A physics-based model explains the prion-like features of neurodegeneration in Alzheimer’s disease, Parkinson’s disease, and amyotrophic lateral sclerosis
Prion disease is characterized by a chain reaction in which infectious misfolded proteins force native proteins into a similar pathogenic structure. Recent studies have reinforced the hypothesis that the prion paradigm–the templated growth and spreading of misfolded proteins–could help explain a var...
Glavni autori: | Weickenmeier, J, Jucker, M, Goriely, A, Kuhl, E |
---|---|
Format: | Journal article |
Izdano: |
Elsevier
2018
|
Slični predmeti
Slični predmeti
-
Prion-like spreading of Alzheimer's disease within the brain's connectome
od: Fornari, S, i dr.
Izdano: (2019) -
The multiphysics of prion-like diseases: progression and atrophy
od: Weickenmeier, J, i dr.
Izdano: (2018) -
Alzheimer's disease, amyotrophic lateral sclerosis, and transgenic mice.
od: Bajaj, N, i dr.
Izdano: (1998) -
Does interneuronal dysfunction contribute to neurodegeneration in amyotrophic lateral sclerosis?
od: Turner, M, i dr.
Izdano: (2012) -
Concurrent multiple sclerosis and amyotrophic lateral sclerosis: where inflammation and neurodegeneration meet?
od: Li, G, i dr.
Izdano: (2012)