ALS Compendium

Interaction of FUS and HDAC1 regulates DNA damage response and repair in neurons

Death receptor 6 ( DR6 ) antagonist antibody is neuroprotective in the mouse SOD1 G93A model of amyotrophic lateral sclerosis

Establishing a novel C. elegans model to investigate the role of autophagy in amyotrophic lateral sclerosis

Prediction of functional loss of human angiogenin mutants associated with ALS by molecular dynamics simulations

Acidotoxicity and acid-sensing ion channels contribute to motoneuron degeneration. Cell Death and Differentiation

Efficient gene expression from integration-deficient lentiviral vectors in the spinal cord

Genetic analysis of SIGMAR1 as a cause of familial ALS with dementia.

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS