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Biology and Pathobiology of TDP-43 and Emergent Therapeutic Strategies

Cytoplasmic TDP-43 mislocalization and aggregation is a pathological hallmark of amyotrophic lateral sclerosis and frontotemporal lobar degeneration. TDP-43 is an RNA-binding protein (RBP) with a prion-like domain (PrLD) that promotes TDP-43 misfolding. PrLDs possess compositional similarity to cano...

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Publicat a:Cold Spring Harb Perspect Med
Autors principals: Guo, Lin, Shorter, James
Format: Artigo
Idioma:Inglês
Publicat: Cold Spring Harbor Laboratory Press 2017
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5580514/
https://ncbi.nlm.nih.gov/pubmed/27920024
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/cshperspect.a024554
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