Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Vockley

Showing results (51-60 of 62) with videos related to

Pageof 7
Sort By:
Human Molecular Genetics|October 9, 2001
Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouseK B Cox, D A Hamm, D S Millington, et al.
American Journal of Human Genetics|March 7, 2001
Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiencyB A Binzak, R A Wevers, S H Moolenaar, et al.
Journal of Inherited Metabolic Disease|December 18, 2008
Essential fatty acid profiling for routine nutritional assessment unmasks adrenoleukodystrophy in an infant with isovaleric acidaemiaR Bonilla Guerrero, L A Wolfe, N Payne, et al.
Molecular Genetics and Metabolism|September 4, 2016
Triheptanoin treatment in patients with pediatric cardiomyopathy associated with long chain-fatty acid oxidation disordersJ Vockley, J Charrow, J Ganesh, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 23, 1998
Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidationD M Kurtz, P Rinaldo, W J Rhead, et al.
Cell Death & Disease|June 15, 2013
Alterations in c-Myc phenotypes resulting from dynamin-related protein 1 (Drp1)-mediated mitochondrial fissionM Sarin, Y Wang, F Zhang, et al.
Journal of Inherited Metabolic Disease|July 23, 2003
Recurrent vomiting and ethylmalonic aciduria associated with rare mutations of the short-chain acyl-CoA dehydrogenase geneJ Seidel, S Streck, K Bellstedt, et al.
Molecular Genetics and Metabolism|February 13, 2017
UX007 for the treatment of long chain-fatty acid oxidation disorders: Safety and efficacy in children and adults following 24weeks of treatmentJ Vockley, B Burton, G T Berry, et al.
Pediatric Research|January 3, 2001
Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiencyM J Corydon, J Vockley, P Rinaldo, et al.
Clinical Pharmacology and Therapeutics|November 6, 2015
Precision medicine in the age of big data: The present and future role of large-scale unbiased sequencing in drug discovery and developmentP Vicini, O Fields, E Lai, et al.
Pageof 7

Showing results (51-60 of 62) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|October 9, 2001
Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouseK B Cox, D A Hamm, D S Millington, et al.
American Journal of Human Genetics|March 7, 2001
Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiencyB A Binzak, R A Wevers, S H Moolenaar, et al.
Journal of Inherited Metabolic Disease|December 18, 2008
Essential fatty acid profiling for routine nutritional assessment unmasks adrenoleukodystrophy in an infant with isovaleric acidaemiaR Bonilla Guerrero, L A Wolfe, N Payne, et al.
Molecular Genetics and Metabolism|September 4, 2016
Triheptanoin treatment in patients with pediatric cardiomyopathy associated with long chain-fatty acid oxidation disordersJ Vockley, J Charrow, J Ganesh, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 23, 1998
Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidationD M Kurtz, P Rinaldo, W J Rhead, et al.
Cell Death & Disease|June 15, 2013
Alterations in c-Myc phenotypes resulting from dynamin-related protein 1 (Drp1)-mediated mitochondrial fissionM Sarin, Y Wang, F Zhang, et al.
Journal of Inherited Metabolic Disease|July 23, 2003
Recurrent vomiting and ethylmalonic aciduria associated with rare mutations of the short-chain acyl-CoA dehydrogenase geneJ Seidel, S Streck, K Bellstedt, et al.
Molecular Genetics and Metabolism|February 13, 2017
UX007 for the treatment of long chain-fatty acid oxidation disorders: Safety and efficacy in children and adults following 24weeks of treatmentJ Vockley, B Burton, G T Berry, et al.
Pediatric Research|January 3, 2001
Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiencyM J Corydon, J Vockley, P Rinaldo, et al.
Clinical Pharmacology and Therapeutics|November 6, 2015
Precision medicine in the age of big data: The present and future role of large-scale unbiased sequencing in drug discovery and developmentP Vicini, O Fields, E Lai, et al.
Pageof 7