Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
about
Destabilization of human glycine N-methyltransferase by H176N mutationAcetylation of N-terminal valine of glycine N-methyltransferase affects enzyme inhibition by folateGlycine N-methyltransferase-/- mice develop chronic hepatitis and glycogen storage disease in the liverEndocrine-disrupting chemicals and fatty liver disease.Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?Fatty liver and fibrosis in glycine N-methyltransferase knockout mice is prevented by nicotinamide.Polymorphisms and disease: hotspots of inactivation in methyltransferasesGNMT expression increases hepatic folate contents and folate-dependent methionine synthase-mediated homocysteine remethylation.The biochemical and toxicological significance of hypermethionemia: new insights and clinical relevanceDeficiency of glycine N-methyltransferase aggravates atherosclerosis in apolipoprotein E-null mice.S-adenosylmethionine in liver health, injury, and cancer.A novel role of the tumor suppressor GNMT in cellular defense against DNA damage.Role of glycine N-methyltransferase in experimental ulcerative colitis.S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolismThe role of genetics in the establishment and maintenance of the epigenome.A novel tumor suppressor function of glycine N-methyltransferase is independent of its catalytic activity but requires nuclear localizationGlycine N-methyltransferase and regulation of S-adenosylmethionine levels.Functional characterization of glycine N-methyltransferase and its interactive protein DEPDC6/DEPTOR in hepatocellular carcinoma.Inhibition of natural killer cells protects the liver against acute injury in the absence of glycine N-methyltransferase.Human liver methionine cycle: MAT1A and GNMT gene resequencing, functional genomics, and hepatic genotype-phenotype correlationLoss of the glycine N-methyltransferase gene leads to steatosis and hepatocellular carcinoma in miceS-adenosylhomocysteine hydrolase deficiency in a 26-year-old man.Benzo[a]pyrene decreases global and gene specific DNA methylation during zebrafish developmentExcess S-adenosylmethionine reroutes phosphatidylethanolamine towards phosphatidylcholine and triglyceride synthesis.Adenosine kinase deficiency with neurodevelopemental delay and recurrent hepatic dysfunction: A case report.A glycine N-methyltransferase knockout mouse model for humans with deficiency of this enzyme.Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders.Hypermethioninemias of genetic and non-genetic origin: A review.Steatosis in the liver.A DNA methylation signature associated with the epigenetic repression of glycine N-methyltransferase in human hepatocellular carcinoma.Glycine N-methyltransferase expression in the hippocampus and its role in neurogenesis and cognitive performance.Impaired liver regeneration in mice lacking glycine N-methyltransferase.Neuronal damage and memory deficits after seizures are reversed by ascorbic acid?Identification of phosphorylation sites in glycine N-methyltransferase from rat liver.Methionine and methionine sulfoxide treatment induces M1/classical macrophage polarization and modulates oxidative stress and purinergic signaling parameters.
P2860
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P2860
Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
@ast
Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
@en
Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
@nl
type
label
Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
@ast
Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
@en
Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
@nl
prefLabel
Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
@ast
Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
@en
Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
@nl
P2093
P1476
Glycine N -methyltransferase deficiency: a new patient with a novel mutation.
@en
P2093
Augoustides-Savvopoulou P
Patsiaoura K
Stabler SP
P304
P356
10.1023/B:BOLI.0000009978.17777.33
P577
2003-01-01T00:00:00Z
P5875
P6179
1016960121