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Cytosine DNA Methylation Is Found in Drosophila melanogaster but Absent in Saccharomyces cerevisiae, Schizosaccharomyces pombe, and Other Yeast Species

Analytical chemistry (Washington), 2014-04, Vol.86 (8), p.3697-3702

2014

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Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency

Journal of Inherited Metabolic Disease, 2017-01, Vol.40 (1), p.49-74

2017

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Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines

Journal of Inherited Metabolic Disease, 2015-11, Vol.38 (6), p.1007-1019

2015

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No Tryptophan, Tyrosine and Phenylalanine Abnormalities in Children with Attention-Deficit/Hyperactivity Disorder

PloS one, 2016-03, Vol.11 (3), p.e0151100-e0151100

2016

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homocysteine controversy

Journal of inherited metabolic disease, 2011-02, Vol.34 (1), p.93-99

2011

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Adenosine Kinase Deficiency Disrupts the Methionine Cycle and Causes Hypermethioninemia, Encephalopathy, and Abnormal Liver Function

American journal of human genetics, 2011-10, Vol.89 (4), p.507-515

2011

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Promiscuous activity of arginine:glycine amidinotransferase is responsible for the synthesis of the novel cardiovascular risk factor homoarginine

FEBS letters, 2012-10, Vol.586 (20), p.3653-3657

2012

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The effect of diet-induced weight loss on circulating homocysteine levels in people with obesity and type 2 diabetes

Nutrition journal, 2024-01, Vol.23 (1), p.2-2, Article 2

2024

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Overview of homocysteine and folate metabolism. With special references to cardiovascular disease and neural tube defects

Journal of inherited metabolic disease, 2011-02, Vol.34 (1), p.75-81

2011

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Liver and brain differential expression of one-carbon metabolism genes during ontogenesis

Scientific reports, 2021-10, Vol.11 (1), p.21132-21132, Article 21132

2021

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Homocysteine and disease: Causal associations or epiphenomenons?

Molecular aspects of medicine, 2017-02, Vol.53, p.36-42

2017

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Homocysteine lowering by B vitamins and the secondary prevention of deep vein thrombosis and pulmonary embolism: a randomized, placebo-controlled, double-blind trial

Blood, 2007-01, Vol.109 (1), p.139-144

2007

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Choline and Risk of Neural Tube Defects in a Folate-fortified Population

Epidemiology (Cambridge, Mass.), 2009-09, Vol.20 (5), p.714-719

2009

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No evidence for an association of plasma homocysteine levels and refractive error - Results from the population-based Gutenberg Health Study (GHS)

PloS one, 2020-04, Vol.15 (4), p.e0231011-e0231011

2020

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Hemodialysis in MNGIE transiently reduces serum and urine levels of thymidine and deoxyuridine, but not CSF levels and neurological function

Orphanet journal of rare diseases, 2017-08, Vol.12 (1), p.135-4, Article 135

2017

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Homocysteine and methylmalonic acid in Phenylketonuria patients

Genetics and molecular biology, 2023-01, Vol.46 (3 Suppl 1), p.e20230103-e20230103

2023

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Adenosine kinase deficiency: expanding the clinical spectrum and evaluating therapeutic options

Journal of inherited metabolic disease, 2016-03, Vol.39 (2), p.273-283

2016

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Inhibition of Cellular Methyltransferases Promotes Endothelial Cell Activation by Suppressing Glutathione Peroxidase 1 Protein Expression

The Journal of biological chemistry, 2014-05, Vol.289 (22), p.15350-15362

2014

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Benchmarking Outlier Detection Methods for Detecting IEM Patients in Untargeted Metabolomics Data

Metabolites, 2023-01, Vol.13 (1), p.97

2023

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Biotinidase deficiency: Genotype-biochemical phenotype association in Brazilian patients

PloS one, 2017-05, Vol.12 (5), p.e0177503-e0177503

2017

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Folinic Acid Increases Protein Arginine Methylation in Human Endothelial Cells

Nutrients, 2018-03, Vol.10 (4), p.404

2018

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Homocysteine determinants and the evidence to what extent homocysteine determines the risk of coronary heart disease

Pharmacological reviews, 2002-12, Vol.54 (4), p.599-618

2002

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Classical homocystinuria: A common inborn error of metabolism? An epidemiological study based on genetic databases

Molecular genetics & genomic medicine, 2020-06, Vol.8 (6), p.e1214-n/a

2020

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Identification and Characterization of an Inborn Error of Metabolism Caused by Dihydrofolate Reductase Deficiency

American journal of human genetics, 2011-02, Vol.88 (2), p.216-225

2011

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Umbilical choline and related methylamines betaine and dimethylglycine in relation to birth weight

Pediatric research, 2013-06, Vol.73 (6), p.783-787

2013

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Cytosine DNA Methylation Is Found in Drosophila melanogaster but Absent in Saccharomyces cerevisiae, Schizosaccharomyces pombe, and Other Yeast Species

Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency

Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines

No Tryptophan, Tyrosine and Phenylalanine Abnormalities in Children with Attention-Deficit/Hyperactivity Disorder

homocysteine controversy

Adenosine Kinase Deficiency Disrupts the Methionine Cycle and Causes Hypermethioninemia, Encephalopathy, and Abnormal Liver Function

Promiscuous activity of arginine:glycine amidinotransferase is responsible for the synthesis of the novel cardiovascular risk factor homoarginine

The effect of diet-induced weight loss on circulating homocysteine levels in people with obesity and type 2 diabetes

Overview of homocysteine and folate metabolism. With special references to cardiovascular disease and neural tube defects

Liver and brain differential expression of one-carbon metabolism genes during ontogenesis

Homocysteine and disease: Causal associations or epiphenomenons?

Homocysteine lowering by B vitamins and the secondary prevention of deep vein thrombosis and pulmonary embolism: a randomized, placebo-controlled, double-blind trial

Choline and Risk of Neural Tube Defects in a Folate-fortified Population

No evidence for an association of plasma homocysteine levels and refractive error - Results from the population-based Gutenberg Health Study (GHS)

Hemodialysis in MNGIE transiently reduces serum and urine levels of thymidine and deoxyuridine, but not CSF levels and neurological function

Homocysteine and methylmalonic acid in Phenylketonuria patients

Adenosine kinase deficiency: expanding the clinical spectrum and evaluating therapeutic options

Inhibition of Cellular Methyltransferases Promotes Endothelial Cell Activation by Suppressing Glutathione Peroxidase 1 Protein Expression

Benchmarking Outlier Detection Methods for Detecting IEM Patients in Untargeted Metabolomics Data

Biotinidase deficiency: Genotype-biochemical phenotype association in Brazilian patients

Folinic Acid Increases Protein Arginine Methylation in Human Endothelial Cells

Homocysteine determinants and the evidence to what extent homocysteine determines the risk of coronary heart disease

Classical homocystinuria: A common inborn error of metabolism? An epidemiological study based on genetic databases

Identification and Characterization of an Inborn Error of Metabolism Caused by Dihydrofolate Reductase Deficiency

Umbilical choline and related methylamines betaine and dimethylglycine in relation to birth weight

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