Genetic variation of folate-mediated one-carbon transfer pathway predicts susceptibility to choline deficiency in humans.
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Dietary choline requirements of women: effects of estrogen and genetic variationCholine: critical role during fetal development and dietary requirements in adultsCholine: an essential nutrient for public healthEpigenetic mechanisms for nutrition determinants of later health outcomesSex and menopausal status influence human dietary requirements for the nutrient cholineGenetic variants in phosphatidylethanolamine N-methyltransferase and methylenetetrahydrofolate dehydrogenase influence biomarkers of choline metabolism when folate intake is restrictedCommon genetic polymorphisms affect the human requirement for the nutrient cholineBiomarkers of Nutrition for Development-Folate ReviewCholine: clinical nutrigenetic/nutrigenomic approaches for identification of functions and dietary requirementsReduced MTHFD1 activity in male mice perturbs folate- and choline-dependent one-carbon metabolism as well as transsulfurationEnantioselective Effects of Metalaxyl Enantiomers on Breast Cancer Cells Metabolic Profiling Using HPLC-QTOF-Based MetabolomicsDietary and genetic manipulations of folate metabolism differentially affect neocortical functions in mice.A nutrient combination that can affect synapse formationIdentification of new genetic polymorphisms that alter the dietary requirement for choline and vary in their distribution across ethnic and racial groups.The effects of choline on hepatic lipid metabolism, mitochondrial function and antioxidative status in human hepatic C3A cells exposed to excessive energy substrates.Choline intake and genetic polymorphisms influence choline metabolite concentrations in human breast milk and plasma.Metabolomic profiling can predict which humans will develop liver dysfunction when deprived of dietary choline.Choline's role in maintaining liver function: new evidence for epigenetic mechanisms.What choline metabolism can tell us about the underlying mechanisms of fetal alcohol spectrum disorders.Geographical and ethnic distribution of single nucleotide polymorphisms within genes of the folate/homocysteine pathway metabolismWhy randomized controlled trials of calcium and vitamin D sometimes failEarly second trimester maternal plasma choline and betaine are related to measures of early cognitive development in term infantsNutritional genomics: defining the dietary requirement and effects of cholineGenetic epidemiology and insights into interactive genetic and environmental effects in autism spectrum disordersDocosahexaenoic acid in plasma phosphatidylcholine may be a potential marker for in vivo phosphatidylethanolamine N-methyltransferase activity in humans.Choline: clinical nutrigenetic/nutrigenomic approaches for identification of functions and dietary requirements.The supply of choline is important for fetal progenitor cells.Choline intake in a large cohort of patients with nonalcoholic fatty liver disease.Dietary choline deficiency causes DNA strand breaks and alters epigenetic marks on DNA and histones.Evidence for negative selection of gene variants that increase dependence on dietary choline in a Gambian cohortInteraction and exposure modification: are we asking the right questions?Plasma choline metabolites associate with metabolic stress among young overweight men in a genotype-specific manner.Choline metabolites: gene by diet interactions.Choline, Its Potential Role in Nonalcoholic Fatty Liver Disease, and the Case for Human and Bacterial GenesHighlights of the 2012 Research Workshop: Using nutrigenomics and metabolomics in clinical nutrition research.Choline metabolism provides novel insights into nonalcoholic fatty liver disease and its progression.Plasma 1-carbon metabolites and academic achievement in 15-yr-old adolescents.Genetic signatures in choline and 1-carbon metabolism are associated with the severity of hepatic steatosisGene response elements, genetic polymorphisms and epigenetics influence the human dietary requirement for cholineNutrigenomics and metabolomics will change clinical nutrition and public health practice: insights from studies on dietary requirements for choline
P2860
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P2860
Genetic variation of folate-mediated one-carbon transfer pathway predicts susceptibility to choline deficiency in humans.
description
2005 nî lūn-bûn
@nan
2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Genetic variation of folate-me ...... o choline deficiency in humans
@nl
Genetic variation of folate-me ...... choline deficiency in humans.
@ast
Genetic variation of folate-me ...... choline deficiency in humans.
@en
type
label
Genetic variation of folate-me ...... o choline deficiency in humans
@nl
Genetic variation of folate-me ...... choline deficiency in humans.
@ast
Genetic variation of folate-me ...... choline deficiency in humans.
@en
prefLabel
Genetic variation of folate-me ...... o choline deficiency in humans
@nl
Genetic variation of folate-me ...... choline deficiency in humans.
@ast
Genetic variation of folate-me ...... choline deficiency in humans.
@en
P2093
P2860
P356
P1476
Genetic variation of folate-me ...... choline deficiency in humans.
@en
P2093
Kerry-Ann da Costa
Leslie M Fischer
Martin Kohlmeier
P2860
P304
16025-16030
P356
10.1073/PNAS.0504285102
P407
P577
2005-10-18T00:00:00Z