Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Moira L. Ogden"'
Autor:
Daniel E. Hale, Daniel P. Kelly, Alison J. Whelan, Zhifang Zhang, Arnold W. Strauss, S. L. Rutledge, Moira L. Ogden
Publikováno v:
Journal of Inherited Metabolic Disease. 15:171-180
Deficiency of medium-chain acyl-CoA dehydrogenase (MCAD) is an important cause of sudden death in children. The majority of surviving individuals with MCAD deficiency studied to date are homozygous for a single point mutation at bp 985 of the MCAD mR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0bb823d48dd8f353de3a4292407ad5e
https://doi.org/10.1007/bf01799626
https://doi.org/10.1007/bf01799626
Autor:
Ruth Alpers, Moira L. Ogden, L. Dorland, Arnold W. Strauss, Gary Bellus, Daniel P. Kelly, Zhifang Zhang, Niels Gregersen, Alison J. Whelan
Publikováno v:
Proceedings of the National Academy of Sciences. 87:9236-9240
Deficiency of medium-chain acyl-CoA dehydrogenase (MCAD) is a common inherited defect in energy metabolism. Characterization of the mRNA encoding MCAD in a Dutch MCAD-deficient patient revealed an A----G change at nucleotide position 985 of the MCAD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0578a97f5460b3a9bc19ef07f75c8426
https://doi.org/10.1073/pnas.87.23.9236
https://doi.org/10.1073/pnas.87.23.9236
Structural organization and regulatory regions of the human medium-chain acyl-CoA dehydrogenase gene
Autor:
Jung-Ja P. Kim, Daniel P. Kelly, Alison J. Whelan, Moira L. Ogden, Zhifang Zhang, Arnold W. Strauss, Yeqing Zhou
Publikováno v:
Biochemistry. 31(1)
Medium-chain acyl-CoA dehydrogenase (MCAD) is a highly regulated mitochondrial flavo-enzyme that catalyzes the initial reaction in fatty acid beta-oxidation. Deficiency of MCAD is a common inherited defect in energy metabolism. We have previously sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ead07c1f152fcce36e17736cf8a140cf
https://pubmed.ncbi.nlm.nih.gov/1731887
https://pubmed.ncbi.nlm.nih.gov/1731887