Neurochemical evidence that the metabolites accumulating in 3-methylcrotonyl-CoA carboxylase deficiency induce oxidative damage in cerebral cortex of young rats. (Q44638197)

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scientific article published on 28 September 2012

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English	Neurochemical evidence that the metabolites accumulating in 3-methylcrotonyl-CoA carboxylase deficiency induce oxidative damage in cerebral cortex of young rats.	scientific article published on 28 September 2012

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10 March 2020

Neurochemical evidence that the metabolites accumulating in 3-methylcrotonyl-CoA carboxylase deficiency induce oxidative damage in cerebral cortex of young rats (English)

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10 March 2020

3-methylcrotonyl-CoA carboxylase deficiency

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César Augusto João Ribeiro

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10 March 2020

Guilhian Leipnitz

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10 March 2020

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Moacir Wajner

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10 March 2020

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Ângela Zanatta

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10 March 2020

Alana Pimentel Moura

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10 March 2020

Anelise Miotti Tonin

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10 March 2020

Lisiane Aurélio Knebel

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10 March 2020

Mateus Grings

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10 March 2020

Vannessa Araújo Lobato

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10 March 2020

Carlos Severo Dutra-Filho

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10 March 2020

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28 September 2012

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10 March 2020

Cellular and Molecular Neurobiology

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10 March 2020

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10 March 2020

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10 March 2020

137-146

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10 March 2020

Production of reactive oxygen species in brain mitochondria: contribution by electron transport chain and non-electron transport chain sources

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Catalase in vitro

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A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency

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The molecular basis of human 3-methylcrotonyl-CoA carboxylase deficiency

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Consanguineous 3-methylcrotonyl-CoA carboxylase deficiency: early-onset necrotizing encephalopathy with lethal outcome

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Oxygen- or organic hydroperoxide-induced chemiluminescence of brain and liver homogenates

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Protein carbonyl groups as biomarkers of oxidative stress.

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Protein carbonylation: 2,4-dinitrophenylhydrazine reacts with both aldehydes/ketones and sulfenic acids.

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Induction of oxidative stress by the metabolites accumulating in 3-methylglutaconic aciduria in cerebral cortex of young rats.

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Short/branched-chain acyl-CoA dehydrogenase deficiency due to an IVS3+3A>G mutation that causes exon skipping

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Novel mutations in the human MCCA and MCCB gene causing methylcrotonylglycinuria

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Human biotin-containing subunit of 3-methylcrotonyl-CoA carboxylase gene (MCCA): cDNA sequence, genomic organization, localization to chromosomal band 3q27, and expression

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Neurochemical Evidence that Lysine Inhibits Synaptic Na+,K+-ATPase Activity and Provokes Oxidative Damage in Striatum of Young Rats In vivo

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Disruption of redox homeostasis in cerebral cortex of developing rats by acylcarnitines accumulating in medium-chain acyl-CoA dehydrogenase deficiency.

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Identifiers

10.1007/S10571-012-9879-2

1 reference

Europe PubMed Central

PubMed publication ID

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10 March 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

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10 March 2020

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