Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Isabela S Lemos"'
3
Administration of branched-chain amino acids alters epigenetic regulatory enzymes in an animal model of Maple Syrup Urine Disease
Autor: Mariane Bernardo Duarte, Leticia B. Wessler, Fernanda F. Gava, Isabela S Lemos, Emilio L. Streck, Carolina A Torres, Jade de Oliveira, Felipe P Bussular, Matheus Scarpatto Rodrigues, Victoria Linden de Rezende, Samira S. Valvassori, Gabriela Candiotto
Publikováno v: Metabolic Brain Disease. 36:247-254
Maple Syrup Urine Disease (MSUD) is an autosomal recessive inherited disorder that affects the activity of the branched-chainα-keto acid dehydrogenase complex (BCDK). This deficiency on BCDK complex results in the accumulation of branched-chain amin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::92d95d7e07a55b30074d56586ba4f454
https://doi.org/10.1007/s11011-020-00631-1
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4
The metabolic effect of α-ketoisocaproic acid: in vivo and in vitro studies
Autor: Mariane Bernardo Duarte, Jade de Oliveira, Giselli Scaini, Victoria Linden de Rezende, Leticia B. Wessler, Maria Laura Cecconi, Isabela S Lemos, Emilio L. Streck, Hémelin Resende Farias, Joice R Gabriel
Publikováno v: Metabolic Brain Disease. 36:185-192
Maple syrup urine disease (MSUD) is characterized by a deficiency in the mitochondrial branched-chain α-keto acid dehydrogenase complex activity and, consequently, accumulation of the branched-chain amino acids and their respective branched-chain α
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3dc380d1197852e450f614702fd37292
https://doi.org/10.1007/s11011-020-00626-y
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5
Coadministration of tianeptine alters behavioral parameters and levels of neurotrophins in a chronic model of Maple Syrup Urine disease
Autor: Fábio A, Morais, Isabela S, Lemos, Rafaela T, Matiola, Maria Luísa S, Freitas, Carolina G, Alano, Julia, Cabral, Leticia B, Wessler, Jaqueline S, Generoso, Giselli, Scaini, Gislaine Z, Réus, Emilio L, Streck
Publikováno v: Metabolic brain disease. 37(5)
Maple Syrup Urine Disease (MSUD) is caused by the deficiency in the activity of the branched-chain α-ketoacid dehydrogenase complex (BCKDC), resulting in the accumulation of the branched-chain amino acids (BCAA) leucine, isoleucine, and valine, and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::dd3da0f786263c33839c58ac842034aa
https://pubmed.ncbi.nlm.nih.gov/35394251
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6
Administration of branched-chain amino acids alters epigenetic regulatory enzymes in an animal model of Maple Syrup Urine Disease
Autor: Emilio L, Streck, Felipe P, Bussular, Leticia B, Wessler, Mariane B, Duarte, Victoria L, Rezende, Matheus S, Rodrigues, Carolina A, Torres, Isabela S, Lemos, Gabriela, Candiotto, Fernanda F, Gava, Jade, de Oliveira, Samira S, Valvassori
Publikováno v: Metabolic brain disease. 36(2)
Maple Syrup Urine Disease (MSUD) is an autosomal recessive inherited disorder that affects the activity of the branched-chainα-keto acid dehydrogenase complex (BCDK). This deficiency on BCDK complex results in the accumulation of branched-chain amin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d80effd86cd14b670da00d06f3e46914
https://pubmed.ncbi.nlm.nih.gov/33098071
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7
The metabolic effect of α-ketoisocaproic acid: in vivo and in vitro studies
Autor: Hémelin R, Farias, Joice R, Gabriel, Maria Laura, Cecconi, Isabela S, Lemos, Victoria L, de Rezende, Letícia B, Wessler, Mariane B, Duarte, Giselli, Scaini, Jade, de Oliveira, Emilio L, Streck
Publikováno v: Metabolic brain disease. 36(1)
Maple syrup urine disease (MSUD) is characterized by a deficiency in the mitochondrial branched-chain α-keto acid dehydrogenase complex activity and, consequently, accumulation of the branched-chain amino acids and their respective branched-chain α
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a144f01d8fe398ec22bb5fc5872cf2b2
https://pubmed.ncbi.nlm.nih.gov/33034842
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8
Exposure to a high dose of amoxicillin causes behavioral changes and oxidative stress in young zebrafish
Autor: Mariane B D Matias, Eduardo Pacheco Rico, Francine F P Vasconcelos, Jaime Lin, Emilio L. Streck, Gabriela Candiotto, Leticia B. Wessler, Cinara L. Gonçalves, Isabela S Lemos
Publikováno v: Metabolic brain disease. 35(8)
Autistic spectrum disorder (ASD) is a group of early-onset neurodevelopmental disorders characterized by impaired social and communication skills. Autism is widely described as a behavioral syndrome with multiple etiologies where may exhibit neurobio
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60bca2fd85e58af698b1e756cccc4530
https://pubmed.ncbi.nlm.nih.gov/32876824
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