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Jerry Vockley

Showing results (91-100 of 293) with videos related to

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Journal of Inherited Metabolic Disease|February 26, 2022
Characterization of exonic variants of uncertain significance in very long-chain acyl-CoA dehydrogenase identified through newborn screeningOlivia M D'Annibale, Erik A Koppes, Meena Sethuraman, et al.
The Journal of Biological Chemistry|January 30, 2008
Structural basis for substrate fatty acyl chain specificity: crystal structure of human very-long-chain acyl-CoA dehydrogenaseRyan P McAndrew, Yudong Wang, Al-Walid Mohsen, et al.
Molecular Genetics and Metabolism Reports|November 17, 2022
Natural history of propionic acidemia in the Amish populationSarah Ehrenberg, Catherine Walsh Vockley, Paige Heiman, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|August 7, 2018
Liver Transplantation for Propionic Acidemia and Methylmalonic Acidemia: Perioperative Management and Clinical OutcomesKristen Critelli, Patrick McKiernan, Jerry Vockley, et al.
Neuromuscular Disorders : NMD|January 8, 2011
Novel mutation in MYH7 gene associated with distal myopathy and cardiomyopathyHouman Homayoun, Simin Khavandgar, Jacqueline M Hoover, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 7, 2007
Enhanced defense against Pneumocystis carinii mediated by a novel dectin-1 receptor Fc fusion proteinRekha R Rapaka, Eric S Goetzman, Mingquan Zheng, et al.
Analytical Biochemistry|June 14, 2019
An acyl-CoA dehydrogenase microplate activity assay using recombinant porcine electron transfer flavoproteinYuxun Zhang, Al-Walid Mohsen, Catherine Kochersperger, et al.
Molecular Genetics and Metabolism|June 20, 2007
Different spectrum of mutations of isovaleryl-CoA dehydrogenase (IVD) gene in Korean patients with isovaleric acidemiaYong-Wha Lee, Dong Hwan Lee, Jerry Vockley, et al.
Clinical Genetics|August 11, 2025
RePOWER: An International, Prospective, Non-Interventional Registry of Patients With Primary Mitochondrial MyopathyAmel Karaa, Amy Goldstein, Bruce H Cohen, et al.
Pediatric Transplantation|August 27, 2021
Domino transplantation for pediatric liver recipients: Obstacles, challenges, and successesVikram K Raghu, Peter D Carr-Boyd, James E Squires, et al.
Pageof 30

Showing results (91-100 of 293) with videos related to

Sort By:
Pageof 30
Journal of Inherited Metabolic Disease|February 26, 2022
Characterization of exonic variants of uncertain significance in very long-chain acyl-CoA dehydrogenase identified through newborn screeningOlivia M D'Annibale, Erik A Koppes, Meena Sethuraman, et al.
The Journal of Biological Chemistry|January 30, 2008
Structural basis for substrate fatty acyl chain specificity: crystal structure of human very-long-chain acyl-CoA dehydrogenaseRyan P McAndrew, Yudong Wang, Al-Walid Mohsen, et al.
Molecular Genetics and Metabolism Reports|November 17, 2022
Natural history of propionic acidemia in the Amish populationSarah Ehrenberg, Catherine Walsh Vockley, Paige Heiman, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|August 7, 2018
Liver Transplantation for Propionic Acidemia and Methylmalonic Acidemia: Perioperative Management and Clinical OutcomesKristen Critelli, Patrick McKiernan, Jerry Vockley, et al.
Neuromuscular Disorders : NMD|January 8, 2011
Novel mutation in MYH7 gene associated with distal myopathy and cardiomyopathyHouman Homayoun, Simin Khavandgar, Jacqueline M Hoover, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 7, 2007
Enhanced defense against Pneumocystis carinii mediated by a novel dectin-1 receptor Fc fusion proteinRekha R Rapaka, Eric S Goetzman, Mingquan Zheng, et al.
Analytical Biochemistry|June 14, 2019
An acyl-CoA dehydrogenase microplate activity assay using recombinant porcine electron transfer flavoproteinYuxun Zhang, Al-Walid Mohsen, Catherine Kochersperger, et al.
Molecular Genetics and Metabolism|June 20, 2007
Different spectrum of mutations of isovaleryl-CoA dehydrogenase (IVD) gene in Korean patients with isovaleric acidemiaYong-Wha Lee, Dong Hwan Lee, Jerry Vockley, et al.
Clinical Genetics|August 11, 2025
RePOWER: An International, Prospective, Non-Interventional Registry of Patients With Primary Mitochondrial MyopathyAmel Karaa, Amy Goldstein, Bruce H Cohen, et al.
Pediatric Transplantation|August 27, 2021
Domino transplantation for pediatric liver recipients: Obstacles, challenges, and successesVikram K Raghu, Peter D Carr-Boyd, James E Squires, et al.
Pageof 30