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Daniel Leclerc

Showing results (31-40 of 39) with videos related to

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Molecular Genetics and Metabolism|May 16, 2006
Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduriaC Melissa Dobson, Abigail Gradinger, Nicola Longo, et al.
Molecular Neurobiology|October 6, 2018
Early Manifestations of Brain Aging in Mice Due to Low Dietary Folate and Mild MTHFR DeficiencyRenata H Bahous, Marta Cosín-Tomás, Liyuan Deng, et al.
Molecular Nutrition & Food Research|February 8, 2024
Folate Deficiency and/or the Genetic Variant Mthfr<sup>677C >T</sup> Can Drive Hepatic Fibrosis or Steatosis in Mice, in a Sex-Specific MannerDaniel Leclerc, Karen E Christensen, Alaina M Reagan, et al.
Pharmacogenetics and Genomics|June 14, 2008
Altered expression of methylenetetrahydrofolate reductase modifies response to methotrexate in miceBasak Celtikci, Daniel Leclerc, Andrea K Lawrance, et al.
Molecular Genetics and Metabolism|March 21, 2007
Metabolic derangement of methionine and folate metabolism in mice deficient in methionine synthase reductaseC Lee Elmore, Xuchu Wu, Daniel Leclerc, et al.
Nutrients|January 11, 2025
Folic Acid and Methyltetrahydrofolate Supplementation in the <i>Mthfr</i> Mouse Model with Hepatic SteatosisKaren E Christensen, Marie-Lou Faquette, Daniel Leclerc, et al.
Molecular Nutrition & Food Research|November 9, 2018
Mild Methylenetetrahydrofolate Reductase Deficiency Alters Inflammatory and Lipid Pathways in LiverDaniel Leclerc, Karen E Christensen, Olivia Cauvi, et al.
JAMA Neurology|May 7, 2014
Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegiaAlexander Lossos, Omri Teltsh, Tsipi Milman, et al.
Nature Genetics|November 29, 2005
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC typeJordan P Lerner-Ellis, Jamie C Tirone, Peter D Pawelek, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Molecular Genetics and Metabolism|May 16, 2006
Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduriaC Melissa Dobson, Abigail Gradinger, Nicola Longo, et al.
Molecular Neurobiology|October 6, 2018
Early Manifestations of Brain Aging in Mice Due to Low Dietary Folate and Mild MTHFR DeficiencyRenata H Bahous, Marta Cosín-Tomás, Liyuan Deng, et al.
Molecular Nutrition & Food Research|February 8, 2024
Folate Deficiency and/or the Genetic Variant Mthfr<sup>677C >T</sup> Can Drive Hepatic Fibrosis or Steatosis in Mice, in a Sex-Specific MannerDaniel Leclerc, Karen E Christensen, Alaina M Reagan, et al.
Pharmacogenetics and Genomics|June 14, 2008
Altered expression of methylenetetrahydrofolate reductase modifies response to methotrexate in miceBasak Celtikci, Daniel Leclerc, Andrea K Lawrance, et al.
Molecular Genetics and Metabolism|March 21, 2007
Metabolic derangement of methionine and folate metabolism in mice deficient in methionine synthase reductaseC Lee Elmore, Xuchu Wu, Daniel Leclerc, et al.
Nutrients|January 11, 2025
Folic Acid and Methyltetrahydrofolate Supplementation in the <i>Mthfr</i> Mouse Model with Hepatic SteatosisKaren E Christensen, Marie-Lou Faquette, Daniel Leclerc, et al.
Molecular Nutrition & Food Research|November 9, 2018
Mild Methylenetetrahydrofolate Reductase Deficiency Alters Inflammatory and Lipid Pathways in LiverDaniel Leclerc, Karen E Christensen, Olivia Cauvi, et al.
JAMA Neurology|May 7, 2014
Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegiaAlexander Lossos, Omri Teltsh, Tsipi Milman, et al.
Nature Genetics|November 29, 2005
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC typeJordan P Lerner-Ellis, Jamie C Tirone, Peter D Pawelek, et al.
Pageof 4