Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ângela de Mattos Dutra"'
Autor:
Ana Cristina Borba Cunha, Pedro Henrique Mirapalheta Jacques, Rita de Cássia dos Reis Schmidt, Henrique Carvalho Andrade, Ângela de Mattos Dutra
Publikováno v:
Interação. 21:446-467
O presente estudo foi desenvolvido por meio de uma pesquisa aplicada na disciplina de química analítica na Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS. A questão norteadora da pesquisa teve por objetivo avaliar a compr
Autor:
Nicoli T. Henn, Fernanda Rech Zanin, Ângela M. Sgaravatti, Eline Coan Romagna, Francieli J Rockenbach, Carlos Severo Dutra-Filho, Moacir Wajner, Clovis Milton Duval Wannmacher, Angela T. S. Wyse, Ângela de Mattos Dutra, Carolina Didonet Pederzolli
Publikováno v:
Metabolic Brain Disease. 24:283-298
N-acetylaspartic acid (NAA) is the biochemical hallmark of Canavan Disease, an inherited metabolic disease caused by deficiency of aspartoacylase activity. NAA is an immediate precursor for the enzyme-mediated biosynthesis of N-acetylaspartylglutamic
Autor:
Regina Pessoa-Pureur, Ângela de Mattos-Dutra, Moacir Wajner, Susana Tchernin Wofchuk, Tricia Cristine Kommers, Betânia Bevilaqua da Rocha, Renata Bezerra Meirelles
Publikováno v:
Brain Research. 856:111-118
In this study we investigated the effects of methylmalonic acid (MMA) and propionic acid (PA) on the phosphorylation of cytoskeletal proteins of cerebral cortex of rats. Slices of tissue were incubated with 32P-orthophosphate in the presence or absen
Autor:
Marta Sampaio de Freitas, Nadja Schröder, Ângela de Mattos-Dutra, Ana Maria Carina Zilles, Ivan Izquierdo, Regina Pessoa-Pureur, Carla Simone Fogaca Lisboa
Publikováno v:
Brain Research. 749:275-282
Neurofilaments (NF) are the most abundant constituents of the neuronal cytoskeleton, while glial fibrillary acidic protein (GFAP) is a major component of the glial astrocyte cytoskeleton. These proteins can be phosphorylated by different protein kina
Publikováno v:
Developmental Brain Research. 96:76-82
Autor:
Ângela de Mattos Dutra, Andrea Pereira Rosa, Carlos Eduardo Dias Jacques, Carlos Severo Dutra-Filho, Tarsila Barros Moraes, Clovis Milton Duval Wannmacher
Publikováno v:
Cellular and molecular neurobiology. 32(7)
Phenylketonuria is a recessive autosomal disorder that is caused by a deficiency in the activity of phenylalanine-4-hydroxylase, which converts phenylalanine to tyrosine, leading to the accumulation of phenylalanine and its metabolites phenyllactic a
Autor:
Ângela de Mattos-Dutra, Regina Pessoa-Pureur, Moacir Wajner, Carla Simone Fogaca Lisboa, Marta Sampaio de Freitas
Publikováno v:
Neurochemistry international. 33(1)
We studied the e}ects of acute and chronic administration of methylmalonic (MMA) and propionic (PA) acids on the in vitro incorporation of 32 P into neurofilament subunits (NF-M and NF-L), α and β tubulins, from cerebral cortex of rats. In the chro
Autor:
Moacir Wajner, Marta Sampaio de Freitas, Nadja Schröder, Regina Pessoa-Pureur, Carla Simone Fogaca Lisboa, Ângela de Mattos-Dutra
Publikováno v:
Experimental neurology. 147(2)
In the present study we demonstrate that propionic acid (PA), a metabolite that accumulates in large amounts in propionic acidemia, is able to decrease in vitro incorporation of [32P]ATP into neurofilament subunits (NF-M and NF-L) and alpha- and beta
Autor:
Carolina Pederzolli, Francieli Rockenbach, Fernanda Zanin, Nicoli Henn, Eline Romagna, Ângela Sgaravatti, Ângela de Mattos Dutra
Publikováno v:
Metabolic Brain Disease; Jun2009, Vol. 24 Issue 2, p283-298, 16p