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Items where Author is "Roscher, A"

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Article

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, Maier, EM, Heidenreich, SC, Niederer, B, Mayerhofer, PU, Lagler, F, Koch, HG, Santer, R, Fletcher, JM, Ranieri, E, Das, AM, Spiekerkotter, U, Schwab, KO, Potzsch, S, Marquardt, I, Hennermann, JB, Knerr, I, Mercimek-Mahmutoglu, S, Kohlschmidt, N, Liebl, B, Fingerhut, R, Olgemoller, B, Muntau, AC, Roscher, AA and Roschinger, W (2006) Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessment Hum Mutat, 27. pp. 748-759.

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.

Landgraf, P, Mayerhofer, PU, Polanetz, R, Roscher, AA and Holzinger, A (2003) Targeting of the human adrenoleukodystrophy protein to the peroxisomal membrane by an internal region containing a highly conserved motif Eur J Cell Biol, 82. pp. 401-410.

Holzinger, A, Maier, EM, Buck, C, Mayerhofer, PU, Kappler, M, Haworth, JC, Moroz, SP, Hadorn, HB, Sadler, JE and Roscher, AA (2002) Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency Am J Hum Genet, 70. pp. 20-25.

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.

Holzinger, A, Roschinger, W, Lagler, F, Mayerhofer, PU, Lichtner, P, Kattenfeld, T, Thuy, LP, Nyhan, WL, Koch, HG, Muntau, AC and Roscher, AA (2001) Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency Hum Mol Genet, 10. pp. 1299-1306.

Muntau, AC, Mayerhofer, PU, Paton, BC, Kammerer, S and Roscher, AA (2000) Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G Am J Hum Genet, 67. pp. 967-975.

Muntau, AC, Mayerhofer, PU, Albet, S, Schmid, TE, Bugaut, M, Roscher, AA and Kammerer, S (2000) Genomic organization, expression analysis, and chromosomal localization of the mouse PEX3 gene encoding a peroxisomal assembly protein Biol Chem, 381. pp. 337-342.

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.

Holzinger, A, Muntau, A, Mayerhofer, P, Kammerer, S, Albet, S, Bugaut, M and Roscher, AA (1998) The mouse gene encoding the peroxisomal membrane protein 1-like protein (PXMP1-L): cDNA cloning, genomic organization and comparative expression studies FEBS Lett, 433. pp. 179-183.

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