The Wobbler mouse (wr) exhibits the loss of motoneurons especially in the cervical spinal cord, and thus has been studied as a model for human motoneuron diseases. Wobbler mice selected at various ages and stages during the disease process show increased levels of thyrotropin releasing hormone and substance P in spinal cord and brainstem (medulla). Enkephalins (methionine and leucine) also increase in the spinal cord and brainstem. Somatostatin increases in hypothalamus, perhaps accounting partly for the small size of this mutant mouse via its effect on growth hormone.link_to_subscribed_fulltex
Wobbler mice are experimental models for amyotrophic lateral sclerosis. As such they show motoneuron...
Ulbrich-Lesner M, Schmidt VC, Ronsiek M, et al. Genetic modifiers that aggravate the neurological ph...
To identify candidate genes that are responsible for motoneurone degeneration, we combined laser cap...
The present study was undertaken to quantify selected neuropeptides (thyrotropin releasing hormone, ...
The Wobbler mouse possesses an inherited motoneuron disease, which expresses itself primarily at cer...
Enzymatic assays for acetylcholine esterase (AChE) and choline acetyltransferase (ChAT) were applied...
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...
The wobbler mouse is a model of selective motor neuron degeneration in the cervical spinal cord. Com...
Rathke-Hartlieb S, Schmidt VC, Jockusch H, Schmitt-John T, Bartsch JW. Spatiotemporal progression of...
The Wobbler mouse, a mutant characterized by motoneuron degeneration in the cervical spinal cord, ha...
The Wobbler mouse spinal cord shows vacuolated motoneurons, glial reaction, inflammation and abnorma...
The role of neuropeptides and the significance of peptidergic mechanisms in neurodegenerative diseas...
In wobbler mice, histometric features and the response to injury in the less affected hindlimb nerve...
Profound alteration of the oxygen consumption rate (QO2) is present in the cervical spinal cord (CS)...
Wobbler mice are experimental models for amyotrophic lateral sclerosis. As such they show motoneuron...
Ulbrich-Lesner M, Schmidt VC, Ronsiek M, et al. Genetic modifiers that aggravate the neurological ph...
To identify candidate genes that are responsible for motoneurone degeneration, we combined laser cap...
The present study was undertaken to quantify selected neuropeptides (thyrotropin releasing hormone, ...
The Wobbler mouse possesses an inherited motoneuron disease, which expresses itself primarily at cer...
Enzymatic assays for acetylcholine esterase (AChE) and choline acetyltransferase (ChAT) were applied...
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...
The wobbler mouse is a model of selective motor neuron degeneration in the cervical spinal cord. Com...
Rathke-Hartlieb S, Schmidt VC, Jockusch H, Schmitt-John T, Bartsch JW. Spatiotemporal progression of...
The Wobbler mouse, a mutant characterized by motoneuron degeneration in the cervical spinal cord, ha...
The Wobbler mouse spinal cord shows vacuolated motoneurons, glial reaction, inflammation and abnorma...
The role of neuropeptides and the significance of peptidergic mechanisms in neurodegenerative diseas...
In wobbler mice, histometric features and the response to injury in the less affected hindlimb nerve...
Profound alteration of the oxygen consumption rate (QO2) is present in the cervical spinal cord (CS)...
Wobbler mice are experimental models for amyotrophic lateral sclerosis. As such they show motoneuron...
Ulbrich-Lesner M, Schmidt VC, Ronsiek M, et al. Genetic modifiers that aggravate the neurological ph...
To identify candidate genes that are responsible for motoneurone degeneration, we combined laser cap...