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Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosis
BACKGROUND: A pathological hallmark of most amyotrophic lateral sclerosis (ALS) cases are intracellular aggregates of the protein TDP-43. The pathophysiological relevance of TDP-43 is underlined by familial ALS cases caused by TDP-43 mutations. TDP-43 is involved in processing of both coding RNAs an...
Gorde:
| Egile Nagusiak: | , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2013
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3893596/ https://ncbi.nlm.nih.gov/pubmed/24252274 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2051-5960-1-42 |
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