Labile methyl group balances in the human: the role of sarcosine.
about
Interaction between dietary methionine and methyl donor intake on rat liver betaine-homocysteine methyltransferase gene expression and organization of the human geneTranssulfuration in an adult with hepatic methionine adenosyltransferase deficiencyCholine: critical role during fetal development and dietary requirements in adultsEpigenetic mechanisms for nutrition determinants of later health outcomesSex and menopausal status influence human dietary requirements for the nutrient cholineGenome-wide association study of selenium concentrationsThe Molecular and Cellular Effect of Homocysteine Metabolism Imbalance on Human HealthHepatic phosphatidylethanolamine N-methyltransferase, unexpected roles in animal biochemistry and physiologyLocalization-independent regulation of homocysteine secretion by phosphatidylethanolamine N-methyltransferaseTissue distribution of glycine N-methyltransferase, a major folate-binding protein of liverIsolated persistent hypermethioninemia.Folding of dimeric methionine adenosyltransferase III: identification of two folding intermediates.Effect of nicotinic acid administration on hepatic very low density lipoprotein-triglyceride production.Dealing with methionine/homocysteine sulfur: cysteine metabolism to taurine and inorganic sulfurGlycine N-methyltransferase is a folate binding protein of rat liver cytosol.S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolismFunctional proteomics of nonalcoholic steatohepatitis: mitochondrial proteins as targets of S-adenosylmethionine.Glycine N-methyltransferase and regulation of S-adenosylmethionine levels.Redox-based epigenetic status in drug addiction: a potential contributor to gene priming and a mechanistic rationale for metabolic intervention.Hepatic methionine adenosyltransferase deficiency in a 31-year-old man.Human liver methionine cycle: MAT1A and GNMT gene resequencing, functional genomics, and hepatic genotype-phenotype correlationSulfur as a signaling nutrient through hydrogen sulfide.Perinatal choline influences brain structure and function.An allosteric mechanism for switching between parallel tracks in mammalian sulfur metabolismGene response elements, genetic polymorphisms and epigenetics influence the human dietary requirement for cholineSupplementation with Folic Acid, but Not Creatine, Increases Plasma Betaine, Decreases Plasma Dimethylglycine, and Prevents a Decrease in Plasma Choline in Arsenic-Exposed Bangladeshi AdultsHomocysteine imbalance: a pathological metabolic markerThe Pediatric Methionine Requirement Should Incorporate Remethylation Potential and Transmethylation Demands.sar: a genetic mouse model for human sarcosinemia generated by ethylnitrosourea mutagenesisImportance of methyl donors during reproduction.Methoxistasis: integrating the roles of homocysteine and folic acid in cardiovascular pathobiology.Quantitative lipid metabolomic changes in alcoholic micropigs with fatty liver disease.Hypermethioninemias of genetic and non-genetic origin: A review.Biochemical basis for the dominant inheritance of hypermethioninemia associated with the R264H mutation of the MAT1A gene. A monomeric methionine adenosyltransferase with tripolyphosphatase activity.Plasma homocysteine is regulated by phospholipid methylation.High sodium chloride intake decreases betaine-homocysteine S-methyltransferase expression in guinea pig liver and kidney.Effects of creatine supplementation on homocysteine levels and lipid peroxidation in rats.Metabolomic profiles of arsenic (+3 oxidation state) methyltransferase knockout mice: effect of sex and arsenic exposure.Flavouring Group Evaluation 74 (FGE.74): Consideration of Simple Aliphatic Sulphides and Thiols evaluated by JECFA (61st meeting) Structurally related to Aliphatic and Alicyclic Mono-, Di-, Tri-, and Polysulphides with or without Additional Oxygen...Biochemical and behavioral phenotype of AGAT and GAMT deficient mice following long-term Creatine monohydrate supplementation.
P2860
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P2860
Labile methyl group balances in the human: the role of sarcosine.
description
1980 nî lūn-bûn
@nan
1980 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1980 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1980年の論文
@ja
1980年論文
@yue
1980年論文
@zh-hant
1980年論文
@zh-hk
1980年論文
@zh-mo
1980年論文
@zh-tw
1980年论文
@wuu
name
Labile methyl group balances in the human: the role of sarcosine.
@ast
Labile methyl group balances in the human: the role of sarcosine.
@en
Labile methyl group balances in the human: the role of sarcosine.
@nl
type
label
Labile methyl group balances in the human: the role of sarcosine.
@ast
Labile methyl group balances in the human: the role of sarcosine.
@en
Labile methyl group balances in the human: the role of sarcosine.
@nl
prefLabel
Labile methyl group balances in the human: the role of sarcosine.
@ast
Labile methyl group balances in the human: the role of sarcosine.
@en
Labile methyl group balances in the human: the role of sarcosine.
@nl
P1433
P1476
Labile methyl group balances in the human: the role of sarcosine.
@en
P2093
P304
P356
10.1016/0026-0495(80)90192-4
P577
1980-08-01T00:00:00Z