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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Andreas Holzinger

Department of Pediatrics

Division of Clinical Chemistry and Metabolism

Dr. v. Hauner Children's Hospital

Ludwig-Maximilian-University

Germany

[email]@*.med.uni-muenchen.de

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Pediatrics, Division of Clinical Chemistry and Metabolism, Dr. v. Hauner Children's Hospital, Ludwig-Maximilian-University, Germany. 1999 - 2002
  • Dr. v. Hauner Children's Hospital, Department of Clinical Chemistry and Biochemistry, Ludwig-Maximilian-University, Munich, Germany. 1997 - 2001
  • Dr. von Hauner Children's Hospital, Ludwig-Maximilian-University, Department of Pediatrics, Munich, Germany. 1998

References

  1. Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency. Holzinger, A., Maier, E.M., Bück, C., Mayerhofer, P.U., Kappler, M., Haworth, J.C., Moroz, S.P., Hadorn, H.B., Sadler, J.E., Roscher, A.A. Am. J. Hum. Genet. (2002) [Pubmed]
  2. Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency. Holzinger, A., Röschinger, W., Lagler, F., Mayerhofer, P.U., Lichtner, P., Kattenfeld, T., Thuy, L.P., Nyhan, W.L., Koch, H.G., Muntau, A.C., Roscher, A.A. Hum. Mol. Genet. (2001) [Pubmed]
  3. 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. Holzinger, A., Mayerhofer, P., Berger, J., Lichtner, P., Kammerer, S., Roscher, A.A. Biochem. Biophys. Res. Commun. (1999) [Pubmed]
  4. Genomic organization and chromosomal localization of the human peroxisomal membrane protein-1-like protein (PXMP1-L) gene encoding a peroxisomal ABC transporter. Holzinger, A., Roscher, A.A., Landgraf, P., Lichtner, P., Kammerer, S. FEBS Lett. (1998) [Pubmed]
  5. The mouse gene encoding the peroxisomal membrane protein 1-like protein (PXMP1-L): cDNA cloning, genomic organization and comparative expression studies. Holzinger, A., Muntau, A., Mayerhofer, P., Kammerer, S., Albet, S., Bugaut, M., Roscher, A.A. FEBS Lett. (1998) [Pubmed]
  6. Primary structure of human PMP69, a putative peroxisomal ABC-transporter. Holzinger, A., Kammerer, S., Roscher, A.A. Biochem. Biophys. Res. Commun. (1997) [Pubmed]
  7. cDNA cloning and mRNA expression of the human adrenoleukodystrophy related protein (ALDRP), a peroxisomal ABC transporter. Holzinger, A., Kammerer, S., Berger, J., Roscher, A.A. Biochem. Biophys. Res. Commun. (1997) [Pubmed]
 
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