Exploring neuroinflammatory processes in a mouse model of amyotrophic lateral sclerosis
<p>Amyotrophic lateral sclerosis (ALS) is a devastating degenerative disease, affecting both upper and lower motor neurons in the CNS. Around 10% of ALS cases are classed as familial, and around 20% of these are due to a mutation in the gene superoxide dismutase-1 (SOD1). The SOD1G93A mouse is...
मुख्य लेखकों: | Evans, M, Mr Matthew C Evans |
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अन्य लेखक: | Turner, M |
स्वरूप: | थीसिस |
भाषा: | English |
प्रकाशित: |
2012
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विषय: |
समान संसाधन
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The genetics of amyotrophic lateral sclerosis
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In vitro transgenic models to elucidate the molecular mechanisms of TDP-43 pathology in amyotrophic lateral sclerosis
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Model systems for exploring new therapeutic interventions and disease mechanisms in spinal muscular atrophies (SMAs)
द्वारा: Sleigh, JN
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Investigating TDP43 biological dysfunction through the characterisation of Tardbp ENU mouse mutants: implications for neurodegeneration
द्वारा: De Sao Jose Martinho De Oliveira, H, और अन्य
प्रकाशित: (2014) -
Molecular mechanisms of OXR1 function
द्वारा: Liu, K
प्रकाशित: (2014)