(Q24658050)

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Genetic variants in phosphatidylethanolamine N-methyltransferase and methylenetetrahydrofolate dehydrogenase influence biomarkers of choline metabolism when folate intake is restricted

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scholarly article

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Genetic variants in phosphatidylethanolamine N-methyltransferase and methylenetetrahydrofolate dehydrogenase influence biomarkers of choline metabolism when folate intake is restricted (English)

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1 reference

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author name string

Alexandre Ivanov

1

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Susan Nash-Barboza

2

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Sabrina Hinkis

3

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Marie A Caudill

4

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language of work or name

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publication date

February 2009

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Journal of the American Dietetic Association

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109

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2

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313-8

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Phosphatidylethanolamine N-methyltransferase (PEMT) gene expression is induced by estrogen in human and mouse primary hepatocytes

1 reference

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Choline: critical role during fetal development and dietary requirements in adults

1 reference

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Common genetic polymorphisms affect the human requirement for the nutrient choline

1 reference

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Genetic variation of folate-mediated one-carbon transfer pathway predicts susceptibility to choline deficiency in humans

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Polymorphism of the PEMT gene and susceptibility to nonalcoholic fatty liver disease (NAFLD)

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Choline availability modulates human neuroblastoma cell proliferation and alters the methylation of the promoter region of the cyclin-dependent kinase inhibitor 3 gene

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A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects

1 reference

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The ratio of phosphatidylcholine to phosphatidylethanolamine influences membrane integrity and steatohepatitis

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Biochemical and evolutionary significance of phospholipid methylation

1 reference

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Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2655101

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Phosphatidylethanolamine N-methyltransferase from liver

1 reference

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Choline, an essential nutrient for humans

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Genetic and epigenetic contributions to human nutrition and health: managing genome-diet interactions

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Personalized nutrition: nutritional genomics as a potential tool for targeted medical nutrition therapy

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Folate intake and the MTHFR C677T genotype influence choline status in young Mexican American women

1 reference

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Polymorphisms of MTHFD, plasma homocysteine levels, and risk of gastric cancer in a high-risk Chinese population.

1 reference

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The fetal origins of memory: the role of dietary choline in optimal brain development

1 reference

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Periconceptional dietary intake of choline and betaine and neural tube defects in offspring

1 reference

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Elevated serum creatine phosphokinase in choline-deficient humans: mechanistic studies in C2C12 mouse myoblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2655101

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Perturbations in choline metabolism cause neural tube defects in mouse embryos in vitro

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2655101

28 September 2017

https://api.crossref.org/works/10.1016%2FJ.JADA.2008.10.046

7 January 2021

based on heuristic

inferred from DOI database lookup

Disruption of the murine gene encoding phosphatidylethanolamine N-methyltransferase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2655101

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High performance liquid chromatography method for rapid and accurate determination of homocysteine in plasma and serum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2655101

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Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2655101

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Choline and homocysteine interrelations in umbilical cord and maternal plasma at delivery

1 reference

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Insights into the requirement of phosphatidylcholine synthesis for liver function in mice

1 reference

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Methylenetetrahydrofolate Reductase 677C→T Variant Modulates Folate Status Response to Controlled Folate Intakes in Young Women

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2655101

28 November 2018

Plasma homocysteine is regulated by phospholipid methylation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2655101

28 November 2018

Quantitation of choline and its metabolites in tissues and foods by liquid chromatography/electrospray ionization-isotope dilution mass spectrometry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2655101

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Choline and human nutrition.

1 reference

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Choline deficiency: a cause of hepatic steatosis during parenteral nutrition that can be reversed with intravenous choline supplementation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19167960

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https://pubmed.ncbi.nlm.nih.gov/19167960

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Rapid and accurate HPLC assay for plasma total homocysteine and cysteine in a clinical laboratory setting

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https://pubmed.ncbi.nlm.nih.gov/19167960

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Is it time to reevaluate methyl balance in humans?

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https://pubmed.ncbi.nlm.nih.gov/19167960

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Identification of 197 genetic variations in six human methyltranferase genes in the Japanese population

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inferred from PubMed ID database lookup

Identifiers

10.1016/J.JADA.2008.10.046

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