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Results 1-10 of 127 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2007Fragile sitesSutherland, G.
2008Deletion of Glu155 causes a deficiency of glutathione transferase Omega 1-1 but does not alter sensitivity to arsenic trioxide and other cytotoxic drugsSchmuck, E.; Cappello, J.; Coggan, M.; Brew, J.; Cavanaugh, J.; Blackburn, A.; Baker, R.; Eyre, H.; Sutherland, G.; Board, P.
2007Fragile sites on human chromosomesSutherland, G.
2007The spectrum of SCNIA-related infantile epileptic encephalopathiesHarkin, L.; McMahon, J.; Iona, X.; Dibbens, L.; Pelekanos, J.; Zuberi, S.; Sadleir, L.; Andermann, E.; Gill, D.; Farrell, K.; Connolly, M.; Stanley, T.; Harbord, M.; Andermann, F.; Wang, J.; Batish, S.; Jones, J.; Seltzer, W.; Gardner, A.; Sutherland, G.; et al.
1995The genes encoding the myeloid nuclear differentiation antigen (MNDA) and IFI 16 are closely linked on human chromosome 1q22 but exhibit contrasting expression in haemopoietic cell lnesDawson, M.; Trapani, J.; Briggs, R.; Nicholl, J.; Sutherland, G.; Baker, E.
1995Chromosomal mapping of the human proteinase inhibitor 6 (PI6) gene to 6p25 by fluorescence in situ hybridizationCoughlin, P.; Nicholl, J.; Sun, J.; Salem, H.; Bird, P.; Sutherland, G.
1996Molecular Characterization of a Nonneuronal Human Unc18 HomologZiegler, S.; Mortrud, M.; Swartz, A.; Baker, E.; Sutherland, G.; Burmeister, M.; Mulligan, J.
1995Assignment of the gene encoding human galanin receptor (GALNR) to 18q23 by in situ hybridisationNicholl, J.; Kofler, B.; Sutherland, G.; Shine, J.; Iismaa, T.
1996Chromosomal mapping of the gene (INPP5A) encoding the 43-kDa membrane-associated inositol polyphosphate 5-phosphatase to 10q26.3 by fluorescence in situ hybridizationMitchell, C.; Speed, C.; Nicholl, J.; Sutherland, G.
1995Gene duplication of the human peptide YY gene (PYY) generated the pancreatic polypeptide gene (PPY) on chromosome 17q21.1Hort, Y.; Baker, E.; Sutherland, G.; Shine, J.; Herzog, H.