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Blood|August 9, 2001
Defective hematopoiesis and hepatic steatosis in mice with combined deficiencies of the genes encoding Fancc and Cu/Zn superoxide dismutaseS Hadjur, K Ung, L Wadsworth, et al.
Plos Genetics|August 22, 2009
Osteo-chondroprogenitor-specific deletion of the selenocysteine tRNA gene, Trsp, leads to chondronecrosis and abnormal skeletal development: a putative model for Kashin-Beck diseaseCharlene M Downey, Chelsea R Horton, Bradley A Carlson, et al.
International Journal for Parasitology|April 16, 2013
Murine autoimmune arthritis is exaggerated by infection with the rat tapeworm, Hymenolepis diminutaRabea Graepel, Gabriella Leung, Arthur Wang, et al.
The Journal of Physiology|November 13, 2013
Image-based assessment of microvascular function and structure in collagen XV- and XVIII-deficient miceC B Rygh, G Løkka, R Heljasvaara, et al.
Oncogene|July 10, 1997
Base transitions dominate the mutational spectrum of a transgenic reporter gene in MSH2 deficient miceS E Andrew, A H Reitmair, J Fox, et al.
Nature Immunology|June 10, 2008
PTEN functions to 'prioritize' chemotactic cues and prevent 'distraction' in migrating neutrophilsBryan Heit, Stephen M Robbins, Charlene M Downey, et al.
Mutation Research|October 25, 1996
A novel lacI transgenic mutation-detection system and its application to establish baseline mutation frequencies in the scid mouseS E Andrew, S Pownall, J Fox, et al.
Carcinogenesis|February 19, 2008
Mgmt deficiency alters the in vivo mutational spectrum of tissues exposed to the tobacco carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)Linda E Sandercock, Jennifer N Hahn, Li Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 1998
Tissues of MSH2-deficient mice demonstrate hypermutability on exposure to a DNA methylating agentS E Andrew, M McKinnon, B S Cheng, et al.
Osteoarthritis and Cartilage|May 11, 2005
Degenerative knee joint disease in mice lacking 3'-phosphoadenosine 5'-phosphosulfate synthetase 2 (Papss2) activity: a putative model of human PAPSS2 deficiency-associated arthrosisAlice F Ford-Hutchinson, Zenobia Ali, Ruth A Seerattan, et al.
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