The wobbler mouse is a model of selective motor neuron degeneration in the cervical spinal cord. Comparing cervical and lumbar tracts of control and diseased mice at the early stage of pathology by proteomic analysis, we identified 31 proteins by peptide mass fingerprint after tryptic digestion and MALDI-TOF analysis, that were differently represented among the four experimental groups. In healthy mice, patterns of protein expression differed between cervical and lumbar tract: proteins of cellular energetic metabolism pathway showed lower expression in the cervical tract, while cellular trafficking proteins were overrepresented. In wobbler mice, these differences disappeared and the expression pattern was similar between cervical and lumbar...
The isolation of synaptoneurosomes (SNs) represents a useful means to study synaptic events. However...
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder, characterised by th...
Krabbe disease is a rare, childhood lysosomal storage disorder caused by a deficiency of galactosylc...
Amyotrophic lateral sclerosis is the most common form of motor neuron disease in adult patients and ...
Staunton L, Jockusch H, Ohlendieck K. Proteomic analysis of muscle affected by motor neuron degenera...
Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease, whose primary mechanisms or cau...
The fatal neurodegenerative disorders amyotrophic lateral sclerosis and spinal muscular atrophy are,...
The fatal neurodegenerative disorders amyotrophic lateral sclerosis and spinal muscular atrophy are,...
S100B is a calcium-binding protein that, in the nervous system, is mainly concentrated in glial cell...
The Wobbler mouse (wr) exhibits the loss of motoneurons especially in the cervical spinal cord, and ...
Profound alteration of the oxygen consumption rate (QO2) is present in the cervical spinal cord (CS)...
Mice are commonly used to study intervertebral disc (IVD) biology and related diseases such as IVD d...
Non-somatic synaptic and axonal compartments of neurons are primary pathological targets in many neu...
The objective of this study was to explore the correlation between the alteration in chondroitin sul...
<div><p>Low back pain is the most common musculoskeletal problem and the single most common cause of...
The isolation of synaptoneurosomes (SNs) represents a useful means to study synaptic events. However...
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder, characterised by th...
Krabbe disease is a rare, childhood lysosomal storage disorder caused by a deficiency of galactosylc...
Amyotrophic lateral sclerosis is the most common form of motor neuron disease in adult patients and ...
Staunton L, Jockusch H, Ohlendieck K. Proteomic analysis of muscle affected by motor neuron degenera...
Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease, whose primary mechanisms or cau...
The fatal neurodegenerative disorders amyotrophic lateral sclerosis and spinal muscular atrophy are,...
The fatal neurodegenerative disorders amyotrophic lateral sclerosis and spinal muscular atrophy are,...
S100B is a calcium-binding protein that, in the nervous system, is mainly concentrated in glial cell...
The Wobbler mouse (wr) exhibits the loss of motoneurons especially in the cervical spinal cord, and ...
Profound alteration of the oxygen consumption rate (QO2) is present in the cervical spinal cord (CS)...
Mice are commonly used to study intervertebral disc (IVD) biology and related diseases such as IVD d...
Non-somatic synaptic and axonal compartments of neurons are primary pathological targets in many neu...
The objective of this study was to explore the correlation between the alteration in chondroitin sul...
<div><p>Low back pain is the most common musculoskeletal problem and the single most common cause of...
The isolation of synaptoneurosomes (SNs) represents a useful means to study synaptic events. However...
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder, characterised by th...
Krabbe disease is a rare, childhood lysosomal storage disorder caused by a deficiency of galactosylc...