ALSOD: The Amyotrophic Lateral Sclerosis Online Database
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SOD1 Transcriptional and Posttranscriptional Regulation and Its Potential Implications in ALSLigand binding and aggregation of pathogenic SOD1Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.Mendelian bases of myopathies, cardiomyopathies, and neuromyopathies.An integrated approach to the interpretation of single amino acid polymorphisms within the framework of CATH and Gene3D.Glial nuclear aggregates of superoxide dismutase-1 are regularly present in patients with amyotrophic lateral sclerosis.Proteins that bind to misfolded mutant superoxide dismutase-1 in spinal cords from transgenic amyotrophic lateral sclerosis (ALS) model mice.An Iranian familial amyotrophic lateral sclerosis pedigree with p.Val48Phe causing mutation in SOD1: a genetic and clinical report.Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mappingChromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.Inhibition of Cytohesins Protects against Genetic Models of Motor Neuron Disease.Effects of Cellular Pathway Disturbances on Misfolded Superoxide Dismutase-1 in Fibroblasts Derived from ALS PatientsObservation of c.260A > G mutation in superoxide dismutase 1 that causes p.Asn86Ser in Iranian amyotrophic lateral sclerosis patient and absence of genotype/phenotype correlation.Low autophagy capacity implicated in motor system vulnerability to mutant superoxide dismutaseSingle-nucleotide Polymorphism rs2275294 in ZNF512B is not Associated with Susceptibility to Amyotrophic Lateral Sclerosis in a Large Chinese CohortEstablishing a novel C. elegans model to investigate the role of autophagy in amyotrophic lateral sclerosis.Regulation of superoxide dismutase genes: implications in disease.The SODyssey: superoxide dismutases from biochemistry, through proteomics, to oxidative stress, aging and nutraceuticals.Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databases.Stress signaling from the endoplasmic reticulum: A central player in the pathogenesis of amyotrophic lateral sclerosis.Disruption of axonal transport in motor neuron diseases.Use of Caenorhabditis elegans as a model to study Alzheimer's disease and other neurodegenerative diseases.Gene discovery in amyotrophic lateral sclerosis: implications for clinical management.Two superoxide dismutase prion strains transmit amyotrophic lateral sclerosis-like disease.Identification of L84F mutation with a novel nucleotide change c.255G > T in the superoxide dismutase gene in a North Indian family with amyotrophic lateral sclerosis.Aberrant association of misfolded SOD1 with Na(+)/K(+)ATPase-α3 impairs its activity and contributes to motor neuron vulnerability in ALS.Oxidative stress induced by loss of Cu,Zn-superoxide dismutase (SOD1) or superoxide-generating herbicides causes axonal degeneration in mouse DRG cultures.Genetic mutations in RNA-binding proteins and their roles in ALS.A novel SOD1 splice site mutation associated with familial ALS revealed by SOD activity analysis.A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS.G127R: A novel SOD1 mutation associated with rapidly evolving ALS and severe pain syndrome.Misfolded superoxide dismutase-1 in CSF from amyotrophic lateral sclerosis patients.Modelling the effects of penetrance and family size on rates of sporadic and familial disease.ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics.Developing the "next generation" of genetic association databases for complex diseases.G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype.Computational investigation of the human SOD1 mutant, Cys146Arg, that directs familial amyotrophic lateral sclerosis.A theoretical study on Zn binding loop mutants instigating destabilization and metal binding loss in human SOD1 protein.NDDVD: an integrated and manually curated Neurodegenerative Diseases Variation Database.Degenerative Myelopathy in a Bernese Mountain Dog with a Novel SOD1 Missense Mutation
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ALSOD: The Amyotrophic Lateral Sclerosis Online Database
description
article
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в січні 2008
@uk
name
ALSOD: The Amyotrophic Lateral Sclerosis Online Database
@en
ALSOD: The Amyotrophic Lateral Sclerosis Online Database
@nl
type
label
ALSOD: The Amyotrophic Lateral Sclerosis Online Database
@en
ALSOD: The Amyotrophic Lateral Sclerosis Online Database
@nl
prefLabel
ALSOD: The Amyotrophic Lateral Sclerosis Online Database
@en
ALSOD: The Amyotrophic Lateral Sclerosis Online Database
@nl
P2093
P1476
ALSOD: The Amyotrophic Lateral Sclerosis Online Database
@en
P2093
Amy Wai-Ling Butler
John F. Powell
Richard Wroe
P304
P356
10.1080/17482960802146106
P577
2008-01-01T00:00:00Z