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Results: 1-8 |
Results: 8

Authors: Ogburn, CE Carlberg, K Ottinger, MA Holmes, DJ Martin, GM Austad, SN
Citation: Ce. Ogburn et al., Exceptional cellular resistance to oxidative damage in long-lived birds requires active gene expression, J GERONT A, 56(11), 2001, pp. B468-B474

Authors: Schriner, SE Ogburn, CE Smith, AC Newcomb, TG Ladiges, WC Dolle, MET Vijg, J Fukuchi, KI Martin, GM
Citation: Se. Schriner et al., Levels of DNA damage are unaltered in mice overexpressing human catalase in nuclei, FREE RAD B, 29(7), 2000, pp. 664-673

Authors: Castro, E Edland, SD Lee, L Ogburn, CE Deeb, SS Brown, G Panduro, A Riestra, R Tilvis, R Louhija, J Penttinen, R Erkkola, R Wang, L Martin, GM Oshima, J
Citation: E. Castro et al., Polymorphisms at the Werner locus: II. 1074Leu/Phe, 1367Cys/Arg, longevity, and atherosclerosis, AM J MED G, 95(4), 2000, pp. 374-380

Authors: Wang, L Ogburn, CE Ware, CB Ladiges, WC Youssoufian, H Martin, GM Oshima, J
Citation: L. Wang et al., Cellular Werner phenotypes in mice expressing a putative dominant-negativehuman WRN gene, GENETICS, 154(1), 2000, pp. 357-362

Authors: Wang, L Evans, AE Ogburn, CE Youssoufian, H Martin, GM Oshima, J
Citation: L. Wang et al., Werner helicase expression in human fetal and adult aortas, EXP GERONT, 34(8), 1999, pp. 935-941

Authors: Prince, PR Ogburn, CE Moser, MJ Emond, MJ Martin, GM Monnat, RJ
Citation: Pr. Prince et al., Cell fusion corrects the 4-nitroquinoline 1-oxide sensitivity of Werner syndrome fibroblast cell lines, HUM GENET, 105(1-2), 1999, pp. 132-138

Authors: Castro, E Ogburn, CE Hunt, KE Tilvis, R Louhija, J Penttinen, R Erkkola, R Panduro, A Riestra, R Piussan, C Deeb, SS Wang, L Edland, SD Martin, GM Oshima, J
Citation: E. Castro et al., Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cy/Arg, and its stability in a population of Finnish centenarians, AM J MED G, 82(5), 1999, pp. 399-403

Authors: Jin, LW Hearn, MG Ogburn, CE Dang, N Nochlin, D Ladiges, WC Martin, GM
Citation: Lw. Jin et al., Transgenic mice over-expressing the C-99 fragment of beta PP with an alpha-secretase site mutation develop a myopathy similar to human inclusion bodymyositis, AM J PATH, 153(6), 1998, pp. 1679-1686
Risultati: 1-8 |