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E C Smith

Showing results (181-190 of 232) with videos related to

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American Journal of Physiology. Renal Physiology|July 24, 2004
Homocysteine clearance and methylation flux rates in health and end-stage renal disease: association with S-adenosylhomocysteineFrank Stam, Coen van Guldener, Piet M ter Wee, et al.
The Journal of Nutritional Biochemistry|April 10, 2007
Red blood cell folate vitamer distribution in healthy subjects is determined by the methylenetetrahydrofolate reductase C677T polymorphism and by the total folate statusYvo M Smulders, Desiree E C Smith, Robert M Kok, et al.
Biochimica Et Biophysica Acta|February 25, 2014
Post-transcriptional regulation of the creatine transporter gene: functional relevance of alternative splicingJoseph D T Ndika, Cristina Martinez-Munoz, Nandaja Anand, et al.
JIMD Reports|March 6, 2024
5,10-methenyltetrahydrofolate synthetase deficiency: An extreme rare defect of folate metabolism in two Dutch siblingsLelde Liepina, Desiree E C Smith, Hidde Huidekoper, et al.
Essays in Biochemistry|April 19, 2024
Sulfate: a neglected (but potentially highly relevant) anionEmil den Bakker, Desiree E C Smith, Martijn J J Finken, et al.
European Journal of Clinical Nutrition|September 10, 2005
[6S]5-methyltetrahydrofolate or folic acid supplementation and absorption and initial elimination of folate in young and middle-aged adultsK de Meer, Y M Smulders, J R Dainty, et al.
Analytical Biochemistry|March 9, 2004
5-Methyltetrahydrofolic acid and folic acid measured in plasma with liquid chromatography tandem mass spectrometry: applications to folate absorption and metabolismR M Kok, D E C Smith, J R Dainty, et al.
Molecular Genetics & Genomic Medicine|February 18, 2025
Loss-of-Function CARS1 Variants in a Patient With Microcephaly, Developmental Delay, and a Brittle Hair PhenotypeChristina Del Greco, Molly E Kuo, Desiree E C Smith, et al.
Connective Tissue Research|January 1, 1990
Changes in vascular extracellular matrix accumulation reflect phenotypic differences between the arterial wall of pigeons resistant and susceptible to the development of spontaneous atherosclerosisH S Park, A C Kniep, S C Smith, et al.
Clinical Genetics|December 14, 2020
Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterizationElisabetta Tabolacci, Clelia Molinario, Giuseppe Marangi, et al.
Pageof 24

Showing results (181-190 of 232) with videos related to

Sort By:
Pageof 24
American Journal of Physiology. Renal Physiology|July 24, 2004
Homocysteine clearance and methylation flux rates in health and end-stage renal disease: association with S-adenosylhomocysteineFrank Stam, Coen van Guldener, Piet M ter Wee, et al.
The Journal of Nutritional Biochemistry|April 10, 2007
Red blood cell folate vitamer distribution in healthy subjects is determined by the methylenetetrahydrofolate reductase C677T polymorphism and by the total folate statusYvo M Smulders, Desiree E C Smith, Robert M Kok, et al.
Biochimica Et Biophysica Acta|February 25, 2014
Post-transcriptional regulation of the creatine transporter gene: functional relevance of alternative splicingJoseph D T Ndika, Cristina Martinez-Munoz, Nandaja Anand, et al.
JIMD Reports|March 6, 2024
5,10-methenyltetrahydrofolate synthetase deficiency: An extreme rare defect of folate metabolism in two Dutch siblingsLelde Liepina, Desiree E C Smith, Hidde Huidekoper, et al.
Essays in Biochemistry|April 19, 2024
Sulfate: a neglected (but potentially highly relevant) anionEmil den Bakker, Desiree E C Smith, Martijn J J Finken, et al.
European Journal of Clinical Nutrition|September 10, 2005
[6S]5-methyltetrahydrofolate or folic acid supplementation and absorption and initial elimination of folate in young and middle-aged adultsK de Meer, Y M Smulders, J R Dainty, et al.
Analytical Biochemistry|March 9, 2004
5-Methyltetrahydrofolic acid and folic acid measured in plasma with liquid chromatography tandem mass spectrometry: applications to folate absorption and metabolismR M Kok, D E C Smith, J R Dainty, et al.
Molecular Genetics & Genomic Medicine|February 18, 2025
Loss-of-Function CARS1 Variants in a Patient With Microcephaly, Developmental Delay, and a Brittle Hair PhenotypeChristina Del Greco, Molly E Kuo, Desiree E C Smith, et al.
Connective Tissue Research|January 1, 1990
Changes in vascular extracellular matrix accumulation reflect phenotypic differences between the arterial wall of pigeons resistant and susceptible to the development of spontaneous atherosclerosisH S Park, A C Kniep, S C Smith, et al.
Clinical Genetics|December 14, 2020
Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterizationElisabetta Tabolacci, Clelia Molinario, Giuseppe Marangi, et al.
Pageof 24