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Jerry Vockley

Showing results (151-160 of 294) with videos related to

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Human Gene Therapy|January 18, 2006
Systemic correction of a fatty acid oxidation defect by intramuscular injection of a recombinant adeno-associated virus vectorThomas J Conlon, Glenn Walter, Renius Owen, et al.
JIMD Reports|March 13, 2013
Infantile hypophosphatasia secondary to a novel compound heterozygous mutation presenting with pyridoxine-responsive seizuresDina Belachew, Traci Kazmerski, Ingrid Libman, et al.
BMJ Evidence-Based Medicine|November 11, 2020
An evidence map of randomised controlled trials evaluating genetic therapiesEric A Apaydin, Andrea S Richardson, Sangita Baxi, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 1, 2022
Whole-genome sequencing holds the key to the success of gene-targeted therapiesJerry Vockley, Annemieke Aartsma-Rus, Jennifer L Cohen, et al.
Molecular Genetics and Metabolism|April 2, 2016
Outcomes of cases with 3-methylcrotonyl-CoA carboxylase (3-MCC) deficiency - Report from the Inborn Errors of Metabolism Information SystemRaeLynn Forsyth, Catherine Walsh Vockley, Mathew J Edick, et al.
International Journal of Molecular Sciences|October 13, 2021
Lipidomic and Proteomic Alterations Induced by Even and Odd Medium-Chain Fatty Acids on Fibroblasts of Long-Chain Fatty Acid Oxidation DisordersKhaled I Alatibi, Stefan Tholen, Zeinab Wehbe, et al.
The Journal of Biological Chemistry|July 16, 2005
Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acidsRegina Ensenauer, Miao He, Jan-Marie Willard, et al.
European Journal of Immunology|January 29, 2014
Follistatin-like protein 1 enhances NLRP3 inflammasome-mediated IL-1β secretion from monocytes and macrophagesYury Chaly, Yu Fu, Anthony Marinov, et al.
The Journal of Pediatrics|August 16, 2011
Liver transplantation for classical maple syrup urine disease: long-term follow-up in 37 patients and comparative United Network for Organ Sharing experienceGeorge V Mazariegos, D Holmes Morton, Rakesh Sindhi, et al.
Plos Genetics|August 27, 2005
Medium-chain acyl-CoA dehydrogenase deficiency in gene-targeted miceRavi J Tolwani, Doug A Hamm, Liqun Tian, et al.
Pageof 30

Showing results (151-160 of 294) with videos related to

Sort By:
Pageof 30
Human Gene Therapy|January 18, 2006
Systemic correction of a fatty acid oxidation defect by intramuscular injection of a recombinant adeno-associated virus vectorThomas J Conlon, Glenn Walter, Renius Owen, et al.
JIMD Reports|March 13, 2013
Infantile hypophosphatasia secondary to a novel compound heterozygous mutation presenting with pyridoxine-responsive seizuresDina Belachew, Traci Kazmerski, Ingrid Libman, et al.
BMJ Evidence-Based Medicine|November 11, 2020
An evidence map of randomised controlled trials evaluating genetic therapiesEric A Apaydin, Andrea S Richardson, Sangita Baxi, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 1, 2022
Whole-genome sequencing holds the key to the success of gene-targeted therapiesJerry Vockley, Annemieke Aartsma-Rus, Jennifer L Cohen, et al.
Molecular Genetics and Metabolism|April 2, 2016
Outcomes of cases with 3-methylcrotonyl-CoA carboxylase (3-MCC) deficiency - Report from the Inborn Errors of Metabolism Information SystemRaeLynn Forsyth, Catherine Walsh Vockley, Mathew J Edick, et al.
International Journal of Molecular Sciences|October 13, 2021
Lipidomic and Proteomic Alterations Induced by Even and Odd Medium-Chain Fatty Acids on Fibroblasts of Long-Chain Fatty Acid Oxidation DisordersKhaled I Alatibi, Stefan Tholen, Zeinab Wehbe, et al.
The Journal of Biological Chemistry|July 16, 2005
Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acidsRegina Ensenauer, Miao He, Jan-Marie Willard, et al.
European Journal of Immunology|January 29, 2014
Follistatin-like protein 1 enhances NLRP3 inflammasome-mediated IL-1β secretion from monocytes and macrophagesYury Chaly, Yu Fu, Anthony Marinov, et al.
The Journal of Pediatrics|August 16, 2011
Liver transplantation for classical maple syrup urine disease: long-term follow-up in 37 patients and comparative United Network for Organ Sharing experienceGeorge V Mazariegos, D Holmes Morton, Rakesh Sindhi, et al.
Plos Genetics|August 27, 2005
Medium-chain acyl-CoA dehydrogenase deficiency in gene-targeted miceRavi J Tolwani, Doug A Hamm, Liqun Tian, et al.
Pageof 30