemento estão associadas à degeneração macular relacionada à idade. Métodos: Pacientes com degeneração macular relacionada à idade a controles pareados realizaram exame oftalmológico completo e imagens de tomografia de coerênc
Arq. Bras. Oftalmol.. Publicado em: 2018-04
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9. Combined genotypes of the MBL2 gene related to low mannose-binding lectin levels are associated with vaso-occlusive events in children with sickle cell anemia
Abstract Sickle cell anemia (SCA) presents heterogenous clinical manifestations that cannot be explained solely by alterations to hemoglobin (Hb); other components such as endothelial adhesion, thrombosis and inflammation may be involved. The mannose-binding lectin (MBL) has an important role in innate immunity and inflammatory diseases. In this report, we d
Genet. Mol. Biol.. Publicado em: 21/08/2017
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10. Participação na democracia brasileira: a hegemonia popular e a inovação do protesto da classe média
Resumo O Brasil se tornou uma referência na participação social após o sucesso do orçamento participativo no início dos anos 1990. A teoria padrão do sucesso da participação aponta seu impacto positivo sobre o sistema político. No entanto, o Brasil tem experimentado algumas mudanças importantes no nível tanto de participação como de representa�
Opin. Publica. Publicado em: 2017-04
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11. Prevalence and antimicrobial susceptibility of non-fermenting Gram-negative bacilli isolated from clinical samples at a tertiary care hospital
Abstract INTRODUCTION: We compared the prevalence and antimicrobial susceptibility of non-fermenting gram-negative bacilli (NFGNB) isolated from clinical samples at a Brazilian tertiary care hospital in 2008 and 2013. METHODS: Collected data included patient’s name, age, sex, inpatient unit, laboratory record number, type of biological material, cultur
Rev. Soc. Bras. Med. Trop.. Publicado em: 2017-03
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12. Mannose-binding lectin 2 (Mbl2) gene polymorphisms are related to protein plasma levels, but not to heart disease and infection by Chlamydia
The presence of the single nucleotide polymorphisms in exon 1 of the mannose-binding lectin 2 (MBL2) gene was evaluated in a sample of 159 patients undergoing coronary artery bypass surgery (71 patients undergoing valve replacement surgery and 300 control subjects) to investigate a possible association between polymorphisms and heart disease with Chlamydia i
Braz J Med Biol Res. Publicado em: 12/12/2016