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PreviewIssue DateTitleAuthor(s)
2002Asparagine hydroxylation of the HIF transactivation domain: A hypoxic switchLando, D.; Peet, D.; Whelan, D.; Gorman, J.; Whitelaw, M.
2002The nucleotide-binding site of human sphingosine kinase 1Pitson, S.; Moretti, P.; Zebol, J.; Zareie, R.; Derian, C.; Darrow, A.; Qi, J.; D'Andrea, R.; Bagley, C.; Vadas, M.; Wattenberg, B.
2002Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): A Y210C mutation causes either altered protein handling or altered protein function of N-acetylgalactosamine 4-sulfatase at multiple points in the vacuolar networkBradford, T.; Litjens, T.; Parkinson, E.; Hopwood, J.; Brooks, D.
2002Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndromeLower, K.; Turner, G.; Kerr, B.; Mathews, K.; Shaw, M.; Gedeon, A.; Schelley, S.; Hoyme, H.; White, S.; Delatycki, M.; Lampe, A.; Clayton-Smith, J.; Stewart, H.; van Ravenswaay, C.; de Vries, B.; Cox, B.; Grompe, M.; Ross, S.; Thomas, P.; Mulley, J.; et al.
2002Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsyStromme, P.; Mangelsdorf, M.; Shaw, M.; Lower, K.; Lewis, S.; Bruyere, H.; Lutcherath, V.; Gedeon, A.; Wallace, R.; Scheffer, I.; Turner, G.; Partington, M.; Frints, S.; Fryns, J.; Sutherland, G.; Mulley, J.; Gecz, J.
2002A novel androgen receptor mutant, A748T, exhibits hormone concentration-dependent defects in nuclear accumulation and activity despite normal hormone-binding affinityJames, A.; Agoulnik, I.; Harris, J.; Buchanan, G.; Tilley, W.; Marcelli, M.; Lamb, D.; Weigel, N.
2002Biomarkers of genetic damage for cancer epidemiologyFenech, M.
2002The mutator phenotype theory can explain the complex morphology and behaviour of cancersBignold, L.

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