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Journal of Neurochemistry, ISSN 0022-3042, 05/2011, Volume 117, Issue 3, pp. 375 - 387
Journal Article
AMERICAN JOURNAL OF CLINICAL NUTRITION, ISSN 0002-9165, 11/2016, Volume 104, Issue 5, pp. 1459 - 1469
Background: Moderately high folic acid intake in pregnant women has led to concerns about deleterious effects on the mother and fetus. Common polymorphisms in... 
high folate | NEURAL-TUBE DEFECTS | embryo | POLYMORPHISM | birth defects | METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY | CHOLINE METABOLISM | S-ADENOSYLMETHIONINE | methylenetetrahydrofolate reductase | PREGNANT CANADIAN WOMEN | NUTRITION & DIETETICS | PLASMA | developmental defects | MTHFD1 | placenta | GENETIC RISK-FACTOR | LOW DIETARY-FOLATE | folic acid | FORTIFICATION | S-Adenosylhomocysteine - metabolism | Folic Acid - pharmacology | Methylenetetrahydrofolate Dehydrogenase (NADP) - deficiency | Aminohydrolases - deficiency | Multienzyme Complexes - metabolism | Methylenetetrahydrofolate Reductase (NADPH2) - metabolism | Aminohydrolases - genetics | Multienzyme Complexes - deficiency | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Female | Embryo, Mammalian - enzymology | Methylenetetrahydrofolate Dehydrogenase (NADP) - genetics | Methylenetetrahydrofolate Dehydrogenase (NADP) - metabolism | Formate-Tetrahydrofolate Ligase - deficiency | Logistic Models | Mice, Transgenic | Placenta - abnormalities | Placenta - enzymology | Multienzyme Complexes - genetics | Pregnancy | Formate-Tetrahydrofolate Ligase - metabolism | Animals | Choline - pharmacology | Formate-Tetrahydrofolate Ligase - genetics | Aminohydrolases - metabolism | Mice | Polymorphism, Single Nucleotide | Embryonic Development - drug effects | Dietary Supplements | S-Adenosylmethionine - metabolism | Ligases | Genetic variation | Pregnancy, Complications of | Development and progression | Genetic aspects | Health aspects | Folic acid
Journal Article
American Journal of Physiology - Endocrinology And Metabolism, ISSN 0193-1849, 01/2010, Volume 298, Issue 1, pp. 49 - 58
Insulin resistance in skeletal muscle in obesity and T2DM is associated with reduced muscle oxidative capacity, reduced expression in nuclear genes responsible... 
β-oxidation | Insulin resistance | Cardiolipin | Trichloroacetic acid cycle | Reduced nicotinamide adenine dinucleotide/nicotinamide adenine dinucleotide ratio | RESPIRATORY-CHAIN | PHYSIOLOGY | PHOSPHORYLATION | trichloroacetic acid cycle | WEIGHT-LOSS | cardiolipin | EXERCISE | reduced nicotinamide adenine dinucleotide/nicotinamide adenine dinucleotide ratio | FAT OXIDATION | BIOGENESIS | beta-oxidation | MALONYL-COA | INSULIN-RESISTANCE | ENDOCRINOLOGY & METABOLISM | PHYSICAL-ACTIVITY | ENERGY-METABOLISM | insulin resistance | Mitochondria - enzymology | DNA, Mitochondrial - metabolism | Humans | Middle Aged | 3-Hydroxyacyl CoA Dehydrogenases - metabolism | Oxidative Phosphorylation | Multienzyme Complexes - metabolism | Cardiolipins - metabolism | Diabetes Mellitus, Type 2 - metabolism | Mitochondria - pathology | Trichloroacetic Acid - metabolism | Obesity - metabolism | Biopsy | Insulin Resistance - physiology | Adult | Citrate (si)-Synthase - metabolism | Electron Transport - physiology | Blood Glucose - metabolism | NADH, NADPH Oxidoreductases - metabolism | Quadriceps Muscle - metabolism | Quadriceps Muscle - pathology | Lipid Metabolism - physiology | NAD - metabolism | Type 2 diabetes | Physiological aspects | Muscles | Obesity | Genetic aspects | Electron transport | reduced nicotinamide adenine dinucleotide | nicotinamide adenine dinucleotide ratio
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 09/2012, Volume 21, Issue 18, pp. 3969 - 3983
Biallelic mutations in the gene encoding DHOdehase [dihydroorotate dehydrogenase (DHODH)], an enzyme required for de novo pyrimidine biosynthesis, have been... 
DIHYDROOROTATE-DEHYDROGENASE | GENE | PHOSPHORYLATION | CLONING | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | TERATOGENICITY | MUTATIONS | LEFLUNOMIDE | SYNDROME TYPE RODRIGUEZ | PRENATAL-DIAGNOSIS | ROBIN-SEQUENCE | Limb Deformities, Congenital - enzymology | Limb Buds - pathology | Limb Deformities, Congenital - genetics | Mandibulofacial Dysostosis - urine | Schizosaccharomyces - growth & development | Humans | Child, Preschool | Micrognathism - enzymology | Multienzyme Complexes - metabolism | Infant | Male | Mutation, Missense | Genetic Complementation Test | Embryo, Mammalian - metabolism | Oxidoreductases Acting on CH-CH Group Donors - deficiency | Schizosaccharomyces - genetics | Mandibulofacial Dysostosis - genetics | Reference Standards | Micrognathism - urine | DNA Mutational Analysis | Gene Expression Regulation, Developmental | Base Sequence | Limb Deformities, Congenital - urine | Mandibulofacial Dysostosis - enzymology | Orotate Phosphoribosyltransferase - metabolism | Female | Oxidoreductases Acting on CH-CH Group Donors - genetics | Abnormalities, Multiple - genetics | Orotidine-5'-Phosphate Decarboxylase - metabolism | Orotic Acid - analogs & derivatives | Embryo, Mammalian - pathology | Schizosaccharomyces pombe Proteins - genetics | Genetic Association Studies | Abnormalities, Multiple - urine | Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing) - metabolism | Micrognathism - genetics | Orotate Phosphoribosyltransferase - genetics | Multienzyme Complexes - genetics | Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing) - genetics | Oxidoreductases Acting on CH-CH Group Donors - metabolism | Orotidine-5'-Phosphate Decarboxylase - genetics | Animals | Limb Buds - metabolism | Pedigree | Abnormalities, Multiple - enzymology | Mice | Gas Chromatography-Mass Spectrometry - standards | Orotic Acid - urine | Complementation
Journal Article
Journal Article
Nature, ISSN 0028-0836, 07/2007, Volume 447, Issue 7147, pp. 1017 - 1020
AMP-activated protein kinase (AMPK, also known as SNF1A) has been primarily studied as a metabolic regulator that is activated in response to energy... 
CYTOKINESIS | MUTANTS | ROLES | DISC | MULTIDISCIPLINARY SCIENCES | LIGHT-CHAIN | MYOSIN-II | NONMUSCLE MYOSIN | Protein Kinases - metabolism | Cell Polarity | Protein-Serine-Threonine Kinases - deficiency | Phosphorylation | Protein Kinases - genetics | Mitosis | Humans | Multienzyme Complexes - metabolism | Male | Drosophila Proteins - metabolism | Drosophila melanogaster - genetics | AMP-Activated Protein Kinases | Multienzyme Complexes - deficiency | Female | Protein Kinases - deficiency | Protein-Serine-Threonine Kinases - metabolism | Cell Line | Drosophila melanogaster - cytology | Protein-Serine-Threonine Kinases - genetics | Multienzyme Complexes - genetics | Phenotype | Animals | Energy Metabolism | Drosophila Proteins - deficiency | Drosophila melanogaster - enzymology | Drosophila melanogaster - growth & development | Myosin Light Chains - metabolism | Drosophila Proteins - genetics | Physiological aspects | Usage | Cell physiology | Research | Protein kinases | Drosophila | Chemistry | Biochemistry | Cellular biology | Kinases | Proteins | Control | Deprivation | Polarity | Mathematical models | Activation energy | Drosophila Proteins | Multienzyme Complexes | Protein-Serine-Threonine Kinases | Biochemistry, Molecular Biology | Cellular Biology | Life Sciences | Protein Kinases | Myosin Light Chains | Drosophila melanogaster
Journal Article
Nature Reviews Cancer, ISSN 1474-175X, 03/2003, Volume 3, Issue 3, pp. 193 - 202
Mitochondrial defects have been associated with neurological disorders, as well as cancers. Two ubiquitously expressed mitochondrial enzymes - succinate... 
RESPIRATORY-CHAIN | GERM-LINE MUTATIONS | ONCOLOGY | LEIGH-SYNDROME | C-OXIDASE DEFICIENCY | HEREDITARY PARAGANGLIOMA | SACCHAROMYCES-CEREVISIAE | RENAL-CELL CANCER | DNA MUTATIONS | RET PROTOONCOGENE | COMPLEX-I DEFICIENCY | Mitochondria - enzymology | Protein Subunits | Kidney Neoplasms - genetics | Humans | Mitochondrial Encephalomyopathies - enzymology | Carcinoma, Renal Cell - genetics | Pheochromocytoma - enzymology | Apoptosis - genetics | Oxidoreductases - physiology | Fumarate Hydratase - deficiency | Electron Transport Complex II | Multienzyme Complexes - deficiency | Carcinoma, Renal Cell - enzymology | Neoplastic Syndromes, Hereditary - genetics | Oxidoreductases - deficiency | Paraganglioma - enzymology | Free Radicals | Neovascularization, Physiologic - genetics | Oxidoreductases - genetics | Paraganglioma - genetics | Fumarate Hydratase - physiology | Mitochondrial Encephalomyopathies - genetics | Multienzyme Complexes - genetics | Fumarate Hydratase - genetics | Forecasting | Succinate Dehydrogenase - deficiency | Homozygote | Neovascularization, Physiologic - physiology | Citric Acid Cycle - genetics | Succinate Dehydrogenase - genetics | Energy Metabolism | Kidney Neoplasms - enzymology | Multienzyme Complexes - physiology | Neoplastic Syndromes, Hereditary - enzymology | Heterozygote | Pheochromocytoma - genetics | Apoptosis - physiology | Mutation | Succinate Dehydrogenase - physiology | Leiomyomatosis - enzymology | Leiomyomatosis - genetics | Enzymes | Mitochondria | Gene mutations | Physiological aspects | Genetic aspects | Research | Health aspects | Cancer
Journal Article
Essays in Biochemistry, ISSN 0071-1365, 07/2018, Volume 62, Issue 3, pp. 271 - 286
Journal Article