Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida - Wikidata - thesis-toulmin - TriplyDB

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida

http://www.wikidata.org/entity/Q24632031

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Metabolic derangement of methionine and folate metabolism in mice deficient in methionine synthase reductase Maternal genetic mutations as gestational and early life influences in producing psychiatric disease-like phenotypes in mice.118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects Genome-wide association study of maternal and inherited loci for conotruncal heart defects.Evaluation of potential modifiers of the palatal phenotype in the 22q11.2 deletion syndrome.Genetic and lifestyle variables associated with homocysteine concentrations and the distribution of folate derivatives in healthy premenopausal women.Maternal genome-wide DNA methylation patterns and congenital heart defects.Variants of folate metabolism genes and risk of left-sided cardiac defects.Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defects.A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism Variants of folate metabolism genes and the risk of conotruncal cardiac defects.An integrative computational approach for prioritization of genomic variants Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations An epidemiologic study of mitochondrial membrane transporter protein gene polymorphism and risk factors for neural tube defects in Shanxi, China.Folic acid and human reproduction-ten important issues for clinicians Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population Approaches for the identification of genetic modifiers of nutrient dependent phenotypes: examples from folate.Polymorphic variants of genes involved in homocysteine metabolism in celiac disease.Incidence and Risk Factors of Neural Tube Defects in Kashan, Central Iran Proteomic Analysis of One-carbon Metabolism-related Marker in Liver of Rat Offspring.Genetic variation in genes of folate metabolism and neural-tube defect risk.Acquired and inherited disorders of cobalamin and folate in children.A Three-Way Interaction among Maternal and Fetal Variants Contributing to Congenital Heart Defects.Polymorphisms in 1-carbon metabolism, epigenetics and folate-related pathologies.Vitamin B(12) metabolism during pregnancy and in embryonic mouse models.Neural tube defects, folic acid and methylation Gene-nutrient interactions: importance of folic acid and vitamin B12 during early embryogenesis.The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.Pharmacogenetics of drug-induced birth defects: what is known so far?Genetic defects in folate and cobalamin pathways affecting the brain.Folate and epigenetic mechanisms in neural tube development and defects.Multiple sclerosis-like diagnosis as a complication of previously treated malaria in an iron and vitamin D deficient Nigerian patient.Nicotinamide N-methyl transferase (NNMT) gene polymorphisms and risk for spina bifida.Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene.Anencephaly-exencephaly sequence and congenital diaphragmatic hernia in a fetus with 46, XX karyotype: Early prenatal diagnosis, necropsy, and maternal folate pathway genetic analysis.Relationship between methionine synthase, methionine synthase reductase genetic polymorphisms and deep vein thrombosis among South Indians.Association between 5,10-methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and conotruncal heart defects.Genome-wide detection and characterization of mating asymmetry in human populations.Neural tube closure depends on nitric oxide synthase activity.Occurrence of fetal choroid plexus cysts in siblings.

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Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida

http://www.wikidata.org/entity/Q24632031

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2002 nî lūn-bûn

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2002 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2002 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2002年の論文

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Maternal genetic effects, exer ...... uence the risk of spina bifida

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Maternal genetic effects, exer ...... uence the risk of spina bifida

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Maternal genetic effects, exer ...... uence the risk of spina bifida

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Maternal genetic effects, exer ...... uence the risk of spina bifida

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Maternal genetic effects, exer ...... uence the risk of spina bifida

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Maternal genetic effects, exer ...... uence the risk of spina bifida

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Maternal genetic effects, exer ...... uence the risk of spina bifida

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Maternal genetic effects, exer ...... uence the risk of spina bifida

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Maternal genetic effects, exer ...... uence the risk of spina bifida

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American Journal of Human Genetics

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Maternal genetic effects, exer ...... uence the risk of spina bifida

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Alexander S Whitehead

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Katy Hoess

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Laura E Mitchell

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Maeve McDonnell

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Marie-Therese Doolin

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P2860

The transmission/disequilibrium test: history, subdivision, and admixture

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

The TDT and other family-based tests for linkage disequilibrium and association

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations

A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting.

Allowing for missing parents in genetic studies of case-parent triads

A note on the application of the transmission disequilibrium test when a parent is missing.

Methionine synthase and neural tube defects

Testing for linkage disequilibrium, maternal effects, and imprinting with (In)complete case-parent triads, by use of the computer program LEM.

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10.1086/344209

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