검색결과 : 5건
| No. | Article |
|---|---|
| 1 |
X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype Maier EM, Mayerhofer PU, Asheuer M, Kohler W, Rothe M, Muntau AC, Roscher AA, Holzinger A, Aubourg P, Berger J Biochemical and Biophysical Research Communications, 377(1), 176, 2008 |
| 2 |
Targeted inactivation of the murine Abca3 gene leads to respiratory failure in newborns with defective lamellar bodies Hammel M, Michel G, Hoefer C, Klaften M, Muller-Hocker J, de Angelis MH, Holzinger A Biochemical and Biophysical Research Communications, 359(4), 947, 2007 |
| 3 |
Mitochondrial targeting signals and mature peptides of 3-methylcrotonyl-CoA carboxylase Stadler SC, Polanetz R, Meier S, Mayerhofer PU, Herrmann JM, Anslinger K, Roscher AA, Roschinger W, Holzinger A Biochemical and Biophysical Research Communications, 334(3), 939, 2005 |
| 4 |
The human PEX3 gene encoding a peroxisomal assembly protein: Genomic organization, positional mapping, and mutation analysis in candidate phenotypes Muntau AC, Holzinger A, Mayerhofer PU, Gartner J, Roscher AA, Kammerer S Biochemical and Biophysical Research Communications, 268(3), 704, 2000 |
| 5 |
Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p Gloeckner CJ, Mayerhofer PU, Landgraf P, Muntau AC, Holzinger A, Gerber JK, Kammerer S, Adamski J, Roscher AA Biochemical and Biophysical Research Communications, 271(1), 144, 2000 |