Glutathione metabolism in cobalamin deficiency type C (cblC). (Q39437913)

12 September 2017

Glutathione metabolism in cobalamin deficiency type C (cblC). (English)

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12 September 2017

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8

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12 September 2017

7

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Fiorella Piemonte

3

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Anna Pastore

Gianna Di Giovamberardino

1

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Gianna Di Giovamberardino

6

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Giulia Tozzi

Giulia Tozzi

4

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Carlo Dionisi-Vici

Carlo Dionisi-Vici

9

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Diego Martinelli

2

Diego Martinelli

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12 September 2017

Sara Boenzi

5

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12 September 2017

9 April 2013

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Journal of Inherited Metabolic Disease

12 September 2017

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12 September 2017

37

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12 September 2017

125-129

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1

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https://scigraph.springernature.com/pub.10.1007/s10545-013-9605-3

12 September 2017

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cites work

Inherited disorders affecting mitochondrial function are associated with glutathione deficiency and hypocitrullinemia

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Glutathione dysregulation and the etiology and progression of human diseases.

21 January 2018

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A novel role for vitamin B(12): Cobalamins are intracellular antioxidants in vitro

21 January 2018

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Mitochondrial dysfunction in mut methylmalonic acidemia

21 January 2018

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S-glutathionylation: from redox regulation of protein functions to human diseases.

21 January 2018

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

21 January 2018

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The X-ray crystal structure of glutathionylcobalamin revealed.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10545-013-9605-3

The MMACHC proteome: hallmarks of functional cobalamin deficiency in humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9605-3

Protection of aquo/hydroxocobalamin from reduced glutathione by a B12 trafficking chaperone

21 January 2018

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Branched chain amino acids induce apoptosis in neural cells without mitochondrial membrane depolarization or cytochrome c release: implications for neurological impairment associated with maple syrup urine disease

21 January 2018

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Decyanation of vitamin B12 by a trafficking chaperone

21 January 2018

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

21 January 2018

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Regulation of glutathione synthesis

21 January 2018

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Cobalamin C defect: natural history, pathophysiology, and treatment.

21 January 2018

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Profiling of oxidative stress in patients with inborn errors of metabolism

21 January 2018

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The quantitatively important relationship between homocysteine metabolism and glutathione synthesis by the transsulfuration pathway and its regulation by redox changes

21 January 2018

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S-Glutathionylation signaling in cell biology: progress and prospects

21 January 2018

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Analysis of glutathione: implication in redox and detoxification

21 January 2018

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

21 January 2018

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Oxidative stress and apoptosis in homocystinuria patients with genetic remethylation defects

21 January 2018

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Oxidative stress in patients with phenylketonuria.

21 January 2018

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Studies on the formation of glutathionylcobalamin: any free intracellular aquacobalamin is likely to be rapidly and irreversibly converted to glutathionylcobalamin

21 January 2018

1 reference

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Fully automated assay for total homocysteine, cysteine, cysteinylglycine, glutathione, cysteamine, and 2-mercaptopropionylglycine in plasma and urine.

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23568438

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10545-013-9605-3

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12 September 2017

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PubMed ID

23568438