Rathke-Hartlieb S, Schlomann U, Heimann P, Meisler MH, Jockusch H, Bartsch JW. Progressive loss of striatal neurons causes motor dysfunction in MND2 mutant mice and is not prevented by Bcl-2. Experimental Neurology. 2002;175(1):87-97.The mouse mutant "motoneuron disease 2" (MND2, mnd2 on Chr 6) was originally characterized as a spinal muscular atrophy (SMA) because degenerating motoneurons were observed in late stages of the disease. MND2 mutants exhibit a progressive phenotype with neurological symptoms that begin at postnatal day (dP) 20 and include involuntary movements, abnormal postures, akinesis, and death between dP 30 and 40. Unexpectedly, there was no induction of acetylcholine receptor alpha subunit mRNA in skeletal muscle of MND2...
Loss of the survival motor neuron gene (SMN1) is responsible for spinal muscular atrophy (SMA), the ...
\(\textbf {Background:}\) Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder ...
Objective: Motor neurons (MNs) die in amyotrophic lateral sclerosis (ALS), a clinically heterogeneou...
The autosomal recessive mutation mnd2 results in early onset motor neuron disease with rapidly progr...
The autosomal recessive mutation mnd2 results in early onset motor neuron disease with rapidly progr...
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease leading to motor impai...
AbstractApoptosis is a hallmark of motoneuron diseases such as amyotrophic lateral sclerosis (ALS) a...
International audienceThe molecular events leading to motoneuronal death are still poorly understood...
To identify candidate genes that are responsible for motoneurone degeneration, we combined laser cap...
Amyotrophic lateral sclerosis (ALS) involves motor neuron degeneration, skeletal muscle atrophy, par...
Spinal muscular atrophy (SMA), which is caused by inactivating mutations in the survival motor neuro...
AbstractBcl-2 is a major regulator of programmed cell death, a critical process in shaping the devel...
It is becoming evident that microglia, the resident immune cells of the central nervous system (CNS)...
\(\textbf {Background:}\) Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder ...
International audienceAmyotrophic lateral sclerosis (ALS) is the most frequent adult onset motor neu...
Loss of the survival motor neuron gene (SMN1) is responsible for spinal muscular atrophy (SMA), the ...
\(\textbf {Background:}\) Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder ...
Objective: Motor neurons (MNs) die in amyotrophic lateral sclerosis (ALS), a clinically heterogeneou...
The autosomal recessive mutation mnd2 results in early onset motor neuron disease with rapidly progr...
The autosomal recessive mutation mnd2 results in early onset motor neuron disease with rapidly progr...
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease leading to motor impai...
AbstractApoptosis is a hallmark of motoneuron diseases such as amyotrophic lateral sclerosis (ALS) a...
International audienceThe molecular events leading to motoneuronal death are still poorly understood...
To identify candidate genes that are responsible for motoneurone degeneration, we combined laser cap...
Amyotrophic lateral sclerosis (ALS) involves motor neuron degeneration, skeletal muscle atrophy, par...
Spinal muscular atrophy (SMA), which is caused by inactivating mutations in the survival motor neuro...
AbstractBcl-2 is a major regulator of programmed cell death, a critical process in shaping the devel...
It is becoming evident that microglia, the resident immune cells of the central nervous system (CNS)...
\(\textbf {Background:}\) Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder ...
International audienceAmyotrophic lateral sclerosis (ALS) is the most frequent adult onset motor neu...
Loss of the survival motor neuron gene (SMN1) is responsible for spinal muscular atrophy (SMA), the ...
\(\textbf {Background:}\) Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder ...
Objective: Motor neurons (MNs) die in amyotrophic lateral sclerosis (ALS), a clinically heterogeneou...