It is well known that transgenic mice overexpressing human tau protein with P301S mutation driven by the mouse prion protein promoter show clasping and limb retraction, hunched back and paralysis, followed by inability to feed that results in death around 12 months of age. To understand these motor deficits, we have carried out rotarod tests on PS19 line and demonstrated how they worsened during aging. Then, we have analyzed if these phenotypic characteristics correlate with sciatic nerve degeneration. We first demonstrated by western blot and immunohistochemistry that the sciatic nerve expresses the transgenic tau protein; then, electron microscopy studies showed alterations in myelin, mainly a detachment of myelin lamellae at Schmidt-Lant...
Lower motor neurons of the peripheral nervous system are responsible for innervating skeletal muscle...
Background: Myelination, degeneration and regeneration are implicated in crucial responses to injury...
Intracellular tau aggregates are the neuropathological hallmark of several neurodegenerative disease...
Tauopathies include a variety of neurodegenerative diseases associated with the pathological aggrega...
In disorders known as ‘dying-back’ neuropathies, the distal nerves appear to degenerate first and th...
Several neurodegenerative diseases are characterized by both cognitive and motor deficits associated...
Mutations in the coding and intronic regions of the tau gene cause frontotemporal dementia and parki...
Mutations in the human tau gene cause frontotemporal dementia and parkinsonism linked to chromosome ...
Pathological hyperphosphorylated tau is a key feature of Alzheimer's disease (AD) and Frontotemporal...
Transgenic mice expressing human tau containing the P301L tau mutation (JNPL3; tau mice) develop mot...
Tau is a microtubule-associated protein functionally known to bind microtubules and to be critical i...
Neurodegenerative diseases characterized by brain and spinal cord involvement often show widespread ...
This study investigates changes with respect to increasing protein levels in dystrophic nerves of tw...
Myotonic dystrophy type 1 (DM1) is a multisystem disorder with a variable phenotype. The involvement...
AbstractFilamentous tau aggregates are hallmarks of tauopathies, e.g., frontotemporal dementia with ...
Lower motor neurons of the peripheral nervous system are responsible for innervating skeletal muscle...
Background: Myelination, degeneration and regeneration are implicated in crucial responses to injury...
Intracellular tau aggregates are the neuropathological hallmark of several neurodegenerative disease...
Tauopathies include a variety of neurodegenerative diseases associated with the pathological aggrega...
In disorders known as ‘dying-back’ neuropathies, the distal nerves appear to degenerate first and th...
Several neurodegenerative diseases are characterized by both cognitive and motor deficits associated...
Mutations in the coding and intronic regions of the tau gene cause frontotemporal dementia and parki...
Mutations in the human tau gene cause frontotemporal dementia and parkinsonism linked to chromosome ...
Pathological hyperphosphorylated tau is a key feature of Alzheimer's disease (AD) and Frontotemporal...
Transgenic mice expressing human tau containing the P301L tau mutation (JNPL3; tau mice) develop mot...
Tau is a microtubule-associated protein functionally known to bind microtubules and to be critical i...
Neurodegenerative diseases characterized by brain and spinal cord involvement often show widespread ...
This study investigates changes with respect to increasing protein levels in dystrophic nerves of tw...
Myotonic dystrophy type 1 (DM1) is a multisystem disorder with a variable phenotype. The involvement...
AbstractFilamentous tau aggregates are hallmarks of tauopathies, e.g., frontotemporal dementia with ...
Lower motor neurons of the peripheral nervous system are responsible for innervating skeletal muscle...
Background: Myelination, degeneration and regeneration are implicated in crucial responses to injury...
Intracellular tau aggregates are the neuropathological hallmark of several neurodegenerative disease...