Abstract Background Amyotrophic Lateral Sclerosis (ALS) is a lethal disorder characterized by progressive degeneration of motor neurons in the brain and spinal cord. Diagnosis is mainly based on clinical symptoms, and there is currently no therapy to stop the disease or slow its progression. Since access to spinal cord tissue is not possible at disease onset, we investigated changes in gene expression profiles in whole blood of ALS patients. Results Our transcriptional study showed dramatic changes in blood of ALS patients; 2,300 probes (9.4%) showed significant differential expression in a discovery dataset consisting of 30 ALS patients and 30 healthy controls. Weighted gene co-expression network analysis (WGCNA) was used to find disease-r...
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by dam...
Amyotrophic lateral sclerosis (ALS) is an incurable neurodegenerative disease that primarily affects...
BackgroundDespite the discovery of familial cases with mutations in Cu/Zn-superoxide dismutase (SOD1...
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease defined by motor neuron (MN) loss...
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease of motor neurons resulting in pro...
<div><p>The biological pathways involved in amyotrophic lateral sclerosis (ALS) remain elusive and d...
Amyotrophic lateral sclerosis (ALS) is a fatal late-onset motor neuron disease characterized by the ...
The biological pathways involved in amyotrophic lateral sclerosis (ALS) remain elusive and diagnosti...
Abstract Amyotrophic lateral sclerosis (ALS) is a neurodegenerativedisease with strong genetic compo...
The biological pathways involved in amyotrophic lateral sclerosis (ALS) remain elusive and diagnosti...
Abstract Background Sporadic amyotrophic lateral sclerosis (sALS) is a motor neuron disease with poo...
The aim of the present study is to investigate the molecular pathways underlying amyotrophic lateral...
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive and ultimately fatal neurodegenerative ...
AbstractAmyotrophic lateral sclerosis (ALS) is a rapidly progressive and ultimately fatal neurodegen...
<p>WGCNA analysis identified six gene networks which were dysregulated between <i>C9ORF72</i>-ALS an...
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by dam...
Amyotrophic lateral sclerosis (ALS) is an incurable neurodegenerative disease that primarily affects...
BackgroundDespite the discovery of familial cases with mutations in Cu/Zn-superoxide dismutase (SOD1...
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease defined by motor neuron (MN) loss...
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease of motor neurons resulting in pro...
<div><p>The biological pathways involved in amyotrophic lateral sclerosis (ALS) remain elusive and d...
Amyotrophic lateral sclerosis (ALS) is a fatal late-onset motor neuron disease characterized by the ...
The biological pathways involved in amyotrophic lateral sclerosis (ALS) remain elusive and diagnosti...
Abstract Amyotrophic lateral sclerosis (ALS) is a neurodegenerativedisease with strong genetic compo...
The biological pathways involved in amyotrophic lateral sclerosis (ALS) remain elusive and diagnosti...
Abstract Background Sporadic amyotrophic lateral sclerosis (sALS) is a motor neuron disease with poo...
The aim of the present study is to investigate the molecular pathways underlying amyotrophic lateral...
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive and ultimately fatal neurodegenerative ...
AbstractAmyotrophic lateral sclerosis (ALS) is a rapidly progressive and ultimately fatal neurodegen...
<p>WGCNA analysis identified six gene networks which were dysregulated between <i>C9ORF72</i>-ALS an...
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by dam...
Amyotrophic lateral sclerosis (ALS) is an incurable neurodegenerative disease that primarily affects...
BackgroundDespite the discovery of familial cases with mutations in Cu/Zn-superoxide dismutase (SOD1...