Decreased Levels of Foldase and Chaperone Proteins Are Associated with an Early-Onset Amyotrophic Lateral Sclerosis
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Decreased Levels of Foldase and Chaperone Proteins Are Associated with an Early-Onset Amyotrophic Lateral Sclerosis
Authors
Keywords
-
Journal
Frontiers in Molecular Neuroscience
Volume 10, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2017-04-06
DOI
10.3389/fnmol.2017.00099
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Hsp90 directly interacts, in vitro , with amyloid structures and modulates their assembly and disassembly
- (2016) Claire Schirmer et al. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
- New Insights on the Mechanisms of Disease Course Variability in ALS from Mutant SOD1 Mouse Models
- (2016) Giovanni Nardo et al. BRAIN PATHOLOGY
- Proteostasis impairment in ALS
- (2016) Céline Ruegsegger et al. BRAIN RESEARCH
- ALS‐linked protein disulfide isomerase variants cause motor dysfunction
- (2016) Ute Woehlbier et al. EMBO JOURNAL
- Factors predicting survival in ALS: a multicenter Italian study
- (2016) Andrea Calvo et al. JOURNAL OF NEUROLOGY
- Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases
- (2016) Valeria Crippa et al. Scientific Reports
- Peptidylprolyl isomerase A governs TARDBP function and assembly in heterogeneous nuclear ribonucleoprotein complexes
- (2015) Eliana Lauranzano et al. BRAIN
- Marinesco-Sjögren syndrome protein SIL1 regulates motor neuron subtype-selective ER stress in ALS
- (2015) Audrey Filézac de L'Etang et al. NATURE NEUROSCIENCE
- Differences in protein quality control correlate with phenotype variability in 2 mouse models of familial amyotrophic lateral sclerosis
- (2015) Marianna Marino et al. NEUROBIOLOGY OF AGING
- De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients
- (2015) Annemarie Hübers et al. NEUROBIOLOGY OF AGING
- DJ-1 Knockout Augments Disease Severity and Shortens Survival in a Mouse Model of ALS
- (2015) Nirit Lev et al. PLoS One
- Casein Kinase II Induced Polymerization of Soluble TDP-43 into Filaments Is Inhibited by Heat Shock Proteins
- (2014) Yari Carlomagno et al. PLoS One
- Plasma amino acids patterns and age of onset of amyotrophic lateral sclerosis
- (2014) Matteo Cecchi et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Transcriptomic indices of fast and slow disease progression in two mouse models of amyotrophic lateral sclerosis
- (2013) Giovanni Nardo et al. BRAIN
- Hsp90 Inhibits α-Synuclein Aggregation by Interacting with Soluble Oligomers
- (2013) Soumya Daturpalli et al. JOURNAL OF MOLECULAR BIOLOGY
- Large-scale gene function analysis with the PANTHER classification system
- (2013) Huaiyu Mi et al. Nature Protocols
- The role of heat shock proteins in Amyotrophic Lateral Sclerosis: The therapeutic potential of Arimoclomol
- (2013) Bernadett Kalmar et al. PHARMACOLOGY & THERAPEUTICS
- Whole-blood global DNA methylation is increased in amyotrophic lateral sclerosis independently of age of onset
- (2013) Lucio Tremolizzo et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Are professional soccer players at higher risk for ALS?
- (2013) Ettore Beghi Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Trauma and amyotrophic lateral sclerosis: a case-control study from a population-based registry
- (2012) E. Pupillo et al. EUROPEAN JOURNAL OF NEUROLOGY
- EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans
- (2012) Annelies Van Hoecke et al. NATURE MEDICINE
- Amyotrophic Lateral Sclerosis Multiprotein Biomarkers in Peripheral Blood Mononuclear Cells
- (2011) Giovanni Nardo et al. PLoS One
- The epidemiology and treatment of ALS: Focus on the heterogeneity of the disease and critical appraisal of therapeutic trials
- (2010) Ettore Beghi et al. Amyotrophic Lateral Sclerosis
- Suppression of Expression of Endoplasmic Reticulum Chaperones byHelicobacter pyloriand Its Role in Exacerbation of Non-steroidal Anti-inflammatory Drug-induced Gastric Lesions
- (2010) Takushi Namba et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- A role for motoneuron subtype–selective ER stress in disease manifestations of FALS mice
- (2009) Smita Saxena et al. NATURE NEUROSCIENCE
- Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation
- (2009) Adriano Chiò et al. NEUROBIOLOGY OF AGING
- Characterization of Detergent-Insoluble Proteins in ALS Indicates a Causal Link between Nitrative Stress and Aggregation in Pathogenesis
- (2009) Manuela Basso et al. PLoS One
- DJ-1 Changes in G93A-SOD1 Transgenic Mice: Implications for Oxidative Stress in ALS
- (2008) Nirit Lev et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Arimoclomol at dosages up to 300 mg/day is well tolerated and safe in amyotrophic lateral sclerosis
- (2008) Merit E. Cudkowicz et al. MUSCLE & NERVE
- Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis
- (2008) Julie D. Atkin et al. NEUROBIOLOGY OF DISEASE
- DJ-1 Modulates α-Synuclein Aggregation State in a Cellular Model of Oxidative Stress: Relevance for Parkinson's Disease and Involvement of HSP70
- (2008) Sara Batelli et al. PLoS One
- Proteomic map of peripheral blood mononuclear cells
- (2008) Daniele Vergara et al. PROTEOMICS
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started