Rosenthal S S - OmicsDI

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CHEBI ID

CHEBI:17234 (3)
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(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol (1)
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Study type

Transcription profiling by array (54)
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Lab affiliation

Basic Immune System of Plants / Protein Mass Spectrometry Max Planck Institute for Plant Breeding Research Carl-von-Linne-Weg 10, 50829 Cologne, Germany (1)
Department of Cancer Research and Molecular Medicine Faculty of Medicine Laboratory Centre, 5th floor. Erling Skjalgssons gt. 1 Norwegian University of Science and Technology NTNU 7006 Trondheim, Norway Tel: +47 72573076; Fax: +47 72576400 Cell. phone: +47 91825455 (1)
Department of Molecular Mechanisms of Disease, University of Zurich, CH-8057 Zurich, Switzerland (1)
Department of Molecular Mechanisms of Disease, University of Zurich, Switzerland (1)
Department of Pharmacology and Toxicology University of Texas Medical Branch Galveston, TX 77555 USA (1)
Institute for Cell Engineering, Department of Neurology, Johns Hopkins University School of Medicine (1)
Istituto superiore di sanità (1)
Johns Hopkins University School of Medicine (1)
Max Planck Institute for Terrestrial Microbiology Karl-von-Frisch Str. 10 35043 Marburg Germany (1)
Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Department of Neurology (1)
Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Department of Neurology, Johns Hopkins University (1)
Professor of Neurobiology, University of Alabama at Birmingham, USA (1)
Tel Aviv University (1)
The University of Melbourne (1)
UCSF (1)

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Composition of Rosenthal fibers in Alexander disease patients and mouse models

Alexander disease (AxD) is a fatal neurodegenerative disorder characterized by the presence in astrocytes of protein aggregates called Rosenthal fibers (RFs). In this work, we used a new biochemical fractionation method to enrich for RFs followed by analysis of this fraction using quantitative iTRA...

ORGANISM(S): Mus musculus (Mouse) Homo sapiens (Human)

2016-05-23 | PXD002448 | Pride

Composition of Rosenthal Fibers, the Protein Aggregate Hallmark of Alexander Disease.

Not available

S-EPMC5036859 | biostudies-literature

Melkersson-Rosenthal Syndrome with Genitalia Involved in a 12-Year-Old Boy.

Not available

S-EPMC4828388 | biostudies-literature

Melkersson⁻Rosenthal Syndrome in Childhood: Report of Three Paediatric Cases and a Review of the Literature.

Not available

S-EPMC6479526 | biostudies-literature

S-nitrosothiol signaling regulates liver development and improves outcome following toxic liver injury.

Not available

S-EPMC4008725 | biostudies-literature

Discovery of s-nitrosoglutathione reductase inhibitors: potential agents for the treatment of asthma and other inflammatory diseases.

Not available

S-EPMC4018076 | biostudies-literature

The S-Factor, a New Measure of Disease Severity in Spinocerebellar Ataxia: Findings and Implications.

Not available

S-EPMC10363993 | biostudies-literature

SYNTHESIS OF THE INTERSPECIES SIGNALING MOLECULE AUTOINDUCER-2 PLAYS AN IMPORTANT ROLE IN THE ANTI-MICROBIAL EFFECT OF BIFIDOBACTERIA

In the present study we show that a functional luxS gene is present in all members of the genus Bifidobacterium and that AI-2 production by Bifidobacterium breve UCC2003 is necessary to confer protection against Salmonella infection in Caenorhabditis elegans. Mutants carrying a disrupted luxS gene c...

ORGANISM(S): Bifidobacterium breve UCC2003

2015-12-31 | E-GEOD-49880 | biostudies-arrayexpress

Genes involved in synthesis of lipoteichoic acids are induced when Bifidobacterium animalis subsp. lactis BB12 is incubated with Human Enterocyte-Like Caco-2 Cells

Bifidobacterium animalis subsp. lactis BB12 is a widely used probiotic bacterium. However the molecular mechanism by which this bacterium confers positive health effects to the host is largely unknown. The importance of lipoteichoic acids (LTA) in the cross-talk between the bacteria and human entero...

ORGANISM(S): Bifidobacterium animalis subsp. lactis BB-12

2012-07-31 | E-GEOD-21588 | biostudies-arrayexpress

Chromosome deletion of 14q32.33 detected by array comparative genomic hybridization in a patient with features of dubowitz syndrome.

Not available

S-EPMC3447229 | biostudies-literature

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