Jeremy M. Van Raamsdonk, Ph.D.

Affiliations: 
Michigan State University, East Lansing, MI 
Area:
aging, neurodegeneration
Google:
"Jeremy Van Raamsdonk"
Mean distance: (not calculated yet)
 
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

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
See more...