Berger, Johannes

Peroxisomal very long-chain fatty acid transport is targeted by herpesviruses and the antiviral host response

Weinhofer, I., Buda, A., Kunze, M., Palfi, Z., Traunfellner, M., Hesse, S., Villoria-Gonzalez, A., Hofmann, J., Hametner, S., Regelsberger, G., et al. (2022) · Communications Biology

Cytomegalovirus and herpesvirus researchHerpesvirus Infections and Treatments

Cited by 20

Formation of GABAA receptor complexes containing α1 and α5 subunits is paralleling a multiple T-maze learning task in mice

Ghafari, M., Falsafi, S. K., Szodorai, E., Kim, E.-J., Li, L., Höger, H., Berger, J., Fuchs, K., Sieghart, W., & Lubec, G. (2017) · Brain Structure and Function

Neuroscience and Neuropharmacology ResearchMemory and Neural Mechanisms

Cited by 19

Immune response of BV-2 microglial cells is impacted by peroxisomal beta-oxidation

Tawbeh, A., Raas, Q., Tahri-Joutey, M., Keime, C., Kaiser, R., Trompier, D., Nasser, B., Bellanger, E., Dessard, M., Hamon, Y., et al. (2023) · Frontiers in Molecular Neuroscience

Neuroinflammation and Neurodegeneration MechanismsInflammasome and immune disorders

Cited by 18

CD1 Gene Polymorphisms and Phenotypic Variability in X-Linked Adrenoleukodystrophy

Barbier, M., Sabbagh, A., Kasper, E., Asheuer, M., Ahouansou, O., Pribill, I., Forss-Petter, S., Vidaud, M., Berger, J., & Aubourg, P. (2012) · PLoS ONE

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 18

Rat adrenoleukodystrophy-related (ALDR) gene: full-length cDNA sequence and new insight in expression

Albet, S., Bentejac, M., Savary, S., Gondcaille, C., Netik, A., Berger, J., Szpirer, C., Troffer-Charlier, N., & Bugaut, M. (2001) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 18

Association of X-Linked Adrenoleukodystrophy with HLA DRB1 Alleles

Berger, J., Bernheimer, H., Fae, I., Braun, A., Roscher, A., Molzer, B., & Fischer, G. (1995) · Biochemical and Biophysical Research Communications

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 16

ABCD1 Transporter Deficiency Results in Altered Cholesterol Homeostasis

Buda, A., Forss-Petter, S., Hua, R., Jaspers, Y., Lassnig, M., Waidhofer-Söllner, P., Kemp, S., Kim, P., Weinhofer, I., & Berger, J. (2023) · Biomolecules

Metabolism and Genetic DisordersCholesterol and Lipid Metabolism

Cited by 14

Ether lipid transfer across the blood-brain and placental barriers does not improve by inactivation of the most abundant ABC transporters.

Dorninger, F., Vaz, F. M., Waterham, H. R., Klinken, J. B. V., Zeitler, G., Forss-Petter, S., Berger, J., & Wiesinger, C. (2022) · Brain Research Bulletin

Drug Transport and Resistance MechanismsBarrier Structure and Function Studies

Cited by 12

Evaluation of Retinoids for Induction of the Redundant Gene ABCD2 as an Alternative Treatment Option in X-Linked Adrenoleukodystrophy

Weber, F. D., Weinhofer, I., Einwich, A., Forss-Petter, S., Muneer, Z., Maier, H., Weber, W. H. A., & Berger, J. (2014) · PLoS ONE

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 8

Involvement of Human Peroxisomes in Biosynthesis and Signaling of Steroid and Peptide Hormones

Weinhofer, I., Kunze, M., Forss-Petter, S., & Berger, J. (2013) · Subcellular Biochemistry

Metabolism and Genetic DisordersCellular transport and secretion

Cited by 8