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Agouni, A, Owen, C, Czopek, A, Mody, N and Delibegovic, M (2010) In vivo differential effects of fasting, re-feeding, insulin and insulin stimulation time course on insulin signaling pathway components in peripheral tissues. Biochem Biophys Res Commun, 401 (1). pp. 104-111.

Maier, EM, Mayerhofer, PU, Asheuer, M, Kohler, W, Rothe, M, Muntau, AC, Roscher, AA, Holzinger, A, Aubourg, P and Berger, J (2008) X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype Biochem Biophys Res Commun, 377. pp. 176-180.

Stadler, SC, Polanetz, R, Meier, S, Mayerhofer, PU, Herrmann, JM, Anslinger, K, Roscher, AA, Roschinger, W and Holzinger, A (2005) Mitochondrial targeting signals and mature peptides of 3-methylcrotonyl-CoA carboxylase Biochem Biophys Res Commun, 334. pp. 939-946.

Mayerhofer, PU, Kattenfeld, T, Roscher, AA and Muntau, AC (2002) Two splice variants of human PEX19 exhibit distinct functions in peroxisomal assembly Biochem Biophys Res Commun, 291. pp. 1180-1186.

Gloeckner, CJ, Mayerhofer, PU, Landgraf, P, Muntau, AC, Holzinger, A, Gerber, JK, Kammerer, S, Adamski, J and Roscher, AA (2000) Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p Biochem Biophys Res Commun, 271. pp. 144-150.

Muntau, AC, Holzinger, A, Mayerhofer, PU, Gartner, J, Roscher, AA and Kammerer, S (2000) The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypes Biochem Biophys Res Commun, 268. pp. 704-710.

Holzinger, A, Mayerhofer, P, Berger, J, Lichtner, P, Kammerer, S and Roscher, AA (1999) Full length cDNA cloning, promoter sequence, and genomic organization of the human adrenoleukodystrophy related (ALDR) gene functionally redundant to the gene responsible for X-linked adrenoleukodystrophy Biochem Biophys Res Commun, 258. pp. 436-442.

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