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References

  • Andersen P. M. (2006) Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene. Curr. Neurol. Neurosci. Rep. 6, 3746.
  • Boyce M., Bryant K. F., Jousse C., Long K., Harding H. P., Scheuner D., Kaufman R. J., Ma D., Ron D. and Yuan J. (2005) A selective inhibitor of eIF2alpha dephosphorylation protects cells from ER stress. Science 307, 935959.
  • Brown R. H. Jr (1998) SOD1 aggregates in ALS: cause, correlate or consequence? Nat. Med. 4, 13621364.
  • Bruijn L. I., Miller T. M. and Cleveland D. W. (2004) Unraveling the mechanisms involved in motor neuron degeneration in ALS. Annu. Rev. Neurosci. 27, 723749.
  • Chaudhuri T. K. and Paul S. (2006) Protein-misfolding diseases and chaperone-based therapeutic approaches. FEBS J. 273, 13311349.
  • Cleveland D. W. and Rothstein J. D. (2001) From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS. Nat. Rev. Neurosci. 2, 806819.
  • Gonatas N. K., Stieber A. and Gonatas J. O. (2006) Fragmentation of Golgi apparatus in neurodegenerative diseases and cell death. J. Neurol. Sci. 246, 2130.
  • Haass C. and Selkoe D. J. (2007) Soluble protein oligomers in neurodegeneration: lessions from the Alzheimer’s amyloid beta-peptide. Nat. Rev. Mol. Cell Biol. 8, 101112.
  • Iwawaki T., Akai R., Kohno K. and Miura M. (2004) A transgenic mouse model for monitoring endoplasmic reticulum stress. Nat. Med. 10, 98102.
  • Julien J. P. and Kritz J. (2006) Transgenic mouse models of amyotrophic lateral sclerosis. Biochim. Biophys. Acta 1762, 10131024.
  • Kabashi E. and Durham H. D. (2006) Failure of protein quality control in amyotrophic lateral sclerosis. Biochim. Biophys. Acta 1762, 10381050.
  • Kikuchi H., Almer G., Yamashita S., Guegan C., Nagai M., Xu Z., Sosunov A. A., McKhann G. M. II and Przedborski S. (2006) Spinal cord endoplasmic reticulum stress associated with a microsomal accumulation of mutant superoxide dismutase-1 in an ALS model. Proc. Natl Acad. Sci. USA 103, 60256030.
  • Lansbury P. T. and Lashuel H. A. (2006) A century-old debate on protein aggregation and neurodegeneration enters the clinic. Nature 443, 774779.
  • Lee J. P., Gerin V. P., Bindokas V. P., Miller R., Ghadge G. and Roos R. P. (2002) No correlation between aggregates of Cu/Zn superoxide dismutase and cell death in familial amyotrophic lateral sclerosis. J. Neurochem. 82, 12291238.
  • Lindholm D., Wootz H. and Korhonen L. (2006) ER stress and neurodegenerative diseases. Cell Death Differ. 13, 385392.
  • McGeer E. G. and McGeer P. P. (2005) Pharmacological approaches to the treatment of amyotrophic lateral sclerosis. BioDrugs 19, 3137.
  • Meusser B., Hirsch C., Jarosch E. and Sommer T. (2005) ERAD: the long road to destruction. Nat. Cell Biol. 8, 766772.
  • Momoi T. (2004) Caspases involved in ER stress-mediated cell death. J. Chem. Neuroanat. 28, 101105.
  • Morishima N., Nakanishi K., Tsuchiya K., Shibata T. and Seiwa E. (2004) Translocation of Bim to the endoplasmic reticulum (ER) mediates ER stress signaling for activation of caspase-12 during ER stress-induced apoptosis. J. Biol. Chem. 279, 5037550381.
  • Nakagawa T., Zhu H., Morishima N., Li E., Xu J., Yankner B. A. and Yuan J. (2000) Caspase-12 mediates endoplasmic-reticulum-specific apoptosis and cytotoxicity by amyloid-β. Nature 403, 98103.
  • Ross C. A. and Pickart C. M. (2004) The ubiquitin-proteasome pathway in Parkinson’s disease and other neurodegenerative diseases. Trends Cell Biol. 14, 703711.
  • Ross C. A. and Poirier M. A. (2004) Protein aggregation and neurodegenerative disease. Nat. Med. 10, s10s17.
  • Rutkowski D. T. and Kaufman R. J. (2004) A trip to the ER: coping with stress. Trends Cell Biol. 14, 2028.
  • Shastry B. S. (2003) Neurodegenerative disorders of protein aggregation. Neurochem. Int. 43, 17.
  • Shen X., Zhang K. and Kaufman R. J. (2004) The unfolded protein response – a stress signaling pathway of the endoplasmic reticulum. J. Chem. Neuroanat. 28, 7992.
  • Tobisawa S., Hozumi Y., Arawaka S., Koyama S., Wada M., Nagai M., Aoki M., Itoyama Y., Goto K. and Kato T. (2003) Mutant SOD1 linked to familial amyotrophic lateral sclerosis, but not wild-type SOD1, induces ER stress in COS7 cells and transgenic mice. Biochem. Biophys. Res. Commun. 303, 496503.
  • Wootz H., Hansson I., Korhonen L., Näpänkangas U. and Lindholm D. (2004) Caspase-12 cleavage and increased oxidative stress during motoneuron degeneration in transgenic mouse model of ALS. Biochem. Biophys. Res. Commun. 322, 281286.
  • Yoneda T., Imaizumi K., Oono K., Yui D., Gomi F., Katayama T. and Tohyama M. (2001) Activation of caspase-12, an endoplasmic reticulum (ER) resident caspase, through tumor necrosis factor receptor-associated factor 2-dependent mechanism in response to the ER stress. J. Biol. Chem. 276, 1393513940.
  • Yoshida H., Mtsui T., Yamamoto A., Okada T. and Mori K. (2001) XBP1 mRNA is induced by ATF6 and spliced by IRE1 in response to ER stress to produce a highly active transcription factor. Cell 107, 881891.