Polymorphism of the PEMT gene and susceptibility to nonalcoholic fatty liver disease (NAFLD) - Wikidata - wikimedia - TriplyDB

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

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

http://www.wikidata.org/entity/Q24535745

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Dietary choline requirements of women: effects of estrogen and genetic variation Choline intake, plasma riboflavin, and the phosphatidylethanolamine N-methyltransferase G5465A genotype predict plasma homocysteine in folate-deplete Mexican-American men with the methylenetetrahydrofolate reductase 677TT genotype Choline: critical role during fetal development and dietary requirements in adults Choline metabolism and risk of breast cancer in a population-based study Genetic variants in phosphatidylethanolamine N-methyltransferase and methylenetetrahydrofolate dehydrogenase influence biomarkers of choline metabolism when folate intake is restricted Common genetic polymorphisms affect the human requirement for the nutrient choline Genetic, metabolic and environmental factors involved in the development of liver cirrhosis in Mexico Genetic background in nonalcoholic fatty liver disease: A comprehensive review Egg phospholipids and cardiovascular health Hepatic phosphatidylethanolamine N-methyltransferase, unexpected roles in animal biochemistry and physiology Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum Impaired de novo choline synthesis explains why phosphatidylethanolamine N-methyltransferase-deficient mice are protected from diet-induced obesity Aberrant estrogen regulation of PEMT results in choline deficiency-associated liver dysfunction Sphingolipids and phospholipids in insulin resistance and related metabolic disorders.Dietary docosahexaenoic acid supplementation modulates hippocampal development in the Pemt-/- mouse.Lack of association between peroxisome proliferator-activated receptors alpha and gamma2 polymorphisms and progressive liver damage in patients with non-alcoholic fatty liver disease: a case control study NAFLD Susceptibility Genes and their Association with Type 2 Diabetes and Obesity in a New Mexico Population.In-vivo31P-MRS of skeletal muscle and liver: A way for non-invasive assessment of their metabolism.The Association between Pediatric NAFLD and Common Genetic Variants.Choline intake and genetic polymorphisms influence choline metabolite concentrations in human breast milk and plasma.Molecular analysis of the Retinoic Acid Induced 1 gene (RAI1) in patients with suspected Smith-Magenis syndrome without the 17p11.2 deletion.Metabolomic profiling can predict which humans will develop liver dysfunction when deprived of dietary choline.Effects of choline on health across the life course: a systematic review.Higher dietary choline intake is associated with lower risk of nonalcoholic fatty liver in normal-weight Chinese women.Specificity and rate of human and mouse liver and plasma phosphatidylcholine synthesis analyzed in vivo.Genetic variants in PNPLA3 and risk of non-alcoholic fatty liver disease in a Han Chinese population.Common genetic variations in CLOCK transcription factor are associated with nonalcoholic fatty liver disease Hepatic methionine homeostasis is conserved in C57BL/6N mice on high-fat diet despite major changes in hepatic one-carbon metabolism.Association between composition of the human gastrointestinal microbiome and development of fatty liver with choline deficiency.Genetic determinants of hepatic steatosis in man.Genetic Variation in Choline-Metabolizing Enzymes Alters Choline Metabolism in Young Women Consuming Choline Intakes Meeting Current Recommendations.Docosahexaenoic acid in plasma phosphatidylcholine may be a potential marker for in vivo phosphatidylethanolamine N-methyltransferase activity in humans.Association of genetic variation in adaptor protein APPL1/APPL2 loci with non-alcoholic fatty liver disease Improved method for quantitative analysis of methylated phosphatidylethanolamine species and its application for analysis of diabetic-mouse liver samples.Choline intake in a large cohort of patients with nonalcoholic fatty liver disease.A distinct and replicable variant of the squamous cell carcinoma gene inositol polyphosphate-5-phosphatase modifies the susceptibility of arsenic-associated skin lesions in Bangladesh.Heritability of nonalcoholic fatty liver disease.Plasma choline metabolites associate with metabolic stress among young overweight men in a genotype-specific manner.Genetic analysis of nonalcoholic fatty liver disease within a Caribbean-Hispanic population.Choline, Its Potential Role in Nonalcoholic Fatty Liver Disease, and the Case for Human and Bacterial Genes

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

http://www.wikidata.org/entity/Q24535745

description

2005 nî lūn-bûn

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2005 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2005 թվականի օգոստոսին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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name

Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Polymorphism of the PEMT gene ...... ic fatty liver disease (NAFLD)

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Jiannan Song

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Kerry Ann da Costa

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Leslie M Fischer

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Lester Kwock

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Martin Kohlmeier

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Shuli Wang

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P2860

An unexpected requirement for phosphatidylethanolamine N-methyltransferase in the secretion of very low density lipoproteins

Phosphatidylethanolamine N-methyltransferase from liver

Choline, an essential nutrient for humans

Biochemical and evolutionary significance of phospholipid methylation

Kinetic mechanism of phosphatidylethanolamine N-methyltransferase

The active synthesis of phosphatidylcholine is required for very low density lipoprotein secretion from rat hepatocytes

Molecular mediators of hepatic steatosis and liver injury

Concentrations of choline-containing compounds and betaine in common foods.

Clinical features and natural history of nonalcoholic steatosis syndromes.

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