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One or more keywords matched the following items that are connected to Ghadge, Ghanashyam
Item TypeName
Concept Amyotrophic Lateral Sclerosis
Concept Multiple Sclerosis
Academic Article Mutant superoxide dismutase-1-linked familial amyotrophic lateral sclerosis: molecular mechanisms of neuronal death and protection.
Academic Article The role of immunophilins in mutant superoxide dismutase-1linked familial amyotrophic lateral sclerosis.
Academic Article Truncated wild-type SOD1 and FALS-linked mutant SOD1 cause neural cell death in the chick embryo spinal cord.
Academic Article Glutamate carboxypeptidase II inhibition protects motor neurons from death in familial amyotrophic lateral sclerosis models.
Academic Article Mutant SOD1 forms ion channel: implications for ALS pathophysiology.
Academic Article A protein critical for a Theiler's virus-induced immune system-mediated demyelinating disease has a cell type-specific antiapoptotic effect and a key role in virus persistence.
Academic Article No correlation between aggregates of Cu/Zn superoxide dismutase and cell death in familial amyotrophic lateral sclerosis.
Academic Article Single chain variable fragment antibodies block aggregation and toxicity induced by familial ALS-linked mutant forms of SOD1.
Academic Article Palmitoylation of superoxide dismutase 1 (SOD1) is increased for familial amyotrophic lateral sclerosis-linked SOD1 mutants.
Academic Article S-acylation of SOD1, CCS, and a stable SOD1-CCS heterodimer in human spinal cords from ALS and non-ALS subjects.
Academic Article Poloxamer 188 decreases membrane toxicity of mutant SOD1 and ameliorates pathology observed in SOD1 mouse model for ALS.
Academic Article Single chain variable fragment antibodies directed against SOD1 ameliorate disease in mutant SOD1 transgenic mice.
Academic Article Knockdown of GADD34 in neonatal mutant SOD1 mice ameliorates ALS.
Academic Article RNA-binding protein altered expression and mislocalization in MS.
Academic Article A C. elegans model of C9orf72-associated ALS/FTD uncovers a conserved role for eIF2D in RAN translation.
Academic Article Machine learning predicts translation initiation sites in neurologic diseases with nucleotide repeat expansions.
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