Molecular analysis of a human liver mitochondrial ornithine transcarbamylase deficiency-Reference-Cited by-同舟云学术

Molecular analysis of a human liver mitochondrial ornithine transcarbamylase deficiency

Published:1991-01 Issue:1 Volume:14 Page:29-36
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Berrez J.-M.,Bardot O.,Thiard M.-C.,Alvarez F.,Latruffe N.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://www.springerlink.com/index/pdf/10.1007/BF01804385

Reference22 articles.

1. Argan, C. and Shore, G. G. The precursor of ornithine carbamyltransferase is transported to mitochondria as a 5S complex containing an import factor.Biochem. Biophys. Res. Commun. 131 (1985) 289–298

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3. Briand, P., Baudoin, F., Rabier, D. and Cathelineau, L. Ornithine transcarbamylase deficiencies in human males. Kinetic and immunochemical classification.Biochim. Biophys. Acta 704 (1982) 100–106

4. Burnette, W. N. ‘Western blotting’. Electrophoretic transfer of protein from sodium dodecyl sulfate polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A.Anal. Biochem. 112 (1981) 195–205

5. Corral, M., Paris, B., Corcos, D. Guguen-Guillouzo, C., Kruh, J. and Defer, N. Increased expression of the N-myc gene during normal and neoplastic rat liver growth.Exp. Cell Res. 174 (1985) 107–115

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