Coincident thresholds of mutant protein for paralytic disease and protein aggregation caused by restrictively expressed superoxide dismutase cDNA
- 31 December 2005
- journal article
- Published by Elsevier BV in Neurobiology of Disease
- Vol. 20 (3), 943-952
- https://doi.org/10.1016/j.nbd.2005.06.005
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Increased cytotoxic potential of microglia from ALS‐transgenic miceGlia, 2004
- D90A-SOD1 mediated amyotrophic lateral sclerosis: A single founder for all cases with evidence for aCis-acting disease modifier in the recessive haplotypeHuman Mutation, 2002
- Inflammatory processes in amyotrophic lateral sclerosisMuscle & Nerve, 2002
- Multiple Transcripts of the Human Cu,Zn Superoxide Dismutase GeneBiochemical and Biophysical Research Communications, 2000
- A vector for expressing foreign genes in the brains and hearts of transgenic miceGenetic Analysis: Biomolecular Engineering, 1996
- Familial Alzheimer's Disease–Linked Presenilin 1 Variants Elevate Aβ1–42/1–40 Ratio In Vitro and In VivoNeuron, 1996
- Microglia: a sensor for pathological events in the CNSTrends in Neurosciences, 1996
- Trinucleotide repeat expansion in neurological diseaseAnnals of Neurology, 1994
- Amyotrophic lateral sclerosis: Theories and therapiesAnnals of Neurology, 1994
- Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisNature, 1993