Publications by authors named "F de Oliveira Santos"

The negative effects of land-use changes on biodiversity significantly contribute to climate change. Primates are among the animals most affected by these changes, because of their high dependence on forest cover where a lack of forest connectivity can limit their dispersal and segregate their populations. In this sense, protected areas (PAs) are crucial for conserving endangered primates, especially endemic species.

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This publication aims to provide guidelines of the knowledge required and the potential research to be conducted in order to understand the mode of action of antimethanogenic feed additives (AMFA). In the first part of the paper, we classify AMFA into 4 categories according to their mode of action: (1) lowering dihydrogen (H) production; (2) inhibiting methanogens; (3) promoting alternative H-incorporating pathways; and (4) oxidizing methane (CH). The second part of the paper presents questions that guide the research to identify the mode of action of an AMFA on the rumen CH production from 5 different perspectives: (1) microbiology; (2) cell and molecular biochemistry; (3) microbial ecology; (4) animal metabolism; and (5) cross-cutting aspects.

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Chikungunya virus (CHIKV) is mainly transmitted by the invasive mosquito () in tropical and subtropical regions worldwide. However, genetic adaptations of the virus to the peri domestic mosquito vector () has resulted in enhanced vector competence and associated epidemics and may contribute to further geographic expansion of CHIKV. However, evidence-based data on the relative role of in CHIKV transmission dynamics are scarce, especially in regions where is the main vector, such as in Brazil.

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Background: One of the challenges for professional football players is injuries. Due to their influence on their teams, injuries greatly impact the sports business. This research aims to assess predictive models of injury risk in male professional football players.

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Compound (4-(3,5-di-tert-butyl-4-hydroxybenzylamine)benzenesulfonamide) (LQFM275) was designed and synthesized from darbufelone and sulfanilamide as a new multi-target for the treatment of inflammatory diseases. LQFM275 showed a great range of safe cytotoxicity profile (100-400 μM) evaluated by MTT assay, preventing damage induced by lipopolysaccharide (LPS) in EA.hy926 cell line.

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