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John M Scott

Showing results (71-80 of 100) with videos related to

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The American Journal of Clinical Nutrition|September 28, 2004
Determining bioavailability of food folates in a controlled intervention studyMary P Hannon-Fletcher, Nicola C Armstrong, John M Scott, et al.
American Journal of Medical Genetics. Part A|May 9, 2007
The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish populationAnne Parle-McDermott, Faith Pangilinan, James L Mills, et al.
American Journal of Medical Genetics. Part A|September 18, 2008
Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish populationFaith Pangilinan, Kerry Geiler, Jessica Dolle, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Association between the NAT1 1095C > A polymorphism and homocysteine concentrationAnna Stanisławska-Sachadyn, Liselotte E Jensen, Carmel Kealey, et al.
Clinical Immunology (Orlando, Fla.)|July 24, 2009
Folate/homocysteine phenotypes and MTHFR 677C>T genotypes are associated with serum levels of monocyte chemoattractant protein-1Andrea L Hammons, Carolyn M Summers, Jayne V Woodside, et al.
The Journal of Nutrition|January 29, 2016
Evidence from a Randomized Trial That Exposure to Supplemental Folic Acid at Recommended Levels during Pregnancy Does Not Lead to Increased Unmetabolized Folic Acid Concentrations in Maternal or Cord BloodKristina Pentieva, Jacob Selhub, Ligi Paul, et al.
Molecular Genetics and Metabolism|January 9, 2008
Evidence for sex differences in the determinants of homocysteine concentrationsAnna Stanisławska-Sachadyn, Jayne V Woodside, Karen S Brown, et al.
Human Genetics|February 6, 2008
An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in womenAnna Stanisławska-Sachadyn, Karen S Brown, Laura E Mitchell, et al.
American Journal of Human Genetics|October 18, 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 GroupLawrence C Brody, Mary Conley, Christopher Cox, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study populationTonia C Carter, Faith Pangilinan, James F Troendle, et al.
Pageof 10

Showing results (71-80 of 100) with videos related to

Sort By:
Pageof 10
The American Journal of Clinical Nutrition|September 28, 2004
Determining bioavailability of food folates in a controlled intervention studyMary P Hannon-Fletcher, Nicola C Armstrong, John M Scott, et al.
American Journal of Medical Genetics. Part A|May 9, 2007
The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish populationAnne Parle-McDermott, Faith Pangilinan, James L Mills, et al.
American Journal of Medical Genetics. Part A|September 18, 2008
Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish populationFaith Pangilinan, Kerry Geiler, Jessica Dolle, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Association between the NAT1 1095C > A polymorphism and homocysteine concentrationAnna Stanisławska-Sachadyn, Liselotte E Jensen, Carmel Kealey, et al.
Clinical Immunology (Orlando, Fla.)|July 24, 2009
Folate/homocysteine phenotypes and MTHFR 677C>T genotypes are associated with serum levels of monocyte chemoattractant protein-1Andrea L Hammons, Carolyn M Summers, Jayne V Woodside, et al.
The Journal of Nutrition|January 29, 2016
Evidence from a Randomized Trial That Exposure to Supplemental Folic Acid at Recommended Levels during Pregnancy Does Not Lead to Increased Unmetabolized Folic Acid Concentrations in Maternal or Cord BloodKristina Pentieva, Jacob Selhub, Ligi Paul, et al.
Molecular Genetics and Metabolism|January 9, 2008
Evidence for sex differences in the determinants of homocysteine concentrationsAnna Stanisławska-Sachadyn, Jayne V Woodside, Karen S Brown, et al.
Human Genetics|February 6, 2008
An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in womenAnna Stanisławska-Sachadyn, Karen S Brown, Laura E Mitchell, et al.
American Journal of Human Genetics|October 18, 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 GroupLawrence C Brody, Mary Conley, Christopher Cox, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study populationTonia C Carter, Faith Pangilinan, James F Troendle, et al.
Pageof 10