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TARA >
Browsing by Author SCOTT, JOHN MARTIN
Showing results 9 to 28 of 35
| Preview | Issue Date | Title | Author(s) | | 2007 | Effect of a voluntary food fortification policy on folate, related B vitamin status, and homocysteine in healthy adults. | MOLLOY, ANNE MARIE; SCOTT, JOHN MARTIN |
| 2007 | Evidence of unmetabolised folic acid in cord blood of newborn and serum of 4-day-old infants | MCPARTLIN, JOSEPH; SCOTT, JOHN MARTIN; WEIR, DONALD |
| 2004 | Facts and recommendations about total homocysteine determinations: an expert opinion | MCPARTLIN, JOSEPH; SCOTT, JOHN MARTIN |
| 2009 | Folate/homocysteine phenotypes and MTHFR 677C>T genotypes are associated with serum levels of monocyte chemoattractant protein-1. | SCOTT, JOHN MARTIN |
| 2007 | Folic acid fortification and public health: report on threshold doses above which unmetabolised folic acid appear in serum | MOLLOY, ANNE MARIE; SCOTT, JOHN MARTIN; MC PARTLIN, JOSEPH |
| 2003 | Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults | MCPARTLIN, JOSEPH; SCOTT, JOHN MARTIN |
| 2003 | Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults | SCOTT, JOHN MARTIN |
| 2008 | Homocysteine concentration, related B vitamins, and betaine in pregnant women recruited to the Seychelles Child Development Study. | MOLLOY, ANNE MARIE; SCOTT, JOHN MARTIN |
| 1999 | Homocysteine, folate enzymes and neural tube defects | SCOTT, JOHN MARTIN; MOLLOY, ANNE MARIE |
| 2004 | Impact of the MTHFR C677T polymorphism on risk of neural tube defects:case-control study | MOLLOY, ANNE MARIE; SCOTT, JOHN MARTIN |
| 2002 | Impaired functioning of thermolabile methylenetetrahydrofolate reductase is dependent on riboflavin status: implications for riboflavin requirements | MCPARTLIN, JOSEPH; SCOTT, JOHN MARTIN |
| 2009 | Lack of Association between Folate-Receptor Autoantibodies and Neural-Tube Defects | MOLLOY, ANNE MARIE; SCOTT, JOHN MARTIN |
| 2004 | Maternal homocysteine before conception and throughout pregnancy predicts fetal homocysteine and birth weight. | MOLLOY, ANNE MARIE; SCOTT, JOHN MARTIN |
| 2009 | Maternal vitamin B12 status and risk of neural tube defects in a population with high neural tube defect prevalence and no folic Acid fortification | MOLLOY, ANNE MARIE; SCOTT, JOHN MARTIN |
| 2009 | Persistent circulating unmetabolised folic acid in a setting of liberal voluntary folic acid fortification. Implications for further mandatory fortification? | SCOTT, JOHN MARTIN |
| 2009 | Personalised nutrition Genetic variation and disease risk: new advances | SCOTT, JOHN MARTIN |
| 2005 | A polymorphism in the MTHFD1 gene increases a mother's risk of having an unexplained second trimester pregnancy loss. | MOLLOY, ANNE MARIE; SCOTT, JOHN MARTIN |
| 2002 | A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth Defects Research Group | MOLLOY, ANNE MARIE; SCOTT, JOHN MARTIN |
| 2002 | The pregnancy-related decrease in fasting plasma homocysteine is not explained by folic acid supplementation, hemodilution, or a decrease in albumin in a longitudinal study | MCPARTLIN, JOSEPH; SCOTT, JOHN MARTIN |
| 2009 | The reduced folate carrier (SLC19A1) c.80G>A polymorphism is associated with red cell folate concentrations among women. | SCOTT, JOHN MARTIN |
Showing results 9 to 28 of 35
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