Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Gustavo C. Ferreira"'
Autor:
Lorena O. Fernandes-Siqueira, Fabiana A. P. Ferreira, Bruna G. Sousa, Nathane C. Mebus-Antunes, Thais C. Neves-Martins, Fabio C. L. Almeida, Gustavo C. Ferreira, Didier Salmon, Luciana S. Wermelinger, Andrea T. Da Poian
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-14 (2022)
Abstract The Covid-19 pandemic, caused by SARS-CoV-2, has resulted in over 6 million reported deaths worldwide being one of the biggest challenges the world faces today. Here we present optimizations of all steps of an enzyme-linked immunosorbent ass
Externí odkaz:
https://doaj.org/article/3b2218a2321c433fbb4b44938012e554
Autor:
Lorena O. Fernandes-Siqueira, Bruna G. Sousa, Carlos E. Cleto, Luciana S. Wermelinger, Beatriz L.L. Caetano, Agatha R. Pacheco, Simone M. Costa, Fabio C.L. Almeida, Gustavo C. Ferreira, Didier Salmon, Ada M.B. Alves, Andrea T. Da Poian
Publikováno v:
Journal of Clinical Virology Plus, Vol 2, Iss 4, Pp 100121- (2022)
Background: Vaccination against COVID-19 was implemented very quickly, but the emergence of new variants that can evade the previous acquired immunological protection highlights the importance of understanding the mechanisms involved in the immune re
Externí odkaz:
https://doaj.org/article/b9920b9f634a4c629aa5cd026992bb9d
Publikováno v:
Revista Brasileira de Farmácia Hospitalar e Serviços de Saúde, Vol 12, Iss 2 (2021)
Objetivo: O presente estudo tem como objetivo principal a validação de mensagens de alertas, para os prescritores, sobre possíveis interações medicamentosas graves. Métodos: Trata-se de um estudo descritivo documental, sendo utilizado a lista d
Externí odkaz:
https://doaj.org/article/4e099d35e0ef4987a8e42e5bf2b82c72
Autor:
Ernesto A. Macongonde, Naithan L.F. Costa, Bruna K. Ferreira, Mairis S. Biella, Marisa J.S. Frederico, Marcos R. de Oliveira, Silvio Ávila Júnior, Fátima R.M.B. Silva, Gustavo C. Ferreira, Emilio L. Streck, Patrícia F. Schuck
Publikováno v:
Anais da Academia Brasileira de Ciências, Vol 87, Iss 2 suppl, Pp 1451-1459 (2015)
Fructose accumulates in tissue and body fluids of patients affected by hereditary fructose intolerance (HFI), a disorder caused by the deficiency of aldolase B. We investigated the effect of acute fructose administration on the biochemical profile an
Externí odkaz:
https://doaj.org/article/0587adb19c9c445bba9818249ebd063a
Publikováno v:
Anais da Academia Brasileira de Ciências, Vol 87, Iss 2 suppl, Pp 1409-1414 (2015)
Inherited metabolic diseases are a heterogeneous group of diseases caused by a punctual defect in cell metabolism, resulting in the accumulation of toxic intermediate metabolites or in the lack of important biomolecules for adequate cell functioning.
Externí odkaz:
https://doaj.org/article/cf7871eb658d41529c81b9db605f2670
Autor:
CARINE A. GUIMARÃES, MAIRIS S. BIELLA, ABIGAIL LOPES, PEDRO F. DEROZA, MARIANA B. OLIVEIRA, TAMIRES P. MACAN, EMILIO L. STRECK, GUSTAVO C. FERREIRA, ALEXANDRA I. ZUGNO, PATRÍCIA F. SCHUCK
Publikováno v:
Anais da Academia Brasileira de Ciências, Vol 86, Iss 4, Pp 1919-1926 (2014)
Increased fructose concentrations are the biochemical hallmark of fructosemia, a group of inherited disorders on the metabolic pathway of this sugar. The main clinical findings observed in patients affected by fructosemia include neurological abnorma
Externí odkaz:
https://doaj.org/article/f5691b1faac3412a9927ce08059fcf8a
Autor:
Danielle Dias Pinto Ferreira, Ricardo Augusto de Melo Reis, Mariana Nunes Marinho Ritter Ferreira, Pâmella de Moura, Maurício Dos Santos Pereira, Gustavo C. Ferreira, Thais da Rosa Valli, Regina Célia Cussa Kubrusly, Vladimir Pedro Borges-Martins, Robertta Silva Martins, Alex C. Manhães, Matheus F. Sathler
Publikováno v:
Neurotoxicity Research. 39:1946-1958
The spontaneously hypertensive rat (SHR) is an excellent animal model that mimics the behavioral and neurochemical phenotype of attention-deficit/hyperactivity disorder (ADHD). Here, we characterized the striatal GABA transport of SHR and investigate
Publikováno v:
Journal of Neurochemistry. 157:1946-1962
There is little information on metabolism in developing cerebellum despite the known importance of this region in cognition and motor tasks. Ex vivo 1 H- and 13 C-NMR spectroscopy were used to determine metabolism during late postnatal development in
Autor:
Rafaela Antonini, Mariane B D Matias, Gustavo C. Ferreira, Emilio L. Streck, Giselli Scaini, Felipe Dal-Pizzol, Monique Michels, Jade de Oliveira, Patrícia F. Schuck
Publikováno v:
Metabolic Brain Disease. 35:295-303
Tyrosinemia type II is an autosomal recessive inborn error of metabolism caused by hepatic cytosolic tyrosine aminotransferase deficiency. Importantly, this disease is associated with neurological and developmental abnormalities in many patients. Con
Autor:
Gustavo C. Ferreira, Alinny Rosendo Isaac, Hércules Rezende Freitas, Ricardo Augusto de Melo Reis, Isis Hara Trevenzoli, Belmira Lara da Silveira Andrade-da-Costa, Mariana M. Almeida, Patrícia Fernanda Schuck
Publikováno v:
Frontiers in Neuroscience
Frontiers in Neuroscience, Vol 15 (2021)
Frontiers in Neuroscience, Vol 15 (2021)
The endocannabinoid system (ECS) is an important brain modulatory network. ECS regulates brain homeostasis throughout development, from progenitor fate decision to neuro- and gliogenesis, synaptogenesis, brain plasticity and circuit repair, up to lea