Sanders et al. (2014) demonstrate in this issue of Neuron that the natively unfolded protein tau can propagate indefinitely in distinct stable strains, therefore supporting the general idea that tau has prion-like properties, with implications for Alzheimer’s disease and other tauopathies
Prion-like propagation of tau aggregation might underlie the stereotyped progression of neurodegener...
Abstract Since 2009, evidence has accumulated to suggest that Tau aggregates form firs...
SummaryMany neurodegenerative diseases are characterized by the accumulation of insoluble protein ag...
SummaryPrion-like propagation of tau aggregation might underlie the stereotyped progression of neuro...
Tauopathies are a diverse set of neurodegenerative diseases that feature the progressive accumulatio...
Recent findings have suggested that tau pathology may spread in the brain by a prion-like mechanism....
Tauopathies are a heterogeneous group of pathologies characterized by tau aggregation inside neurons...
Abstract Tauopathies are a heterogeneous group of pathologies characterized by tau aggregation insid...
Emerging experimental evidence suggests that the spread of tau pathology in the brain in Tauopathies...
Tauopathies are neurodegenerative diseases characterized by neurofibrillary tangles and/or paired he...
Neurodegenerative tauopathies are characterized by the abnormal accumulation of tau protein inside n...
Neurodegenerative tauopathies are characterized by the abnormal accumulation of tau protein inside n...
International audienceThe term “propagon” is used to define proteins that may transmit misfolding in...
The inter-cellular propagation of tau aggregates in several neurodegenerative diseases involves, in ...
A shared property of several neurodegenerative diseases is the neuronal accumulation of aggregated t...
Prion-like propagation of tau aggregation might underlie the stereotyped progression of neurodegener...
Abstract Since 2009, evidence has accumulated to suggest that Tau aggregates form firs...
SummaryMany neurodegenerative diseases are characterized by the accumulation of insoluble protein ag...
SummaryPrion-like propagation of tau aggregation might underlie the stereotyped progression of neuro...
Tauopathies are a diverse set of neurodegenerative diseases that feature the progressive accumulatio...
Recent findings have suggested that tau pathology may spread in the brain by a prion-like mechanism....
Tauopathies are a heterogeneous group of pathologies characterized by tau aggregation inside neurons...
Abstract Tauopathies are a heterogeneous group of pathologies characterized by tau aggregation insid...
Emerging experimental evidence suggests that the spread of tau pathology in the brain in Tauopathies...
Tauopathies are neurodegenerative diseases characterized by neurofibrillary tangles and/or paired he...
Neurodegenerative tauopathies are characterized by the abnormal accumulation of tau protein inside n...
Neurodegenerative tauopathies are characterized by the abnormal accumulation of tau protein inside n...
International audienceThe term “propagon” is used to define proteins that may transmit misfolding in...
The inter-cellular propagation of tau aggregates in several neurodegenerative diseases involves, in ...
A shared property of several neurodegenerative diseases is the neuronal accumulation of aggregated t...
Prion-like propagation of tau aggregation might underlie the stereotyped progression of neurodegener...
Abstract Since 2009, evidence has accumulated to suggest that Tau aggregates form firs...
SummaryMany neurodegenerative diseases are characterized by the accumulation of insoluble protein ag...