ALS Compendium
Homozygosity analysis in amyotrophic lateral sclerosis
Selective Forelimb Impairment in Rats Expressing a Pathological TDP-43 25 kDa C-terminal Fragment to Mimic Amyotrophic Lateral Sclerosis
Exome sequencing to identify de novo mutations in sporadic ALS trios
The modest impact of transcription factor Nrf2 on the course of disease in an ALS animal model. Laboratory Investigation
Synergistic Effects of GDNF and VEGF on Lifespan and Disease Progression in a Familial ALS Rat Model
Viral Delivery of Antioxidant Genes as a Therapeutic Strategy in Experimental Models of Amyotrophic Lateral Sclerosis
FUS-regulated region- and cell-type-specific transcriptome is associated with cell selectivity in ALS/ FTLD
Sequestosome-1 ( SQSTM1 ) sequence variants in ALS cases in the UK : prevalence and coexistence of SQSTM1 mutations in ALS kindred with PDB
Therapeutic AAV9-mediated Suppression of Mutant SOD1 Slows Disease Progression and Extends Survival in Models of Inherited ALS
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