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UnknownDifferential role of C-terminal truncations on alpha-synuclein pathology and Lewy body formation.
Not available
S-EPMC12381302 | biostudies-literature
UnknownMutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis.
Not available
S-EPMC4000579 | biostudies-literature
UnknownA hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Not available
S-EPMC3200438 | biostudies-literature
UnknownMechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data.
Not available
S-EPMC11605688 | biostudies-literature
UnknownAssociation of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis.
Not available
S-EPMC8406220 | biostudies-literature
UnknownGenome-wide Analyses Identify KIF5A as a Novel ALS Gene.
Not available
S-EPMC5867896 | biostudies-literature
UnknownLiraglutide and Cardiovascular Outcomes in Type 2 Diabetes.
Not available
S-EPMC4985288 | biostudies-literature
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