Enzymatic assays for acetylcholine esterase (AChE) and choline acetyltransferase (ChAT) were applied to dorsal and ventral cervical spinal cord regions taken from the Wobbler mouse, a model for inherited motoneuron disease. Early in the disease, ChAT (but not AChE) activity is significantly greater compared with the control littermate specimens. The high ChAT activity correlates with the high thyrotropin releasing hormone (also leucine-enkephalin) concentrations measured in the Wobbler ventral horn early in the disease. Late in the motoneuron disease, both AChE and ChAT activities are significantly lower than in the control littermate specimens. These data correlate with the high substance P, methionine and leucine enkephalin concentrations...
The wobbler mouse is a model of selective motor neuron degeneration in the cervical spinal cord. Com...
Lack of dystrophin in brain structures have been involved with impaired cognitive functions. Acethyl...
To identify candidate genes that are responsible for motoneurone degeneration, we combined laser cap...
The Wobbler mouse (wr) exhibits the loss of motoneurons especially in the cervical spinal cord, and ...
The Wobbler mouse possesses an inherited motoneuron disease, which expresses itself primarily at cer...
The present study was undertaken to quantify selected neuropeptides (thyrotropin releasing hormone, ...
<p>(A) Motoneurons stained by an anti-choline acetyltransferase antibody (red) at the anterior horn ...
The Wobbler mouse is used as a model of human motoneuron disease (MND). During the disease progress,...
The Wobbler mouse possesses an inherited autosomal recessive form of motoneuron disease. The most ch...
Ts65Dn mice, trisomic for a portion of chromosome 16 segmentally homologous to human chromosome 21, ...
Sporadic and familiar amyotrophic lateral sclerosis (ALS) cases presented lower cholinergic activity...
The cholinoacetyltransferase activity (CAT) in diaphragm of mice of Bar Harbor strain (129 ReJ dγ/dγ...
<div><p>Motor neurons in the ventral spinal cord were labeled with ChAT staining (A), and the number...
Profound alteration of the oxygen consumption rate (QO2) is present in the cervical spinal cord (CS)...
Plastic changes have been reported in the SOD1-G93A mouse model of amyotrophic lateral sclerosis, a ...
The wobbler mouse is a model of selective motor neuron degeneration in the cervical spinal cord. Com...
Lack of dystrophin in brain structures have been involved with impaired cognitive functions. Acethyl...
To identify candidate genes that are responsible for motoneurone degeneration, we combined laser cap...
The Wobbler mouse (wr) exhibits the loss of motoneurons especially in the cervical spinal cord, and ...
The Wobbler mouse possesses an inherited motoneuron disease, which expresses itself primarily at cer...
The present study was undertaken to quantify selected neuropeptides (thyrotropin releasing hormone, ...
<p>(A) Motoneurons stained by an anti-choline acetyltransferase antibody (red) at the anterior horn ...
The Wobbler mouse is used as a model of human motoneuron disease (MND). During the disease progress,...
The Wobbler mouse possesses an inherited autosomal recessive form of motoneuron disease. The most ch...
Ts65Dn mice, trisomic for a portion of chromosome 16 segmentally homologous to human chromosome 21, ...
Sporadic and familiar amyotrophic lateral sclerosis (ALS) cases presented lower cholinergic activity...
The cholinoacetyltransferase activity (CAT) in diaphragm of mice of Bar Harbor strain (129 ReJ dγ/dγ...
<div><p>Motor neurons in the ventral spinal cord were labeled with ChAT staining (A), and the number...
Profound alteration of the oxygen consumption rate (QO2) is present in the cervical spinal cord (CS)...
Plastic changes have been reported in the SOD1-G93A mouse model of amyotrophic lateral sclerosis, a ...
The wobbler mouse is a model of selective motor neuron degeneration in the cervical spinal cord. Com...
Lack of dystrophin in brain structures have been involved with impaired cognitive functions. Acethyl...
To identify candidate genes that are responsible for motoneurone degeneration, we combined laser cap...