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List of works by Johannes Berger

A Novel FRET Approach Quantifies the Interaction Strength of Peroxisomal Targeting Signals and Their Receptor in Living Cells

scientific article published on 30 October 2020

A de novo adrenoleukodystrophy gene (ABCD1) mutation S636I without detectable ABCD1 protein and a R104C mutation with normal amounts of protein from an Austrian patient collective

scientific article published on 01 December 2000

A new polymorphism of arylsulfatase A within the coding region

scientific article published on 01 September 1996

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

scientific article

ABCA8 Regulates Cholesterol Efflux and High-Density Lipoprotein Cholesterol Levels.

scientific article

Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient mice

scientific article

Acyl-CoA synthetase activity links wild-type but not mutant alpha-synuclein to brain arachidonate metabolism

scientific journal article

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

scientific article

Alterations in the Plasma Levels of Specific Choline Phospholipids in Alzheimer's Disease Mimic Accelerated Aging.

scientific article published in January 2018

Association of X-linked adrenoleukodystrophy with HLA DRB1 alleles

scientific article published on 01 November 1995

CD1 gene polymorphisms and phenotypic variability in X-linked adrenoleukodystrophy

scientific article

Coincidence of two novel arylsulfatase A alleles and mutation 459+1G>A within a family with metachromatic leukodystrophy: molecular basis of phenotypic heterogeneity

scientific article

Development of HIV encephalitis in AIDS and TNF-alpha regulatory elements

scientific article published in November 1998

Dietary magnesium restriction reduces amygdala-hypothalamic GluN1 receptor complex levels in mice

scientific article

Distinct modulatory roles for thyroid hormone receptors TRalpha and TRbeta in SREBP1-activated ABCD2 expression

scientific article published in October 2008

Distribution and cellular localization of adrenoleukodystrophy protein in human tissues: implications for X-linked adrenoleukodystrophy

scientific article

Drebrin depletion alters neurotransmitter receptor levels in protein complexes, dendritic spine morphogenesis and memory-related synaptic plasticity in the mouse hippocampus

scientific article published on 29 April 2015

Dysferlin is a new marker for leaky brain blood vessels in multiple sclerosis.

scientific article published in September 2006

Eight novel ABCD1 gene mutations and three polymorphisms in patients with X-linked adrenoleukodystrophy: The first polymorphism causing an amino acid exchange.

scientific article published in January 2001

Elevated sulfatide excretion in compound heterozygotes of metachromatic leukodystrophy and ASA-pseudodeficiency allele

scientific article published on 01 June 1997

Ether Lipid Deficiency in Mice Produces a Complex Behavioral Phenotype Mimicking Aspects of Human Psychiatric Disorders

scientific article published on 13 August 2019

Ether lipid deficiency does not cause neutropenia or leukopenia in mice and men.

scientific article published on May 2015

Evaluation of retinoids for induction of the redundant gene ABCD2 as an alternative treatment option in X-linked adrenoleukodystrophy

scientific article

Evaluation of the therapeutic potential of PPARalpha agonists for X-linked adrenoleukodystrophy.

scientific article

Expression of Hypoxia-related Tissue Factors Correlates with Diminished Survival of Adjuvantly Treated Patients with Chromosome 1p Aberrant Oligodendroglial Neoplasms and Therapeutic Implications

scientific article published on 01 October 2004

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

scientific article published on 7 May 2016

From peroxisomal disorders to common neurodegenerative diseases - the role of ether phospholipids in the nervous system.

scientific article

High prevalence of I179S mutation in patients with late-onset metachromatic leukodystrophy

scientific article published on 01 May 2002

Hippocampal proteoglycans brevican and versican are linked to spatial memory of Sprague-Dawley rats in the morris water maze

scientific article

Homeostasis of phospholipids - The level of phosphatidylethanolamine tightly adapts to changes in ethanolamine plasmalogens.

scientific article

Human leukocyte antigens and cytokine expression in cerebral inflammatory demyelinative lesions of X-linked adrenoleukodystrophy and multiple sclerosis

scientific article published in May 1997

Impaired neurotransmission in ether lipid-deficient nerve terminals ⬇️

scientific article published on March 8, 2012

Impaired plasmalogen synthesis dysregulates liver X receptor-dependent transcription in cerebellum

scientific article published on 28 May 2019

Impaired plasticity of macrophages in X-linked adrenoleukodystrophy

scientific article published on 01 August 2018

Impaired very long-chain acyl-CoA β-oxidation in human X-linked adrenoleukodystrophy fibroblasts is a direct consequence of ABCD1 transporter dysfunction.

scientific article published on 13 May 2013

Investigations of micro-organic brain damage (MOBD) in heterozygotes of metachromatic leukodystrophy.

scientific article

Involvement of human peroxisomes in biosynthesis and signaling of steroid and peptide hormones.

scientific article published on January 2013

LXR antagonists induce ABCD2 expression

scientific article published on 01 February 2014

Lack of adrenoleukodystrophy protein enhances oligodendrocyte disturbance and microglia activation in mice with combined Abcd1/Mag deficiency

scientific article published on 9 September 2007

Late-onset metachromatic leukodystrophy: genotype strongly influences phenotype

scientific article published in September 2006

Liver X receptor alpha interferes with SREBP1c-mediated Abcd2 expression. Novel cross-talk in gene regulation.

scientific article

Mechanistic insights into PTS2-mediated peroxisomal protein import: the co-receptor PEX5L drastically increases the interaction strength between the cargo protein and the receptor PEX7

scientific article

Microvascularization and expression of VEGF and its receptors in recurring meningiomas: pathobiological data in favor of anti-angiogenic therapy approaches.

scientific article

Molecular and phenotypic characteristics of metachromatic leukodystrophy patients from Poland.

scientific article published in July 2005

Mouse very long-chain Acyl-CoA synthetase 3/fatty acid transport protein 3 catalyzes fatty acid activation but not fatty acid transport in MA-10 cells

scientific journal article

Murine bubblegum orthologue is a microsomal very long-chain acyl-CoA synthetase ⬇️

scientific article published on January 1, 2004

Mutational analysis of functional domains in the HIV-1 rev trans-regulatory protein ⬇️

scientific article published on August 1, 1991

Mutations c.459+1G>A and p.P426L in the ARSA gene: prevalence in metachromatic leukodystrophy patients from European countries

scientific article published on 02 September 2005

Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophy

scientific article published in March 1997

Pathophysiology of X-linked adrenoleukodystrophy

scientific article

Peroxisomal alterations in Alzheimer's disease

scientific article

Peroxisomal cholesterol biosynthesis and Smith-Lemli-Opitz syndrome

scientific article published on 25 April 2006

Peroxisomal localization of the proopiomelanocortin-derived peptides beta-lipotropin and beta-endorphin

scientific article

Peroxisome-derived lipids are self antigens that stimulate invariant natural killer T cells in the thymus

scientific article published on 18 March 2012

Peroxisomes in brain development and function

scientific article

Plasmalogens, platelet-activating factor and beyond - Ether lipids in signaling and neurodegeneration

scientific article published on 28 August 2020

Proteome profiling in the rat Harderian gland.

scientific article published on July 2006

Proteomics characterization of mouse kidney peroxisomes by tandem mass spectrometry and protein correlation profiling

scientific journal article

Rare Human Missense Variants can affect the Function of Disease-Relevant Proteins by Loss and Gain of Peroxisomal Targeting Motifs

scientific article published on 17 September 2019

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

scientific article

Reduced muscle strength in ether lipid-deficient mice is accompanied by altered development and function of the neuromuscular junction

scientific article published on 29 May 2017

Revised nomenclature for the mammalian long-chain acyl-CoA synthetase gene family

scientific article

Simultaneous detection of the two most frequent metachromatic leukodystrophy mutations

scientific article published on 01 October 1993

Structural requirements for interaction of peroxisomal targeting signal 2 and its receptor PEX7.

scientific article published on 5 November 2011

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

scientific article published on December 1, 1997

Targeting foam cell formation in inflammatory brain diseases by the histone modifier MS-275

scientific article published on 30 September 2020

The TMEM189 gene encodes plasmanylethanolamine desaturase which introduces the characteristic vinyl ether double bond into plasmalogens

scientific article published on 24 March 2020

The difference in recognition of terminal tripeptides as peroxisomal targeting signal 1 between yeast and human is due to different affinities of their receptor Pex5p to the cognate signal and to residues adjacent to it.

scientific article

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

scientific article published in October 1999

The genetic landscape of X-linked adrenoleukodystrophy: inheritance, mutations, modifier genes, and diagnosis ⬇️

scientific article

The similarity between N-terminal targeting signals for protein import into different organelles and its evolutionary relevance

scientific article

Thyroid hormone induction of the adrenoleukodystrophy-related gene (ABCD2).

scientific article published in June 2003

Very long-chain acyl-CoA synthetase 3: overexpression and growth dependence in lung cancer

scientific article (publication date: 2013)

X-linked adrenoleukodystrophy mice demonstrate abnormalities in cholesterol metabolism

scientific article

X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype

scientific article published on 01 October 2008

X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.

scientific article

X-linked adrenoleukodystrophy: clinical, metabolic, genetic and pathophysiological aspects.

scientific article published on 28 March 2012

X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism is severely impaired in monocytes but not in lymphocytes.

scientific article published on 20 December 2013

cDNA cloning and analysis of tissue-specific expression of mouse peroxisomal straight-chain acyl-CoA oxidase

scientific article published in February 2000

cDNA cloning and mRNA distribution of a mouse very long‐chain acyl‐CoA synthetase ⬇️

scientific article published on March 27, 1998

cDNA cloning and mRNA expression of the human adrenoleukodystrophy related protein (ALDRP), a peroxisomal ABC transporter.

scientific article

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