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Jerry Vockley

Showing results (181-190 of 294) with videos related to

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Molecular Genetics and Metabolism|April 10, 2018
Pegvaliase for the treatment of phenylketonuria: A pivotal, double-blind randomized discontinuation Phase 3 clinical trialCary O Harding, R Stephen Amato, Mary Stuy, et al.
Medrxiv : the Preprint Server for Health Sciences|April 29, 2025
Rapid Genome Sequencing Compared to a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic EvaluationTara A Lavelle, Jill L Maron, Stephen F Kingsmore, et al.
The Journal of Biological Chemistry|August 16, 2015
c-Myc programs fatty acid metabolism and dictates acetyl-CoA abundance and fateLia R Edmunds, Lokendra Sharma, Audry Kang, et al.
Journal of Inherited Metabolic Disease|September 4, 2020
The mitochondrial-targeted reactive species scavenger JP4-039 prevents sulfite-induced alterations in antioxidant defenses, energy transfer, and cell death signaling in striatum of ratsNícolas Manzke Glänzel, Mateus Grings, Nevton Teixeira da Rosa-Junior, et al.
The Journal of Biological Chemistry|July 24, 2014
c-Myc programs fatty acid metabolism and dictates acetyl-CoA abundance and fateLia R Edmunds, Lokendra Sharma, Audry Kang, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|May 6, 2025
Metformin restores mitochondrial bioenergetics and redox homeostasis through modulation of mitochondrial biogenesis and dynamics in patient derived cultured fibroblasts and an animal model of molybdenum cofactor deficiencyMorgana Brondani, Rafael T Ribeiro, Camila V Pinheiro, et al.
The Journal of Pediatrics|November 2, 2025
Rapid Genome Sequencing Compared with a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic EvaluationTara A Lavelle, Jill L Maron, Stephen F Kingsmore, et al.
Clinical & Translational Immunology|July 1, 2021
Pervasive inflammatory activation in patients with deficiency in very-long-chain acyl-coA dehydrogenase (VLCADD)Abbe N Vallejo, Henry J Mroczkowski, Joshua J Michel, et al.
Molecular Genetics and Metabolism|August 2, 2016
221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism CollaborativeKristi Bentler, Shaohui Zhai, Sara A Elsbecker, et al.
Biorxiv : the Preprint Server for Biology|July 28, 2023
Loss of the mitochondrial carrier, <i>SLC25A1,</i> during embryogenesis induces a unique senescence program controlled by p53Anna Kasprzyk-Pawelec, Mingjun Tan, Raneen Rahhal, et al.
Pageof 30

Showing results (181-190 of 294) with videos related to

Sort By:
Pageof 30
Molecular Genetics and Metabolism|April 10, 2018
Pegvaliase for the treatment of phenylketonuria: A pivotal, double-blind randomized discontinuation Phase 3 clinical trialCary O Harding, R Stephen Amato, Mary Stuy, et al.
Medrxiv : the Preprint Server for Health Sciences|April 29, 2025
Rapid Genome Sequencing Compared to a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic EvaluationTara A Lavelle, Jill L Maron, Stephen F Kingsmore, et al.
The Journal of Biological Chemistry|August 16, 2015
c-Myc programs fatty acid metabolism and dictates acetyl-CoA abundance and fateLia R Edmunds, Lokendra Sharma, Audry Kang, et al.
Journal of Inherited Metabolic Disease|September 4, 2020
The mitochondrial-targeted reactive species scavenger JP4-039 prevents sulfite-induced alterations in antioxidant defenses, energy transfer, and cell death signaling in striatum of ratsNícolas Manzke Glänzel, Mateus Grings, Nevton Teixeira da Rosa-Junior, et al.
The Journal of Biological Chemistry|July 24, 2014
c-Myc programs fatty acid metabolism and dictates acetyl-CoA abundance and fateLia R Edmunds, Lokendra Sharma, Audry Kang, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|May 6, 2025
Metformin restores mitochondrial bioenergetics and redox homeostasis through modulation of mitochondrial biogenesis and dynamics in patient derived cultured fibroblasts and an animal model of molybdenum cofactor deficiencyMorgana Brondani, Rafael T Ribeiro, Camila V Pinheiro, et al.
The Journal of Pediatrics|November 2, 2025
Rapid Genome Sequencing Compared with a Gene Panel in Critically Ill Infants with a Suspected Genetic Disorder: An Economic EvaluationTara A Lavelle, Jill L Maron, Stephen F Kingsmore, et al.
Clinical & Translational Immunology|July 1, 2021
Pervasive inflammatory activation in patients with deficiency in very-long-chain acyl-coA dehydrogenase (VLCADD)Abbe N Vallejo, Henry J Mroczkowski, Joshua J Michel, et al.
Molecular Genetics and Metabolism|August 2, 2016
221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism CollaborativeKristi Bentler, Shaohui Zhai, Sara A Elsbecker, et al.
Biorxiv : the Preprint Server for Biology|July 28, 2023
Loss of the mitochondrial carrier, <i>SLC25A1,</i> during embryogenesis induces a unique senescence program controlled by p53Anna Kasprzyk-Pawelec, Mingjun Tan, Raneen Rahhal, et al.
Pageof 30