It has recently been established that the ubiquitinated neuronal inclusions and neurites observed in frontotemporal lobar degeneration (FTLD) contain the TAR DNA-binding protein, TDP-43. It is not uncommon for genetic variation of genes that encode proteins that accumulate in neurodegenerative conditions to increase risk for disease. We therefore examined whether variation of the TDP-43 locus was associated with an increased risk of disease in the Manchester FTLD cohort. We found no evidence of TDP-43 variation increasing risk for FTLD in this cohort. These data suggest that TDP-43 accumulation is a consequence of the disease process underlying FTLD
To further characterize the neuropathology of the heterogeneous molecular disorder frontotemporal lo...
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The ...
Frontotemporal lobar degeneration (FTLD) is a highly heterogenous group of progressive neurodegenera...
A new study has identified novel genes involved in sporadic frontotemporal lobar degeneration with n...
Major discoveries have been made in the recent past in the genetics, biochemistry and neuropathology...
The nuclear TAR DNA binding protein (TDP-43) is deposited in ubiquitin-positive inclusions in fronto...
International audienceTDP-43 (TAR-DNA binding protein) aggregates in neuronal inclusions in motoneur...
Aggregation of misfolded TAR DNA-binding protein 43 (TDP-43) is a striking hallmark of neurodegenera...
TAR DNA-binding protein of 43 kDa (TDP-43) is a major component of the pathological inclusions of fr...
Frontotemporal lobar degeneration with neuronal inclusions of the TAR DNA-binding protein 43 (FTLD-T...
Abstract The identification of the TAR DNA-binding protein 43 (TDP-43) as the ubiquitinated cytoplas...
has recently been associated with a risk of frontotemporal lobar degeneration (FTLD) in North Ameri...
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The ...
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The ...
The BrainNet Europe consortium assessed the reproducibility in the assignment of the type of frontot...
To further characterize the neuropathology of the heterogeneous molecular disorder frontotemporal lo...
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The ...
Frontotemporal lobar degeneration (FTLD) is a highly heterogenous group of progressive neurodegenera...
A new study has identified novel genes involved in sporadic frontotemporal lobar degeneration with n...
Major discoveries have been made in the recent past in the genetics, biochemistry and neuropathology...
The nuclear TAR DNA binding protein (TDP-43) is deposited in ubiquitin-positive inclusions in fronto...
International audienceTDP-43 (TAR-DNA binding protein) aggregates in neuronal inclusions in motoneur...
Aggregation of misfolded TAR DNA-binding protein 43 (TDP-43) is a striking hallmark of neurodegenera...
TAR DNA-binding protein of 43 kDa (TDP-43) is a major component of the pathological inclusions of fr...
Frontotemporal lobar degeneration with neuronal inclusions of the TAR DNA-binding protein 43 (FTLD-T...
Abstract The identification of the TAR DNA-binding protein 43 (TDP-43) as the ubiquitinated cytoplas...
has recently been associated with a risk of frontotemporal lobar degeneration (FTLD) in North Ameri...
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The ...
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The ...
The BrainNet Europe consortium assessed the reproducibility in the assignment of the type of frontot...
To further characterize the neuropathology of the heterogeneous molecular disorder frontotemporal lo...
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The ...
Frontotemporal lobar degeneration (FTLD) is a highly heterogenous group of progressive neurodegenera...