Genetic and cellular studies of oxidative stress in methylmalonic aciduria (MMA) cobalamin deficiency type C (cblC) with homocystinuria (MMACHC). (Q35003560)

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English	Genetic and cellular studies of oxidative stress in methylmalonic aciduria (MMA) cobalamin deficiency type C (cblC) with homocystinuria (MMACHC).	scientific article

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Genetic and cellular studies of oxidative stress in methylmalonic aciduria (MMA) cobalamin deficiency type C (cblC) with homocystinuria (MMACHC) (English)

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Lourdes R Desviat

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Celia Pérez-Cerdá

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Belén Pérez

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7 February 2020

Adult-onset combined methylmalonic aciduria and homocystinuria (cblC).

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Vitamin B6 suppresses apoptosis of NM-1 bovine endothelial cells induced by homocysteine and copper.

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Late-onset cobalamin-C disorder: a challenging diagnosis.

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Cobalamin (Cbl) C/D deficiency: clinical, neurophysiological and neuroradiologic findings in 14 cases.

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Mitochondrial dysfunction in mut methylmalonic acidemia

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Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition

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Cerebral vascular dysfunction mediated by superoxide in hyperhomocysteinemic mice.

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Genetic and phenotypic aspects of phenylalanine hydroxylase deficiency in Spain: molecular survey by regions

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Hyperhomocysteinemia, oxidative stress, and cerebral vascular dysfunction

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Propionic and L-methylmalonic acids induce oxidative stress in brain of young rats.

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Apoptosis in CADASIL: an in vitro study of lymphocytes and fibroblasts from a cohort of Italian patients.

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A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status.

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Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNA.

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Processing of alkylcobalamins in mammalian cells: A role for the MMACHC (cblC) gene product

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Elevation in S-Adenosylhomocysteine and DNA Hypomethylation: Potential Epigenetic Mechanism for Homocysteine-Related Pathology

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Homocysteine enhances apoptosis in human bone marrow stromal cells

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Decyanation of vitamin B12 by a trafficking chaperone

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Evaluation of the probe 2',7'-dichlorofluorescin as an indicator of reactive oxygen species formation and oxidative stress

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Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

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Imaging of the brain, including diffusion-weighted imaging in methylmalonic acidemia

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Spectrum of MMACHC mutations in Italian and Portuguese patients with combined methylmalonic aciduria and homocystinuria, cblC type.

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10.1002/HUMU.21107

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7 February 2020

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