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Showing results (221-230 of 226) with videos related to

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The Journal of Biological Chemistry|January 18, 2024
Restoration of the ER stress response protein TDAG51 in hepatocytes mitigates NAFLD in miceTamana R Yousof, Celeste C Bouchard, Mihnea Alb, et al.
Journal of the American Heart Association|May 21, 2013
Deficiency of TDAG51 protects against atherosclerosis by modulating apoptosis, cholesterol efflux, and peroxiredoxin-1 expressionGazi S Hossain, Edward G Lynn, Kenneth N Maclean, et al.
Journal of Inherited Metabolic Disease|March 12, 2020
Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh diseaseMarisa W Friederich, Abdallah F Elias, Alice Kuster, et al.
Journal of Inherited Metabolic Disease|March 16, 2019
Biomarkers of oxidative stress, inflammation, and vascular dysfunction in inherited cystathionine β-synthase deficient homocystinuria and the impact of taurine treatment in a phase 1/2 human clinical trialJohan L K Van Hove, Cynthia L Freehauf, Can Ficicioglu, et al.
Journal of Inherited Metabolic Disease|January 28, 2026
A Nonketotic Hyperglycinemia Mouse Shows Wide-Ranging Biochemical Consequences of Elevated Glycine, Reduced Folate One-Carbon Charging, and Serine DeficiencyMichael A Swanson, Hua Jiang, Lakshmi Divya Kolora, et al.
Brain : a Journal of Neurology|December 17, 2013
Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5Peter R Baker, Marisa W Friederich, Michael A Swanson, et al.
Pageof 23

Showing results (221-230 of 226) with videos related to

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Pageof 23
You have reached the last page of results.This site can display upto 226 results.
The Journal of Biological Chemistry|January 18, 2024
Restoration of the ER stress response protein TDAG51 in hepatocytes mitigates NAFLD in miceTamana R Yousof, Celeste C Bouchard, Mihnea Alb, et al.
Journal of the American Heart Association|May 21, 2013
Deficiency of TDAG51 protects against atherosclerosis by modulating apoptosis, cholesterol efflux, and peroxiredoxin-1 expressionGazi S Hossain, Edward G Lynn, Kenneth N Maclean, et al.
Journal of Inherited Metabolic Disease|March 12, 2020
Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh diseaseMarisa W Friederich, Abdallah F Elias, Alice Kuster, et al.
Journal of Inherited Metabolic Disease|March 16, 2019
Biomarkers of oxidative stress, inflammation, and vascular dysfunction in inherited cystathionine β-synthase deficient homocystinuria and the impact of taurine treatment in a phase 1/2 human clinical trialJohan L K Van Hove, Cynthia L Freehauf, Can Ficicioglu, et al.
Journal of Inherited Metabolic Disease|January 28, 2026
A Nonketotic Hyperglycinemia Mouse Shows Wide-Ranging Biochemical Consequences of Elevated Glycine, Reduced Folate One-Carbon Charging, and Serine DeficiencyMichael A Swanson, Hua Jiang, Lakshmi Divya Kolora, et al.
Brain : a Journal of Neurology|December 17, 2013
Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5Peter R Baker, Marisa W Friederich, Michael A Swanson, et al.
Pageof 23