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Published in 2021 at "Acta neurologica Belgica"
DOI: 10.1007/s13760-021-01743-w
Abstract: Skeletal muscle pathology is thought to have an important role in the onset and/or progression of amyotrophic lateral sclerosis (ALS), which is a neurodegenerative disorder characterized by progressive muscle weakness. Since miRNAs are recognized as…
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Keywords:
skeletal muscle;
muscle;
mirnas patients;
expressed mirnas ... See more keywords
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Published in 2020 at "Cell systems"
DOI: 10.1016/j.cels.2020.10.010
Abstract: Induced pluripotent stem cell (iPSC)-derived neural cultures from amyotrophic lateral sclerosis (ALS) patients can model disease phenotypes. However, heterogeneity arising from genetic and experimental variability limits their utility, impacting reproducibility and the ability to track…
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Keywords:
early convergent;
disease;
cross comparison;
sporadic als ... See more keywords
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Published in 2017 at "Neurobiology of Aging"
DOI: 10.1016/j.neurobiolaging.2017.06.007
Abstract: Genetic variants are implicated in the development of amyotrophic lateral sclerosis (ALS), but it is unclear whether the burden of rare variants in ALS genes has an effect on survival. We performed whole genome sequencing…
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Keywords:
als genes;
burden rare;
variants als;
sporadic als ... See more keywords
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Published in 2020 at "Genes"
DOI: 10.3390/genes11040448
Abstract: Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease that causes compromised function of motor neurons and neuronal death. However, oculomotor neurons are largely spared from disease symptoms. The underlying causes for sporadic ALS as well…
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Keywords:
gene expression;
oculomotor neurons;
sporadic als;
spinal oculomotor ... See more keywords