Berger J - Search Results

1

Neurofilament light chain as a potential biomarker for monitoring neurodegeneration in X-linked adrenoleukodystrophy.

Weinhofer I, Rommer P, Zierfuss B, Altmann P, Foiani M, Heslegrave A, Zetterberg H, Gleiss A, Musolino PL, Gong Y, Forss-Petter S, Berger T, Eichler F, Aubourg P, Köhler W, Berger J. Weinhofer I, et al. Among authors: berger j, berger t. Nat Commun. 2021 Mar 22;12(1):1816. doi: 10.1038/s41467-021-22114-2. Nat Commun. 2021. PMID: 33753741 Free PMC article.

2

Association of X-linked adrenoleukodystrophy with HLA DRB1 alleles.

Berger J, Bernheimer H, Faé I, Braun A, Roscher A, Molzer B, Fischer G. Berger J, et al. Biochem Biophys Res Commun. 1995 Nov 13;216(2):447-51. doi: 10.1006/bbrc.1995.2643. Biochem Biophys Res Commun. 1995. PMID: 7488132

3

X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypes.

Berger J, Molzer B, Faé I, Bernheimer H. Berger J, et al. Biochem Biophys Res Commun. 1994 Dec 30;205(3):1638-43. doi: 10.1006/bbrc.1994.2855. Biochem Biophys Res Commun. 1994. PMID: 7811247

4

Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice.

Forss-Petter S, Werner H, Berger J, Lassmann H, Molzer B, Schwab MH, Bernheimer H, Zimmermann F, Nave KA. Forss-Petter S, et al. Among authors: berger j. J Neurosci Res. 1997 Dec 1;50(5):829-43. doi: 10.1002/(SICI)1097-4547(19971201)50:5<829::AID-JNR19>3.0.CO;2-W. J Neurosci Res. 1997. PMID: 9418970

5

cDNA cloning and mRNA distribution of a mouse very long-chain acyl-CoA synthetase.

Berger J, Truppe C, Neumann H, Forss-Petter S. Berger J, et al. FEBS Lett. 1998 Mar 27;425(2):305-9. doi: 10.1016/s0014-5793(98)00255-5. FEBS Lett. 1998. PMID: 9559670 Free article.

6

A novel relative of the very-long-chain acyl-CoA synthetase and fatty acid transporter protein genes with a distinct expression pattern.

Berger J, Truppe C, Neumann H, Forss-Petter S. Berger J, et al. Biochem Biophys Res Commun. 1998 Jun 18;247(2):255-60. doi: 10.1006/bbrc.1998.8770. Biochem Biophys Res Commun. 1998. PMID: 9642112

7

Adrenoleukodystrophy-related protein can compensate functionally for adrenoleukodystrophy protein deficiency (X-ALD): implications for therapy.

Netik A, Forss-Petter S, Holzinger A, Molzer B, Unterrainer G, Berger J. Netik A, et al. Among authors: berger j. Hum Mol Genet. 1999 May;8(5):907-13. doi: 10.1093/hmg/8.5.907. Hum Mol Genet. 1999. PMID: 10196381

8

The four murine peroxisomal ABC-transporter genes differ in constitutive, inducible and developmental expression.

Berger J, Albet S, Bentejac M, Netik A, Holzinger A, Roscher AA, Bugaut M, Forss-Petter S. Berger J, et al. Eur J Biochem. 1999 Oct;265(2):719-27. doi: 10.1046/j.1432-1327.1999.00772.x. Eur J Biochem. 1999. PMID: 10504404 Free article.

9

Rolipram does not normalize very long-chain fatty acid levels in adrenoleukodystrophy protein-deficient fibroblasts and mice.

Netik A, Hobel A, Rauschka H, Molzer B, Forss-Petter S, Berger J. Netik A, et al. Among authors: berger j. J Inherit Metab Dis. 2000 Sep;23(6):615-24. doi: 10.1023/a:1005686114356. J Inherit Metab Dis. 2000. PMID: 11032336

10

Co-expression of mutated and normal adrenoleukodystrophy protein reduces protein function: implications for gene therapy of X-linked adrenoleukodystrophy.

Unterrainer G, Molzer B, Forss-Petter S, Berger J. Unterrainer G, et al. Among authors: berger j. Hum Mol Genet. 2000 Nov 1;9(18):2609-16. doi: 10.1093/hmg/9.18.2609. Hum Mol Genet. 2000. PMID: 11063720

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