Associated Papers
Aggregation of E121K mutant D-amino acid oxidase and ubiquitination-mediated autophagy mechanisms leading to amyotrophic lateral sclerosis.
Dave U et al.
Journal of the Neurological Sciences, 2024
Characterization of E121K mutation of D-amino acid oxidase - Insights into mechanisms leading to amyotrophic lateral sclerosis.
Dave U et al.
Biochimica Et Biophysica Acta. Proteins and Proteomics, 2023
Human d-amino acid oxidase: The inactive G183R variant.
Murtas G et al.
Biochimica Et Biophysica Acta. Proteins and Proteomics, 2018
Focus on the Role of D-serine and D-amino Acid Oxidase in Amyotrophic Lateral Sclerosis/Motor Neuron Disease (ALS).
Kondori NR et al.
Frontiers in Molecular Biosciences, 2018
Biochemical Properties of Human D-amino Acid Oxidase Variants and Their Potential Significance in Pathologies.
Sacchi S et al.
Frontiers in Molecular Biosciences, 2018
Human D-Amino Acid Oxidase: Structure, Function, and Regulation.
Pollegioni L et al.
Frontiers in Molecular Biosciences, 2018
Structure-function relationships in human d-amino acid oxidase variants corresponding to known SNPs.
Cappelletti P et al.
Biochimica Et Biophysica Acta, 2015
Characterization of human DAAO variants potentially related to an increased risk of schizophrenia.
Caldinelli L et al.
Biochimica Et Biophysica Acta, 2013
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