Pages that link to "Q57234841"
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The following pages link to Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects (Q57234841):
Displaying 50 items.
- Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studies (Q21089859) (← links)
- Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida (Q24632031) (← links)
- A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects (Q24632141) (← links)
- Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L (Q24632653) (← links)
- Methylenetetrahydrofolate reductase and transcobalamin genetic polymorphisms in human spontaneous abortion: biological and clinical implications (Q24799429) (← links)
- Methionine synthase (MTR) 2756 (A --> G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome (Q28202213) (← links)
- Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models (Q29547388) (← links)
- Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke (Q30414223) (← links)
- Maternal periconceptional folic acid intake and risk of autism spectrum disorders and developmental delay in the CHARGE (CHildhood Autism Risks from Genetics and Environment) case-control study (Q30515879) (← links)
- Domain duplication, divergence, and loss events in vertebrate Msx paralogs reveal phylogenomically informed disease markers (Q33401099) (← links)
- [6S]-5-methyltetrahydrofolate increases plasma folate more effectively than folic acid in women with the homozygous or wild-type 677C-->T polymorphism of methylenetetrahydrofolate reductase (Q33595354) (← links)
- Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome (Q33608633) (← links)
- Effect of including environmental data in investigations of gene-disease associations in the presence of qualitative interactions (Q33612514) (← links)
- Genetic and epigenetic contributions to human nutrition and health: managing genome-diet interactions (Q33647210) (← links)
- Neural tube defects, folate, and immune modulation (Q33739571) (← links)
- Genomic DNA methylation changes in response to folic acid supplementation in a population-based intervention study among women of reproductive age (Q34098137) (← links)
- Primary prevention of neural-tube defects and some other major congenital abnormalities: recommendations for the appropriate use of folic acid during pregnancy (Q34111808) (← links)
- A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism (Q34115389) (← links)
- Red blood cell folate as a risk factor for breast cancer among patients at a tertiary hospital in Uganda: a case control study (Q34136073) (← links)
- Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome (Q34142627) (← links)
- Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations (Q34144199) (← links)
- Biological and clinical implications of the MTHFR C677T polymorphism (Q34204929) (← links)
- MTHFR 677TT genotype and disease risk: is there a modulating role for B-vitamins? (Q34378098) (← links)
- Association between MTHFR polymorphisms and congenital heart disease: a meta-analysis based on 9,329 cases and 15,076 controls (Q34628733) (← links)
- Significant association of MTHFD1 1958G>A single nucleotide polymorphism with nonsyndromic cleft lip and palate in Indian population (Q34654198) (← links)
- Shmt1 and de novo thymidylate biosynthesis underlie folate-responsive neural tube defects in mice (Q34674474) (← links)
- Prenatal vitamins, one-carbon metabolism gene variants, and risk for autism (Q35049905) (← links)
- The prevention of congenital anomalies with periconceptional folic acid supplementation (Q35063481) (← links)
- Quantitative assessment of maternal biomarkers related to one-carbon metabolism and neural tube defects (Q35133992) (← links)
- Maternal dietary uridine causes, and deoxyuridine prevents, neural tube closure defects in a mouse model of folate-responsive neural tube defects (Q35239518) (← links)
- Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects (Q35311051) (← links)
- Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population (Q35445213) (← links)
- Approaches for the identification of genetic modifiers of nutrient dependent phenotypes: examples from folate (Q35596531) (← links)
- Dietary folate, but not choline, modifies neural tube defect risk in Shmt1 knockout mice (Q35615230) (← links)
- Insights into metabolic mechanisms underlying folate-responsive neural tube defects: a minireview (Q35619839) (← links)
- Sulfur containing amino acids and human disease (Q35636141) (← links)
- Neural tube defects between folate metabolism and genetics (Q35749281) (← links)
- Maternal Mthfd1 disruption impairs fetal growth but does not cause neural tube defects in mice (Q35826415) (← links)
- MTHFD1 gene polymorphisms as risk factors involved in orofacial cleft: an independent case-control study and a meta-analysis. (Q35870890) (← links)
- Detecting gene-environment interactions in human birth defects: Study designs and statistical methods (Q35957563) (← links)
- Maternal folate and vitamin b(12) status and neural tube defects in northern iran: a case control study (Q36244461) (← links)
- The role of pharmacogenetics in cancer therapeutics (Q36536674) (← links)
- Current perspectives on the genetic causes of neural tube defects (Q36581497) (← links)
- Various pharmacogenetic aspects of antiepileptic drug therapy: a review (Q36729620) (← links)
- Polymorphisms in 1-carbon metabolism, epigenetics and folate-related pathologies (Q36966016) (← links)
- Family-based association study between SLC2A1, HK1, and LEPR polymorphisms with myelomeningocele in Chile. (Q37154169) (← links)
- Syndromes, disorders and maternal risk factors associated with neural tube defects (IV). (Q37208056) (← links)
- Neural tube defects, folic acid and methylation (Q37236998) (← links)
- Mapping eQTLs in the Norfolk Island genetic isolate identifies candidate genes for CVD risk traits. (Q37368024) (← links)
- The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects. (Q37399043) (← links)