1. Adelaide Research & Scholarship

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Results 21-30 of 41 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
1996Type X collagen is colocalized with a proteoglycan epitope to form distinct morphological structures in bovine growth cartilageGibson, G.; Lin, D.; Francki, F.; Caterson, B.; Foster, B.
1996Structure and sequence of the human sulphamidase geneKarageorgos, L.; Guo, X.H.; Blanch, L.; Weber, B.; Anson, D.; Scott, H.; Hopwood, J.
1996Positional cloning of the Fanconi anaemia group A geneApostolou, S.; Whitmore, S.; Crawford, J.; Lennon, G.; Sutherland, G.; Callen, D.; Ianzano, L.; Savino, M.; d'Apolito, M.; Notarangelo, A.; Memeo, E.; Piemontese, M.; Zelante, L.; Savoia, A.; Gibson, R.; Tipping, A.; Morgan, N.; Hassock, S.; Jansen, S.; de Ravel, T.; et al.
1996A novel X-linked gene, G4.5. is responsible for Barth SyndromeBione, S.; D'Adamo, P.; Maestrini, E.; Gedeon, A.; Bolhuis, P.; Toniolo, D.
1996Identification of the gene FMR2, associated with FRAXE mental retardationGecz, J.; Gedeon, A.; Sutherland, G.; Mulley, J.
1996Stable inheritance of an HLA-"blank" phenotype associated with a structural mutation in the HLA-A*0301 geneLienert, K.; Russ, G.; Lester, S.; Bennet, G.; Gao, X.; McCluskey, J.
1996Multiple alleles encoding a virus-like particle protein in the ichneumonid endoparasitoid Venturia canescensHellers, M.; Beck, M.; Theopold, U.; Kamei, M.; Schmidt, O.
1996Production of a human epidermal growth factor fusion protein and its degradation in rat gastrointestinal flushingsXian, C.; Upton, Z.; Goddard, C.; Shoubridge, C.; McNeil, K.; Wallace, J.; Read, L.; Francis, G.
1996Cloning and Expression of the Gene Involved in Sanfilippo B Syndrome (Mucopolysaccharidosis III B)Weber, B.; Blanch, L.; Clements, P.; Scott, H.; Hopwood, J.

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