<p>(<b>A</b>) Immunohistochemistry with SEDI anti-SOD1 antibody on 120 day lumbar spinal cord from female mice showed no reactivity in WT tissue and punctate staining in G93A and DBLE. Scale bar 50 µm (<b>B</b>) Immunofluorescence of G93A or DBLE 90 day spinal cord from female mice, as indicated, showed enhanced ubiquitin staining (green) in motor neuron cell bodies and processes labelled with βIII tubulin antibody (red). Nuclei were stained with DAPI visible in MERGE panel. Scale bar 20 µm.</p
<p>KS expression in the spinal cords of SOD1<sup>G93A</sup> mice, age-matched non-Tg and SOD1<sup>G9...
<p>Histological characterization of ATF4<sup>−/−</sup>/SOD1<sup>G86R</sup> spinal cord. (<b>A</b>) I...
Mutations in the Cu,Zn-superoxide dismutase (SOD1) gene cause a familial form of amyotrophic lateral...
<p>(<b>A</b>) Representative Western blot with anti-SOD1 (C4F6) of spinal cord lysates from male tra...
<p>(<b>A</b>) Representative immunofluorescence image showing co-localization of mutant GFP-SOD1 (SO...
<p>(<b>A</b>) Typical examples of motor unit traces are shown from the EDL muscle of WT, hHSJ1a, G93...
<p>The FLAG-tagged SOD1 and the ligand proteins were immunoprecipitated using the FLAG affinity resi...
<p>(<b>A</b>) Representative Western blot showing total levels of HSJ1 expression in G93A and DBLE t...
<p>(<b>A</b>) Serial gallocynanin stained sections of the L2–L6 region from 90 day old spinal cord f...
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by the selec...
Mutations in SOD1 cause selective motor neuron degeneration in familial amyotrophic lateral sclerosi...
<p>Representative Toluidine blue stain (left column) and GFAP immunofluorescence (red, right column)...
Mutations in the Cu, Zn superoxide dismutase (SOD1) gene cause a familial form of amyotrophic latera...
Mutations in SOD1 cause selective motor neuron degeneration in familial amyotrophic lateral sclerosi...
<p>Lumbar spinal cord sections from different ages of SOD1<sup>G93A</sup> mice (<i>G93A</i>) and non...
<p>KS expression in the spinal cords of SOD1<sup>G93A</sup> mice, age-matched non-Tg and SOD1<sup>G9...
<p>Histological characterization of ATF4<sup>−/−</sup>/SOD1<sup>G86R</sup> spinal cord. (<b>A</b>) I...
Mutations in the Cu,Zn-superoxide dismutase (SOD1) gene cause a familial form of amyotrophic lateral...
<p>(<b>A</b>) Representative Western blot with anti-SOD1 (C4F6) of spinal cord lysates from male tra...
<p>(<b>A</b>) Representative immunofluorescence image showing co-localization of mutant GFP-SOD1 (SO...
<p>(<b>A</b>) Typical examples of motor unit traces are shown from the EDL muscle of WT, hHSJ1a, G93...
<p>The FLAG-tagged SOD1 and the ligand proteins were immunoprecipitated using the FLAG affinity resi...
<p>(<b>A</b>) Representative Western blot showing total levels of HSJ1 expression in G93A and DBLE t...
<p>(<b>A</b>) Serial gallocynanin stained sections of the L2–L6 region from 90 day old spinal cord f...
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by the selec...
Mutations in SOD1 cause selective motor neuron degeneration in familial amyotrophic lateral sclerosi...
<p>Representative Toluidine blue stain (left column) and GFAP immunofluorescence (red, right column)...
Mutations in the Cu, Zn superoxide dismutase (SOD1) gene cause a familial form of amyotrophic latera...
Mutations in SOD1 cause selective motor neuron degeneration in familial amyotrophic lateral sclerosi...
<p>Lumbar spinal cord sections from different ages of SOD1<sup>G93A</sup> mice (<i>G93A</i>) and non...
<p>KS expression in the spinal cords of SOD1<sup>G93A</sup> mice, age-matched non-Tg and SOD1<sup>G9...
<p>Histological characterization of ATF4<sup>−/−</sup>/SOD1<sup>G86R</sup> spinal cord. (<b>A</b>) I...
Mutations in the Cu,Zn-superoxide dismutase (SOD1) gene cause a familial form of amyotrophic lateral...