Jeremy M. Van Raamsdonk, Ph.D.

Michigan State University, East Lansing, MI 
aging, neurodegeneration
"Jeremy Van Raamsdonk"
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Schaar CE, Dues DJ, Spielbauer KK, et al. (2015) Mitochondrial and cytoplasmic ROS have opposing effects on lifespan. Plos Genetics. 11: e1004972
Van Raamsdonk JM, Hekimi S. (2012) Superoxide dismutase is dispensable for normal animal lifespan. Proceedings of the National Academy of Sciences of the United States of America. 109: 5785-90
Van Raamsdonk JM, Hekimi S. (2010) Reactive Oxygen Species and Aging in Caenorhabditis elegans: Causal or Casual Relationship? Antioxidants & Redox Signaling. 13: 1911-53
Van Raamsdonk JM, Meng Y, Camp D, et al. (2010) Decreased energy metabolism extends life span in Caenorhabditis elegans without reducing oxidative damage. Genetics. 185: 559-71
Van Raamsdonk JM, Hekimi S. (2009) Deletion of the mitochondrial superoxide dismutase sod-2 extends lifespan in Caenorhabditis elegans. Plos Genetics. 5: e1000361
Van Raamsdonk JM, Pearson J, Murphy Z, et al. (2006) Wild-type huntingtin ameliorates striatal neuronal atrophy but does not prevent other abnormalities in the YAC128 mouse model of Huntington disease. Bmc Neuroscience. 7: 80
Zhang Y, Leavitt BR, van Raamsdonk JM, et al. (2006) Huntingtin inhibits caspase-3 activation. The Embo Journal. 25: 5896-906
Van Raamsdonk JM, Gibson WT, Pearson J, et al. (2006) Body weight is modulated by levels of full-length huntingtin. Human Molecular Genetics. 15: 1513-23
Leavitt BR, van Raamsdonk JM, Shehadeh J, et al. (2006) Wild-type huntingtin protects neurons from excitotoxicity. Journal of Neurochemistry. 96: 1121-9
Van Raamsdonk JM, Murphy Z, Slow EJ, et al. (2005) Selective degeneration and nuclear localization of mutant huntingtin in the YAC128 mouse model of Huntington disease. Human Molecular Genetics. 14: 3823-35
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