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PreviewIssue DateTitleAuthor(s)
1999Testisin, a new human serine proteinase expressed by premeiotic testicular germ cells and lost in testicular germ cell tumorsHooper, J.; Nicol, D.; Dickinson, J.; Eyre, H.; Scarman, A.; Normyle, J.; Stuttgen, M.; Douglas, M.; Loveland, K.; Sutherland, G.; Antalis, T.
2001HPP1: A transmembrane protein-encoding gene commonly methylated in colorectal polyps and cancersYoung, J.; Biden, K.; Simms, L.; Huggard, P.; Karamatic, R.; Eyre, H.; Sutherland, G.; Herath, N.; Barker, M.; Anderson, G.; Fitzpatrick, D.; Ramm, G.; Jass, J.; Leggett, B.
2001MUC13, a novel human cell surface mucin expressed by epithelial and hemopoietic cellsWilliams, S.; Wreschner, D.; Tran, M.; Eyre, H.; Sutherland, G.; McGuckin, M.
2001Cloning and characterization of the human activity-dependent neuroprotective proteinZamostiano, R.; Pinhasov, A.; Gelber, E.; Steingart, R.; Seroussi, E.; Giladi, E.; Bassan, M.; Wollman, Y.; Eyre, H.; Mulley, J.; Brenneman, D.; Gozes, I.
2001Identification of a novel human tankyrase through its interaction with the adaptor protein Grb14Lyons, R.; Deane, R.; Lynch, D.; Ye, Z.; Sanderson, G.; Eyre, H.; Sutherland, G.; Daly, R.
1999Molecular cloning and characterization of a cDNA encoding the human leucocyte vacuolar protein sorting (h1Vps45)Rajasekariah, P.; Eyre, H.; Stanley, K.; Walls, R.; Sutherland, G.
1997Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeatYu, S.; Mangelsdorf, M.; Hewett, D.; Hobson, L.; Baker, E.; Eyre, H.; Lapsys, N.; Le Paslier, D.; Doggett, N.; Sutherland, G.; Richards, R.
1998FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesisHewett, D.; Handt, O.; Hobson, L.; Mangelsdorf, M.; Eyre, H.; Baker, E.; Sutherland, G.; Schuffenhauer, S.; Mao, J.I.; Richards, R.
1995Molecular cloning of the cDNA encoding human skeletal muscle triadin and its localisation to chromosome 6q22-6q23Taske, N.; Eyre, H.; O'Brien, R.; Sutherland, G.; Denborough, M.; Foster, P.
1998The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.Kortschak, R.; Reimann, H.; Zimmer, M.; Eyre, H.; Saint, R.; Jenne, D.