(Q37246124)

19 August 2017

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title

Folate and vitamin B12 metabolism: overview and interaction with riboflavin, vitamin B6, and polymorphisms (English)

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19 August 2017

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Barry Shane

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19 August 2017

publication date

1 June 2008

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Food and Nutrition Bulletin

19 August 2017

published in

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19 August 2017

volume

29

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19 August 2017

issue

2 Suppl

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19 August 2017

page(s)

S5-16; discussion S17-9

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Glutamate carboxypeptidase II: a polymorphism associated with lower levels of serum folate and hyperhomocysteinemia.

19 August 2017

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Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption

21 January 2018

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Internalization and intracellular transport of folate-binding protein in rat kidney proximal tubule

21 January 2018

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Retrovirally mediated complementation of the glyB phenotype. Cloning of a human gene encoding the carrier for entry of folates into mitochondria

21 January 2018

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Purification and properties of human cytosolic folylpoly-gamma-glutamate synthetase and organization, localization, and differential splicing of its gene

21 January 2018

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New perspectives on folate catabolism

21 January 2018

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Molecular cloning, characterization, and regulation of the human mitochondrial serine hydroxymethyltransferase gene

21 January 2018

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Vitamin B12-folate interrelationships

21 January 2018

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Homocysteine and cardiovascular disease

21 January 2018

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Composite organization of the cobalamin binding and cubilin recognition sites of intrinsic factor

21 January 2018

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Transfer of cobalamin from intrinsic factor to transcobalamin II

21 January 2018

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Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1

21 January 2018

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The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless

21 January 2018

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Megalin-mediated endocytosis of transcobalamin-vitamin-B12 complexes suggests a role of the receptor in vitamin-B12 homeostasis

21 January 2018

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Defective lysosomal release of vitamin B12 (cb1F): a hereditary cobalamin metabolic disorder associated with sudden death.

21 January 2018

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Human methionine synthase. cDNA cloning, gene localization, and expression

21 January 2018

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The structure of the C-terminal domain of methionine synthase: presenting S-adenosylmethionine for reductive methylation of B12

21 January 2018

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Characterization of a succinyl-CoA radical-cob(II)alamin spin triplet intermediate in the reaction catalyzed by adenosylcobalamin-dependent methylmalonyl-CoA mutase

21 January 2018

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Cobalamin-dependent methionine synthase: the structure of a methylcobalamin-binding fragment and implications for other B12-dependent enzymes

21 January 2018

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Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria

21 January 2018

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Current concepts in cobalamin deficiency

21 January 2018

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Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage

21 January 2018

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Prevalence of intrinsic factor antibodies and vitamin B12 malabsorption in older patients admitted to a rehabilitation hospital

21 January 2018

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Helicobacter pylori infection and food-cobalamin malabsorption

21 January 2018

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Cobalamin deficiency and the pathogenesis of nervous system disease

21 January 2018

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Methylation deficiency causes vitamin B12-associated neuropathy in the pig.

21 January 2018

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Impact of folic acid fortification of the US food supply on the occurrence of neural tube defects

21 January 2018

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Neural tube defect rates before and after food fortification with folic acid.

21 January 2018

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Transposable elements: targets for early nutritional effects on epigenetic gene regulation

21 January 2018

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A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

21 January 2018

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Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

21 January 2018

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

21 January 2018

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A common mutation in the methylenetetrahydrofolate reductase gene is associated with an accumulation of formylated tetrahydrofolates in red blood cells

21 January 2018

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The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia

21 January 2018

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Polymorphisms in the methylenetetrahydrofolate reductase gene are associated with susceptibility to acute leukemia in adults

21 January 2018

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https://api.crossref.org/works/10.1177%2F15648265080292S103

A polymorphism in the MTHFD1 gene increases a mother's risk of having an unexplained second trimester pregnancy loss

21 January 2018

1 reference

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Transcobalamin II 775G>C polymorphism and indices of vitamin B12 status in healthy older adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F15648265080292S103

10.1177/15648265080292S103

21 January 2018

Identifiers

DOI

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1 reference