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Investigations on the mode of action of gephyronic acid, an inhibitor of eukaryotic protein translation from myxobacteria

PloS one, 2018-07, Vol.13 (7), p.e0201605

2018

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Alopecia and male infertility in oligotriche mutant mice are caused by a deletion on distal chromosome 9

Mammalian genome, 2008-12, Vol.19 (10-12), p.691-702

2008

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dominant vimentin mutant upregulates Hsp70 and the activity of the ubiquitin-proteasome system, and causes posterior cataracts in transgenic mice

Journal of cell science, 2008-11, Vol.121 (22), p.3737-3746

2008

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Absence of 2-Hydroxylated Sphingolipids Is Compatible with Normal Neural Development But Causes Late-Onset Axon and Myelin Sheath Degeneration

The Journal of neuroscience, 2008-09, Vol.28 (39), p.9741-9754

2008

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Down-regulation of Polysialic Acid Is Required for Efficient Myelin Formation

The Journal of biological chemistry, 2007-06, Vol.282 (22), p.16700-16711

2007

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A spontaneously immortalized Schwann cell line to study the molecular aspects of metachromatic leukodystrophy

Journal of neuroscience methods, 2007-04, Vol.161 (2), p.223-233

2007

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Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71rco12 and Krt71rco13

Mammalian genome, 2006-12, Vol.17 (12), p.1172-1182

2006

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Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13

Mammalian genome, 2006-12, Vol.17 (12), p.1172-1182

2006

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Keratin 5 knockout mice reveal plasticity of keratin expression in the corneal epithelium

European journal of cell biology, 2006-08, Vol.85 (8), p.803-811

2006

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Expression pattern and functional characterization of connexin29 in transgenic mice

Glia, 2006-04, Vol.53 (6), p.601-611

2006

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Grey, a novel mutation in the murine Lyst gene, causes the beige phenotype by skipping of exon 25

Mammalian genome, 2006-03, Vol.17 (3), p.203-210

2006

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Loss-of-Function Mutations in the Keratin 5 Gene Lead to Dowling-Degos Disease

American journal of human genetics, 2006-03, Vol.78 (3), p.510-519

2006

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Oligodendrocyte-specific ceramide galactosyltransferase (CGT) expression phenotypically rescues CGT-deficient mice and demonstrates that CGT activity does not limit brain galactosylceramide level

Glia, 2005-11, Vol.52 (3), p.190-198

2005

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Structure determination of human proteins and protein complexes

GBM Annual Fall meeting Berlin/Potsdam 2005, 2005-09, Vol.2005 (Fall), Article 1326

2005

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Reversal of non-hydroxy : [alpha]-hydroxy galactosylceramide ratio and unstable myelin in transgenic mice overexpressing UDP-galactose : ceramide galactosyltransferase

Journal of neurochemistry, 2005-07, Vol.94 (2), p.469

2005

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Reversal of non‐hydroxy : α‐hydroxy galactosylceramide ratio and unstable myelin in transgenic mice overexpressing UDP‐galactose : ceramide galactosyltransferase

Journal of neurochemistry, 2005-07, Vol.94 (2), p.469-481

2005

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Missense mutations as a cause of metachromatic leukodystrophy. Degradation of arylsulfatase A in the endoplasmic reticulum

The FEBS journal, 2005-03, Vol.272 (5), p.1179-1188

2005

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Missense mutations as a cause of metachromatic leukodystrophy

The FEBS journal, 2005-03, Vol.272 (5), p.1179-1188

2005

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Exocytosis of storage material in a lysosomal disorder

Biochemical and biophysical research communications, 2005-02, Vol.327 (3), p.663-667

2005

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X-ray structure of fumarylacetoacetate hydrolase family member Homo sapiens FLJ36880

Biological chemistry, 2004-10, Vol.385 (10), p.935-942

2004

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Functional Integration of Embryonic Stem Cell-Derived Neurons In Vivo

The Journal of neuroscience, 2004-06, Vol.24 (22), p.5258-5268

2004

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Crystal structure of Homo sapiens protein hp14.5

Proteins, structure, function, and bioinformatics, 2004-05, Vol.55 (3), p.783-783

2004

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Functional expression of connexin57 in horizontal cells of the mouse retina

The European journal of neuroscience, 2004-05, Vol.19 (10), p.2633-2640

2004

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X-ray structure of human gankyrin, the product of a gene linked to hepatocellular carcinoma

Proteins, structure, function, and bioinformatics, 2004-04, Vol.55 (1), p.214-217

2004

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Crystal structure of Homo sapiens protein hp14.5

Proteins, structure, function, and bioinformatics, 2004-03, Vol.54 (4), p.797-800

2004

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Investigations on the mode of action of gephyronic acid, an inhibitor of eukaryotic protein translation from myxobacteria

Alopecia and male infertility in oligotriche mutant mice are caused by a deletion on distal chromosome 9

dominant vimentin mutant upregulates Hsp70 and the activity of the ubiquitin-proteasome system, and causes posterior cataracts in transgenic mice

Absence of 2-Hydroxylated Sphingolipids Is Compatible with Normal Neural Development But Causes Late-Onset Axon and Myelin Sheath Degeneration

Down-regulation of Polysialic Acid Is Required for Efficient Myelin Formation

A spontaneously immortalized Schwann cell line to study the molecular aspects of metachromatic leukodystrophy

Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71rco12 and Krt71rco13

Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13

Keratin 5 knockout mice reveal plasticity of keratin expression in the corneal epithelium

Expression pattern and functional characterization of connexin29 in transgenic mice

Grey, a novel mutation in the murine Lyst gene, causes the beige phenotype by skipping of exon 25

Loss-of-Function Mutations in the Keratin 5 Gene Lead to Dowling-Degos Disease

Oligodendrocyte-specific ceramide galactosyltransferase (CGT) expression phenotypically rescues CGT-deficient mice and demonstrates that CGT activity does not limit brain galactosylceramide level

Structure determination of human proteins and protein complexes

Reversal of non-hydroxy : [alpha]-hydroxy galactosylceramide ratio and unstable myelin in transgenic mice overexpressing UDP-galactose : ceramide galactosyltransferase

Reversal of non‐hydroxy : α‐hydroxy galactosylceramide ratio and unstable myelin in transgenic mice overexpressing UDP‐galactose : ceramide galactosyltransferase

Missense mutations as a cause of metachromatic leukodystrophy. Degradation of arylsulfatase A in the endoplasmic reticulum

Missense mutations as a cause of metachromatic leukodystrophy

Exocytosis of storage material in a lysosomal disorder

X-ray structure of fumarylacetoacetate hydrolase family member Homo sapiens FLJ36880

Functional Integration of Embryonic Stem Cell-Derived Neurons In Vivo

Crystal structure of Homo sapiens protein hp14.5

Functional expression of connexin57 in horizontal cells of the mouse retina

X-ray structure of human gankyrin, the product of a gene linked to hepatocellular carcinoma

Crystal structure of Homo sapiens protein hp14.5

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