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The EMBO Journal|April 15, 1994
The mouse lethal nonagouti (a(x)) mutation deletes the S-adenosylhomocysteine hydrolase (Ahcy) geneM W Miller, D M Duhl, B M Winkes, et al.
American Journal of Physiology. Cell Physiology|April 13, 2004
Role of mitochondrial superoxide dismutase in contraction-induced generation of reactive oxygen species in skeletal muscle extracellular spaceA McArdle, J van der Meulen, G L Close, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 16, 2001
Failed retrograde transport of NGF in a mouse model of Down's syndrome: reversal of cholinergic neurodegenerative phenotypes following NGF infusionJ D Cooper, A Salehi, J D Delcroix, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 1999
Mitochondrial disease in superoxide dismutase 2 mutant miceS Melov, P Coskun, M Patel, et al.
Nature Genetics|December 1, 1995
Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutaseY Li, T T Huang, E J Carlson, et al.
The Journal of Biological Chemistry|April 12, 2001
Manganese superoxide dismutase signals matrix metalloproteinase expression via H2O2-dependent ERK1/2 activationA C Ranganathan, K K Nelson, A M Rodriguez, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 12, 1996
Developmental abnormalities and age-related neurodegeneration in a mouse model of Down syndromeD M Holtzman, D Santucci, J Kilbridge, et al.
Human Molecular Genetics|December 14, 2004
The cerebellar transcriptome during postnatal development of the Ts1Cje mouse, a segmental trisomy model for Down syndromeL Dauphinot, R Lyle, I Rivals, et al.
American Journal of Human Genetics|October 9, 2001
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromesK E Heath, A Campos-Barros, A Toren, et al.
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