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Extracellular truncated tau causes early presynaptic dysfunction associated with Alzheimer’s disease and other tauopathies
The largest part of tau secreted from AD nerve terminals and released in cerebral spinal fluid (CSF) is C-terminally truncated, soluble and unaggregated supporting potential extracellular role(s) of NH(2) -derived fragments of protein on synaptic dysfunction underlying neurodegenerative tauopathies,...
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| Pubblicato in: | Oncotarget |
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| Autori principali: | , , , , , , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Impact Journals LLC
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5630290/ https://ncbi.nlm.nih.gov/pubmed/29029390 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.17371 |
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