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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 aciduria
C 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 Deficiency
Renata 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 Manner
Daniel 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 mice
Basak 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 reductase
C 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 Steatosis
Karen 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 Liver
Daniel 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 paraplegia
Alexander Lossos, Omri Teltsh, Tsipi Milman, et al.
Nature Genetics
|
November 29, 2005
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type
Jordan P Lerner-Ellis, Jamie C Tirone, Peter D Pawelek, et al.
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of 4
Search research articles
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Showing results (31-40 of 39) with videos related to
Sort By:
Page
of 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 aciduria
C 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 Deficiency
Renata 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 Manner
Daniel 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 mice
Basak 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 reductase
C 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 Steatosis
Karen 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 Liver
Daniel 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 paraplegia
Alexander Lossos, Omri Teltsh, Tsipi Milman, et al.
Nature Genetics
|
November 29, 2005
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type
Jordan P Lerner-Ellis, Jamie C Tirone, Peter D Pawelek, et al.
Page
of 4