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Results: 1-7 |
Results: 7
Genomic organization, expression analysis, and chromosomal localization ofthe mouse PEX3 gene encoding a peroxisomal assembly protein
Authors: Muntau, AC Mayerhofer, PU Albet, S Schmid, TE Bugaut, M Roscher, AA Kammerer, S
Citation: Ac. Muntau et al., Genomic organization, expression analysis, and chromosomal localization ofthe mouse PEX3 gene encoding a peroxisomal assembly protein, BIOL CHEM, 381(4), 2000, pp. 337-342
Carrier assessment in families with Lowe oculocerebrorenal syndrome: Novelmutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examination
Authors: Roschinger, W Muntau, AC Rudolph, G Roscher, AA Kammerer, S
Citation: W. Roschinger et al., Carrier assessment in families with Lowe oculocerebrorenal syndrome: Novelmutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examination, MOL GEN MET, 69(3), 2000, pp. 213-222
Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p
Authors: Gloeckner, CJ Mayerhofer, PU Landgraf, P Muntau, AC Holzinger, A Gerber, JK Kammerer, S Adamski, J Roscher, AA
Citation: Cj. Gloeckner et al., Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p, BIOC BIOP R, 271(1), 2000, pp. 144-150
The human PEX3 gene encoding a peroxisomal assembly protein: Genomic organization, positional mapping, and mutation analysis in candidate phenotypes
Authors: Muntau, AC Holzinger, A Mayerhofer, PU Gartner, J Roscher, AA Kammerer, S
Citation: Ac. Muntau et al., The human PEX3 gene encoding a peroxisomal assembly protein: Genomic organization, positional mapping, and mutation analysis in candidate phenotypes, BIOC BIOP R, 268(3), 2000, pp. 704-710
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G
Authors: Muntau, AC Mayerhofer, PU Paton, BC Kammerer, S Roscher, AA
Citation: Ac. Muntau et al., Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G, AM J HU GEN, 67(4), 2000, pp. 967-975
Prenatal diagnosis of X-linked adrenoleukodystrophy combining biochemical,immunocytochemical and DNA analyses
Authors: Maier, EM Roscher, AA Kammerer, S Mehnert, K Conzelmann, E Holzinger, A
Citation: Em. Maier et al., Prenatal diagnosis of X-linked adrenoleukodystrophy combining biochemical,immunocytochemical and DNA analyses, PRENAT DIAG, 19(4), 1999, pp. 364-368
Full length cDNA cloning, promoter sequence, and genomic organization of the human adrenoleukodystrophy related (ALDR) gene functionally redundant tothe gene responsible for x-linked adrenoleukodystrophy
Authors: Holzinger, A Mayerhofer, P Berger, J Lichtner, P Kammerer, S Roscher, AA
Citation: A. Holzinger et al., Full length cDNA cloning, promoter sequence, and genomic organization of the human adrenoleukodystrophy related (ALDR) gene functionally redundant tothe gene responsible for x-linked adrenoleukodystrophy, BIOC BIOP R, 258(2), 1999, pp. 436-442
Risultati: 1-7 |