Protein Nitration in a Mouse Model of Familial Amyotrophic Lateral Sclerosis
Open Access
- 1 April 2005
- journal article
- Published by Elsevier
- Vol. 280 (16) , 16295-16304
- https://doi.org/10.1074/jbc.m413111200
Abstract
No abstract availableKeywords
This publication has 54 references indexed in Scilit:
- CHIP promotes proteasomal degradation of familial ALS‐linked mutant SOD1 by ubiquitinating Hsp/Hsc70Journal of Neurochemistry, 2004
- Focal dysfunction of the proteasome: a pathogenic factor in a mouse model of amyotrophic lateral sclerosisJournal of Neurochemistry, 2004
- Protein aggregation in motor neurone disordersNeuropathology and Applied Neurobiology, 2003
- Proteomic identification of oxidatively modified proteins in Alzheimer's disease brain. Part II: dihydropyrimidinase‐related protein 2, α‐enolase and heat shock cognate 71Journal of Neurochemistry, 2002
- Signal transduction by protein tyrosine nitration: competition or cooperation with tyrosine phosphorylation-dependent signaling events?,Published by Elsevier ,2002
- Widespread Nitration of Pathological Inclusions in Neurodegenerative SynucleinopathiesThe American Journal of Pathology, 2000
- Three-Dimensional Imaging by Deconvolution MicroscopyMethods, 1999
- Effects of peroxynitrite‐induced protein modifications on tyrosine phosphorylation and degradationFEBS Letters, 1996
- Rapid identification of proteins by peptide-mass fingerprintingCurrent Biology, 1993
- Subcellular distribution of ubiquitin–protein conjugates in the hippocampus following transient ischemiaJournal of Neuroscience Research, 1992