Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jeffrey C. Brackett"'
Autor:
Jeffrey C. Brackett, Daniel E. Hale, Cynthia K. Powell, Arnold W. Strauss, Harold F. Sims, Ajay Ahuja, Melissa M. Anderson
Publikováno v:
Proceedings of the National Academy of Sciences. 92:10496-10500
beta-Oxidation of long-chain fatty acids provides the major source of energy in the heart. Defects in enzymes of the beta-oxidation pathway cause sudden, unexplained death in childhood, acute hepatic encephalopathy or liver failure, skeletal myopathy
Autor:
Jeffrey C. Brackett, Michael J. Bennett, Piero Rinaldo, H F Sims, C. K. Powell, Arnold W. Strauss, S Shapiro
Publikováno v:
Journal of Clinical Investigation. 95:2076-2082
Human trifunctional protein catalyzes three steps in mitochondrial beta-oxidation of fatty acids, including the long chain 3-hydroxyacyl-CoA dehydrogenase step. Deficiency of this heterocomplex, which contains 4 alpha and 4 beta subunits, causes sudd
Autor:
Rana Ziadeh, Eric P. Hoffman, Rita C. Hoop, David N. Finegold, Arnold W. Strauss, Jeffrey C. Brackett, Edwin W. Naylor
Publikováno v:
Pediatric research. 37(5)
Medium chain acyl-CoA dehydrogenase deficiency (MCAD) is a defect in the mitochondrial oxidation of fatty acids. The disorder typically presents with episodes of vomiting and hypoglycemia, sometimes with changes in mental status and hepatic failure.
Autor:
Michael E. Silverman, Jeffrey C. Brackett, Michael R. Gold, Michael D. Pressel, Salvatore S. Lauria, Stephen S. Gottlieb
Publikováno v:
The American journal of cardiology. 75(7)
Studies of electrocardiographic predictors of mortality in patients with chronic heart failure have reached varying conclusions. Differences in the characteristics of the patients studied may explain the conflicting results regarding both a prolonged
Autor:
Daniel E. Hale, Arnold W. Strauss, Scott Shapiro, William R. Treem, Beverly Gibson, Harold F. Sims, Cynthia K. Powell, Jeffrey C. Brackett, Michael J. Bennett
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 92(3)
Mitochondrial long chain fatty acid beta-oxidation provides the major source of energy in the heart. Deficiencies of human beta-oxidation enzymes produce sudden, unexplained death in childhood, acute hepatic encephalopathy, skeletal myopathy, or card
Autor:
Robert D. Steiner, M Nunge, Arnold W. Strauss, Rachel Slaugh, Jeffrey C. Brackett, Piero Rinaldo, H F Sims, E M Zimmerman, B deMartinville
Publikováno v:
Scopus-Elsevier
Medium chain acyl-CoA dehydrogenase (MCAD) deficiency is the most common known genetic disorder of fatty acid oxidation. Most (approximately 80%) cases are homozygous for a single mutation: A to G replacement at nucleotide 985 (A985G). MCAD deficienc
Autor:
Michael L. Fisher, Stephen S. Gottlieb, Michelle Weinberg, Jeffrey C. Brackett, Gary C. Brown
Publikováno v:
Journal of the American College of Cardiology. 17(2)