טוען...
Mutant Superoxide Dismutase 1 Forms Aggregates in the Brain Mitochondrial Matrix of Amyotrophic Lateral Sclerosis Mice
An increasing body of evidence suggests that mitochondrial dysfunction plays an important role in the pathogenesis of familial amyotrophic lateral sclerosis associated with “gain of function” mutations in Cu/Zn superoxide dismutase 1 (SOD1). SOD1 is mostly a cytosolic protein, but a portion of SOD1...
שמור ב:
| הוצא לאור ב: | J Neurosci |
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| Main Authors: | , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Society for Neuroscience
2005
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6725162/ https://ncbi.nlm.nih.gov/pubmed/15758154 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4385-04.2005 |
| תגים: |
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