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UnknownEvaluation of a biomarker for amyotrophic lateral sclerosis derived from a hypomethylated DNA signature of human motor neurons.
Not available
S-EPMC11734586 | biostudies-literature
UnknownThe Effect of SMN Gene Dosage on ALS Risk and Disease Severity.
Not available
S-EPMC8048961 | biostudies-literature
UnknownALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function.
Not available
S-EPMC6983933 | biostudies-literature
UnknownStructural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis.
Not available
S-EPMC8799638 | biostudies-literature
UnknownTelomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data.
Not available
S-EPMC9799999 | biostudies-literature
UnknownGenetic variability in sporadic amyotrophic lateral sclerosis.
Not available
S-EPMC10473563 | biostudies-literature
UnknownRare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene.
Not available
S-EPMC7710676 | biostudies-literature
UnknownGenome-wide identification of the genetic basis of amyotrophic lateral sclerosis.
Not available
S-EPMC9017397 | biostudies-literature
UnknownATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization.
Not available
S-EPMC7425293 | biostudies-literature
UnknownNEK1 variants confer susceptibility to amyotrophic lateral sclerosis.
Not available
S-EPMC5560030 | biostudies-literature
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