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Results 11-20 of 37 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1996Feline mucopolysaccharidosis type VI - characterization of recombinant N-acetylgalactosamine 4-sulfatase and identification of a mutation causing the diseaseYogalingam, G.; Litjens, T.; Bielicki, J.; Crawley, A.; Muller, V.; Anson, D.; Hopwood, J.
1999Myeloid DAP12-associating lectin (MDL)-1 is a cell surface receptor involved in the activation of myeloid cellsBaker, E.; Sutherland, G.; Phillips, J.; Lanier, L.
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.
1996Molecular cloning of the cDNA and chromosome localization of the gene for human ubiquitin-conjugating enzyme 9Wang, Z.; Qiu, Q.; Seufert, W.; Taguchi, T.; Testa, J.; Whitmore, S.; Callen, D.; Welsh, D.; Shenk, T.; Deuel, T.
1996Further characterization of proteins associated with elastic fiber microfibrils including the molecular cloning of MAGP-2 (MP25)Gibson, M.; Hatzinikolas, G.; Kumaratilake, J.; Sandberg, L.; Nicholl, J.; Sutherland, G.; Cleary, E.
1997LAIR-1, a novel inhibitory receptor expressed on human mononuclear leukocytesMeyaard, L.; Adema, G.; Chang, C.; Woollatt, E.; Sutherland, G.; Lanier, L.; Phillips, J.
1997Isolation and identification of homeobox genes from the human placenta including a novel member of the Distal-less family, DLX4Quinn, L.; Johnson, B.; Nicholl, J.; Sutherland, G.; Kalionis, B.
1996DNAM-1, a novel adhesion molecule involved in the cytolytic function of T lymphocytesShibuya, A.; Campbell, D.; Hannum, C.; Yssel, H.; Franz-Bacon, K.; McClanahan, T.; Kitamura, T.; Nicholl, J.; Sutherland, G.; Lanier, L.; Phillips, J.
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.
2002α-Mannosidosis in the guinea pig: cloning of the lysosomal α-mannosidase cDNA and identification of a missense mutation causing α-mannosidosisBerg, T.; Hopwood, J.