Mutations in the tau gene have been described in families affected by frontotemporal dementia with parkinsonism linked to chromosome 17. The authors performed a genetic and biochemical analysis of this gene and its product in the parkinsonism dementia complex of Guam, a disorder characterized by the extensive formation of neurofibrillary tangles. The tau gene is not a primary cause of the parkinsonism dementia complex of Guam
Progressive supranuclear palsy (PSP) is a tau deposition neurodegenerative disorder which usually oc...
The tauopathies are a group of neurodegenerative diseases characterized by abnormal tau neuropatholo...
AbstractTau is the major component of the neurofibrillar tangles that are a pathological hallmark of...
Mutations in the tau gene have been described in families affected by frontotemporal dementia with p...
Tau protein is deposited as neurofibrillary tangles in Alzheimer's disease and in a range of other n...
A number of related conditions, including progressive supranuclear palsy (PSP), corticobasal degener...
Frontotemporal dementia (FTD) is considered to have a heterogeneous aetiology. To date the tau gene ...
Abundant cytoplasmic inclusions consisting of aggregated hyperphosphorylated protein tau a...
Frontotemporal dementia (FTD) is next to Alzheimer's disease one of the common causes of early onset...
An Australian family with autosomal dominant presenile nonspecific dementia was recently described. ...
Frontotemporal dementia (FTD) and Alzheimer's disease (AD) are two frequent causes of dementia that ...
BACKGROUND: Frontotemporal dementia (FTD) is an important cause of neurodegenerative dementia, parti...
Abstract Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) is an autosomal ...
The neural microtubule-associated protein tau binds directly to microtubules and regulates their dyn...
BACKGROUND: While mechanistic links between tau abnormalities and neurodegeneration have been proven...
Progressive supranuclear palsy (PSP) is a tau deposition neurodegenerative disorder which usually oc...
The tauopathies are a group of neurodegenerative diseases characterized by abnormal tau neuropatholo...
AbstractTau is the major component of the neurofibrillar tangles that are a pathological hallmark of...
Mutations in the tau gene have been described in families affected by frontotemporal dementia with p...
Tau protein is deposited as neurofibrillary tangles in Alzheimer's disease and in a range of other n...
A number of related conditions, including progressive supranuclear palsy (PSP), corticobasal degener...
Frontotemporal dementia (FTD) is considered to have a heterogeneous aetiology. To date the tau gene ...
Abundant cytoplasmic inclusions consisting of aggregated hyperphosphorylated protein tau a...
Frontotemporal dementia (FTD) is next to Alzheimer's disease one of the common causes of early onset...
An Australian family with autosomal dominant presenile nonspecific dementia was recently described. ...
Frontotemporal dementia (FTD) and Alzheimer's disease (AD) are two frequent causes of dementia that ...
BACKGROUND: Frontotemporal dementia (FTD) is an important cause of neurodegenerative dementia, parti...
Abstract Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) is an autosomal ...
The neural microtubule-associated protein tau binds directly to microtubules and regulates their dyn...
BACKGROUND: While mechanistic links between tau abnormalities and neurodegeneration have been proven...
Progressive supranuclear palsy (PSP) is a tau deposition neurodegenerative disorder which usually oc...
The tauopathies are a group of neurodegenerative diseases characterized by abnormal tau neuropatholo...
AbstractTau is the major component of the neurofibrillar tangles that are a pathological hallmark of...