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Faith Pangilinan

Showing results (1-10 of 49) with videos related to

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Annual Review of Nutrition|June 20, 2017
Genetic Risk Factors for Folate-Responsive Neural Tube DefectsAnne M Molloy, Faith Pangilinan, Lawrence C Brody
Communications Biology|November 19, 2022
Mito-SiPE is a sequence-independent and PCR-free mtDNA enrichment method for accurate ultra-deep mitochondrial sequencingDarren J Walsh, David J Bernard, Faith Pangilinan, et al.
European Journal of Clinical Investigation|March 9, 2016
Association of a transcobalamin II genetic variant with falsely low results for the holotranscobalamin immunoassayAgata Sobczyńska-Malefora, Faith Pangilinan, Gordon T Plant, et al.
Molecular Genetics and Metabolism Reports|July 11, 2018
The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolitesJessica O'Reilly, Faith Pangilinan, Karsten Hokamp, et al.
BMC Medical Genetics|April 24, 2012
Genotyping of a tri-allelic polymorphism by a novel melting curve assay in MTHFD1L: an association study of nonsyndromic Cleft in IrelandStefano Minguzzi, Anne M Molloy, Kirke Peadar, et al.
Molecular Genetics and Metabolism Reports|October 24, 2019
Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsyRemi Stevelink, Faith Pangilinan, Floor E Jansen, et al.
American Journal of Medical Genetics. Part A|June 7, 2005
Folate-related genes and omphaloceleJames L Mills, Charlotte M Druschel, Faith Pangilinan, et al.
Biological Research for Nursing|February 7, 2015
Association of Transcobalamin II (TCN2) and Transcobalamin II-Receptor (TCblR) Genetic Variations With Cobalamin Deficiency Parameters in Elderly WomenEmma L Kurnat-Thoma, Faith Pangilinan, Amy M Matteini, et al.
Human Genetics|January 9, 2009
Analysis of the MTHFD1 promoter and risk of neural tube defectsNicola Carroll, Faith Pangilinan, Anne M Molloy, et al.
PNAS Nexus|April 1, 2024
Vitamin B12 status and folic acid supplementation influence mitochondrial heteroplasmy levels in miceDarren J Walsh, David J Bernard, Joanna L Fiddler, et al.
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
Annual Review of Nutrition|June 20, 2017
Genetic Risk Factors for Folate-Responsive Neural Tube DefectsAnne M Molloy, Faith Pangilinan, Lawrence C Brody
Communications Biology|November 19, 2022
Mito-SiPE is a sequence-independent and PCR-free mtDNA enrichment method for accurate ultra-deep mitochondrial sequencingDarren J Walsh, David J Bernard, Faith Pangilinan, et al.
European Journal of Clinical Investigation|March 9, 2016
Association of a transcobalamin II genetic variant with falsely low results for the holotranscobalamin immunoassayAgata Sobczyńska-Malefora, Faith Pangilinan, Gordon T Plant, et al.
Molecular Genetics and Metabolism Reports|July 11, 2018
The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolitesJessica O'Reilly, Faith Pangilinan, Karsten Hokamp, et al.
BMC Medical Genetics|April 24, 2012
Genotyping of a tri-allelic polymorphism by a novel melting curve assay in MTHFD1L: an association study of nonsyndromic Cleft in IrelandStefano Minguzzi, Anne M Molloy, Kirke Peadar, et al.
Molecular Genetics and Metabolism Reports|October 24, 2019
Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsyRemi Stevelink, Faith Pangilinan, Floor E Jansen, et al.
American Journal of Medical Genetics. Part A|June 7, 2005
Folate-related genes and omphaloceleJames L Mills, Charlotte M Druschel, Faith Pangilinan, et al.
Biological Research for Nursing|February 7, 2015
Association of Transcobalamin II (TCN2) and Transcobalamin II-Receptor (TCblR) Genetic Variations With Cobalamin Deficiency Parameters in Elderly WomenEmma L Kurnat-Thoma, Faith Pangilinan, Amy M Matteini, et al.
Human Genetics|January 9, 2009
Analysis of the MTHFD1 promoter and risk of neural tube defectsNicola Carroll, Faith Pangilinan, Anne M Molloy, et al.
PNAS Nexus|April 1, 2024
Vitamin B12 status and folic acid supplementation influence mitochondrial heteroplasmy levels in miceDarren J Walsh, David J Bernard, Joanna L Fiddler, et al.
Pageof 5