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Biochimie|December 10, 2013
Pathophysiology of X-linked adrenoleukodystrophyJ Berger, S Forss-Petter, F S EichlerCurrent Opinion in Neurology|May 24, 2001
Leukodystrophies: recent developments in genetics, molecular biology, pathogenesis and treatmentJ Berger, H W Moser, S Forss-PetterFEBS Letters|April 29, 1998
cDNA cloning and mRNA distribution of a mouse very long-chain acyl-CoA synthetaseJ Berger, C Truppe, H Neumann, et al.Human Molecular Genetics|November 7, 2000
Co-expression of mutated and normal adrenoleukodystrophy protein reduces protein function: implications for gene therapy of X-linked adrenoleukodystrophyG Unterrainer, B Molzer, S Forss-Petter, et al.Biochemical and Biophysical Research Communications|June 27, 1998
A novel relative of the very-long-chain acyl-CoA synthetase and fatty acid transporter protein genes with a distinct expression patternJ Berger, C Truppe, H Neumann, et al.Human Molecular Genetics|April 10, 1999
Adrenoleukodystrophy-related protein can compensate functionally for adrenoleukodystrophy protein deficiency (X-ALD): implications for therapyA Netik, S Forss-Petter, A Holzinger, et al.Journal of Inherited Metabolic Disease|October 14, 2000
Rolipram does not normalize very long-chain fatty acid levels in adrenoleukodystrophy protein-deficient fibroblasts and miceA Netik, A Hobel, H Rauschka, et al.Journal of Neuroscience Research|January 1, 1986
Neuron-specific enolase: complete structure of rat mRNA, multiple transcriptional start sites, and evidence suggesting post-transcriptional controlS Forss-Petter, P Danielson, J G SutcliffeEuropean Journal of Biochemistry|October 3, 1999
The four murine peroxisomal ABC-transporter genes differ in constitutive, inducible and developmental expressionJ Berger, S Albet, M Bentejac, et al.Journal of Neuroscience Research|January 7, 1998
Targeted inactivation of the X-linked adrenoleukodystrophy gene in miceS Forss-Petter, H Werner, J Berger, et al.Pageof 151