Acads gene deletion in BALB/cByJ mouse strain occurred after 1981 and is not present in BALB/cByJ-fld mutant mice (original) (raw)
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References
- Amendt, B.A., Greene, C., Sweetman, L., Cloherty, J., Shih, V., Moon, A., Teel, L., Rhead, W.J. (1987). Short-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical studies in two patients. J. Clin. Invest. 79, 1303–1309.
Article PubMed CAS Google Scholar - Amendt, B.A., Freneaux, E., Reece, C., Wood, P.A., Rhead, W.J. (1992). Short-chain acyl-coenzyme A dehydrogenase activity, antigen, and biosynthesis are absent in the BALB/cByJ mouse. Pediatr. Res. 31, 552–556.
Article PubMed CAS Google Scholar - Coates, P.M., Hale, D.E., Finocchiaro, G., Tanaka, K., Winter, S.M. (1988). Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weakness. J. Clin. Invest. 81, 171–175.
Article PubMed CAS Google Scholar - Hinsdale, M.E., Kelly, C.L., Wood, P.A. (1993). Null allele at Bcd-1 locus in BALB/cByJ mice is due to a deletion in the short-chain acyl-CoA dehydrogenase gene and results in missplicing of mRNA. Genomics 16, 605–611.
Article PubMed CAS Google Scholar - Langner, CA., Birkenmeier, E.H., Ben-Zeev, O., Schotz, M.C., Sweet, H.O., Davisson, M.T., Gordon, J.I. (1989). The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities. J. Biol. Chem. 264, 7994–8003.
PubMed CAS Google Scholar - Reue, K., Rehnmark, S., Cohen, R.D., Doolittle, M.H. (1994). The fatty liver dystrophy (fld) mutation: A developmental abnormality in fatty acid oxidation. Circulation 90, I-80.
Google Scholar - Schiffer, S.P., Prochazka, M., Jezyk, P.F., Roderick, T.H., Yudkoff, M., Patterson, D.F. (1989). Organic aciduria and butyryl CoA dehydrogenase deficiency in BALB/cByJ mice. Biochem. Genet. 27, 47–58.
Article PubMed CAS Google Scholar - Taylor, B.A. (1989). Recombinant inbred strains. In Genetic Variants and Strains of the Laboratory Mouse, M.F. Lyon, A.G. Searle, eds. (Oxford: Oxford University Press), pp. 773–796.
Google Scholar - Wood, P.A., Amendt, B.A., Rhead, W.J., Millington, D.S., Inoue, F., Armstrong, D. (1989). Short-chain acyl-coenzyme A dehydrogenase deficiency in mice. Pediatr. Res. 25, 38–43.
Article PubMed CAS Google Scholar - Wood, P.A., Hinsdale, M.E., Kelly, C.L. (1993). Molecular detection of the Bcd-1 null allele in BALB/cByJ mice by polymerase chain reaction: a simple assay for genetic monitoring. Mouse Genome 91, 342–344.
Google Scholar