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Items where Author is "Kammerer, S"

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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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